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Kathy R Phipps a School of Dentistry, Oregon Health Sciences
University, 611 SW Campus Drive, Portland, OR 97201, USA, b School of Medicine,
Oregon Health Sciences University, 3181 SW Sam Jackson Park Road,
Portland, c Department of Epidemiology, School of Public Health,
University of Pittsburgh, 130 DeSoto Street, Crabtree A524, Pittsburgh,
PA 15261, USA
Correspondence to: K R Phipps
phippsk{at}ohsu.edu
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Abstract |
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Objective:
To determine whether fluoridation
influences bone mineral density and fractures in older women.
In 1945 Grand Rapids, Michigan, increased the fluoride
concentration of its water supply to 1.0 ppm and became the first city to implement water fluoridation. After 15 years children in Grand Rapids had a 56% reduction in rates of dental decay.1
Since 1950 the number of individuals drinking fluoridated water has steadily increased. Today an estimated 300 million people are exposed
to fluoridated water, including 5.5 million in the United Kingdom and
144 million in the United States.2
While the benefit of fluoridation in the prevention of dental caries
has been overwhelmingly substantiated, the effect of fluoridation on
bone mineral density and rates of fracture is inconsistent. Ecological
studies that compare rates of fracture specific for age and sex between
fluoridated and non-fluoridated communities have variously found that
exposure to fluoridated water increases the risk of hip
fracture,3-5 increases the risk of proximal humerus and
distal forearm fracture,6 has no effect on fracture
risk,7-10 and decreases the risk of hip
fracture.
11 12
Ecological studies, however, have a major
design flaw We determined, on an individual level, whether older women with long
term exposure to fluoridated water had different bone mass and rates of
fracture compared with women with no exposure. Given our widespread
exposure to fluoridation, the impact of fluoride on rates of fracture
is an important public health issue. In a previous study in which we
found no effect of fluoridation on bone mass or risk of fracture in
women we had limited power to look at individual fractures and had a
relatively small proportion of women exposed to fluoride for long
duration.13 In the current study we increased power to
look at individual fractures by increasing the number of participants,
including more women with long term exposure to fluoride, and following
the population for a longer period of time.
Participants Exposure to fluoridated water Measurement of bone mass Assessment of risk factors Ascertainment of incident non-spinal fractures Ascertainment of prevalent and incident vertebral
fractures Statistical analysis Characteristics of the study
population
Table 1.
Table 2.
Design:
Multicentre prospective study on risk factors for osteoporosis and fractures.
Setting:
Four community based centres in the United States.
Participants:
9704 ambulatory women without bilateral
hip replacements enrolled during 1986-8; 7129 provided information on
exposure to fluoride.
Main outcome measures:
Bone mineral density of the
lumbar spine, proximal femur, radius, and calcaneus plus incident
fractures (fractures that occurred during the study) of vertebrae, hip, wrist, and humerus.
Results:
Women were classified as exposed or not
exposed or having unknown exposure to fluoride for each year from 1950 to 1994. Outcomes were compared in women with continuous exposure to
fluoridated water for the past 20 years (n=3218) and women with no
exposure during the past 20 years (n=2563). In women with continuous
exposure mean bone mineral density was 2.6% higher at the femoral neck
(0.017 g/cm2, P<0.001), 2.5% higher at the lumbar spine
(0.022 g/cm2, P<0.001), and 1.9% lower at the distal
radius (0.007 g/cm2, P=0.002). In women with continuous
exposure the multivariable adjusted risk of hip fracture was slightly
reduced (risk ratio 0.69, 95% confidence interval 0.50 to 0.96, P=0.028) as was the risk of vertebral fracture (0.73, 0.55 to 0.97, P=0.033). There was a non-significant trend toward an increased risk of
wrist fracture (1.32, 1.00 to 1.71, P=0.051) and no difference in risk of humerus fracture (0.85, 0.58 to 1.23, P=0.378).
Conclusions:
Long term exposure to fluoridated
drinking water does not increase the risk of fracture.
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Introduction
Top
Abstract
Introduction
Methods
Results
Discussion
References
they are based on community level data and cannot control
for confounding variables at the individual level.
