You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


  Vol. 118 No. 3, March 2000 TABLE OF CONTENTS
  Archives
  •  Online Features
  Epidemiology and Biostatistics
 This Article
 •Abstract
 •PDF
 • Reply to article
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Citing articles on ISI (57)
 •Contact me when this article is cited
 Related Content
 •Related article
 •Similar articles in this journal
 Topic Collections
 •Articles for Residents
 •Ophthalmology, Other
 •Alert me on articles by topic

Dietary Fat and Fish Intake and Age-Related Maculopathy

Wayne Smith, BMed, BMath, MPH, PhD, FAFPHM; Paul Mitchell, MD, FRACO, FRCOphth; Stephen R. Leeder, MB, BS, PhD

Arch Ophthalmol. 2000;118:401-404.

ABSTRACT

Objective  To assess whether dietary intake of fat or fish is associated with age-related maculopathy (ARM) prevalence.

Design  Cross-sectional, urban population–based study.

Participants  People (N = 3654) aged 49 years or older.

Main Outcome Measures  Subjects with ARM were identified from masked grading of retinal photographs. A 145-item self-administered, semiquantitative food frequency questionnaire was completed adequately by 88.8% of participants and was used to assess intakes of dietary fat and fish.

Results  A higher frequency of fish consumption was associated with decreased odds of late ARM (odds ratio for frequency of consumption more than once per week compared with less than once per month, 0.5). Subjects with higher energy-adjusted intakes of cholesterol were significantly more likely to have late ARM, with an increased risk for late ARM for the highest compared with the lowest quintile of intake (odds ratio, 2.7).

Conclusion  The amount and type of dietary fat intake may be associated with ARM.



INTRODUCTION
 Jump to Section
 •Top
 •Introduction
 •Subjects and methods
 •Results
 •Comment
 •Author information
 •References

AGE-RELATED maculopathy (ARM) is a leading cause of irreversible blindness in Australia1 and the United States.2 The causes of ARM are not known, but there are many hypothesized risk factors. In addition to smoking,3-7 a number of cardiovascular diseases and risk factors previously have been found to have statistically significant associations with ARM. These include systemic hypertension,8-9 past diagnosis of vascular disease,9-10 presence of carotid or lower extremity arterial disease,11 high serum cholesterol level,4, 12 body mass index (calculated as the weight in kilograms divided by the square of the height in meters),12-13 and plasma fibrinogen level.13 However, few cardiovascular associations found in individual studies have been reproduced consistently. An association between early ARM and a high intake of saturated fat and cholesterol was reported from the Beaver Dam Eye Study.14 The relation between diet and atherosclerosis is unproven.15 However, reasonable evidence suggests that dietary fat intake, particularly dietary intake of saturated fat and cholesterol, is associated with an increased risk for atherosclerosis.16 It is biologically plausible that higher dietary saturated fat intake promotes atherosclerosis to increase the risk for ARM.

The human retina and macula contain a high proportion of polyunsaturated {omega}-3 fatty acids, particularly docosahexaenoic acid.17-18 Docosahexaenoic acid is found predominantly in oily fish and offal and appears to play an important role in the normal functioning of the retina.19 Increased consumption of fish and fish oils containing {omega}-3 fatty acids has been associated with antiatherosclerotic effects in a number of studies,20-22 although not all.23-24

Few previous studies have examined associations between dietary fat or fish consumption and ARM. In the only study to assess fish consumption, the intake of fish in the population with ARM was relatively low.14 In the Blue Mountains Eye Study (BMES) population,25 considerable diversity of fish intake was recorded. Our objective, therefore, is to assess whether dietary intake of fish or fat was associated with ARM.


SUBJECTS AND METHODS
 Jump to Section
 •Top
 •Introduction
 •Subjects and methods
 •Results
 •Comment
 •Author information
 •References

The BMES is a population-based survey of vision and common eye diseases in an urban population of 3654 people aged 49 years or older (participation rate, 82.4%). A questionnaire including medical history, smoking history, and family history of late ARM was administered, and subjects underwent a detailed eye examination, including stereoscopic macular photography of at least 1 eye in 3582 participants (98.0%). Details of the survey method and procedures have been described previously.25

The Wisconsin Age-Related Maculopathy Grading System26 was used to grade individual ARM lesions. Age-related maculopathy can be divided into early and late stages. The International ARM Epidemiological Study Group27 described 2 types of late ARM, neovascular and atrophic ARM degeneration. There were 72 cases of late ARM, including 50 neovascular and 22 atrophic cases, identified in the BMES. Early ARM was defined by the presence of soft indistinct or reticular drusen and retinal pigmentary abnormalities, in the absence of late ARM in either eye.25 There were 240 early ARM cases identified in the BMES.

