Review article
Genetic susceptibility to age related macular degeneration
John R W Yatesa, Anthony T Mooreb
a Department of
Medical Genetics, University of Cambridge, Box 134, Addenbrooke's
Hospital, Cambridge CB2 2QQ, UK, b Department of Ophthalmology, Box 41, Addenbrooke's Hospital, Cambridge CB2 2QQ, UK
Correspondence to: Dr Yates
Age related macular degeneration (AMD) is the leading cause of
visual impairment in the elderly and a major cause of blindness in the
developed world. The disease can take two forms, geographic atrophy and
choroidal neovascularisation. The pathogenesis of AMD is poorly
understood. There are undoubtedly environmental and other risk factors
involved and the adverse effect of smoking is well established. Several
studies have shown that genetic factors are important but leave
uncertainty about the magnitude and nature of the genetic component and
whether it varies with the type of AMD. Several hereditary retinal
dystrophies show similarities to AMD and these genes are potential
candidate susceptibility genes. Particular interest has focused on the
ABCR gene which is responsible for autosomal
recessive Stargardt macular dystrophy. It has been claimed that
heterozygotes for ABCR mutations are predisposed to AMD but the data are conflicting. Studies of the genes
responsible for autosomal dominant Sorsby fundus dystrophy, Doyne
honeycomb retinal dystrophy, and Best disease have given negative
results. In one large AMD family, linkage has been reported to markers
in 1q25-q31. Recent data suggest that the ApoE
4 allele may be
associated with reduced risk of AMD. A better understanding of the
genetic factors in AMD would contribute to understanding the
pathogenesis. If those at risk could be identified it may be possible
to modify lifestyle or develop novel therapies in the presymptomatic
stage to prevent disease or decrease its severity.
Keywords: age related macular degeneration; genetic susceptibility
© 2000 by J Med Genet
This article has been cited by other articles:
-
Kim, N. R., Kang, J. H., Kwon, O. W., Lee, S. J., Oh, J. H., Chin, H. S.
(2008). Association between Complement Factor H Gene Polymorphisms and Neovascular Age-Related Macular Degeneration in Koreans. IOVS
49: 2071-2076
[Abstract] [Full Text] -
Jones, M. M., Manwaring, N., Wang, J. J., Rochtchina, E., Mitchell, P., Sue, C. M.
(2007). Mitochondrial DNA Haplogroups and Age-Related Maculopathy. Arch Ophthalmol
125: 1235-1240
[Abstract] [Full Text] -
Bora, N. S., Kaliappan, S., Jha, P., Xu, Q., Sivasankar, B., Harris, C. L., Morgan, B. P., Bora, P. S.
(2007). CD59, a Complement Regulatory Protein, Controls Choroidal Neovascularization in a Mouse Model of Wet-Type Age-Related Macular Degeneration. J. Immunol.
178: 1783-1790
[Abstract] [Full Text] -
Thakkinstian, A., Bowe, S., McEvoy, M., Smith, W., Attia, J.
(2006). Association between Apolipoprotein E Polymorphisms and Age-related Macular Degeneration: A HuGE Review and Meta-Analysis. Am J Epidemiol
164: 813-822
[Abstract] [Full Text] -
Thakkinstian, A., Han, P., McEvoy, M., Smith, W., Hoh, J., Magnusson, K., Zhang, K., Attia, J.
(2006). Systematic review and meta-analysis of the association between complementary factor H Y402H polymorphisms and age-related macular degeneration. Hum Mol Genet
15: 2784-2790
[Abstract] [Full Text] -
Bora, N. S., Kaliappan, S., Jha, P., Xu, Q., Sohn, J.-H., Dhaulakhandi, D. B., Kaplan, H. J., Bora, P. S.
(2006). Complement Activation via Alternative Pathway Is Critical in the Development of Laser-Induced Choroidal Neovascularization: Role of Factor B and Factor H. J. Immunol.
177: 1872-1878
[Abstract] [Full Text] -
Sepp, T., Khan, J. C., Thurlby, D. A., Shahid, H., Clayton, D. G., Moore, A. T., Bird, A. C., Yates, J. R. W., the Genetic Factors in AMD Study Group,
(2006). Complement Factor H Variant Y402H Is a Major Risk Determinant for Geographic Atrophy and Choroidal Neovascularization in Smokers and Nonsmokers. IOVS
47: 536-540
[Abstract] [Full Text] -
Bora, P. S., Sohn, J.-H., Cruz, J. M. C., Jha, P., Nishihori, H., Wang, Y., Kaliappan, S., Kaplan, H. J., Bora, N. S.
(2005). Role of Complement and Complement Membrane Attack Complex in Laser-Induced Choroidal Neovascularization. J. Immunol.
174: 491-497
[Abstract] [Full Text] -
Zarbin, M. A.
(2004). Current Concepts in the Pathogenesis of Age-Related Macular Degeneration. Arch Ophthalmol
122: 598-614
[Abstract] [Full Text] -
Ida, H., Boylan, S. A., Weigel, A. L., Hjelmeland, L. M.
(2003). Age-related changes in the transcriptional profile of mouse RPE/choroid. Physiol. Genomics
15: 258-262
[Abstract] [Full Text] -
Espinosa-Heidmann, D. G., Suner, I. J., Hernandez, E. P., Monroy, D., Csaky, K. G., Cousins, S. W.
(2003). Macrophage Depletion Diminishes Lesion Size and Severity in Experimental Choroidal Neovascularization. IOVS
44: 3586-3592
[Abstract] [Full Text] -
Owen, C G, Fletcher, A E, Donoghue, M, Rudnicka, A R
(2003). How big is the burden of visual loss caused by age related macular degeneration in the United Kingdom?. Br J Ophthalmol
87: 312-317
[Abstract] [Full Text] -
Rakoczy, P. E., Zhang, D., Robertson, T., Barnett, N. L., Papadimitriou, J., Constable, I. J., Lai, C.-M.
(2002). Progressive Age-Related Changes Similar to Age-Related Macular Degeneration in a Transgenic Mouse Model. Am. J. Pathol.
161: 1515-1524
[Abstract] [Full Text] -
Finnemann, S. C., Leung, L. W., Rodriguez-Boulan, E.
(2002). The lipofuscin component A2E selectively inhibits phagolysosomal degradation of photoreceptor phospholipid by the retinal pigment epithelium. Proc. Natl. Acad. Sci. USA
99: 3842-3847
[Abstract] [Full Text] -
Stone, E. M., Sheffield, V. C., Hageman, G. S.
(2001). Molecular genetics of age-related macular degeneration. Hum Mol Genet
10: 2285-2292
[Abstract] [Full Text] -
Sauer, C. G, White, K., Stohr, H., Grimm, T., Hutchinson, A., Bernstein, P. S, Lewis, R. A., Simonelli, F., Pauleikhoff, D., Allikmets, R., Weber, B. H F
(2001). Evaluation of the G protein coupled receptor-75 (GPR75) in age related macular degeneration. Br J Ophthalmol
85: 969-975
[Abstract] [Full Text]
Register for free content
The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.
Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.
