Fluoride: A Statement of Concern
by Paul Connett, PhD
Waste Not #459
January 2000 Introduction.
1.
I have been researching the literature on fluoride for just over
three years. I approached this issue with an open mind. If I had
any bias when I set out it was that those who were opposed to fluoridation
were `crackpots'.
2. However, the more I have read the more concerned I have become
over the dangers posed by fluoride and the very poor science underpinning
its supposed efficacy in protecting children's teeth. How we ever
allowed such a toxic substance into the drinking water is staggering.
Even though fluoride's toxicity is rated higher than lead, the US
Environmental Protection Agency's (EPA) maximum contaminant level
for lead in water is 15 ppb (parts per billion) whereas the level
allowed for fluoride is 4,000 ppb. The recommended level for artificial
fluoridation of the drinking water of 1 part per million (1 ppm
= 1,000 ppb) was established in 1945, and it hasn't been changed
since, even though today we (and our children) are getting fluoride
from many other additional sources, including toothpaste, other
dental products, mouthwashes, processed food, some vitamin tablets,
and beverages.
The benefits to teeth are questionable.
3. The key initial studies which purported to
show that fluoride was a benefit to teeth, conducted in Grand Rapids,
Michigan (1945), Newburgh, New York (1945), Evanston, Illinois (1947),
and Brantford, Ontario, Canada (1945), were of a very dubious scientific
quality. This is fully and thoroughly documented by Dr. Philip Sutton
in his book, "The Greatest Fraud: Fluoridation" (1). While
the science was dubious, the confidence of the US Public Health
Service (PHS) was enormous. In April 1951, before any single fluoridation
trial had been completed, the US Surgeon General, Leonard Scheele,
was telling a Senate Subcommittee on Appropriations, "During
the past year our studies progressed to the point where we could
announce an unqualified endorsement of the fluoridation of the public
water supplies as a mass procedure for reducing tooth decay by two
thirds" (2). Subsequent Surgeon Generals have continued to
act as cheerleaders for this procedure. Their passionate promotion
bears little relation to the quality of the science involved in
fluoridation, either to its efficacy or to its safety. Another Surgeon
General, Thomas Parran, stated, "I consider water fluoridation
to be the greatest single advance in dental health made in our generation"
(3). Such an opinion sharply contrasts with that of former US EPA
scientist, Dr. Robert Carton, who after he examined the evidence
declared, "Fluoridation is a scientific fraud, probably the
greatest fraud of the century" (4).
4. According to Dr. John Lee, a bone specialist from California,
"Certain crucial errors common to fluoride studies that claim
benefit have been identified and, when applied to any or all fluoridation
trials claiming to prove benefit, are sufficient to nullify them.
I challenge fluoridationists to find just one trial that can stand
a critical review in the light of the errors I describe. If they
cannot, they should use their authority to help rid our water supply
of this useless toxin" (5).
5. Lee continues, "It is important to understand that in health
matters, everything is interrelated and multifactorial. This presents
a challenge to all health research: the factor being studied is
just one factor among many that may confound the study. If the other
factors can not be held constant (or their presence be kept equal
in all groups being observed), the role of the single factor being
studied can be confused... In the case of dental caries, the various
factors include oral sugar and other fermentable carbohydrates,
lysine and other amino acids, calcium and other minerals, vitamins,
fiber, saliva flow and oral pH, dental hygiene, sunlight, genetic
or constitutional factors, immune factors, use of antibiotics which
may inhibit plague bacteria and others" (5). Lee lists the
statistical misinterpretations common to the "fluoridation
trials": a) using "percent reductions" instead of
"rate of change" of decay; b) selection bias; and c) outright
fudging of the data (5).
6. Why were these early studies so poorly designed?
In some cases it may simply have been the result of over-zealous
promotion. For example, in the Grand Rapids, Michigan, study the
control city was dropped six years into the study, supposedly because
they wanted the children in this city to get the benefits as well.
In the case of Hastings, New Zealand, this study was unmistakably
fraudulent. Here the control city of Napier was dropped after only
two years and the method of diagnosing tooth decay was changed during
the course of the study, which quite artificially inflated the drop
in decay. This change in diagnosis was made without this being stated
in the final report (6). I am not aware of any double blind examination
to investigate the efficacy of water fluoridation (i.e. one in which
neither investigator nor subject is aware of which subjects have
been exposed and which have not).
7. Meanwhile, considerable evidence has accumulated that the state
of children's permanent teeth in non-fluoridated communities, as
measured by their DMFT (decayed, missing and filled teeth) values,
is just as good as (if not better than) those in fluoridated communities.
For example, in 1995 the teeth of the children in fluoridated Newburgh
were again compared to those in still unfluoridated Kingston (this
study started in 1945) and there was little difference in the DMFT
values across the 7-14 years age range. If an average is taken the
children in unfluoridated Kingston had slightly better DMFT values.
However, there was one big difference: the average levels of dental
fluorosis was about twice as high in fluoridated Newburgh as it
was in unfluoridated Kingston (7). Dental fluorosis is a mottling
of the teeth. In its mildest form it consists of white patches or
streaks. As the severity increases the color of the patches changes
from white to yellow, to orange and then to brown. In its severest
form dental fluorosis results in loss of tooth enamel and extreme
brittleness. The only known cause of dental fluorosis is exposure
to fluoride and the rates are increasing. The argument used by the
pro-fluoride authors of the Newburgh-Kingston study is that the
improvement in DMFTs in non-fluoridated Kingston is due to exposure
to fluoride from other sources: fluoridated toothpaste, beverages
and processed food. If we accept this argument at face value then
it completely undermines the need to add fluoride to the drinking
water since a better result (i.e. slightly better DMFTs and less
dental fluorosis) was achieved in Kingston without fluoridation.
8. In 1986-87 a survey was conducted by the National Institute
for Dental Research (NIDR) at a cost of $3.6 million to the US taxpayer.
The raw data from this study had to be pried out of this institution
by Dr. John Yiamouyiannis using the Freedom of Information Act.
From this data he was able to show that there was little difference
in the DMFT values for approximately 40,000 children, whether they
grew up in fluoridated, non-fluoridated or partially fluoridated
communities (8). Pro-fluoridationists have argued that this data
(or a sub-set of it) indicates 25% lower DMFT in fluoridated communities.
Even if we take this argument at face value, with current DMFT values
(about 2.0 or less) this represents less than half a tooth. Hardly
an achievement to compensate for the increase in dental fluorosis
which goes hand in hand with the measure and possibly other more
serious health effects discussed below. According to Dr. Hardy Limeback,
the Head of Preventive Dentistry at the University of Toronto, fluoridation
of water, "has contributed to the birth of a multi-billion
dollar industry of tooth bleaching and cosmetic dentistry. More
money is being spent now on the treatment of dental fluorosis than
what would be spent on dental decay if water fluoridation were halted"
(9).
9. Another large and important study was carried
out in New Zealand. What makes this work important is that under
the New Zealand National Health Service plan every child between
the ages of 12 and 13 years has his or her teeth examined, so here
we are looking at a complete set of data, not a selected sample.
Again, it was found that the teeth of children in non-fluoridated
cities were slightly better than those in the fluoridated cities,
and again the levels of dental fluorosis was much higher in the
fluoridated cities (10).
10. In Europe, where nearly all the countries remain unfluoridated,
the average DMFTs for the children are actually lower (i.e. better)
than those for children in the US. Moreover, Ireland, the only country
in Europe with significant fluoridation (about 73% of the population
drink fluoridated water), rates sixth in a table of national average
DMFTs in Europe (11).
11. How can this be? People in the US have been told again and
again that children drinking fluoridated water have far better teeth
than those who don't. What explains this conflict between claim
and reality? What emerges from impartial study is that the quality
of children's teeth in industrialized countries has been steadily
improving from the 1930s to the 1990s, independent of whether fluoride
has been added to the water supply or not. Thus, unless a control
community was chosen extremely carefullywhich they were notimprovements
were erroneously assigned to fluoride addition rather than to the
overall improvement that was taking place in both fluoridated and
non-fluoridated communities.
12. Proponents of water fluoridation argue that these overall improvements
in children's teeth in non-flouridated communities have been caused
by the introduction of fluoridized toothpaste and other sources
(see paragraph 7). However, these improvements (i.e. lower DMFT
scores) occurred before the introduction of fluoridized toothpaste
and other dental products, and they have continued long after the
supposed benefits of both the use of water fluoridation and dental
products would have been maximized (12,13). John Colquhoun, using
a simple but very elegant graph (see Figure), has shown that there has been little
change in the steady downward movement in DMFTs over the period
1930-1990 in New Zealand's 5-year olds as a consequence of the addition
of fluoride or the introduction of fluoridized toothpaste (14).
As Lee observes, "A decline in the rate of decay rates after
fluoridation is relatively meaningless unless one knows the rate
of change prior to fluoridation" (5).