Participants also completed a 145-item, semiquantitative food frequency questionnaire (FFQ) modified from an early FFQ by Willett et al28 for Australian diet and vernacular. The FFQ was attempted and returned by 3267 participants (89.4%), with 2900 (88.8%) usable FFQs, including 46 by participants with late ARM and 182 by participants with early ARM. Characteristics of the FFQ respondents and exclusion criteria have been published previously.29-30 This FFQ was also found to be reliable and to have reasonable concurrent validity compared with weighed food records collected for 1 year in the BMES population.29

Energy-adjusted nutrient intakes from food were calculated using the method described by Willett et al.31 Associations between ARM and categories of nutrient intake for total fat, saturated fat, cholesterol, and monounsaturated and polyunsaturated fats were investigated using logistic regression (SAS [Statistical Analysis System], version 6.12; SAS Institute Inc, Cary, NC) and adjusting for age, sex, current smoking, and family history of late ARM. Tests for trend over quintiles were performed by substituting quintile median values in the adjusted logistic regression models.


RESULTS
 Jump to Section
 •Top
 •Introduction
 •Subjects and methods
 •Results
 •Comment
 •Author information
 •References

Characteristics of subjects who consumed relatively little fish are shown in Table 1. Low fish consumption was crudely associated with increasing age, female sex, smoking, and a history of angina. More frequent consumption of fish appeared to protect against late ARM, after adjusting for age, sex, and smoking. As shown in Table 2, the protective effect of fish intake commenced at a relatively low frequency of consumption (odds ratio [OR] for intake 1-3 times per month compared with intake <1 time per month, 0.23) and overall had an OR of 0.5. However, there was little evidence of protection against early ARM.


View this table:
[in this window]
[in a new window]
Table 1. Subjects With and Without Relevant Cardiovascular Disease Factors Reporting Low Fish Consumption*



View this table:
[in this window]
[in a new window]
Table 2. Associations Between Intake of Fish and ARM*


Total and saturated fat intake were associated with a borderline significant increase in risk for early ARM (ORs for highest compared with lowest quintiles of intake, 1.60 and 1.50, respectively), and there was a significant association (P for trend, .05) for increasing prevalence of early ARM with increasing monounsaturated fat intake, as shown in Table 3. Cholesterol intake was associated with a borderline significant increase in risk for late ARM (OR for highest compared with lowest quintiles of intake, 2.71; P for trend, .04).


View this table:
[in this window]
[in a new window]
Table 3. Associations Between ARM and Dietary Fat Intake*



COMMENT
 Jump to Section
 •Top
 •Introduction
 •Subjects and methods
 •Results
 •Comment
 •Author information
 •References

We found a significant protective association between the frequency of consuming fresh or frozen fish and ARM. Although not significant for all categories of increased consumption, the protection against late ARM due to fish consumption (OR for consumption frequency of more than compared with less than once per month, approximately 0.5) is of the same order of magnitude as the statistically borderline protective effect of higher quintiles of polyunsaturated fat (OR, 0.40). The protective associations between ARM and the frequency of fish consumption and the higher polyunsaturated fat intake have not been reported previously. The Beaver Dam Eye Study reported no associations between ARM and seafood consumption, used as a proxy for {omega}-3 fatty acid intake,14 and Sanders et al19 found no association using plasma {omega}-3 fatty acids. However, as noted in the Beaver Dam Eye Study report, consumption of fish in that population may have been too infrequent to identify differences. In contrast, fish intake in our population is likely to be a reasonable marker for dietary {omega}-3 fatty acid intake, as a considerable proportion of our population report frequent fish consumption (Table 2). Our data suggest the possibility of a threshold protective effect at low levels of fish intake, with no increased protection from ARM at increased fish intake. This is consistent with current interpretation of the published associations between fish intake and cardiovascular disease.22 Consumption of high-fish diets by the elderly has been shown to compromise the status of vitamin E, an important antioxidant needed by the retina32; this could explain the threshold protective effect from dietary fish.

