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Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process

机译:对全基因组关联研究的荟萃分析确定了影响拔罐和青光眼过程的新基因座

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Glaucoma is characterized by irreversible optic nerve degeneration and is the most frequent cause of irreversible blindness worldwide. Here, the International Glaucoma Genetics Consortium conducts a meta-analysis of genome-wide association studies of vertical cup-disc ratio (VCDR), an important disease-related optic nerve parameter. In 21,094 individuals of European ancestry and 6,784 individuals of Asian ancestry, we identify 10 new loci associated with variation in VCDR. In a separate risk-score analysis of five case-control studies, Caucasians in the highest quintile have a 2.5-fold increased risk of primary open-angle glaucoma as compared with those in the lowest quintile. This study has more than doubled the known loci associated with optic disc cupping and will allow greater understanding of mechanisms involved in this common blinding condition.
机译:青光眼的特征是不可逆性视神经变性,是全世界不可逆性失明的最常见原因。在这里,国际青光眼遗传学协会对垂直杯碟比(VCDR)(一种与疾病相关的重要视神经参数)进行全基因组关联研究的荟萃分析。在21,094个欧洲血统的个体和6,784个亚洲血统的个体中,我们确定了10个与VCDR变异相关的新基因座。在对五项病例对照研究的单独风险评分分析中,处于最高五分位数的白种人与处于最低五分位数的白种人相比,其原发性开角型青光眼的风险增加了2.5倍。这项研究使与视盘拔罐相关的已知基因座增加了一倍以上,并将使人们更加了解这种常见的致盲条件所涉及的机制。

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