DNA methylation age of blood predicts future onset of lung cancer in the women's health initiative

被引:215
|
作者
Levine, Morgan E. [1 ,2 ]
Hosgood, H. Dean [3 ]
Chen, Brian [4 ]
Absher, Devin [5 ]
Assimes, Themistocles [6 ,7 ]
Horvath, Steve [1 ,8 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Human Genet, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Ctr Neurobehav Genet, Los Angeles, CA 90095 USA
[3] Albert Einstein Coll Med, Dept Epidemiol & Populat Hlth, Bronx, NY 10461 USA
[4] NIA, Longitudinal Study Sect, Translat Gerontol Branch, Intramural Res Program,NIH, Bethesda, MD 20892 USA
[5] HudsonAlpha Inst Biotechnol, Huntsville, AL 35806 USA
[6] Stanford Univ, Sch Med, Dept Med, Stanford, CA 94305 USA
[7] Stanford Univ, Sch Med, Stanford, CA 94305 USA
[8] Univ Calif Los Angeles, Sch Publ Hlth, Biostat, Los Angeles, CA 90095 USA
来源
AGING-US | 2015年 / 7卷 / 09期
基金
美国国家卫生研究院;
关键词
epigenetic clock; biological age; lung cancer; T-CELLS; SUSCEPTIBILITY LOCUS; 15Q25; RISK; IMMUNOSENESCENCE; CENTENARIANS; MORTALITY; VARIANTS;
D O I
10.18632/aging.100809
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Lung cancer is considered an age-associated disease, whose progression is in part due to accumulation of genomic instability as well as age-related decline in system integrity and function. Thus even among individuals exposed to high levels of genotoxic carcinogens, such as those found in cigarette smoke, lung cancer susceptibility may vary as a function of individual differences in the rate of biological aging. We recently developed a highly accurate candidate biomarker of aging based on DNA methylation (DNAm) levels, which may prove useful in assessing risk of aging-related diseases, such as lung cancer. Using data on 2,029 females from the Women's Health Initiative, we examined whether baseline measures of "intrinsic epigenetic age acceleration" (IEAA) predicted subsequent lung cancer incidence. We observed 43 lung cancer cases over the nearly twenty years of follow-up. Results showed that standardized measures of IEAA were significantly associated with lung cancer incidence (HR: 1.50, P= 3.4x10(-3)). Furthermore, stratified Cox proportional hazard models suggested that the association may be even stronger among older individuals (70 years or above) or those who are current smokers. Overall, our results suggest that IEAA may be a useful biomarker for evaluating lung cancer susceptibility from a biological aging perspective.
引用
收藏
页码:690 / 700
页数:11
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