The biological plausibility of a protective effect of {omega}-3 fatty acids against the development of ARM is supported by the high level of polyunsaturated fatty acids in the retina,17-18 where they may be active in the maintenance of cell membrane and the constant renewal of retinal components after oxidative damage.33-34 Protection against ARM may also be provided by {omega}-3 fatty acids through a direct or indirect antiatherosclerotic effect.35-37

The relatively large proportion of people with late ARM who did not return usable FFQs (26/72 [36.1%]) provides a potential source of bias. However, there was no significant association between late ARM and return of a usable FFQ, after adjusting for age and sex.30 It is unlikely that this nondifferential nonresponse has led to a major bias. Antioxidant vitamin intake was not a confounder in any of the associations between ARM and dietary fat and fish intake. A previous report30 found no significant associations between antioxidant vitamin intake and late or early ARM in this population. Table 1 shows a relatively strong association between decreasing fish intake and increasing age. The logistic regression may have controlled inadequately for age in the adjusted model investigating the association between ARM and lower fish intake, as both are strongly age-related characteristics. This could have resulted in a spurious association, although this is unlikely, as the analysis includes sufficient numbers of subjects without ARM in the older age groups.

For associations between ARM and dietary fat intake, our results are similar to those reported from the Beaver Dam Eye Study.14 In Beaver Dam, associations were found between the highest compared with the lowest quintile of saturated fat intake and early (OR, 1.8) and late ARM (OR, 1.5). Our equivalent estimates of ORs of 1.50 and 1.61, respectively, agree closely. Similarly, the Beaver Dam Eye Study reported associations between highest compared with lowest quintile of cholesterol intake and early (OR, 1.6) and late ARM (OR, 1.4). These ORs compare reasonably with our estimated ORs of 1.40 and 2.71, respectively. The consistency of the magnitude of these associations across both studies lends credence to the contention that a higher dietary intake of saturated fats and cholesterol may confer an increased risk for ARM.

A survivor cohort effect may explain the failure of many studies to find associations between cardiovascular disease and ARM, if such an association truly exists. Subjects in whom cardiovascular disease develops will often die before late ARM, a relatively rare disease before the age of 70 years, develops. People with severe cardiovascular disease may thus die before they could be included in cross-sectional and case-control studies investigating associations between cardiovascular diseases and ARM. If there is a true association between atherosclerosis and ARM, subjects who survive to development of ARM are likely to be protected from the worst consequences of atherosclerosis, which may remain undetectable. However, dietary fat intake differences still may be detectable among survivors and may be found to be associated with ARM when atherosclerosis appears not to be associated.

Despite a likely survivor cohort effect, some studies9-11,38 have found increased risk for ARM with a history of a cardiovascular event or diagnostic signs, but other studies12-13 have found no associations with vascular events.

The causal pathway of higher saturated dietary fat intake, leading to increased atherosclerosis and development of ARM, is a plausible explanation for our finding of an association between dietary fat intake and ARM. Together with the protective association found for ARM with increasing frequency of fish consumption, our findings suggest that the amount and type of dietary fat intake are associated with ARM.

This cross-sectional study, although supported by findings from the Beaver Dam Eye Study, provides insufficient evidence of dietary fat intake to join tobacco smoking as an accepted, preventable risk factor for ARM. Evidence from large, prospective studies is required to confirm these findings. Identifying preventable risk factors for ARM, now the most common cause of blindness in western countries, may be the only way of reducing the burden of this disease, as current treatments are rarely effective in the longer term.


AUTHOR INFORMATION
 Jump to Section
 •Top
 •Introduction
 •Subjects and methods
 •Results
 •Comment
 •Author information
 •References

Accepted for publication August 26, 1999.

This study was supported by a Research and Development Grant Advisory Committee grant from the Australian Department of Health and Family Services, the Save Sight Institute, University of Sydney, Sydney, New South Wales, Australia.

Reprints: Wayne Smith, BMed, BMath, MPH, PhD, FAFPHM, National Centre for Epidemiology and Population Health, Australian National University, Australian Capital Territory, 0200 Australia (e-mail: wayne.smith{at}anu.edu.au).

From the National Centre for Epidemiology and Population Health, Australian National University, Australian Capital Territory (Dr Smith); and the Department of Ophthalmology, Westmead Hospital (Dr Mitchell), and the Department of Public Health and Community Medicine (Dr Leeder), University of Sydney, Sydney, New South Wales, Australia.


