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晚期年龄相关性黄斑变性与补体因子 H Y402H 多态性的生态相关性研究。

An ecological correlation study of late age-related macular degeneration and the complement factor H Y402H polymorphism.

机构信息

Department of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, United Kingdom.

出版信息

Invest Ophthalmol Vis Sci. 2010 May;51(5):2393-402. doi: 10.1167/iovs.09-4228. Epub 2009 Dec 30.

DOI:10.1167/iovs.09-4228
PMID:20042653
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2868481/
Abstract

PURPOSE

To investigate whether variation in the distribution of the risk allele frequency of the Y402H single-nucleotide polymorphism (SNP) across various ethnicities and geographic regions reflects differences in the prevalence of late age-related macular degeneration (AMD) in those ethnicities.

METHODS

Published data were obtained via a systematic search. Study samples were grouped into clusters by ethnicity and geographic location and the Spearman correlation coefficient of the prevalence of late AMD and risk allele frequencies was calculated across clusters.

RESULTS

Across all ethnicities, AMD prevalence was seen to increase with age. Populations of European descent had both higher risk allele frequencies and prevalence of late AMD than did Japanese, Chinese, and Hispanic descendants. Results for African descendants were anomalous: although allele frequency was similar to that in European populations, the age-specific prevalence of late AMD was considerably lower. The correlation coefficient for the association between allele frequency and AMD prevalence was 0.40 (95% confidence interval [CI] = -0.36 to 0.84, P = 0.28) in all populations combined and 0.71 (95% CI = 0.02-0.94, P = 0.04) when people of African descent were excluded.

CONCLUSIONS

Evidence was found at the population level to support a positive association between the Y204H risk allele and the prevalence of AMD after exclusion of studies undertaken on persons of African ancestry. Data in African, Middle Eastern, and South American populations are needed to provide a better understanding of the association of late AMD genetic risk across ethnicities.

摘要

目的

探究 Y402H 单核苷酸多态性(SNP)风险等位基因频率在不同种族和地理区域的分布差异是否反映了这些种族中晚期年龄相关性黄斑变性(AMD)的流行率存在差异。

方法

通过系统检索获取已发表的数据。根据种族和地理位置将研究样本分为聚类,计算跨聚类的晚期 AMD 患病率和风险等位基因频率的斯皮尔曼相关系数。

结果

在所有种族中,AMD 的患病率均随年龄增长而增加。欧洲裔人群的风险等位基因频率和晚期 AMD 的患病率均高于日本、中国和西班牙裔后裔。非洲裔后裔的结果则异常:尽管等位基因频率与欧洲人群相似,但晚期 AMD 的年龄特异性患病率明显较低。将等位基因频率与 AMD 患病率之间的关联进行合并分析的相关系数为 0.40(95%置信区间[CI]为-0.36 至 0.84,P=0.28),当排除非洲裔人群的研究后,该相关系数为 0.71(95% CI=0.02-0.94,P=0.04)。

结论

在排除了针对非洲裔人群的研究后,在人群水平上发现了 Y204H 风险等位基因与 AMD 患病率之间存在正相关的证据。需要来自非洲、中东和南美洲人群的数据,以更好地了解不同种族中晚期 AMD 遗传风险的关联。

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