THE LANCET
May 27, 1972; Pages 1135-1138
FLUORIDE, WATER HARDNESS, AND ENDEMIC GOITRE
by T. K. DAY & P. R. POWELL-JACKSON
East Wing,
Guy's Hospital, London S.E.1
Summary
The prevalence of goitre in 17 Himalayan villages has been estimated.
Water-samples from each village were taken, and levels of iodine,
fluoride, and hardness determined. In 13 villages wide variations
in goitre prevalence were not attributable to differences in iodine
intake, which remained constant within a narrow range. Instead,
variations in goitre prevalence were found to correlate closely
with the fluoride content (p=0-74; P<0-01) and with the hardness
(p=0.77; P<0-01) of the water in each village. The effects
of fluoride and water hardness seem to be independent.
Introduction
Goitre prevalence in a number of endemic areas has been shown
to depend on factors other than iodine deficiency (1-3).
The role of water hardness in endemic goitre in man and experimental
goitre in animals is well established (1). That fluoride may be
another important factor has long been suspected. Goitre has been
produced in experimental animals by feeding fluoride salts (5-7),
and fluoride exerts an antithyroid effect in man when used in
the treatment of thyrotoxicosis (8,9).
However, epidemiological evidence of an association between fluoride
and endemic goitre is contradictory. While areas in which the
water contains an unusually high level of fluoride, or in which
dental fluorosis is pronounced, have been shown to coincide with
the regional distribution of endemic goitre (10-13), the absence
of endemic goitre in other areas where the fluoride levels are
equally high has been noted (14-16).
It has been suggested that a high intake of iodine may offset
the goitrogenic effect of fluoride, and this might explain the
absence of goitre in some high fluoride areas. Iodine levels were
consequently measured during surveys (4,17-20), in which goitre
prevalence in centres of relatively high and low fluoride intake
was compared. Unfortunately, iodine intake was generally high,
and varied widely from one centre to another, so no true estimate
could be made of the independent effect of fluoride. Several workers
(4,18,20) felt that the possible goitrogenic effect of fluoride
coule only be usefully studied in an area of low iodine intake
and of high goitre prevalence.
Our study was performed in such an area, and provides data upon
the relation between fluoride and endemic goitre under conditions
of constant low iodine intake. In addition, further evidence is
provided in support of the association between endemic gotire
and water hardness.
Methods
Area of Survey
The survey was conducted in Chintang panchayat, Nepal, in conjunction
with a B.C.G. inoculation programme. The panchayat covers an area
of approximately 25 square miles of hill-country of 500-6000 ft.,
with a population of 10,000 people.
The population is uniform with respect to race, occupations,
and eating habits. The diet is based upon rice, pulse, vegetables,
and spices. It is low in iodine and lacks the common vegetable
goitrogens. Iodised salt is not available locally.
17 villages were visited and 736 people examined. 4 villages
had relatively high water-iodine levels and were excluded. Our
study is based upon data from the remaining 13 (648 people) which
had a water-iodine concentration of 0-001 p.p.m. or less.
Sample Selection and Goitre Assessment
The prevalence of goitre in each village was estimated on a sample
representing about a third of the population. The samples consisted
of all children attending for B.C.G. inoculation plus all accompanying
adults. The same selection procedure was followed in each village.
Goitres were graded into three sizes by inspection, according
to the method of Perez et al. (21), the age and sex of each subject
being noted.
Water Sampling and Analysis
Each of the villages in the survey depended upon one source of
water, in most cases a soil well. A sample of water was taken
from each source into a 50 ml. High density polyethylene bottle,
which had been washed in distilled water. The bottles did not
contaminate or absorb ions from test solutions.
Estimations of fluoride, calcium, magnesium, and iodine were
performed in London, after completion of the goitre survey, in
the laboratory of the Government Chemist. Fluoride was determined
by the specific-ion electrode (22); calcium and magnesium by atomic
absorption spectrophotometry; and iodine by Dubravcic's modification
of the ceric-ion-reduction technique (23). Water hardness was
derived from the calcium and magnesium levels, and expressed as
the concentration of a pure solution of calcium carbonate having
the same degree of hardness as the sample.