13. John Colquhoun's work is both revealing and
inspiring. In the 1960's and 1970's in New Zealand as both local
councilor and Principal Dental Officer for the city of Auckland
(New Zealand's largest city) he had been an avid promoter of fluoridation.
He was so successful in fact that in 1980 he was asked by his superiors
to take a 4-month sabbatical and tour the world in order to collect
supporting evidence for the efficacy of water fluoridation. He did
so. He visited Australia, the US, Canada, the UK, and several other
countries in Europe and Asia. From talking behind the scenes with
dental researchers he found, to his chagrin, that the evidence was
not there. When he returned to New Zealand and examined the national
statistics the evidence was not there either. He might have left
the issue to rest at this point had it not been for the fact that
his colleagues were discovering high levels of dental fluorosis
in the fluoridated cities. He had the courage to change his mind
on the issue and began publicly working for a halt to fluoridation.
His position is well summarized in his paper, "Why I Changed
My Mind on Fluoridation" (14). He later joined Mark Diesendorf
and several other authors, including a former Minister of Health
from Australia, to write another important paper, "New Evidence
on Fluoridation" (15).
14. In May 1998, I had the privilege of making a videotaped interview
with Dr. Colquhoun in his Auckland home less than a year before
he died. Seldom have I been so impressed with the integrity of anyone
as I was with Dr. Colquhoun. I simply cannot believe that any dentist
or scientist who watches this taped interview with an open mind
could continue to promote fluoridation. (This taped interview can
be obtained from GG Video, 82 Judson Street, Canton, NY 13617).
15. Some of the reasons offered for the decline in tooth decay
have included: a) a better standard of living; b) better education;
c) better dental hygiene; d) more refrigeration; e) more fresh fruits
and vegetables in diet; f) more cheese in diet; g) exposure to antibiotics
in processed food; and h) less exposure to environmental lead.
16. The theory behind fluoride's purported benefit to teeth is
that the fluoride ion displaces the hydroxide ion from the calcium
hydroxyapatite in the tooth enamel, forming the substance calcium
fluorapatite, which is more resistant to acid attack. A second suggestion
is that fluoride kills some of the decay causing bacteria in the
mouth by poisoning their enzymes (16). However, these mechanisms
pose three huge questions, which have plagued this matter for over
50 years.
1) Can you poison the enzymes in the oral bacteria, without poisoning
some of the enzymes in the rest of the body? Nearly every single
chemical reaction in the body is steered by enzymes (enzymes are
biological catalysts).
2) As far as the tooth is concerned, can you strengthen the enamel
on the outside of the tooth without damaging the tooth cells on
the inside? In other words, will chemical intervention with the
enamel on the surface of the tooth be accompanied by biological
interference with the enzymes which lay down that enamel?
3) What will this constant exposure to fluoride do to our bones?
They, too, contain calcium hydroxyapatite. Will the formation
of calcium fluorapatite in our bones make them more or less vulnerable
to fracture? Does fluoride poison the enzymes involved in bone
growth and turnover? Are there any other ways fluoride could damage
bone growth and structure?
Some of these questions will be addressed below.
17. The large increase in dental fluorosis in both
fluoridated and non-fluoridated communities testifies to the fact
that an unacceptably high number of children are now being overdosed
on fluoride. In a NIDR study of nearly 40,000 children in the US
it was found that the incidence of dental fluorosis increased in
a dose-related fashion with the level of fluoride in the drinking
water. It was found that
- at less than 0.3 ppm, 13.5% of the children had dental fluorosis,
- between 0.3 to 0.7 ppm, 21.7% had fluorosis,
- between 0.7 to 1.2 ppm, 29.9 % had fluorosis,
- and above 1.2 ppm, 41.4 % had fluorosis.
It was also found that each category
of severity (based on Dean's classification) increased in a similar
dose related fashion (17). Putting these numbers into perspective,
it means that for every three children who might have their tooth
enamel strengthened by the addition of fluoride to drinking water
at 0.7 to 1.2 ppm, approximately one child will have its tooth enamel
damaged by dental fluorosis.
18. Moreover, the fact that children today are getting dental fluorosis
in non-fluoridated areas means other exposures to fluoride can also
cause this same damage. Pendrys et al (18) have shown that there
is a significant difference in the incidence of dental fluorosis
in non-fluoridated areas, between children who brush their teeth
twice a day with fluoridated toothpaste and those who brush just
once a day. Thus, in conjunction with efforts to eliminate fluoridation
of the drinking water, a major effort has to be made to force toothpaste
manufacturers to make available non-fluoridated versions of each
of their major brands. In Canada, there is a non-fluoridated version
of Pepsodent, and Boots, the largest chain of pharmacies in the
UK, also has a brand which contains no fluoride. In the US, one
usually has to go to health food stores or to catalogs to find a
brand without fluoride.
19. To argue that dental fluorosis is merely a "cosmetic effect,"
as some US government agencies do, is a blatant example of "linguistic
detoxification" (19). In actual fact, dental fluorosis indicates
that fluoride has interfered with the enzymes laying down the tooth
enamel. Thus dental fluorosis is the visible flag of fluoride's
toxicity. This observation should raise the question, what other
enzymes and processes in the body are being affected by fluoride
for which we do not have a visible flag? Up until 1983 dental fluorosis
was defined as an adverse health effect due to overexposure to fluoride.
It was redefined as a "cosmetic effect" to accommodate
the US EPA's Recommended Maximum Contaminant Level [RMCL] of 4 .0
mg/L for fluoride in drinking water. According to Bette Hileman,
RCML's are set to "prevent known or anticipated
adverse health effects with an adequate margin of safety... A
special committee convened by the Surgeon General in 1983 to guide
EPA in setting its fluoride standard wrote in the first draft
of its report that moderate to severe dental fluorosis per se
is a health effect. The second draft, presented to the Surgeon
General in September 1983, said that moderate to severe dental
fluorosis is only a cosmetic effectthe position long held
by political advocates of fluoridation. This rationale allowed
EPA to ignore dental fluorosis in setting the RMCL for fluoride"
(20, p 34).
20. Many researchers now agree that fluoride's benefits
(if they exist) come largely from topical application and not
from systemic exposure (i.e. ingestion) (21). Despite this recognition
of the primacy of topical application, and the knowledge of a
marked increase in dental fluorosis, there are still many doctors
who are prescribing fluoride tablets for pregnant women and young
babies, i.e. before the baby's teeth have erupted. Another concern
is that women who bottle feed their babies and who live in fluoridated
communities are not being adequately warned that they should be
using non-fluoridated bottled water, not tap water, to make up
the formula.
21. Underlining the concerns in paragraph 20,
is the fact that fluoride levels in mothers' milk is naturally very
low, averaging approximately 0.01 ppm (22, p 301), which is one
hundred times lower than fluoridated tap water. Even when the mother
herself is drinking fluoridated water, very little of it gets passed
on in her breast milk. One has to wonder then, if fluoride is necessary
for healthy tooth development, how it was that God (or evolutionary
forces) "failed" in this important development by limiting
the supply of fluoride to the newly born baby. Why is it that human
milk provides the baby with such low levels of fluoride if much
higher levels are deemed necessary for healthy teeth? Who is correct:
"God" or the US Public Health Service?
The threat to our bones.
22. If we now turn from teeth to bones, it is shocking to see how
little investigation of the long term effect of fluoride on bones
has been undertaken. For example, there has been no comprehensive
attempt to determine the levels of fluoride in the bones of people
living in the US. This, despite the fact that we know the following:
1) fluoridation has continued for over 50 years;
2) approximately half of the fluoride we ingest each day is deposited
in our bones;
3) there is a steady accumulation of fluoride in our bones over
our lifetime;
4) serious bone diseases have occurred to people with excessive
exposure, especially in workers in the aluminum industry and in
areas of countries like India and China; and
5) we are being exposed to more sources of fluoride today than
we were in the 1940s and 1950s.
By now, if American health authorities had done
their job properly we should have had a wealth of data. We should
know the bone levels as a function of many variables: location,
fluoridation, hardness of water supply, diet, disease status, smoking,
etc. We have practically nothing. Instead, when American agencies
consider what levels may cause bone damage they go back to studies
carried out with cryolite (the mineral used in the smelting of aluminum)
workers in Denmark in 1937. Even though Kaj Roholm's study is a
classic (23), it should not substitute today for a comprehensive
study of the bones of the American people. According toa 1993 report
from the Agency for Toxic Substances and Disease Registry (ATSDR),
"Fluoride is found in all bone, with the concentration
depending on total fluoride exposure. The amount varies among
different bones. Levels of fluoride in human bone are generally
determined by biopsy of the iliac crest bone, and are generally
reported as ppm of bone ash. Normal bone contains 500-1,000 ppm
fluoride... Bone from people with preclinical skeletal fluorosis...
contains 3,500-5,500 ppm... The fluoride concentration in bone
increases with age. In a group of five people ages 64-85 who had
lived for at least 10 years in an area with water containing 1
ppm fluoride, the average fluoride concentration of the iliac
crest bone was 2,250 ppm of bone ash" (24, pp. 53-54).