REFERENCES
 Jump to Section
 •Top
 •Introduction
 •Subjects and methods
 •Results
 •Comment
 •Author information
 •References

1. Cooper RL. Blind registrations in Western Australia: a five-year study. Aust N Z J Ophthalmol. 1989;107:875-879.
2. Klein R, Klein BE, Jensen SC, Meuer SM. The five-year incidence and progression of age-related maculopathy. Ophthalmology. 1997;104:7-21. ISI | PUBMED
3. Klein R, Klein BE, Linton KL, DeMets DL. The Beaver Dam Eye Study: the relation of age-related maculopathy to smoking. Am J Epidemiol. 1993;137:190-200. FREE FULL TEXT
4. Eye Disease Case-Control Study Group. Risk factors for neovascular age-related macular degeneration. Arch Ophthalmol. 1992;110:1701-1708. ABSTRACT
5. Vingerling JR, Hofman A, Grobbee DE, de Jong PT. Age-related macular degeneration and smoking: the Rotterdam Study. Arch Ophthalmol. 1996;114:1193-1196. ABSTRACT
6. Smith W, Mitchell P, Leeder SR. Smoking and age-related maculopathy: the Blue Mountains Eye Study. Arch Ophthalmol. 1996;114:1518-1523. ABSTRACT
7. Delcourt C, Diaz J, Ponton-Sanchez A, Papoz L. Smoking and age-related macular degeneration: the POLA Study. Arch Ophthalmol. 1998;116:1031-1035. FREE FULL TEXT
8. Sperduto R, Hiller R. Systemic hypertension and age-related maculopathy in the Framingham Study. Arch Ophthalmol. 1986;104:216-219. ABSTRACT
9. Goldberg J, Flowerdew G, Smith E, Brody J, Tso M. Factors associated with age-related macular degeneration. Am J Epidemiol. 1988;128:700-710. FREE FULL TEXT
10. Hyman LG, Lilienfeld AM, Ferris FL III, Fine SL. Senile macular degeneration: a case-control study. Am J Epidemiol. 1983;118:213-227. FREE FULL TEXT
11. Vingerling JR, Dielemans I, Bots ML, Hofman A, Grobbee DE, de Jong PT. Age-related macular degeneration is associated with atherosclerosis: the Rotterdam Study. Am J Epidemiol. 1995;142:404-409. FREE FULL TEXT
12. Klein R, Klein BE, Franke T. The relationship of cardiovascular disease and its risk factors to age-related maculopathy. Ophthalmology. 1993;100:406-414. ISI | PUBMED
13. Smith W, Mitchell P, Leeder SR, Wang JJ. Plasma fibrinogen levels, other cardiovascular risk factors, and age-related maculopathy. Arch Ophthalmol. 1998;116:583-588. FREE FULL TEXT
14. Mares Perlman JA, Brady WE, Klein R, VandenLangenberg GM, Klein BE, Palta M. Dietary fat and age-related maculopathy. Arch Ophthalmol. 1995;113:743-748. ABSTRACT
15. Ascherio A, Rimm EB, Giovannucci EL, Spiegelman D, Stampfer M, Willett WC. Dietary fat and risk of coronary heart disease in men. BMJ. 1996;313:84-90. FREE FULL TEXT
16. Willett WC. Diet and health: what should we eat? Science. 1994;264:532-537. FREE FULL TEXT
17. van Kuijk FJ, Buck P. Fatty acid composition of the human macula and peripheral retina. Invest Ophthalmol Vis Sci. 1992;33:3493-3496. FREE FULL TEXT
18. Robison W, Kuwabara T, Bieri J. The roles of vitamin E and unsaturated fatty acids in the visual process. Retina. 1982;2:263-281. FULL TEXT | ISI | PUBMED
19. Sanders TA, Haines AP, Wormald R, Wright LA, Obeid O. Essential fatty acids, plasma cholesterol, and fat-soluble vitamins in subjects with age-related maculopathy and matched control subjects. Am J Clin Nutr. 1993;57:428-433. FREE FULL TEXT