Results
The prevalence of clearly visible goitre - grades two and three
of Perez' classification (21) was calculated for each village.
Grades two and three include only those goitres which are easily
discernible without extension of the neck.
The age and
sex distribution of goitre in the 13 villages is given in table
I. There is a pronounced rise in prevalence with age, but
the sexes are affected almost equally, which is characteristic
of a hyperendemic area (1).
Though a constant very low iodine intake was common to the people
of all the villages, goitre prevalence varied widely from village
to village. This variation correlated closely with corresponding
variations in both water hardness and fluoride content (P <0-01)
(table II). Since water hardness and fluoride
levels are themselves intercorrelated, it is not possible on these
data to decide whether the association between fluoride and goitre
is independent of that between hardness and goitre. A more complex
analysis of the data involving the use of partial correlation
coefficients would not be justified, as assumptions would need
to be made about the linearity of association and the normal distribution
of variables. However, some indication that the effect of fluoride
is independent of that of hardness is provided when the data are
grouped as in the accompanying figure.
It can be seen that the lowest goitre prevalence occurs in soft-water/low-fluoride
villages, whilst goitre prevalence is higher when the water either
is harder or contains more fluoride. The highest prevalence of
all is in villages with both hard-water and high-fluoride levels.
Unlike McCarrison (l), we found no striking inverse relation
between altitude and goitre prevalence. Nor was there an obvious
association between the type of water source and goitre. All villages
were supplied by shallow soil wells except F, H, and M (streams)
and J (river).
Discussion
Water Hardness
The occurrence of endemic
goitre in hard-water areas has often been noted (4). Experimental
work in rats supports the idea (24) that calcium salts exacerbate
an underlying state of iodine deficiency. Where iodine is not
plentiful, the hardness of water may be more important in determining
goitre prevalence than the absolute level of iodine: in the U.K.,
hard waters, though containing a greater concentration of iodine,
are associated with a higher goitre prevalence than soft (4).
Our results show that, with constant low-iodine levels, a very
close correlation may be demonstrated between the degree of hardness
and goitre prevalence.
Although the goitrogenic effect of calcium salts has been elucidated
by experiment (4), the action of magnesium ions on thyroid function
has been little investigated. In our data magnesium levels are
more closely correlated with goitre prevalence than calcium levels,
but this does not necessarily mean that magnesium is a more potent
goitrogen. Indeed, the correlation may reflect only the fact that
the two elements tend to occur together in the rocks and soil
of the region of the survey.
Fluoride
Suspicions of an aetiological connection between fluoride and
goitre, raised by the observation of a high incidence of goitre
in areas of endemic fluorosis (10-13), have not been substantiated
by epidemiological studies (17-20) conducted in relatively non-goitrous
regions.
However, the possibility that fluoride may influence the prevalence
of goitre in an area where goitre is endemic has not previously
been investigated. Our results show a close quantitative association
between fluoride and goitre under these circumstances.
This association is unlikely to be due to chance, but it may
be indirect, and not the result of fluoride exerting a goitrogenic
effect. That the association is probably causal is suggested by
the fact that fluoride produces goitre when fed to animals (1-7).
However, the doses of fluoride used in animal experiments have
been large compared to the doses normally consumed by man (25).
Further experimental work is needed, using lower doses of fluoride,
and iodine-deficient partially goitrous animals, to justify the
conclusion that fluoride is normally goitrogenic under circumstances
of iodine deficiency.
Experimental work should also be directed towards discovering
the site of action of fluoride in thyroid function. Many workers
have suggested that it affects iodine metabolism, but there is
little conclusive evidence of such a mechanism (26,27).
Possibly the influence of fluoride is upon the aminoacid precursors
of thyroxine-tyrosine and its metabolites-rather than upon iodine.