![]()
Methods
Top
Abstract
Introduction
Methods
Results
Discussion
References
This study was ancillary to the study of
osteoporotic fractures, a multicentre study of risk factors for
osteoporosis and fractures. During 1986-8 we recruited 9704 white women
aged at least 65 years in Portland, Oregon; Minneapolis, Minnesota; Baltimore, Maryland; and the Monongahela Valley (an area with several
small communities) in Pennsylvania. Recruitment sources included lists
for jury selection and registration of voters, motor vehicle records,
and membership records of health plans. Men and black women were
excluded as were white women who were unable to walk without assistance
and women who had a bilateral hip replacement.
Exposure to fluoridated water
was assessed with a questionnaire on residence history. Women were
asked to list each address (street, city, state, and postal code),
years they lived at that address, and the type of water supply (public,
well, spring, etc) for each of their residences from 1950 to 1994. Water system maps and the 1992 fluoridation census2 were
used to link street addresses with water system and fluoridation
status. If a question arose, the appropriate water district was
contacted to ascertain water source and fluoride content. For each year
women were coded as being exposed or not exposed or having unknown
exposure. The coding of unknown was used for residences outside the
United States, incomplete addresses, and private wells in areas with
naturally occurring fluoride. The questionnaire was sent to the 7612 women still active in the study and 94% (7129) completed it. To assess
the reliability of the residence history, duplicate histories were
completed by a randomly selected group of 103 women. The
statistic
for agreement between fluoride exposure was 0.94.
Bone mineral density
(g/cm2) of the distal radius, proximal radius,
and calcaneus were measured with single photon absorptiometry
(Osteo-Analyzer, Siemens-Osteon, Wahiawa, Hawaii). Bone mineral density
of the lumbar spine and proximal femur were measured with dual energy
x ray absorptiometry (QDR 1000, Hologic Inc, Waltham, Massachusetts).
Information on medical history,
drugs and supplements, reproductive history, menopause, alcohol consumption, exercise, smoking, caffeine intake, and history of fractures was obtained through a questionnaire. Dietary calcium was
assessed by a food frequency questionnaire administered by an
interviewer.14 Women were also asked about walking, time spent sitting or lying down, and the amount of difficulty experienced with activities of daily living. Height and weight were also
measured.15
During the
study participants were contacted every four months to inquire if a
fracture had occurred (incident fracture). About 99% of these contacts
were completed.16 If a fracture was reported the woman was
interviewed and a copy of the radiographic report obtained. To be coded
as a fracture the report had to mention the occurrence of an acute
fracture. Fractures due to major trauma were excluded. All fractures
that occurred up until 1 December 1995 were included (average follow up
of 7.0 years).
Lateral radiographs of the thoracic and lumbar spine
were taken during the first clinical visit. A vertebral body was
considered to have a prevalent fracture (fracture that had occurred
before the study) if any of the following ratios were more than 3SD
below the mean: the ratio of anterior to posterior height, mid-height to posterior height, and anterior height to the anterior height of the
adjacent vertebrae.17 Repeat radiographs were obtained from 7238 women (average follow up of 4.0 years). The following definition of an incident vertebral fracture was used: a 20% reduction in the vertebral height of the anterior, middle, or posterior dimension
of a vertebral body and at least a 4 mm decrease in the vertebral
height of a dimension.
To evaluate the effect of long term
fluoride exposure we statified data by fluoride exposure. Women with no
exposure during 1971-90 (n=2563) were compared with women with continuous exposure (n=3218) and women with mixed exposure
(n=1348). A 20 year period was selected because information on
residence history for dates before 1971 was less reliable. We used
2 tests of homogeneity and analysis of variance and
covariance to compare mean bone mineral density and other covariates
across the exposure groups. We used proportional hazard and logistic regression models to assess the relation between fluoride and incident
fractures. Multivariable models included those factors that differed
between the fluoride exposure groups plus factors previously shown to
be significantly related to skeletal health in the study of
osteoporotic fractures.
18 19
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Results
Top
Abstract
Introduction
Methods
Results
Discussion
References
Compared with women with continuous exposure, women
with no exposure were older and heavier, were more likely to have had a
surgical menopause, reported a higher use of both thiazide diuretics
and thyroid hormones, drank less alcohol, had lower calcium intakes,
had higher muscle strength at the knee but lower grip strength, and
were less likely to have more than a high school education (table 1).