20. Kromhout D, Bosschieter EB, de Lezenne Coulander C. The inverse relation between fish consumption and 20-year mortality from coronary heart disease. N Engl J Med. 1985;312:1205-1209. ABSTRACT
21. Sanders TA, Sullivan DR, Reeve J, Thompson GR. Triglyceride-lowering effect of marine polyunsaturates in patients with hypertriglyceridemia. Arteriosclerosis. 1985;5:459-465. FREE FULL TEXT
22. Katan MB. Fish and heart disease. N Engl J Med. 1995;332:1024-1025. FREE FULL TEXT
23. Orencia AJ, Daviglus ML, Dyer AR, Shekelle RB, Stamler J. Fish consumption and stroke in men. Stroke. 1996;27:204-209. FREE FULL TEXT
24. Pietinen P, Ascherio A, Korhonen P, et al. Intake of fatty acids and risk of coronary heart disease in a cohort of Finnish men: The Alpha-Tocopherol, Beta-Carotene Cancer Prevention Study. Am J Epidemiol. 1997;145:876-887. FREE FULL TEXT
25. Mitchell P, Smith W, Attebo K, Wang JJ. Prevalence of age-related maculopathy in Australia. Ophthalmology. 1995;102:1450-1460. ISI | PUBMED
26. Klein R, Davis M, Magli Y, Segal P, Klein B, Hubbard L. The Wisconsin Age-Related Maculopathy Grading System. Ophthalmology. 1991;98:1128-1134. ISI | PUBMED
27. The International ARM Epidemiological Study Group. An international classification and grading system for age-related maculopathy and age-related macular degeneration. Surv Ophthalmol. 1995;39:367-374. ISI | PUBMED
28. Willett W, Sampson L, Browne M, et al. The use of a self-administered questionnaire to assess diet four years in the past. Am J Epidemiol. 1988;127:188-199. FREE FULL TEXT
29. Smith WT, Mitchell P, Reay EM, Webb K, Harvey PWJ. Validity and repeatability of a self-administered food frequency questionnaire in older people. Aust N Z J Public Health. 1998;22:456-463. ISI | PUBMED
30. Smith W, Mitchell P, Webb K, Leeder SR. Dietary antioxidants and age-related maculopathy. Ophthalmology. 1999;106:761-767. FULL TEXT | ISI | PUBMED
31. Willett W, Sampson L, Stampfer M, et al. Reproducibility and validity of a semi-quantitative food frequency questionnaire. Am J Epidemiol. 1985;122:51-65. FREE FULL TEXT
32. Meydani M. Vitamin E. Lancet. 1995;345:170-175. FULL TEXT | ISI | PUBMED
33. Diplock AT. Antioxidant nutrients and disease prevention: an overview. Am J Clin Nutr. 1991;53(suppl 1):189S-193S.
34. Young R. Pathophysiology of age-related macular degeneration. Surv Ophthalmol. 1987;31:291-306. FULL TEXT | ISI | PUBMED
35. Williams PT, Fortmann SP, Terry RB, Garay SC, Vranizan KM, Ellsworth N. Associations of dietary fat, regional adiposity and blood pressure in men. JAMA. 1987;257:3251-3256. ABSTRACT
36. Morals MC, Manson JE, Rosner B, Buring JE, Willett WC, Hennekens CH. Fish consumption and cardiovascular disease in the Physicians' Health Study: a prospective study. Am J Epidemiol. 1995;142:166-175. FREE FULL TEXT
37. Tell GS, Evans GW, Folsom AR, Shimakawa T, Carpenter MA, Heiss G. Dietary fat intake and carotid artery wall thickness: the Atherosclerosis Risk in Communities (ARIC) Study. Am J Epidemiol. 1994;139:979-989. FREE FULL TEXT
38. Kahn HA, Leibowitz HM, Ganley JP, et al. The Framingham Eye Study, II: association of ophthalmic pathology with single variables previously measured in the Framingham Heart Study. Am J Epidemiol. 1977;106:33-41. FREE FULL TEXT