It is extraordinary to me that a leading US agency should be relying
on measurements made on "five people". The sad truth of
the matter is that the US PHS has spent many more millions of dollars
promoting fluoridation than it has on investigating the effect that
fluoridation has had on the American people.
23. Belatedly, an investigation has been carried out comparing
the fluoride levels in the iliac crest bone in citizens in Montreal
(non-fluoridated) and Toronto (fluoridated). The initial results
of this study by Dr. Limeback and colleagues have been reported
to the annual meeting of the International Association for Dental
Research in 1999. These results indicate that the levels are about
twice as high in the bones of the Toronto residents. This is a disturbing
finding, since Toronto was only fluoridated in 1963. We have yet
to have any human being on this planet exposed to artificially fluoridated
water for a lifetime. We have little idea what levels of fluoride
will be in the bones of someone who lives into their 60s, 70s, 80s
or 90s who has had lifetime exposure to fluoridated water as well
as all the other sources we are exposed to today. It is incredible
that despite the importance of this Canadian study its funding has
been discontinued. If governmental authorities in fluoridated countries
wish to retain any semblance of credibility on this issue, these
type of studies need to be carried out with greater intensity, not
less. The fear is that the increases in dental fluorosis in our
children today may foreshadow the damage to their bones that will
come in the future.
24. Meanwhile, there are numerous studies in the
published literature (four published in the Journal of the American
Medical Association alone) which demonstrate an association between
water fluoridation, or naturally occurring fluoride, and increased
hip fractures in the elderly, particularly women who were exposed
to fluoride prior to menopause (25-30). In 1993 the ATSDR made the
following comment on the published studies on hip fractures:
"The weight of evidence from these experiments
suggests that fluoride added to water can increase the risk of
hip fractures in both elderly women and men... If this effect
is confirmed, it would mean that hip fracture in the elderly replaces
dental fluorosis in children as the most sensitive endpoint of
fluoride exposure" (24, pp. 56-57).
Yet another study (this one from Finland) has just been published
which demonstrates a correlation between increased hip fracture
rates in elderly women and naturally occurring fluoride (31).
While there are other smaller studies which have not found this
correlation (32-34), and some critics have stressed the weaknesses
inherent in the "ecological" methodology used (study
group and control are distinguished by geographical location and
not by the actual doses received by individuals), the weight of
evidence indicates an association between hip fracture and exposure
to fluoride. Does it make sense to protect our teeth (possibly)
when we are young, and then break our bones (possibly) when we
are old? By whom should such a trade-off be made? This is not
a trivial issue. According to Harold Slavkin, Director of the
National Institute of Dental and Cranofacial Research (formerly
the NIDR), "About one-half of the people with hip fractures
end up in nursing homes, and in the year following the fracture,
20 per cent of them die" (35).
25. Another set of findings which has been outrageously
downplayed in my view is a possible association between water fluoridation
(or fluoride exposure) and osteosarcoma (bone cancer) in young
males. Of particular interest in this matter is a little known
comment which was made by an early reviewer of the medical examinations
of the children studied during the Newburgh-Kingston fluoridation
trial (36). This comment was picked up by the authors of a National
Academy of Sciences report in 1977, and further amplified:
"There was an observation in the Kingston-Newburgh
(Ast et al, 1956) study that was considered spurious and has never
been followed up. There was a 13.5% incidence of cortical defects
in bone in the fluoridated community but only 7.5% in the non-fluoridated
community... Caffey (1955) noted that the age, sex, and anatomical
distribution of these bone defects are `strikingly' similar to
that of osteogenic sarcoma. While progression of cortical defects
to malignancies has not been observed clinically, it would be
important to have direct evidence that osteogenic sarcoma rates
in males under 30 have not increased with fluoridation"
(my emphasis) (37).
26. Surely, if objective government scientists had
been aware of this concern or prediction, they might have taken
far more seriously the studies that followed. For example, in 1990
the National Toxicology Program (NTP) published the results of a
2-year study of rats and mice treated with fluoride in their drinking
water performed by scientists at Battelle laboratories (38). Even
though a peer review of this Battelle study removed some of the
other cancers found (erroneously according to Dr. William Marcus
at the US EPA) (39), it still showed a dose-related increase in
osteosarcoma in the male but not the female rats. Rather
than taking this result as a serious red flag, government scientists
seemed to have done everything they could to downplay it. According
to Dr. William Marcus, who was the senior scientist at US EPA's
Office of Drinking Water in 1990, the NTP studies done by Battelle
"showed that there was an increased level of bone cancer
and other kinds of cancer in the animals. When I got a hold of
the contractor report and reviewed it very carefully and not only
was it reporting cancers in the animals, osteosarcomas, which
bothered me a lot because I've been trying to produce osteosarcomas
in animals for almost 20 years and the only luck I ever had was
with an experiment in dogs and monkeys and the osteosarcomas took
nearly the lifetime of the animals and we were using radium which
specifically produces that in bones and here we have a compound
commonly available (fluoride) that did it in rats in two years
or less. That was upsetting to begin with. Secondarily, there
was a study of, in that same study, there were cancers of the
liver that are very rare according to the board certified veterinary
pathologist at the contractor, Battelle, and those really were
very upsetting because they were hepatocholangiocar-cinoma, a
very rare, rare, liver cancer and when that occurs, something
similar to that occurred with vinyl chloride in a far less well
conducted study and it was determined that it was carcinogenic,
highly carcinogenic. Then there were several other kinds of cancers
found in the jaw and other places and I felt at the time that
the report was very, very interesting. It showed that the levels
of the fluoride that caused the cancers in the animals were actually
lower than those levels seen in people who are ingesting lower
amounts but for longer periods of time and that was very very
worrisome. It meant that the general population could be exposed
to fluoride known to cause cancer in animals and have levels near
the cancer being produced in the bones... I went to a meeting
that was held in Research Triangle Park in April 1990, the latter
part of April, in which the NTP was presenting their review of
the study and I went with several colleagues of mine one of whom
was a board certified veterinary pathologist who had originally
reported hepatocholangiocarcinoma as a separate entity in rats
and mice and I asked him if he would have an opportunity to look
at the slides to see if that really was a tumor or the pathologist
at Battelle had made an error and he told me after looking at
the slide that in fact it was correct and at the meeting every
one of the cancers that was reported by the contractor had been
down-graded by the NTP. Now I've been in the toxicology business
looking at studies of this nature for nearly 25 years and I've
never seen that, never ever seen where every single endpoint that
was a cancer endpoint had been down-graded. I'd seen one or two endpoints argued
over, usually on a definition what is a cancer in that particular
tissue but I've never seen every one of them down-graded. I found
that very suspicious and I went to see an investigator in the
Congress at the suggestion of my friend Bob Carton and this gentleman
and his staff investigated very thoroughly and found out that
the scientists at the NTP down at Research Triangle Park had been
coerced to change their findings." (40)
Some said the results were equivocal. Others said the doses were
so high that they weren't relevant, and yet it is standard toxicological
practice to treat a small group of animals to a large dose of a
toxicant if you are to have a statistical chance of observing any
change in the small sample size. The alternative is to treat a very
large number of animals to a lower dose, which is prohibitively
expensive. The National Research Council (NRC) in a 1993 report
(41) described the result as follows: "The equivocal result
of osteosarcoma in male rats was not supported by results in females
in the same study" (page 122). This is an extraordinary statement
in the context of the concerns raised by the NAS in 1977 (see paragraph
25) because it is precisely the result the authors had feared. The
NRC further downplayed the result based upon a study by Proctor
and Gamble (42) (hardly a disinterested party in these matters)
which hadn't found any osteosarcomas in their rat studies (they
had found osteomas in mice, but they were considered not important
because they were non-malignant). Dr. John Yiamouyiannis used the
Freedom of Information Act to take a closer look at the P&G
studies and found that they had found cancers in their rats as well
as lesions which could lead to cancers (43).
27. A suspicious person might wonder if the US government was maneuvering
around the Delaney Clause, which was operating at that time. This
clause introduced by Congressman Delaney required that no chemical
found to cause cancer in animal studies be added to food. Thus,
if a link had been found between fluoride and cancer in these animal
studies it would have scuttled the whole fluoridation program then
and there.
28. In 1992, a report was published by the New Jersey Department
of Health (44) which indicated that in three fluoridated counties
in NJ, there was a seven-fold increase in osteosarcomas in young
males, compared to non-fluoridated counties. There was no increase
in the females. Again, this is precisely the result feared/anticipated
by the NAS commentators in 1977.
