Racial and Socioeconomic Variation in Genetic Markers of Telomere Length: A Cross-Sectional Study of U.S. Older Adults

被引:24
|
作者
Hamad, Rita [1 ]
Tuljapurkar, Shripad [2 ]
Rehkopf, David H. [1 ]
机构
[1] Stanford Univ, Dept Med, 1070 Arastradero Rd, Palo Alto, CA 94304 USA
[2] Stanford Univ, Dept Biol, Herrin Labs 454, Stanford, CA 94305 USA
来源
EBIOMEDICINE | 2016年 / 11卷
关键词
Telomere; Telomere length; Race; Socioeconomic position; Single nucleotide polymorphism; Polygenic risk score; GENOME-WIDE ASSOCIATION; HEALTH; POPULATION; DISEASE; BIOLOGY; STRESS; LONGER; WHITES; RACE; US;
D O I
10.1016/j.ebiom.2016.08.015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Shorter telomere length (TL) has been associated with stress and adverse socioeconomic conditions, yet U.S. blacks have longer TL than whites. The role of genetic versus environmental factors in explaining TL by race and socioeconomic position (SEP) remains unclear. Methods: We used data from the U.S. Health and Retirement Study (N = 11,934) to test the hypothesis that there are differences in TL-associated SNPs by race and SEP. We constructed a TL polygenic risk score (PRS) and examined its association with race/ethnicity, educational attainment, assets, gender, and age. Results: U.S. blacks were more likely to have a lower PRS for TL, as were older individuals and men. Racial differences in TL were statistically accounted for when controlling for population structure using genetic principal components. The GWAS-derived SNPs for TL, however, may not have consistent associations with TL across different racial/ethnic groups. Conclusions: This study showed that associations of race/ethnicity with TL differed when accounting for population stratification. The role of race/ethnicity for TL remains uncertain, however, as the genetic determinants of TL may differ by race/ethnicity. Future GWAS samples should include racially diverse participants to allow for better characterization of the determinants of TL in human populations. (C) 2016 The Authors. Published by Elsevier B.V.
引用
收藏
页码:296 / 301
页数:6
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