圆锥角膜的遗传学研究进展。

Joshua Wheeler, Michael A Hauser, Natalie A Afshari, R Rand Allingham, Yutao Liu
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引用次数: 72

摘要

圆锥角膜是最常见的角膜膨胀性疾病。遗传和环境因素可能导致其发病。本文就圆锥角膜复杂遗传学的研究现状作一综述。我们讨论了遗传病因学的证据,包括基于家庭的连锁研究、双胞胎研究、基因突变和全基因组关联研究。可能涉及的基因包括VSX1、miR-184、DOCK9、SOD1、RAB3GAP1和HGF。除了编码突变,我们还强调了DNA拷贝数变异在圆锥角膜发病机制中的潜在贡献。最后,对圆锥角膜复杂遗传学的认识及其临床意义提出了今后的遗传学研究方向。随着新的功能性候选圆锥角膜基因的快速发现,圆锥角膜发病机制的分子遗传机制将促进我们对圆锥角膜的认识,并促进新的治疗方法的发展。
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The Genetics of Keratoconus: A Review.

Keratoconus is the most common ectatic disorder of the corneal. Genetic and environmental factors may contribute to its pathogenesis. The focus of this article is to summarize current research into the complex genetics of keratoconus. We discuss the evidence of genetic etiology including family-based linkage studies, twin studies, genetic mutations, and genome-wide association studies. The genes implicated potentially include VSX1, miR-184, DOCK9, SOD1, RAB3GAP1, and HGF. Besides the coding mutations, we also highlight the potential contribution of DNA copy number variants in the pathogenesis of keratoconus. Finally, we present future directions for genetic research in the understanding of the complex genetics of keratoconus and its clinical significance. As new functional, candidate genes for keratoconus are being discovered at a rapid pace, the molecular genetic mechanisms underlying keratoconus pathogenesis will advance our understanding of keratoconus and promote the development of a novel therapy.

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