Department of Ophthalmology, Baylor College of Medicine, Houston, TX, USA.
Adv Exp Med Biol. 2023;1415:61-66. doi: 10.1007/978-3-031-27681-1_10.
Age-related macular degeneration (AMD) is a major cause of irreversible vision loss in the elderly. It is a complex multifactorial disease that is caused by the cumulative impact of genetic predisposition, environmental stress, and advanced aging. Knowledge of genetic risk factors underlying AMD susceptibility has advanced rapidly in the past decade that can be largely credited to genome-wide association studies (GWAS) and next-generation sequencing (NGS) efforts. GWAS have identified 34 genetic risk loci for AMD; the majority of which are in the noncoding genome. Several lines of evidence suggest that a complex trait-associated variant is likely to regulate the gene expression (acting as expression quantitative trait loci (eQTLs)), and there is a significant enrichment of GWAS-associated variants within eQTLs. In the last two years, eQTL studies in AMD-relevant tissues have provided functional interpretation of several AMD-GWAS loci. This review highlights the knowledge gained to date and discusses future directions to bridge the gap between genetic predisposition and biological mechanisms to reap the full benefits of GWAS findings.
年龄相关性黄斑变性(AMD)是老年人不可逆视力丧失的主要原因。它是一种复杂的多因素疾病,由遗传易感性、环境压力和衰老的累积影响引起。在过去的十年中,AMD 易感性的遗传风险因素的知识取得了快速进展,可以主要归功于全基因组关联研究(GWAS)和下一代测序(NGS)的努力。GWAS 已经确定了 34 个 AMD 的遗传风险位点;其中大多数位于非编码基因组中。有几条证据表明,与复杂性状相关的变异可能调节基因表达(作为表达数量性状基因座(eQTLs)),并且 GWAS 相关变异在 eQTLs 中显著富集。在过去的两年中,AMD 相关组织中的 eQTL 研究为几个 AMD-GWAS 位点提供了功能解释。这篇综述强调了迄今为止所获得的知识,并讨论了未来的方向,以缩小遗传易感性和生物学机制之间的差距,充分利用 GWAS 发现的成果。