29. In an earlier national survey under the SEER
program (45) increases in osteosarcomas in young males were
further correlated with fluoridation in two other states. However,
a study in New York, published in 1991, had not found any increase
they could relate to water fluoridation (46). Three other studies
have failed to find a relationship between bone cancer rates and
fluoridation. These are discussed by Dr. John Yiamouyiannis in an
excellent review of the osteosarcoma data for the journal Fluoride
(43). Dr. Yiamouyiannis has pursued the fluoride-cancer connection
more thoroughly than any other scientist alive. For some, the positive
and negative results on osteosarcoma incidence in fluoridated communities
neatly cancel one another out. For me this is too serious an issue
to be so lightly dismissed. In an interview I had with the late
Dr. John Colquhoun he posed the question: "How many cavities
would have to be saved to justify the death of one young man from
osteosarcoma?" (Video interview identified in paragraph 14).
Fluoride's impact on enzymes, soft tissues, the endocrine system,
and the brain.
30. Some of the earliest opponents of fluoridation were biochemists.
One of those early opponents was one of the world's leading authorities
on enzyme chemistry, Nobel laureate Dr. James Sumner at Cornell
University. He said:
"We ought to go slowly. Everybody knows
fluorine and fluorides are very poisonous substances...We use
them in enzyme chemistry to poison enzymes, those vital agents
in the body. That is the reason things are poisoned; because the
enzymes are poisoned and that is why animals and plants die."
31. Dr. James Sumner was one of at least 12 Nobel Prize winners
in Chemistry and Medicine, who have either opposed fluoridation
or expressed reservations about it. These include Giulio Natta
(1963 Nobel Prize in Chemistry), Nikolai Semenov (Chemistry, 1956),
Sir Cyril Norman Hinshelwood (Chemistry, 1956), Hugo Theorell
(Medicine, 1955), Walter Rudolf Hess (Medicine, 1949), Sir Robert
Robinson (Chemistry, 1947), James B. Sumner (Chemistry, 1946),
Artturi Virtanen (Chemistry, 1945), Adolf Butenandt (Chemistry,
1939), Corneille Jean-François Heymans (Medicine, 1938), William
P. Murphy (Medicine, 1934), and Hans von Euler-Chelpin (Chemistry,
1929). This listing makes absurd the ADA's claim that there is
"no scientific debate" over this issue and that the
only people who oppose it are `crackpots'.
32. It is known that many enzymes are inhibited
(poisoned) in test tubes (in vitro) at the levels at which water
is fluoridated (1 ppm) or less (47). One early explanation given
for these observations was that many of the enzymes inhibited had
magnesium ion as a co-factor, and that the fluoride ion interfered
with the enzyme's interaction with the magnesium. A second explanation
from Dr. John Emsley throws more light on how the "humble"
fluoride ion, which is inert from a chemical point of view, can
be so active and so toxic from a biological point of view.
33. In an article published in the Journal of the American Chemical
Society in 1981, Emsley (48) and co-workers showed that fluoride
could form a strong hydrogen bond with the amide function. This
particular function appears throughout proteins and nucleic acids.
The hydrogen bond is the "velcro strip" of biology. It
is a weak bond compared to regular chemical bonds (ionic and covalent),
but when they act in consort they are able to provide the shape
of vitally important molecules and in biochemistry, shape is exquisitely
tied to function. Like the velcro strip when the shape has to be
changed in some important maneuver, like the opening of the two
DNA chains or the interaction between an enzyme and its substrate
(the chemical changed by the enzyme), these bonds can easily be
broken and reformed with little energy input. Thus, fluoride's interference
with hydrogen bonds could cause all sorts of problems at the very
heart of biological functioning. The counter-argument from those
promoting fluoridation is that at 1 ppm fluoride in our drinking
water, fluoride would not reach these concentrations in the soft
tissues. Such statements are usually accompanied with a reference
to the father of toxicology, Paracelsus, who said, " 'tis the
dose that makes the poison." While this ancient observation
remains valid to this day the argument that a concentration of 1
ppm for fluoride (i.e. 1,000 parts per billion) is "harmless"
is extremely arrogant, and I define arrogance as ignorance backed
with over-confidence. We should note that today we are concerned
about very much lower levels of lead in childrens' blood than we
were in the late 1970s. Scientists and government officials were
wrong about lead then, could they be wrong about what constitutes
a safe level of fluoride now?
34. It is interesting to note what the Swedish
Nobel Prize winner Dr. Hugo Theorell said about these concerns in
1958. He wrote:
"Even if with respect to caries fluoride
may be a good prophylactic, it is in larger doses, none the less
a poison. In principle this signifies nothing; in sufficiently
large doses all substances are toxic for the human organism. What
is important is the distance between the therapeutic and the toxic
dose... it may be said that even if the risks from the viewpoint
of enzyme chemistry connected with water fluoridation up to 1
ppm should not be exaggerated, yet the distance to toxic doses
is none the less so short as to justify some hesitation"
(49).
Recognizing that fluoride's target in tooth protection is the
"surface layer of the dental enamel" he suggests that
water fluoridation is "a roundabout way" of delivering
it, because "on its Odyssey through the body fluids most
of the fluoride will be lost in other organs, where it will probably
not do any good, but possibly do damage to enzymes" (49).
35. Recent work from Dr. Jennifer Luke (50-51) indicates that fluoride
reaches one very important gland in the bodythe pineal glandat
very much higher concentrations than 1 ppm. This small gland is
almost at the geometrical center of the brain, between the two hemispheres.
However, it is outside the blood brain barrier. It also has a very
high supply of blood (a perfusion rate second only to the kidney)
and it is a calcifying tissue, laying down crystals of calcium hydroxyapatite
like the teeth and the bone. Because of these observations Luke
argued that one would expect the pineal gland to concentrate fluoride.
When she had the pineal gland from 11 human corpses analyzed she
indeed found this to be the case. The levels of fluoride in the
apatite crystals averaged about 9,000 ppm (and went as high as 21,000
ppm). The average level is as high as you would expect in the bones
of someone afflicted with skeletal fluorosis. The average projected
by Luke for the whole tissue was 300 ppm, well over the 1 ppm found
to inhibit many enzymes.
36. Luke next examined the effect of dosing Mongolian gerbils (the
animal of choice for studying the pineal gland) with fluoride. She
found that animals fed higher doses of fluoride had a significant
decrease in their excretion of melatonin metabolite in their urine.
She also found that the high dose fluoride animals took a shorter
time to reach puberty. This is exactly what you would expect if
melatonin production was lowered. If this result is confirmed by
others it would make fluoride an environmental hormone or endocrine
disrupter, a topic of intense discussion (52) and review by regulatory
agencies in the US and around the world.
37. Another line of evidence which indicates
that fluoride is an endocrine disrupter is the number of studies
that indicate the fluoride may inhibit the functioning of the thyroid
gland. Andreas Schuld, president of a group called Parents of Fluoride
Poisoned Children, has prepared an excellent summary of the evidence
that points in this direction (53, 54). To put the matter as simply
as I can, his group has been able to show that areas of endemic
fluorosis are also areas designated as being endemic with iodine
deficiency disorders (IDD). The group rediscovered studies and documentation
from the European medical literature spanning over 30 years of research
testifying to fluoride's pharmacological effectiveness in the treatment
of hyperthyroidism (the term used to describe an over-functioning
thyroid gland). Thyroid hormones are absolutely essential for normal
growth and development. Hyperthyroidism means that the thyroid gland
is producing too much of the thyroid hormones, T3 and T4. These
two hormones have 3 and 4 iodine atoms respectively. Schuld's group
has also shown that there is a remarkable similarity between the
symptoms listed for hypothyroidism (underactive thyroid gland) and
those reported for fluoride poisoning (55). Putting these two conditions
together, it appears that fluoride decreases the production of thyroid
hormones. If you are suffering from hyperthyroidism, fluoride might
be of some benefit. But for a normal person if you are exposed to
too much fluoride it could result in reducing thyroid hormone production
below normal and necessary levels (i.e., hypothyroidism).
38. It is not clear just how fluoride reduces thyroid hormone production.
It may be that fluoride competes with iodine uptake into this gland.
Alternatively, fluoride might inhibit the enzymes inside the gland
which assemble the hormones from its chemical precursor, the amino
acid tyrosine.
39. Schuld also points to research that fluoride can also stimulate
the thyroid glands, which seems contradictory to the discussion
above. However, stimulation may not lead to production of the hormones
if iodide is in short supply. Such a situation (overstimulation
coupled with iodide shortage) might explain the condition known
as goiter. Here the gland grows and grows producing a swelling in
the neck. The gland grows because it is being stimulated, but because
there are no thyroid hormones produced, there is nothing to switch
off the stimulating signal. In other words, the normal feedback
mechanism is not working. This signal is the hormone (thyrotropin
or thyroid stimulating hormone) which is produced by the pituitary
glandthe master gland as far as hormonal control is concerned.
40. Now this is where the story gets very disturbing. It appears
that fluoride forms a complex with the aluminum ion, in which 4
fluoride ions tightly surround an aluminum ion [AlF4]- and that
this complex looks to the body just like the phosphate ion (PO43-).
Moreover, this [AlF4]- complex is able to bind to G-proteins, which
are part of the signaling mechanism of all water soluble hormones
and many neurotransmitters.