Increased urinary loss of tyrosine is known to occur in men living
in a high-fluoride area (28) and in monkeys receiving low daily
doses of fluoride (29): tyrosine deficiency has been shown to
cause thyroid hypofunction in rats (31). Moreover, the coexistence
of fluorosis and goitre has been noted especially in poor rural
populations consuming diets deficient in protein, and the other
features of fluorosis-tooth and bone changes-are enhanced by malnutrition
(26, 31).
| TABLE
I-DISTRIBUTION OF GOITRE AMONG SCHOOLCHILDREN
AND ADULTS IN 13 HILL VILLAGES ACCORDING TO AGE AND SEX |
| |
Proportion with goitre
as a fraction: |
|
|
| Village |
By age (yr.) |
By sex |
Total |
Prevalence (%) |
| |
0-5 |
6-12 |
13-18 |
19+ |
M |
F |
|
|
| A |
0/11 |
1/13 |
0/6 |
1/8 |
0/21 |
2/17 |
2/38 |
5 |
| B |
0/20 |
4/19 |
0/4 |
2/5 |
1/22 |
5/26 |
6/48 |
12 |
| C |
0/9 |
1/10 |
0/5 |
3/7 |
1/19 |
3/12 |
4/31 |
13 |
| D |
1/11 |
2/14 |
0/8 |
4/7 |
1/19 |
6/21 |
7/40 |
17 |
| E |
1/13 |
2/22 |
7/12 |
0/3 |
2/19 |
8/31 |
10/50 |
20 |
| F |
1/12 |
2/12 |
2/4 |
4/7 |
3/15 |
6/20 |
9/35 |
26 |
| G |
0/8 |
2/13 |
0/3 |
8/12 |
5/19 |
5/17 |
10/36 |
28 |
| H |
2/16 |
0/13 |
3/8 |
14/16 |
7/21 |
12/32 |
19/53 |
36 |
| I |
0/19 |
10/28 |
11/18 |
19/20 |
11/35 |
29/50 |
40/85 |
47 |
| J |
2/11 |
13/29 |
11/23 |
19/26 |
26/52 |
19/37 |
45/89 |
51 |
| K |
2/12 |
6/14 |
3/4 |
12/13 |
13/23 |
10/20 |
23/43 |
53 |
| L |
1/9 |
9/18 |
8/9 |
11/12 |
16/26 |
13/22 |
29/48 |
60 |
| M |
3/10 |
14/20 |
8/10 |
11/12 |
22/26 |
14/26 |
36/52 |
69 |
| |
|
|
|
|
|
|
|
|
| Totals |
13/161 |
66/225 |
53/114 |
108/148 |
108/317 |
132/331 |
240/648 |
|
| |
(8%) |
(29%) |
(46%) |
73% |
(34%) |
(40%) |
(37%) |
|
| TABLE II-GOITRE PREVALENCE
IN RELATION TO THE COMPOSITION OF THE DRINKING-WATER |
| |
|
Water Concentration
in parts per million (p.p.m) of: |
Hardness as CaC03 |
| Village |
Goiter Prevalence (%) |
I |
F |
Ca |
Mg |
(p.p.m) |
| A |
5 |
0.001 |
<0.1 |
6 |
2.0 |
24 |
| B |
12 |
<0.001 |
0.13 |
7 |
1.5 |
24 |
| C |
13 |
<0.001 |
0.13 |
3 |
0.5 |
10 |
| D |
17 |
0.001 |
0.12 |
6 |
1.5 |
21 |
| E |
20 |
<0.001 |
0.19 |
69 |
15.5 |
235 |
| F |
26 |
<0.001 |
0.24 |
108 |
28.5 |
385 |
| G |
28 |
<0.001 |
0.22 |
8 |
3.5 |
33 |
| H |
36 |
<0.001 |
0.28 |
73 |
5.0 |
203 |
| I |
47 |
<0.001 |
0.21 |
12 |
6.0 |
54 |
| J |
51 |
0.001 |
0.19 |
148 |
65 |
630 |
| K |
53 |
<0.001 |
0.36 |
14 |
17 |
102 |
| L |
60 |
0.001 |
0.23 |
121 |
39 |
458 |
| M |
69 |
<0.001 |
0.23 |
145 |
77 |
670 |
| |
|
|
|
|
|
|
| Spearman's p = |
0.74 |
0.78 |
0.83 |
0.77 |
| |
P |
< 0.01 |
<0.01 |
<0.01 |
<0.01 |
| |
|
|
|
|
|
|
We thank Dr. S. J. Patterson and Mr. N. G. Bunton, of the Government
Chemist's laboratory, for performing the water analysis; His Majesty's
Government and the people of Nepal, and the Britain-Nepal Medical
Trust, for help in Nepal; and Dr. Margaret Crawford and Mr. David
Clayton for help with the statistics. The work was supported by
a Searle scholarship of the British Medical Students' Trust.
