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本文引用的文献

1
The genetics of central corneal thickness.中央角膜厚度的遗传学。
Br J Ophthalmol. 2010 Aug;94(8):971-6. doi: 10.1136/bjo.2009.162735. Epub 2009 Jun 24.
2
Heritability of central corneal thickness in nuclear families.核心家庭中中央角膜厚度的遗传力。
Invest Ophthalmol Vis Sci. 2009 Sep;50(9):4087-90. doi: 10.1167/iovs.08-3271. Epub 2009 May 6.
3
Distribution and heritability of intraocular pressure in chinese children: the Guangzhou twin eye study.中国儿童眼压的分布及遗传度:广州双胞胎眼研究
Invest Ophthalmol Vis Sci. 2009 May;50(5):2040-3. doi: 10.1167/iovs.08-3082. Epub 2009 Jan 17.
4
Heritability of intraocular pressure: a classical twin study.眼压的遗传力:一项经典双胞胎研究。
Br J Ophthalmol. 2008 Aug;92(8):1125-8. doi: 10.1136/bjo.2007.133272.
5
Neuropsychological endophenotype approach to genome-wide linkage analysis identifies susceptibility loci for ADHD on 2q21.1 and 13q12.11.全基因组连锁分析的神经心理学内表型方法确定了2q21.1和13q12.11上注意力缺陷多动障碍的易感基因座。
Am J Hum Genet. 2008 Jul;83(1):99-105. doi: 10.1016/j.ajhg.2008.06.006.
6
Heritability of central corneal thickness in Chinese: the Guangzhou Twin Eye Study.中国人中央角膜厚度的遗传度:广州双胞胎眼研究。
Invest Ophthalmol Vis Sci. 2008 Oct;49(10):4303-7. doi: 10.1167/iovs.08-1934. Epub 2008 May 23.
7
Heritability of optic disc and cup measured by the Heidelberg Retinal Tomography in Chinese: the Guangzhou twin eye study.利用海德堡视网膜断层扫描技术测量中国人群视盘和视杯的遗传度:广州双胞胎眼研究
Invest Ophthalmol Vis Sci. 2008 Apr;49(4):1350-5. doi: 10.1167/iovs.07-1146.
8
The heritability of optic disc parameters: a classic twin study.视盘参数的遗传度:一项经典双胞胎研究。
Invest Ophthalmol Vis Sci. 2008 Jan;49(1):77-80. doi: 10.1167/iovs.07-0962.
9
Corneal thickness measurement in the management of primary open-angle glaucoma: a report by the American Academy of Ophthalmology.原发性开角型青光眼治疗中的角膜厚度测量:美国眼科学会报告
Ophthalmology. 2007 Sep;114(9):1779-87. doi: 10.1016/j.ophtha.2007.04.068.
10
Genetic contributions to glaucoma: heritability of intraocular pressure, retinal nerve fiber layer thickness, and optic disc morphology.青光眼的遗传因素:眼压、视网膜神经纤维层厚度和视盘形态的遗传性。
Invest Ophthalmol Vis Sci. 2007 Aug;48(8):3669-76. doi: 10.1167/iovs.06-1519.

开角型青光眼基因发现之路:眼内压、杯盘比和中央角膜厚度的内表型状态。

The path to open-angle glaucoma gene discovery: endophenotypic status of intraocular pressure, cup-to-disc ratio, and central corneal thickness.

机构信息

Department of Genetics, Southwest Foundation for Biomedical Research, San Antonio, Texas, USA.

出版信息

Invest Ophthalmol Vis Sci. 2010 Jul;51(7):3509-14. doi: 10.1167/iovs.09-4786. Epub 2010 Mar 17.

DOI:10.1167/iovs.09-4786
PMID:20237253
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2904007/
Abstract

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.

摘要

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。