41. To appreciate the significance of this we need first to understand
what hormones are and how they function. Hormones are messengers
that regulate body chemistry. They are produced at specific times
and in specific glands, for example the adrenal glands produce adrenaline
when we experience a sudden shock. Once they are produced they are
injected into the bloodstream where they circulate the body until
they find their target tissue: i.e. the tissue which they will regulate.
At this point in our discussion we need to divide hormones into
two groups: those which are soluble in fat and those which are soluble
in water. The fat soluble ones like the steroid hormones (e.g. estrogen
and testosterone) can freely enter the cells of the tissues they
regulate, because the membranes of the cell are made of fat and
these hormones can pass straight through. Once inside the cell they
bind with a protein receptor and change the cell's activity in a
very fundamental way. Water-soluble hormones, on the other hand,
cannot cross the cell membrane and their effect has to be instigated
outside the cell, and this is where the G-proteins play their important
intermediary role. The hormone first combines with a receptor protein
on the outside membrane of the cell. When this event has taken place,
it triggers a response from the G-proteins. The G-proteins have
to take the signal, delivered by the hormone or neurotransmitter,
the so-called "first messenger", across the membrane (transduction),
and excite (or release) a "second messenger", on the internal
surface of the membrane. Once excited (or released) this second
messenger can excite various target molecules like enzymes inside
the cell. Examples of these "second or intracellular messengers"
are cyclic AMP (cAMP) and the Ca2+ion.
42. We will now concentrate on the action of
water soluble hormones and the important role played by the G-proteins
in the transduction process (getting the signal from outside the
cell to the inside). The mechanism of action of the G-proteins is
complicated but fully described in the literature (56,57). For our
purposes we need only examine the key moment when [AlF4]- interferes
with the sequence of events.
43. When the water soluble hormone attaches to its receptor it
triggers a change in the G-protein which allows a phosphate group
to bind to a molecule called guanosine diphosphate (GDP) which sits
in a crevice of the surface of the G-protein. This incoming phosphate
changes the GDP to guanosine triphosphate (GTP). If we envisage
the G-protein as a switch when GDP occupies the crevice the switch
is off, but when the GTP sits in the crevice the switch is on. In
the on position the signal is sent to activate the cell. [AlF4]-
not only performs exactly the same function as the phosphate but
it also does it without the participation of the hormone. Thus in
the absence of the hormone, [AlF4]- is capable of switching on the
signaling mechanism which activates the cell.
44. The possible interference of [AlF4]- is, in my view, one of
the most important developments in fluoride research for many years.
Indications are that the aluminum levels needed for the formation
of [AlF4]- are almost certainly present in our `industrial' diets,
however it may also be that high calcium (Ca2+) and magnesium (Mg2+)
levels may prevent its formation. If this is the case it underlines
the fear that those suffering malnutrition may be especially vulnerable
to fluoride. This point needs urgent recognition by those who advocate
fluoridation to provide dental care for the poor, because it is
the poor who are most likely to be malnourished.
45. The role of G-proteins as intermediaries in signaling by water
soluble hormones (eg insulin, adrenalin, glucogon, thyroid stimulating
hormone, and many others) as well as neurotransmitters is so fundamental
to the proper growth and functioning of mammals that any interference
by aluminum fluoride complexes would be extremely serious indeed.
Interference here would go a long way to explain health problems
associated with fluoride not explained by fluoride's direct inhibition
of enzymes. Anna Strunecká & Jirí Patocka have produced an excellent
review of the potential pathological consequences of human exposure
to [AlF4]- (58).
46. Schuld points out that since the 1994 Nobel Prize in Physiology
or Medicine was awarded to Alfred Gilman and Martin Rodbell for
the discovery of G-proteins and their role in cellular signal transduction,
much attention has been focused on the manifold functions of these
ubiquitous molecules and on the ways in which they can become disordered
in human diseases. Entire data banks have now been established listing
G-protein-coupled receptor mutations or gene rearrangements, and
human diseases caused by such (precocious puberty, neonatal severe
hyperparathyroidism, etc.). The effects of fluorides on these can
be witnessed in hundreds of studies available on Medline and elsewhere.
Schuld's group is providing the key links to these studies via their
website (54).
47. Returning to the pineal gland, Luke postulates
a mechanism which doesn't involve the functioning of the hormone,
but its production. In the production of melatonin in this gland
there are four chemical changes between the amino acid tryptophan
(a nutrient) and melatonin. All four steps are catalyzed by enzymes.
The first two steps yield serotonin, a neurotransmitter, and the
next two convert serotonin into melatonin. Luke argues that one
or more of these enzymes which catalyze these four steps are inhibited
by fluoride (51). Interfering with either the production of serotonin
or melatonin is of extreme significance. A huge amount of research
is ongoing in the attempt to elucidate all the subtle influences
that melatonin has on regulatory mechanisms throughout the body,
including the timing of puberty.
48. Of particular interest, is the knowledge that in the US there
is an earlier onset of puberty, especially in girls, and no one
knows what is causing this (59). There are many possible candidates,
but based upon Luke's work on the pineal gland, fluoride should
be added to the list.
49. Also of interest is the fact that when children were examined
in the Newburgh-Kingston study (already cited) in 1955 (ten years
after fluoridation was begun) they found that the girls in fluoridated
Newburgh reached menstruation five months earlier, on average, than
the girls in non-fluoridated Kingston (36).
50. Our discussion now moves from the pineal gland, which is outside
the blood brain barrier, to the inside of the brain. There have
been several studies which indicate that fluoride can impact mental
behavior. In the 1940s, US scientists working on the Manhattan Project
(the making of the Atomic bomb) were concerned that exposure to
fluoride could threaten the behavior and concentration of the workers
in nuclear plants which were using huge quantities of fluoride in
the separation of uranium isotopes. A request was made by Harold
Hodge, the chief toxicologist of the project, to do a study on the
impact of fluoride on rat behavior. His request was first accepted
and later canceled (60). While discovering this information
from formerly classified documents, researchers Cliff Honicker,
Joel Griffiths and Chris Bryson, also unearthed the fact that one
of the earliest and most important trials of fluoridation, the 1945-55
Newburgh-Kingston study (discussed above), was partially organized
by, and closely watched by, scientists from the Manhattan Project.
Apparently, there was a concern that the government would be facing
lawsuits from communities impacted by fluoride emissions from the
facilities which had manufactured the atomic bomb (60). Among those
concerned was Harold Hodge and in one memo with respect to how to
deal with impacted citizens and farmers, he asked, "Would there
be any use in attempts to counteract the local fear of fluoride...
through lectures on F toxicology and perhaps the usefulness of F
in tooth health?" (60). While the impact of fluoride on teeth
was studied early, Hodge had to wait nearly 50 years before he saw
the rat-behavior experiment performed by Dr. Phyllis Mullenix at
the Forsyth Dental Center in Boston.
51. In 1995, Dr. Phyllis Mullenix resisted an
enormous amount of political pressure to publish her investigation
of the impact of fluoride on rat behavior (61). In her work she
found that fluoride concentrated in the brain and that when the
animals were exposed to fluoride before birth they exhibited behavior
characterized as hyperactive, and when they were dosed after birth
they became hypoactive ("couch potatoes"). In a non peer-reviewed
critique by Gary Whitford, circulated by the Centers for Disease
Control, Division of Oral Health (62), but not submitted to Mullenix
for rebuttal (where are the professional ethics here?), her work
was attacked because of the high levels of fluoride she had used.
52. When Mullenix finally received a copy of Whitford's critique
from a third party she was quickly able to respond. She pointed
out, "These criticisms are without merit because our doses
in rats produce a level of fluoride in the plasma equivalent to
that found in humans drinking 5-10 ppm fluoride in water, or humans
receiving some treatments for osteoporosis. This plasma level is
exceeded ten times over one hour after children receive topical
applications of some dental fluoride gels. Thus, humans are being
exposed to levels of fluoride that we know alter behavior in rats"
(63). Mullenix also pointed out that it is standard toxicological
practice to treat animals with large doses over short periods of
time, in order to tease out an effect with the small number of the
animals being tested. However, before she could administer small
doses over a longer period of time, she was dismissed from the Forsyth
Dental Center. She was told her work had little relevance to dentistry!
While agencies of the US government had shown a lot of interest
in this work (one suspects in order to discredit it) they have not
found it necessary to fund more work in this area. Another example
of politics ruling over science: a sickening thread that runs throughout
this sorrowful 50-year history of fluoride promotion by agencies
of the US Public Health Service.
53. An impartial observer is forced to ask, if the promotion of
fluoride is an honorable cause, why it is that the tactics behind
it have been so despicable? Mullenix is not the only scientist who
has suffered reprisals because of her work on fluoride. In 1992
US EPA fired Dr. William Marcus, the Senior Scientist at EPA's Office
of Drinking Water, for questioning the erroneous downgrading of
cancers in the 1990 NTP fluoride rat study (see paragraph 26). According
to a February 10, 1994, press release from the National Whistleblower
Center in Washington, DC:
"In a precedent-setting ruling, U.S.