Requests for reprints should be addressed to T. K. D.
REFERENCES
1 . McCarrison, R. The Simple Goitres. London, 1928.
2. Young, M., Crabtree, M. G., Mason, E. M. Spec. Rep. Ser.
med. Res. Coun. 1936, no. 217.
3. Pediatrics, Springfield, 1967, 40, 935.
4. Murray, M. M., Ryle, J. A., Simpson, B. W., Wilson, D. C. Med.
Res. Coun. Memo. 1948, no. 18.
5. Maumene, M. E. C. r. hebd. Seanc. Acad. Sci. Paris,
1854, 39, 538.
6. Roholm, K. Fluorine Intoxication; p. 89. Copenhagen, 1937.
7. Hodge, H. C., Smith, F. A. in Fluorine Chemistry (edited
by J. H. Simons); vol. iv, p. 106. London, 1965.
8. Goldemberg, L. Presse med. 1930, 102, 1751.
9. May, W. Klin. Wschr. 1935, 14, 790.
10. von Fellenberg, T. Mitt. Lebensmitt. Hyg. 1938, 29,
276.
11. Wilson, D. C. Lancet, 1941, i, 211.
12. von Hoffmann-Axthelm, W. Dt. zahnirztl. Z. 1953, 8,
757.
13. Steyn, D. G. Leech, Johannesb. 1964, 34, 114.
14. Demole, V., von Fellenberg, T., Held, A. J., Schmid, H. Bull.
schweiz. Akad. med. Wiss. 1951, 7, 440.
15, Leone, N. C., Shimkin, M. B., Arnold, F. R., Stevenson, C.
L., Zimmermann, E. R., Geiser, P. B., Lieberman, J. E. Publ.
Hlth Rep. Wash. 1954, 69, 925.
16. Frada, G., Mentesana, G., Guajana, U. Minerva med.
Roma, 1969, 60, 545.
17. Wespi, H. J. Praxis, 1954, 28, 616.
18. Berry, W. T. C., Whittles, J. H. Mon. Bull. Minist. Hlth,
1963, 22, 50.
19. Gedalia, L, Brand, N. Archs int. Pharmacodyn. Thir.
1963, 142, 312.
20. Siddiqui, A. H. Y. Endocr. 1960, 20, 101.
21. Perez, C., Scrimshaw, N. S., Munoz, J. A. Monograph Ser.
W.H.O. 1960, 44, 369.
22. Patterson, S. J., Bunton, N. G., Crosby, N. T. Wat. Treat.
Examination, 1969, 18, 182.
23. Dubravcic, M. Analyst, Land. 1955, 80, 295.
24. Thompson, J, Archs Path. 1933, 16, 211.
25. Demole, V. Bull. schweiz. Akad. med. Wiss. 1954, 10,
292.
26. Ericsson, Y. Br. dent. J. 1967, 123, 276.
27. Report of the Royal Commission into Fluoridation; p. 153.
Hobart, 1968.
28. Singh, A., Vazirani, S. J., jolly, S. S., Bansal, B. C. Postgrad.
med. J. 1962, 38, 150.
29. Pandit, C. G., Rao, D. N. Indian J. med. Res. 1940,
28, 559.
30. Simon, G., Szilcs, J., Gyetvai, G., Kecskem6ti, V. Acta
physiol. hung. 1962, 21, 335.
31. Murray, M. M., Wilson, D, C. Br. dent. J. 1948, 84,
97.