Department of Genetics, Southwest Foundation for Biomedical Research, San Antonio, Texas, USA.
Invest Ophthalmol Vis Sci. 2010 Jul;51(7):3509-14. doi: 10.1167/iovs.09-4786. Epub 2010 Mar 17.
PURPOSE. Primary open-angle glaucoma (POAG) is a complex disease with a genetic architecture that can be simplified through the investigation of individual traits underlying disease risk. It has been well studied in twin models, and this study was undertaken to investigate the heritability of some of these key endophenotypes in extended pedigrees. METHODS. These data are derived from a large, multicenter study of extended, Caucasian POAG families from Australia and the United States. The study included 1181 people from 22 extended pedigrees. Variance components modeling was used to determine the heritabilities of maximum intraocular pressure (IOP), maximum vertical cup-to-disc ratio (VCDR), and mean central corneal thickness (CCT). Bivariate quantitative genetic analysis between these eye-related phenotypes and POAG itself was performed to determine whether any of these traits represent true endophenotypes. RESULTS. Heritability estimates for IOP, VCDR, and CCT (0.42, 0.66, and 0.72, respectively) were significant and show strong concordance with data in previous studies. Bivariate analysis revealed that both IOP (RhoG = 0.80; P = 9.6 x 10(-6)) and VCDR (RhoG = 0.76; P = 4.8 x 10(-10)) showed strong evidence of genetic correlation with POAG susceptibility. These two traits also correlated genetically with each other (RhoG = 0.45; P = 0.0012). Alternatively, CCT did not correlate genetically with risk of POAG. CONCLUSIONS. All the proposed POAG-related traits have genetic components. However, the significant genetic correlations observed between IOP, VCDR, and POAG itself suggest that they most likely represent true endophenotypes that could aid in the identification of genes underlying POAG susceptibility. CCT did not correlate genetically with disease and is unlikely to be a useful surrogate endophenotype for POAG.
目的。原发性开角型青光眼(POAG)是一种复杂的疾病,其遗传结构可以通过研究疾病风险相关的个体特征来简化。在双胞胎模型中对此已有深入研究,本研究旨在调查这些关键表型在扩展家系中的遗传力。
方法。这些数据来自于澳大利亚和美国的一个大型、多中心的扩展白种人 POAG 家族研究。该研究包括来自 22 个扩展家系的 1181 人。方差成分建模用于确定最大眼内压(IOP)、最大垂直杯盘比(VCDR)和平均中央角膜厚度(CCT)的遗传力。对这些眼部相关表型与 POAG 本身之间的双变量定量遗传分析,以确定这些特征是否代表真正的内表型。
结果。IOP、VCDR 和 CCT 的遗传力估计值分别为 0.42、0.66 和 0.72,均具有统计学意义,与先前研究的数据高度一致。双变量分析显示,IOP(RhoG = 0.80;P = 9.6 x 10(-6))和 VCDR(RhoG = 0.76;P = 4.8 x 10(-10))均与 POAG 易感性具有强烈的遗传相关性。这两个特征彼此之间也存在遗传相关性(RhoG = 0.45;P = 0.0012)。相反,CCT 与 POAG 风险无遗传相关性。
结论。所有提出的与 POAG 相关的特征都具有遗传成分。然而,IOP、VCDR 与 POAG 本身之间观察到的显著遗传相关性表明,它们很可能代表真正的内表型,可以帮助识别 POAG 易感性相关的基因。CCT 与疾病无遗传相关性,不太可能成为 POAG 的有用替代内表型。