Department of Labor (DOL) Secretary Robert B. Reich has ordered
the U.S. Environmental Protection Agency to reinstate toxicologist
Dr. William L. Marcus. Labor found the EPA guilty of falsifying
employment records, discrimination, and retaliation against an
employee whistleblower. It also granted Marcus, the largest compensatory
damage award ever upheld under the federal environment employee
protection statues... The case marks the first time that EPA federal
employees were held to be protected from discrimination under
federal environmental laws. The ruling establishes that all federal
employees are covered under these laws... The decision upheld
an earlier order by a DOL Administrative Law Judge (ALJ) issued
December 3, 1992, supporting Marcus' claim that he was fired for
protected activity... The EPA dismissed the 52-year-old toxicologist
on May 13, 1992 after a four-year investigation of Marcus' outside
activities as an expert trial witness. EPA accused Marcus of improper
use of agency information for private gain, being improperly absent
from work, and engaging in outside employment which appeared to
pose a conflict of interest... Both the ALJ and Reich found many
of the charges to be `unsubstantiated,' and based on apparently
falsified time records and other testimony. Reich disputed the
EPA's position stating, `I agree with the ALJ that this rationale
is pretextual and that the true reason for the discharge was retaliation.'
Both Reich and the ALJ found that Marcus was actually fired for
publicly criticizing and opposing EPA's policy on fluoride in
drinking water."
Dr. Marc Diesendorf describes a similar situation to Mullenix
with respect to the paper he published in Nature (12). He wrote,
"an unpublished covert critique of my
paper... written by a senior member of the Australian Dental Association,
is apparently being circulated to health departments, politicians,
and newspaper editors in several countries, including the U.S.
Recently an overseas newspaper editor sent me a copy, and it was
immediately clear that the critique was easily answered and was
of such a low scientific standard that it would be very difficult
to publish, except perhaps in certain dental journals" (64).
I, myself, have received letters from dentists who have been
threatened because they had the integrity to speak out on this
issue. What makes this kind of bullying even more unacceptable
is that it is supported at the highest levels of government. Mullenix
has described her work and the trouble it sparked in a videotaped
interview (65). Bette Hileman cites several other disturbing
incidents encountered by fluoride researchers, including:
"Phillipe Grandjean, professor of environmental
medicine at Odense University in Denmark, wrote to the Environmental
Protection Agency in June 1985 about a World Health Organization
study on fluorine and fluorides: `Information which could cast
any doubt on the advantage of fluoride supplements was left out
by the Task Group. Unless I had been present myself, I would have
found it hard to believe'" (20, p 36).
54. Meanwhile, Isaacson and his co-workers at SUNY Binghamton,
were conducting low-dose, long-term rat fluoride studies (66).
They found that fluoride administered daily at 1 ppm, either as
aluminum fluoride or sodium fluoride in doubly distilled de-ionized
water, for a period of one year, produced morphological changes
to kidney and brain cells and an increased uptake of aluminum
into the brain. This striking finding has been largely ignored
by US authorities, as have been the studies by Guan et al on the
impact of fluoride on membrane lipids in rat brain (67), and the
studies from China which indicate a lowering of IQ of children
as a function of their exposure to fluoride (68, 69). While it
is possible that these Chinese studies may have not accounted
for some potentially confounding variables, they again wave another
very serious red flag? Are we going to risk damaging our childrens'
brains for the sake of, at most, half a tooth? What would those
who believe in the precautionary principle have to say about that?
55. The work by Isaacson raises a very large
issue: the possibility that because fluoride forms complex ions
with very many metal ions, including toxic metals like radium, uranium,
beryllium, aluminum and lead, it may facilitate the uptake of these
elements into places they would not normally be able to enter. This
may be particularly relevant if fluoride facilitates their crossing
of the blood brain barrier or the placental membrane. Unfortunately,
very few studies have pursued the synergistic effects of fluoride
and other substances like toxic metal ions. In one of those rare
studies that did, it was shown that a combination of lead and fluoride
(the salts were dissolved in the drinking water of rats) proved
to be "much more severely toxic than either compound alone"
and that the fluoride produced significantly higher lead concentrations
in the blood and femur (70). Another more recent study which may
have inadvertently probed the matter is the extraordinary work of
Dr Roger Masters (Professor of Government at Dartmouth) and Myron
Coplan, an environmental engineer from Massachusetts (71). They
have found a correlation between the uptake of lead into children's
blood and the use of hexafluorosilicic acid or its sodium salt to
fluoridate municipal water supplies in Massachusetts. They also
found a correlation between the use of these same agents and the
incidence of violent crime.
56. Masters and Coplan's work also revealed that practically no
toxicological work has been performed on these silcofluorides, which
are used to fluoridate about 90% (72) of the water fluoridated in
the US. Instead, when scientists look at possible problems with
fluoridation they examine the effect of the fluoride ion not the
hexafluorosilicate ion. The assumption being made is that by the
time the hexafluorosilicate ion reaches the tap it will have been
completely converted into silica and the free fluoride ion. Coplan
argues, during a fascinating videotaped interview that I had with
him (and Roger Masters) that this is not likely and that there will
be still some silicon fluoride complexes available at the tap and
these might be the species which facilitate the uptake of the lead
(73).
The source of the fluoride used to fluoridate water in the US.
57. As mentioned above, about 90% of the water
fluoridated in the US contains either hexafluorosilicic acid (H2SiF6)
or its sodium salt (Na2SiF6). These are obtained from the super-phosphate
industry from the scrubbing solution used to remove hydrogen fluoride
from atmospheric releases. By law, these scrubbing liquids cannot
be dumped into the sea, lakes, rivers or streams. However, the US
EPA does allow them to be diluted down to 1 ppm and then to be added
to our drinking water. From there the fluoride can be flushed through
our bodies before it enters rivers and then the sea! According to
one US EPA official this is an excellent way of dealing with "water
and air pollution" problems (74). Canada's leading pro-fluoridation
dental authority, Dr. Hardy Limeback, recently changed his position.
(Limeback's qualifications include: Ph.D in Biochemistry, D.D.S.,
Head of the Department of Preventive Dentistry at the University
of Toronto, and President of the Canadian Association for Dental
Research). In a December 1999 press interview he cited one of the
reasons for his dramatic turn-around:
"the crowning blow was the realization
that we have been dumping contaminated fluoride into water reservoirs
for half a century. The vast majority of all fluoride additives
come from Tampa Bay, Florida smokestack scrubbers. The additives
are a toxic byproduct of the super-phosphate fertilizer industry"
(75).
Barry Forbes, the newspaper reporter who published this interview
with Limeback, wrote:
"Last week, Dr. Hardy Limeback addressed his faculty
and students at the University of Toronto, Department of Dentistry.
In a poignant, memorable meeting, he apologized to those gathered
before him. `Speaking as the head of preventive dentistry, I
told them that I had unintentionally mislead my colleagues and
my students. For the past 15 years, I had refused to study the
toxicology information that is readily available to anyone.
Poisoning our children was the furthest thing from my mind.
The truth,' he confessed to me, `was a bitter pill to swallow.
But swallow it I did' " (75).
Many others, including myself, are outraged that
our health may be put at risk to facilitate the waste disposal needs
of the super-phosphate industry. However, from this industry's narrow
economic point of view it makes a lot of sense. It converts a hazardous
waste disposal cost of about $400 million a year to a profit of
$180 million from sales to the public water works. Citizens like
George Glasser in Florida have raised the issue of the other pollutants
present in these scrubbing solutions (76). Even though they are
diluted at the public water works from about a 24% percent solution
(24 parts per hundred) to a 1 part per million solution of fluoride,
the worry is that even after this dilution certain pollutants and
radioactive isotopes may still be present at unacceptable levels.
Fluoride and the environment.
58. In addition to the threat posed to humans
is the threat posed to the environment. The impact of fluorides
on vegetation (77) and on cattle (78) is well established. Of more
recent concern is the impact of fluoride (from fluoridated water
emerging from wastewater treatment facilities) on spawning salmon
in waterways like the Columbia River (79).
Fluoridation and common sense.
59. Turning to common sense. Pharmaceutical grade fluoride is freely
available via toothpaste, dental products and even vitamin tablets.
Today the bigger danger, as evidenced by the dramatic increase in
dental fluorosis (discussed above), is overdosing our children not
underdosing them. There is no need to add it to the water. Too many
red flags are being waved on possible long-term health threats to
continue the experiment of adding this toxic substance to our drinking
waterespecially in the form of industrial grade hexafluorosilicic
acid.
60. Dr. Robert Carton, formerly with the US EPA and who did so
much to try and expose the fraud that went on at the US EPA when
they established 4 mg/liter as the maximum contaminant level for
fluoride, points out:
"We shouldn't be giving any credence
to the idea that the practice of fluoridation is a matter of weighing
risks and benefits. In keeping with the notion of human rights,
the Safe Drinking Water Act does not allow the weighing of risks
and benefits. It allows you to consider economics and feasibility
only, while the truth about the adverse effects must be stated
clearly. The MCLG (maximum contaminant level goal) is the health
statement which is meant to protect everyoneyoung and old,
healthy and unhealthy, those with failing kidneys, diabetics and
athletes and soldiers who drink massive amounts of water"
(80).
