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青光眼及其相关表型的遗传力:系统评价和荟萃分析。

Heritability of glaucoma and glaucoma-related endophenotypes: Systematic review and meta-analysis.

机构信息

Department of Epidemiology, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.

Department of Ophthalmology, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.

出版信息

Surv Ophthalmol. 2019 Nov-Dec;64(6):835-851. doi: 10.1016/j.survophthal.2019.06.002. Epub 2019 Jun 21.

Abstract

We have systematically extracted all available heritability (h) estimates of glaucoma and related endophenotypes from the literature and summarized the evidence by meta-analysis. Glaucoma endophenotypes were classified into 10 clusters: intraocular pressure, anterior chamber size, central corneal thickness, cup-to-disc ratio, disc size, cup size, corneal hysteresis, retinal nerve fiber layer thickness, cup shape, and peripapillary atrophy. Random-effects meta-analyses were performed for each cluster. For clusters with n ≥ 10 h estimates, we also performed subgroup and meta-regression analyses. The literature search yielded 53 studies. The h of primary open-angle glaucoma ranged from 0.17 to 0.81, and was 0.65 for primary angle-closure glaucoma in a single study. The pooled endophenotype h estimates were intraocular pressure, 0.43 (0.38-0.48); anterior chamber size, 0.67 (0.60-0.74); central corneal thickness, 0.81 (0.73-0.87); cup-to-disc ratio, 0.56 (0.44-0.68); disc size, 0.61 (0.37-0.81); cup size, 0.58 (0.35-0.78); corneal hysteresis, 0.40 (0.29-0.51); retinal nerve fiber layer thickness, 0.73 (0.42-0.91); cup shape, 0.62 (0.22-0.90); and peripapillary atrophy, 0.73 (0.70-0.75). We identified mean age, ethnicity, and study design as major sources of heterogeneity. Our results confirm the strong influence of genetic factors on glaucoma and its endophenotypes. These pooled h estimates provide the most accurate assessment to date of the total genetic variation that can ultimately be explained by gene-finding studies.

摘要

我们系统地从文献中提取了所有可用的青光眼及其相关表型的遗传力(h)估计值,并通过荟萃分析总结了证据。青光眼表型分为 10 个聚类:眼内压、前房大小、中央角膜厚度、杯盘比、视盘大小、杯盘比、角膜滞后、视网膜神经纤维层厚度、杯形和视盘周围萎缩。对每个聚类进行了随机效应荟萃分析。对于 n≥10 个 h 估计值的聚类,我们还进行了亚组和荟萃回归分析。文献检索得到了 53 项研究。原发性开角型青光眼的 h 值范围为 0.17 至 0.81,在一项单独的研究中,原发性闭角型青光眼的 h 值为 0.65。汇总的表型遗传力估计值为眼内压,0.43(0.38-0.48);前房大小,0.67(0.60-0.74);中央角膜厚度,0.81(0.73-0.87);杯盘比,0.56(0.44-0.68);视盘大小,0.61(0.37-0.81);杯盘比,0.58(0.35-0.78);角膜滞后,0.40(0.29-0.51);视网膜神经纤维层厚度,0.73(0.42-0.91);杯形,0.62(0.22-0.90);和视盘周围萎缩,0.73(0.70-0.75)。我们确定平均年龄、种族和研究设计是异质性的主要来源。我们的结果证实了遗传因素对青光眼及其表型的强烈影响。这些汇总的 h 估计值提供了迄今为止对基因发现研究最终可以解释的总遗传变异的最准确评估。

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