Genome-wide association studies: applications and insights gained in Ophthalmology

被引:13
|
作者
Chandra, A. [1 ,2 ]
Mitry, D. [1 ,3 ]
Wright, A. [4 ]
Campbell, H. [3 ]
Charteris, D. G. [1 ]
机构
[1] Moorfields Eye Hosp, Dept Ophthalmol, London EC1V 2PD, England
[2] UCL Inst Ophthalmol, London, England
[3] Univ Edinburgh, Ctr Populat Hlth Sci, Edinburgh, Midlothian, Scotland
[4] Western Gen Hosp, Human Genet Unit, MRC, Edinburgh EH4 2XU, Midlothian, Scotland
关键词
OPEN-ANGLE GLAUCOMA; COMPLEMENT FACTOR-H; NORMAL-TENSION GLAUCOMA; FACTOR HGF GENE; COMPONENT; C2; FACTOR-B BF; MACULAR DEGENERATION; SUSCEPTIBILITY LOCI; PSEUDOEXFOLIATION SYNDROME; EXFOLIATION SYNDROME;
D O I
10.1038/eye.2014.145
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Genome-wide association studies (GWAS) use high-throughput genotyping technologies to genotype thousands of single-nucleotide polymorphisms (SNPs) and relate them to the development of clinical and quantitative traits. Their use has been highly successful in the field of ophthalmology, and since the advent of GWAS in 2005, many genes not previously suspected of having a role in disease have been identified and the findings replicated. We conducted an extensive literature review and describe the concept, design, advantages, and limitations of GWAS and provide a detailed description of the applications and discoveries of GWAS in the field of eye disease to date. There have been many novel findings revealing previously unknown biological insights in a diverse range of common ocular conditions. GWAS have been a highly successful modality for investigating the pathogenesis of a wide variety of ophthalmic conditions. The insights gained into the pathogenesis of disease provide not only a better understanding of underlying disease mechanism but also offer a rationale for targeted treatment and preventative strategies. Expansive international collaboration and standardised phenotyping will permit the continued success of this investigative technique.
引用
收藏
页码:1066 / 1079
页数:14
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