61. If the issue is the protection of human health, as opposed
to the protection of corporate profit, it is imperative that we
stop putting fluoride into our drinking water. If the precautionary
principle applies to anything it should apply to fluoride. Unlike
many other toxic pollutant exposures, this is something we are
doing to ourselves and something we can simply reverse by switching
off a tap. We cannot wait for everything to be proved to a certainty
before we act. There is enough evidence from chemical, biochemical,
animal and epidemiological studies, to indicate that we should
take sensible precautionary action now. Simply put, if in doubt
leave it out. If, on the other hand, any citizen wants to take
the risks they can simply go and get the fluoride for themselvesit
is readily available in every major brand of toothpaste on the
market. No oneand no governmentshould be imposing
these risks on someone else. The only difficult issue left with
the public water supplies is to decide how much of the naturally
occurring fluoride to leave in.
62. Another common sense argument raised against fluoridation is
that it is a very clumsy form of medication. One cannot control
the dose because one cannot control the amount of water people drink
or the other sources of fluoride intake. Thus, when people talk
about 1 ppm of fluoride in the drinking water that simply tells
us that if someone drinks one liter of water a day they would get
1 mg of fluoride per day. What a doctor wants to do is to control
the total dose of medication as either "x" milligrams
a day or "y" mg per kilogram bodyweight per day. The inability
to control the total dose is particularly serious for the most sensitive
and most vulnerable members of our society. Normally, when prescribing
medication to an individual a doctor can prescribe for their special
needs. But with water fluoridation the doctor cannot. This issue
is compounded by the fact that the purported therapeutic dose for
some is a toxic dose for others, as demonstrated by the automatic
increase in dental fluorosis in children whenever water is fluoridated.
The two sides in the debate.
63. The promoters. For over 50 years those promoting fluoridation
have used five tactics: a) they have consistently denied that there
is any debate; b) they usually refuse to appear on a public platform
with opponents of fluoridation, either in debates or public fora;
c) they cite a long list of government agencies and other organizations
that have endorsed fluoridation; d) they stress how many communities
in the US are fluoridated; and e) they dismiss their opponents as
a bunch of crazies. I will deal with each of these tactics in turn.
64. Denial that a debate exists. This position becomes less
and less tenable with each new paper pointing out that there is
little difference between the state of children's teeth in fluoridated
and non-fluoridated communities and with each new paper which points
out some long term health effect which may be associated with fluoride
exposure either in animal studies or in epidemiological studies.
A particularly severe blow was delivered to the notion that there
is "no scientific debate", when, in 1988, the prestigious
weekly journal, Chemical and Engineering News (sent to every member
of the American Chemical Society as part of their membership fee)
ran a seventeen page cover article on this "scientific debate"
(20). This paper, along with the many months of comments which followed
it, is an absolute must for anyone considering the pros and cons
of fluoridation.
65. Refusal to appear on the
same platform as fluoridation opponents. This tactic may work
in the short run, but in the long run most citizens see it for what
it is, a lack of confidence in the substance of their position.
Presumably they believe that they can win the debate with leaflets
or paid advertisements which sell their position in a one-sided
manner. The booklet called "Fluoridation: The Facts" put
out by the American Dental Association (ADA) (81) is a travesty
of science. Perhaps we shouldn't be surprised since this same association
came into existence in the 1830's in order to promote the use of
mercury amalgams, which they have defended ever since, despite the
growing evidence that mercury escapes from these fillings and can
cause health effects. In its fluoride pamphlet the ADA selectively
cites the literature and shamelessly ignores many papers which contradicts
its claims of efficacy and safety. The ADA's standard tactic of
dealing with any study which finds a problem with fluoride is to
attack the methodology used in the paper. An impartial viewer has
to wonder how so many of these papers have made it into peer reviewed
journals if the authors' methodology was as weak as they claim.
Furthermore, such critiques from the ADA don't sit well when they
are not sent to the peer reviewed journals for the authors to concede
or rebut.
66. The long list of endorsements. This long list of endorsements
might look impressive to a newcomer until he or she realizes that
once the US Public Health Service officially endorsed fluoridation,
it was a foregone conclusion that many governmental and non-governmental
agencies (especially those who receive funding from the US PHS)
would fall into line. Many of the other agencies listed are dental
organizations, which have been so partisan on this issue that their
endorsement means very little. Other groups like the pro-fluoridation
and industry-funded American Council on Science and Health are well
known for their pro-industrial position on toxics. After these groups
have been eliminated, the list is less impressive. With those remaining
one has to ask these questions:
1) When did the organization endorse?
2) When did they last review the scientific literature on this
matter?
3) Who in the organization made the endorsement?
4) How much independent review of the literature was made?
5) And finally, what are the responses of those organizations
to the latest scientific information pertaining to fluoride's
impact on: the pineal gland, the thyroid gland, the brain, the
interaction of aluminum fluoride complexes with G-proteins, further
studies associating fluoride with hip fractures, and the vulnerability
of subsets of the population who are especially sensitive to fluoride's
toxicity.
There is an excellent chapter in the book "Fluoridation: The
Great Dilemma" by George Waldbott, Albert
Burgstahler and H. Lewis McKinney (82) which goes into the
dubious nature of some of the early endorsements of fluoridation.
However these endorsements were obtained, the ultimate ruling on
scientific issues like this should be made based upon weighing the
evidence in the published literature and not on the basis of who
says its OK. Otherwise we go back some 300 years when the Pope ruled
over science. In this respect it is noteworthy that in some communities,
where dentists and others have refused open debate, pro-fluoridation
statements by the former Surgeon General Everett Koop, have been
trotted out, either as letters to the editor or in paid advertisements.
This may occur less and less as some of the "ethical shine"
wears off Koop's image (83).
67. Beware of "authorities" which do not do their
homework. When it comes to tarnished authority, the biggest
shock for me personally came when I went to a public hearing on
September 23, 1997, organized by the Food and Nutrition Board, which
is part of the Institute of Medicine, which in turn is a part of
the National Academy of Sciences. Before this day I held these agencies
in some awe. I felt that they were there to arbitrate controversial
scientific issues: to provide judgment above and beyond the sway
of political and economic pressures. On this day I was sadly disillusioned.
Not only had the Food and Nutrition Board included fluoride in a
list of the nutrients, "Calcium, Magnesium, Phosphate and Vitamin
D" but they had recommended an upper tolerance limit (10
mg/day) which is well over the level thought to cause severelet
alone mildbone damage (22). Making matters even more absurd
was the fact that an earlier report from the National Academy of
Science had identified several studies which had shown an increase
in osteosclerosis at levels considerably lower than this (84). To
add salt to this "credibility wound" was the fact that
for eight hours of this meeting, not one single panelist present
could provide answers to the questions that I and Dr. William Hirzy,
from the US EPA, raised about their calculations and the many papers
in the peer-reviewed literature that they had ignored. Another shock:
the chairperson for the committee which determined the upper tolerance
level for fluoride was a gentlemen called Ian Munro, the President
of Cantox. This Canadian consulting company was the very same company
which produced a study on behalf of the Chlorine Industry, which
essentially exonerated organochlorines of causing any health and
environmental problems (85). This whole day is captured on videotape
for diehards who want to see their image of this prestigious body
shattered (86). The journal Fluoride has carried the correspondence
which followed from this meeting (87). Fifteen scientists signed
a letter to the President of the National Academy, Dr. Bruce Alberts,
pointing out the problems with this report. No reply was received.
After several months another letter was sent to Dr. Kenneth Shine,
President of the Institute of Medicine. Again, no reply was received.
Finally, a citizen recruited Senator Arlen Specter who called upon
the Academy to respond. This intervention did finally prompt a reply,
over a year after the initial letter was sent. The end result was
that nothing was changed. The upper tolerance limit for fluoride
remains at ascientifically indefensible10 mg/day.
The daily recommended doses were equally indefensible (88).
68. I have dwelt on this sorry tale because I think it is a very
good example of the danger of relying on "authorities",
however prestigious, to do your thinking for you. In most cases
the reviews performed by government agencies are only as good as
the people they put on the panels. For over 50 years and in several
different countries (US, UK, Australia, NZ, and Canada) the panels
that have been appointed to review the fluoride issue have been
stuffed with scientists and dentists who have held a strong pro-fluoridation
position. Very seldom, if ever, do review panels have people appointed
who have an in-depth knowledge of this issue and have a truly independent
position or an anti-fluoridation position. Such panels are highly
vulnerable to a selective use of the literature in the hands of
the pro-fluoridationists. Thus, the conclusions reached appear to
be a self-fulfilling prophesy designed to save the faces of those
who have promoted this misguided policy for so long. Whatever other
damage fluoride has done, it has certainly damaged the integrity
of some of our leading scientific and governmental agencies.