There was no difference in physical activity, history of falls,
functional status, or smoking. Women with no or mixed exposure were
more likely to have non-insulin dependent diabetes and women with mixed exposure reported a lower use of
oestrogen.
Bone mineral density
Tables 2 and 3 give data on bone
mineral density adjusted for age and other variables for the lumbar spine, proximal femur, radius, and calcaneus stratified by fluoride exposure. Compared with women with no exposure, women with
continuous exposure had significantly higher bone mineral density of
the lumbar spine, femoral neck, and trochanter, but significantly lower density of the radius. Women with mixed exposure tended to have
bone density values between the other exposure
groups.
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Incident fractures
Twenty three per cent of the women
experienced at least one non-vertebral fracture during observation. Women with continuous exposure had fewer fractures of the spine, hip,
and humerus but more wrist fractures than women with no exposure (table
4). After adjustment for potential confounders, women with
continuous exposure had a 31% reduction in risk of hip fracture (P=0.028) and a 27% reduction in risk of vertebral fracture (P=0.033). There was a trend towards fewer fractures of the humerus (P=0.387) and
more fractures of the wrist (P=0.051), but the differences were not
significant. The risk of fracture in women with mixed exposure did not
differ from that in women with no exposure (table 5).
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Discussion |
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Osteoporosis is a major public health problem. In the European Community osteoporosis is responsible for more than one million fractures each year, and the number is expected to increase. Because of this it is imperative that steps be taken to understand the determinants of fracture and to decrease the population's risk of osteoporosis and subsequent fractures.
Strength of study
In the 1950s and 1960s several cross sectional studies
suggested an increase in bone density in individuals living in
fluoridated areas.20-22 These early studies, however,
failed to control for important confounding variables. To overcome this problem, we considered known confounders. In addition, we included only
those fractures confirmed by radiographic report and carefully assessed
long term exposure to fluoridated water. Using a prospective design,
mixed with a retrospective assessment of fluoride exposure, we found
that exposure to fluoridation was associated with an increase in bone
mass at the lumbar spine and proximal femur and a slight decrease in
the risk of hip and vertebral fractures. We also found that women with
long term exposure to fluoridated water had decreased bone mineral
density of the radius. Women with mixed exposure tended to have
fracture risks between those seen in women with no exposure and those
with continuous exposure, especially at the hip and wrist.
Comparisons with recent research
In addition to the definitive concordance we found between bone
mineral density and fractures, our findings are consistent with results
of recent studies that evaluated the impact of fluoridation on bone
mineral density and fractures. In a study of 3222 women Kroger et al
found higher bone mineral density of the lumbar spine (2.7%) and
femoral neck (1.1%) among postmenopausal women exposed to fluoridation
for at least 10 years.23 Hillier et al, however, found no
association between fluoridation and risk of hip fracture risk in a
case-control study of men and women aged 50 years and older (odds ratio
1.0, 95% confidence interval 0.7 to 1.5).24
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What is already known on this topic
Several ecological studies have found that rates of hip fracture are higher in communities with fluoridated drinking water compared with communities without fluoridation These studies, however, have not controlled for several factors known to be associated with rates of fracture including use of oestrogen, smoking, and body weight What this study addsLong term exposure to fluoridation does not increase the risk of osteoporotic fracture among older women In terms of any effect on bone mineral density community water fluoridation as a public health measure for the prevention of dental caries is safe |
Fluoride biomarker
Fluoride is ubiquitous and is found in food, water, air, and
dental products. It is estimated, however, that about 80% of dietary
fluoride is from water and beverages.
28 29
Detailed
histories of residence are the best tool currently available to
estimate long term fluoride exposure. Because concentrations of
environmental fluoride are low, the distinction between the exposed and
the unexposed population is often blurred, making the traditional tool
of epidemiology (questionnaires) less sensitive.30 A
biomarker of exposure could increase sensitivity in studies on the
impact of fluoride on osteoporosis. The only validated biomarker for
long term fluoride exposure is fluoride concentrations in bone. While
bone biopsies provide an accurate concentration of total body burden of
fluoride they are unacceptable to patients. Fluoride concentrations in
fasting plasma, saliva, and nails may be potential measures of
exposure. The development and validation of a fluoride biomarker is an
essential next step in the continued study of the relation between
fluoride and skeletal health.