RELATED ARTICLE

Archives of Ophthalmology Reader's Choice: Continuing Medical Education
Arch Ophthalmol. 2000;118(3):456.
FULL TEXT  


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Age-Related Macular Degeneration
Jager et al.
NEJM 2008;358:2606-2617.
FULL TEXT  

The Importance of the Omega-6/Omega-3 Fatty Acid Ratio in Cardiovascular Disease and Other Chronic Diseases
Simopoulos
Exp. Biol. Med. 2008;233:674-688.
ABSTRACT | FULL TEXT  

Homeostatic Regulation of Photoreceptor Cell Integrity: Significance of the Potent Mediator Neuroprotectin D1 Biosynthesized from Docosahexaenoic Acid The Proctor Lecture
Bazan
IOVS 2007;48:4866-4881.
FULL TEXT  

Eicosapentaenoic Acid Is Anti-Inflammatory in Preventing Choroidal Neovascularization in Mice
Koto et al.
IOVS 2007;48:4328-4334.
ABSTRACT | FULL TEXT  

Association Between Vitamin D and Age-Related Macular Degeneration in the Third National Health and Nutrition Examination Survey, 1988 Through 1994
Parekh et al.
Arch Ophthalmol 2007;125:661-669.
ABSTRACT | FULL TEXT  

The Relationship of Dietary Lipid Intake and Age-Related Macular Degeneration in a Case-Control Study: AREDS Report No. 20
Age-Related Eye Disease Study Research Group
Arch Ophthalmol 2007;125:671-679.
ABSTRACT | FULL TEXT  

Dietary Fatty Acids and the 5-Year Incidence of Age-Related Maculopathy
Chua et al.
Arch Ophthalmol 2006;124:981-986.
ABSTRACT | FULL TEXT  

Cigarette Smoking, Fish Consumption, Omega-3 Fatty Acid Intake, and Associations With Age-Related Macular Degeneration: The US Twin Study of Age-Related Macular Degeneration
Seddon et al.
Arch Ophthalmol 2006;124:995-1001.
ABSTRACT | FULL TEXT  

Potential role of dietary n-3 fatty acids in the prevention of dementia and macular degeneration
Johnson and Schaefer
Am. J. Clin. Nutr. 2006;83:S1494-1498S.
ABSTRACT | FULL TEXT  

Association of Adipose and Red Blood Cell Lipids With Severity of Dominant Stargardt Macular Dystrophy (STGD3) Secondary to an ELOVL4 Mutation.
Hubbard et al.
Arch Ophthalmol 2006;124:257-263.
ABSTRACT | FULL TEXT  

Prospective Study of Dietary Fat and Risk of Cataract Extraction among US Women
Lu et al.
Am J Epidemiol 2005;161:948-959.
ABSTRACT | FULL TEXT  

Nutritional Manipulation of Primate Retinas, I: Effects of Lutein or Zeaxanthin Supplements on Serum and Macular Pigment in Xanthophyll-Free Rhesus Monkeys
Neuringer et al.
IOVS 2004;45:3234-3243.
ABSTRACT | FULL TEXT  

Nutritional Manipulation of Primate Retinas, II: Effects of Age, n-3 Fatty Acids, Lutein, and Zeaxanthin on Retinal Pigment Epithelium
Leung et al.
IOVS 2004;45:3244-3256.
ABSTRACT | FULL TEXT  

Retinal vessel wall signs and the 5 year incidence of age related maculopathy: the Blue Mountains Eye Study
Wang et al.
Br. J. Ophthalmol. 2004;88:104-109.
ABSTRACT | FULL TEXT  

Progression of Age-Related Macular Degeneration: Association With Dietary Fat, Transunsaturated Fat, Nuts, and Fish Intake
Seddon et al.
Arch Ophthalmol 2003;121:1728-1737.
ABSTRACT | FULL TEXT  

Progression of Age-Related Macular Degeneration: Association With Body Mass Index, Waist Circumference, and Waist-Hip Ratio
Seddon et al.
Arch Ophthalmol 2003;121:785-792.
ABSTRACT | FULL TEXT  

Relation of blood homocysteine and its nutritional determinants to age-related maculopathy in the third National Health and Nutrition Examination Survey
Heuberger et al.
Am. J. Clin. Nutr. 2002;76:897-902.
ABSTRACT | FULL TEXT  

Relationship of Dietary Fat to Age-Related Maculopathy in the Third National Health and Nutrition Examination Survey
Heuberger et al.
Arch Ophthalmol 2001;119:1833-1838.
ABSTRACT | FULL TEXT  

Murine High-Fat Diet and Laser Photochemical Model of Basal Deposits in Bruch Membrane
Dithmar et al.
Arch Ophthalmol 2001;119:1643-1649.
ABSTRACT | FULL TEXT  

A Novel Gene for Autosomal Dominant Stargardt-like Macular Dystrophy with Homology to the SUR4 Protein Family
Edwards et al.
IOVS 2001;42:2652-2663.
ABSTRACT | FULL TEXT  

Dietary Fat and Risk for Advanced Age-Related Macular Degeneration
Seddon et al.
Arch Ophthalmol 2001;119:1191-1199.
ABSTRACT | FULL TEXT  

Alternative eye care
ASTBURY
Br. J. Ophthalmol. 2001;85:767-768.
FULL TEXT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 2000 American Medical Association. All Rights Reserved.