69. The number of communities fluoridated. Stressing the
numbers of communities that have been fluoridated in the US is ultimately
self-defeating for the ADA and others, because it leaves them trying
to explain why it is that so many countries have not followed the
American lead. Why is it that practically no country in Europe fluoridates
its drinking water? How come that despite this failure to accept
the "American wisdom" on this matter, that European childrens'
teeth are not full of cavities? No, if numbers convince, then the
ADA loses the debate hands down because they have failed to convince
the vast majority of countries around the world that fluoridation
is an acceptable and sensible public policy. North Americans represent
nearly half of the people worldwide drinking artificially fluoridated
water, which is a very small percentage of the total world population.
70. The opponents of fluoridation are a bunch of crazies.
First of all, bearing in mind the atrocious way opponents of fluoridation
have been treated over the last 50 years, it is surprising to me
that they are not crazy. I think if I had been doing this for 30
years instead of three I would be hanging from the rafters or in
a lunatic asylum! In actual fact over the years there have been
many distinguished people who have either opposed fluoridation or
expressed reservations about it, including dentists, doctors, scientists,
and 12 Noble prize winners (see paragraph 31). Indeed, the most
vocal opponents of fluoridation in the 1950s were professional biochemists
who had used fluoride to poison enzymes in their experiments. During
the debate over fluoridation in New York City in 1963 opponents
collected the signatures of over 1,500 doctors, dentists and scientists
opposed to fluoridation. Unfortunately, this solid, well-informed
and well-reasoned opposition was largely hidden from the public
by slick public relations campaigns. It is a sad part of America's
history that many government agencies have been a part (and still
are) of this public relations effort. And, if you, dear reader,
have felt uneasy even simply reading this paper, this bears testament
to how effective this denigration has been.
71. The opponents I know. Over the last few years I have
been privileged, to meet in person, or correspond with, some of
the leading opponents of fluoridation. These include, Dr. Albert
Burgstahler (Harvard graduate and Professor Emeritus of Organic
Chemistry at the University of Kansas and co-author of "Fluoridation:
The Great Dilemma"), Dr. Robert Carton (formerly with the US
EPA), Dr. John Colquhoun (former Principal Dental Officer of Auckland,
NZ), Dr. Richard Foulkes, M.D. (former adviser to the Government
of British Columbia), Dr. William Hirzy (currently with the US EPA),
Dr. David Kennedy, D.P.H (former President of the International
Academy of Oral Medicine and Toxicology), Dr. Lennart Krook (Professor
Emeritus of Toxicology, Cornell University Department of Veterinary
Medicine), Dr. John Lee, M.D. (Harvard graduate and bone specialist),
Dr. Hardy Limeback (Head of Preventive Dentistry, Toronto University),
Dr. William Marcus (Senior Science Advisor, US EPA), Dr. Roger Masters
(Professor of Government, Dartmouth College), Dr. Phyllis Mullenix
(formerly Head of the Toxicology Department, Forsyth Dental Center),
Dr. Albert Schatz (Co-discoverer of streptomycin), Dr. Bruce Spittle
(Department of Psychological Medicine, University of Otago Medical
School, NZ), Dr. John Yiamouyiannis (author of the Aging Factor),
and numerous remarkable citizens who between them have spent a combined
total of several hundred human years studying this issue. I can
state quite emphatically that these people are not a bunch of crazies.
They are not being paid to oppose fluoridation and have no other
axe to grind. Most of them don't want the hassle that this uphill
task brings to their lives. More than anything else, what they have
done, which many of the proponents have not done, is to do their
homework with an open mind. They may have a minute fraction of the
power and influence of those who have pushed fluoride on the American
people, but, in my view, they have far more integrity. They refuse
to let go until they see justice done and a sound basis of public
policy restored. If readers do likewise, they, too, will find, like
the little boy in Hans Christian Anderson's classic tale, that the
Emperor of Fluoridation has no clothes.
72. If readers do pursue this matter one of the arguments that
they will have to deal with from proponents is that we need to fluoridate
the water to protect the poor who don't have adequate dental services.
On the face of it this seems a very noble sentiment, however, in
practice, it could prove to be extremely pernicious. There is considerable
evidence (from studies in India, for example) that those most vulnerable
to fluoride are those who have a poor diet. The poor are more likely
to have a poor diet. Moreover, the poor in the United States are
also more likely to have been exposed to other pollutants, like
lead, which appear to act synergistically with fluoride. Thus fluoride
could deliver yet another blow to an already compromised section
of the community. If money is going to be spent on dental improvements
for the poor it would be better spent on providing access to better
diets and education on dental hygiene.
73. This raises yet another issue. There are particular subsets
of the population which are, according to ATSDR, "unusually
susceptible to the toxic effects of fluoride and its compounds":
"These populations include the elderly,
people with deficiencies of calcium, magnesium and/or vitamin
C, and people with cardiovascular and kidney problems... Impaired
renal clearance of fluoride has also been found in people with
diabetes mellitus and cardiac insufficiency. People over the age
of 50 often have decreased renal fluoride clearance... Poor nutrition
increases the incidence of dental fluorosis and skeletal fluorosis..."
(24, page 113).
To these must be added those who, in double blind studies, have
been shown to be supersensitive to fluoride (89). How can we as
a society ignore these vulnerable people? How can we put their
interests second to the rest of the community?
A challenge.
74. It is very clear from my experience that the ADA and the US
PHS cannot win this argument in an open public forum. I have challenged
dentists and other proponents of fluoridation to debate this issue
in the UK and several states in the US. Only Representative Tigue
in Pennsylvania (a former Marine) has had the courage to defend
his pro-fluoride position in open public debate. This debate was
held in Scranton, Pa. on October 23, 1999, and was televised by
the Pennsylvanian Cable Network (90). I am not the only one who
has made this kind of challenge. Dr. William Hirzy, of the Union
representing EPA's professionals in Washington D.C., responded to
a particularly nasty attack on the credibility of the Union's anti-fluoride
position paper (91) by challenging the author of the attack, Dr.
Michael Easley, to a public debate. Easley has failed to respond
to the challenge. Let me repeat the challenge. Many of us (Connett,
Mullenix, Hirzy, Carton, and others) are more than willing to take
on representatives of the ADA or the US PHS or other promoters of
fluoridation, in open public debate in any state or in any country.
We need a national campaign to end fluoridation and minimize
fluoride exposure.
75. Finally, fluoridation is a peculiarly American phenomenon.
It was started at a time when there was a tremendous optimism about
what chemicals could do. After World War II, new wonder plastics
were being created and new synthetic pesticides being formulated.
DDT was freely spread around towns and to demonstrate how safe it
was, it was even sprayed over children at picnics and in classrooms!
This was a different age. As with DDT, it is now time to call a
halt. Fluoridation was started in America, let's end it in America.
We need a national campaign to end fluoridation. Actually, we need
more than this. We need to minimize exposure to fluoride from all
sources. We need toothpaste manufacturers to give us a choice. They
need to provide a version of all their major brands with the fluoride
removed. We need the fluoride levels identified on all foods, beverages
and bottled water. Again we need freedom of choice. We need to limit
fluoride air emissions from industry and power stations. We need
to take fluoride air emissions at least as seriously as we do sulfur
oxide and nitrogen oxide emissions. We need to eliminate the use
of fluoride in pesticides and other products. Finally, we need to
pay special attention to the use of cryolite (Na3AlF6) as a "natural
pesticide". However, we will make little progress with all
of these urgent demands until scientists and environmental organizations
take a scientific attitude to this matter and have the courage to
revisit the issue with an open mind. The great moments in history
do not occur when every body jumps up and shouts yes, but when a
few courageous people step out of the crowd and say no. Fluoride
has been a "protected pollutant" (92) for far too long.
Postscript.
In proof reading this paper I realize that I have not done justice
to a number of significant issues relating to fluoride's toxicity,
for example: demonstrations of its mutagenicity; it's ability to
promote cancer in the presence of other carcinogens; its possible
relationship to birth defects like Down's Syndrome; the major work
of Burk and Yiamouyiannis on comparing cancer rates in fluoridated
and non-fluoridated cities in the US; Marier's extensive work on
fluoride's toxicity in conjunction with magnesium deficiency; and
the apparent willingness of the US, Australian and other governments
to downplay or outright ignore the seriousness of industrial fluoride
pollution which has plagued industrial society since the beginning
of the century. However, the important point at this juncture, I
believe, is not to overwhelm the reader with more detail but rather
to encourage them to cut through the layers of public relations,
hype, and name calling, and find out for themselves the prostitution
of science which has taken place on the fluoride issue at the highest
level of government.
Acknowledgements
I would like to thank Dr. Albert Burgstahler, Dr. Robert Carton,
Dr. Richard Foulkes, Peter Meiers, Andreas Schuld, and Ellen Connett,
for taking the time to read this paper and making very useful comments.
Any mistakes left after this process are mine, not theirs.
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