Conclusion
This is the first prospective study with adequate power to examine
the risk of specific fractures associated with fluoride on an
individual rather than a community basis. Our results show that long
term exposure to fluoridation may reduce the risk of fractures of the
hip and vertebrae in older white women. Because the burden of
osteoporosis is largely due to fractures of the hip, this finding may
have enormous importance for public health. If fluoridation does reduce
the risk of hip fracture it may be one of the most cost effective
methods for reducing the incidence of fractures related to
osteoporosis. In addition, our results support the safety of
fluoridation as a public health measure for the control of dental caries.
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Acknowledgments |
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Contributors: KRP (guarantor) developed the study protocols, coordinated the study, and participated in data analysis, interpretation, and writing of the paper. ESO participated in the protocol design, interpretation of the data, and writing of the paper. JDM participated in the design and execution of the study including data collection, data documentation, quality control, and writing of the paper. JAC had the original idea for the present study and participated in data collection, interpretation of the data, and writing of the paper.
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Footnotes |
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Funding: United States National Institutes of Health (DE10814, AG05407, AR35582, AG05394, AR35584, AR35583). United States Environmental Protection Agency, Center for Environmental Epidemiology, University of Pittsburgh. The views expressed are those of the authors and do not necessarily reflect the views or policies of the US Environmental Protection Agency.
Competing interests: None declared.
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References |
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| 1. | Burt BA, Eklund SA. Dentistry, dental practice, and the community. 4th ed. Philadelphia: Saunders, 1992. |
| 2. | Public Health Service, CDC, Division of Oral Health. Fluoridation Census 1992. Atlanta, GA: US Department of Health and Human Services, 1993. |
| 3. | Jacobsen SJ, Goldberg J, Cooper C, Lockwood SA. The association between water fluoridation and hip fracture among white women and men aged 65 years and older. A national ecologic study. Ann Epidemiol 1992; 2: 617-626[Medline]. |
| 4. | Danielson C, Lyon JL, Egger M, Goodenough GK. Hip fractures and fluoridation in Utah's elderly population. JAMA 1992; 268: 746-748[Abstract]. |
| 5. | Jacobsen SJ, Goldberg J, Miles TP, Brody JA, Stiers W, Rimm AA. Regional variation in the incidence of hip fracture. US white women aged 65 years and older. JAMA 1990; 264: 500-502[CrossRef][Medline]. |
| 6. | Karagas MR, Baron JA, Barrett JA, Jacobsen SJ. Patterns of fracture among the United States elderly: geographic and fluoride effects. Ann Epidemiol 1996; 6: 209-216[CrossRef][Medline]. |
| 7. |
Madans J, Kleinman JC, Cornoni-Huntley J.
The relationship between hip fracture and water fluoridation: an analysis of national data.
Am J Public Health
1983;
73:
296-298 |
| 8. | Avorn J, Niessen LC. Relationship between long bone fractures and water fluoridation. Gerodontics 1986; 2: 175-179[Medline]. |
| 9. | Arnala I, Alhava EM, Kivivuori R, Kauranen P. Hip fracture incidence not affected by fluoridation. Osteofluorosis studied in Finland. Acta Orthop Scand 1986; 57: 344-348[Medline]. |
| 10. | Cooper C, Wickham C, Lacey RF, Barker DJ. Water fluoride concentration and fracture of the proximal femur. J Epidemiol Community Health 1990; 44: 17-19[Abstract]. |
| 11. | Simonen O, Laitinen O. Does fluoridation of drinking-water prevent bone fragility and osteoporosis? Lancet 1985; ii: 432-434. |
| 12. |
Jacobsen SJ, O'Fallon WM, Melton LJ.
Hip fracture incidence before and after fluoridation of the public water supply, Rochester, Minnesota.
Am J Public Health
1993;
83:
743-745 |
| 13. | Cauley JA, Murphy PA, Riley TJ, Buhari AM. Effects of fluoridated drinking water on bone mass and fractures: the study of osteoporotic fractures. J Bone Miner Res 1995; 10: 1076-1086[Medline]. |
| 14. |
Cummings SR, Block G, McHenry K, Baron RB.
