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美国健康与退休研究中认知能力加速衰退的遗传易感性。

Genetic susceptibility to accelerated cognitive decline in the US Health and Retirement Study.

作者信息

Zhang Chenan, Pierce Brandon L

机构信息

Department of Health Studies, University of Chicago, Chicago, IL, USA.

Department of Health Studies, University of Chicago, Chicago, IL, USA; University of Chicago Comprehensive Cancer Center, Chicago, IL, USA.

出版信息

Neurobiol Aging. 2014 Jun;35(6):1512.e11-8. doi: 10.1016/j.neurobiolaging.2013.12.021. Epub 2013 Dec 26.

Abstract

Age-related cognitive decline is a major public health concern facing a large segment of the US population. To identify genetic risk factors related to cognitive decline, we used nationally representative longitudinal data from the US Health and Retirement Study to conduct genome-wide association studies with 5765 participants of European ancestry, and 890 participants of African ancestry. Mixed effects models were used to derive cognitive decline phenotypes from data on repeated cognitive assessments and to perform single nucleotide polymorphism-based heritability estimation. We found 2 independent associations among European-Americans in the 19q13.32 region: rs769449 (APOE intron; p = 3.1 × 10(-20)) and rs115881343 (TOMM40 intron; p = 6.6 × 10(-11)). rs769449 was also associated with cognitive decline among African-Americans (p = 0.005), but rs115881343 was not. Cross-sectional cognitive function showed moderate heritability (15%-32%) across several age strata (50-59, 60-69, 70-79 years), but the cognitive decline heritability estimate was low (∼5%). These results indicate that despite multiple association signals for cognitive decline in the 19q13.32 region, inter-individual variation is likely influenced substantially by environmental factors.

摘要

与年龄相关的认知衰退是美国很大一部分人口面临的主要公共卫生问题。为了确定与认知衰退相关的遗传风险因素,我们使用了来自美国健康与退休研究的具有全国代表性的纵向数据,对5765名欧洲血统参与者和890名非洲血统参与者进行全基因组关联研究。混合效应模型用于从重复认知评估数据中得出认知衰退表型,并进行基于单核苷酸多态性的遗传力估计。我们在欧洲裔美国人的19q13.32区域发现了2个独立关联:rs769449(APOE内含子;p = 3.1×10⁻²⁰)和rs115881343(TOMM40内含子;p = 6.6×10⁻¹¹)。rs769449在非裔美国人中也与认知衰退相关(p = 0.005),但rs115881343并非如此。横断面认知功能在几个年龄层(50 - 59岁、60 - 69岁、70 - 79岁)显示出中等遗传力(15% - 32%),但认知衰退遗传力估计值较低(约5%)。这些结果表明,尽管在19q13.32区域有多个与认知衰退相关的关联信号,但个体间差异可能很大程度上受环境因素影响。

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