Evaluation of two food frequency methods of measuring dietary calcium intake.
Am J Epidemiol
1987;
126:
796-802 |
| 15. |
Kelsey JL, Browner WS, Seeley DG, Nevitt MC, Cummings SR.
Risk factors for fractures of the distal forearm and proximal humerus. The study of osteoporotic fractures research group.
Am J Epidemiol
1992;
135:
477-489 |
| 16. |
Cummings SR, Nevitt MC, Browner WS, Stone K, Fox KM, Ensrud KE, et al.
Risk factors for hip fracture in white women. The study of osteoporotic fractures research group.
N Engl J Med
1995;
332:
767-773 |
| 17. | Black DM, Palermo L, Nevitt MC, Genant HK, Epstein R, San Valentin R, et al. Comparison of methods for defining prevalent vertebral fractures: the study of osteoporotic fractures. J Bone Miner Res 1995; 10: 890-902[Medline]. |
| 18. |
Bauer DC, Browner WS, Cauley JA, Orwoll ES, Scott JC, Black DM, et al.
Factors associated with appendicular bone mass in older women. The study of osteoporotic fractures research group.
Ann Intern Med
1993;
118:
657-665 |
| 19. |
Orwoll ES, Bauer DC, Vogt TM, Fox KM.
Axial bone mass in older women. Study of osteoporotic fractures research group.
Ann Intern Med
1996;
124:
187-196 |
| 20. | Leone NC, Stevenson CA, Hilbish TF, Sosman MC. A roentgenologic study of human population exposed to high-fluoride domestic water (a 10-year study). In: McClure FJ, ed. Fluoride drinking waters. Bethesda, MD: National Institute of Dental Research, 1962 (DHEW Publ No (PHS)62-825). |
| 21. | Bernstein DS, Sadowsky N, Hegsted DM, Guri D, Stare FJ. Prevalence of osteoporosis in high- and low-fluoride areas in North Dakota. JAMA 1966; 198: 499-504[CrossRef][Medline]. |
| 22. | Ansell BM, Lawrence JS. Fluoridation and the rheumatic diseases. A comparison of rheumatism in Watford and Leigh. Ann Rheum Dis 1966; 25: 67-75[Medline]. |
| 23. |
Kroger H, Alhava E, Honkanen R, Tuppurainen M, Saarikoski S.
The effect of fluoridated drinking water on axial bone mineral density a population-based study.
Bone Miner
1994;
27:
33-41[Medline].
|
| 24. | Hillier S, Cooper C, Killingray S, Russell G, Hughes H, Coggon D. Fluo-ride in drinking water and risk of hip fracture in the UK: a case-control study. Lancet 2000; 335: 265-269. |
| 25. | Ad-Hoc Subcommittee on Fluoride. Review of fluoride benefits and risks. Bethesda, MD: Public Health Service, Department of Health and Human Services, 1991:17. |
| 26. | Whitford GM. The metabolism and toxicity of fluoride. Monogr Oral Sci 1996; 16(2): 1-153. |
| 27. | Farley JR, Tarbaux N, Hall S, Baylink DJ. Evidence that fluoride-stimulated 3[H]-thymidine incorporation in embryonic chick calvarial cell cultures is dependent on the presence of a bone cell mitogen, sensitive to changes in the phosphate concentration, and modulated by systemic skeletal effectors. Metabolism 1988; 37: 988-995[CrossRef][Medline]. |
| 28. | Dabeka RW, McKenzie AD. Survey of lead, cadmium, fluoride, nickel, and cobalt in food composites and estimation of dietary intakes of these elements by Canadians in 1986-1988. J AOAC Int 1995; 78: 897-909[Medline]. |
| 29. | Lahti SM, Uusitalo U, Feskens E, Haw U, Tuomilehto J, Luoma H. Fluoride and sugar intake among adults and youth in Mauritius: preliminary results. Adv Dent Res 1995; 9: 21-25[Abstract]. |
| 30. |
Silbergeld EK, Davis DL.
Role of biomarkers in identifying and understanding environmentally induced disease.
Clin Chem
1994;
40:
1363-1367 |
(Accepted 5 July 2000)
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