Accelerated epigenetic aging as a risk factor for chronic obstructive pulmonary disease and decreased lung function in two prospective cohort studies

被引:19
作者
Breen, Miyuki [1 ]
Nwanaji-Enwerem, Jamaji C. [2 ,3 ,4 ]
Karrasch, Stefan [5 ,6 ,7 ,8 ]
Flexeder, Claudia [6 ]
Schulz, Holger [6 ,7 ,8 ]
Waldenberger, Melanie [9 ]
Kunze, Sonja [9 ]
Ollert, Markus [10 ,11 ,12 ]
Weidinger, Stefan [13 ]
Colicino, Elena [14 ]
Gao, Xu [15 ]
Wang, Cuicui [2 ]
Shen, Jincheng [16 ]
Just, Allan C. [14 ]
Vokonas, Pantel [17 ]
Sparrow, David [17 ]
Hou, Lifang [18 ]
Schwartz, Joel D. [2 ]
Baccarelli, Andrea A. [15 ]
Peters, Annette [6 ]
Ward-Caviness, Cavin K. [19 ]
机构
[1] US EPA, Oak Ridge Inst Sci & Educ ORISE, Ctr Publ Hlth & Environm Assessment, Chapel Hill, NC 27709 USA
[2] Harvard TH Chan Sch Publ Hlth, Dept Environm Hlth, Boston, MA 02115 USA
[3] Harvard Med Sch, MD PhD Program, Boston, MA 02115 USA
[4] Harvard Kennedy Sch Govt, Belfer Ctr Sci & Int Affairs, Cambridge, MA 02138 USA
[5] Ludwig Maximilians Univ Munchen, Univ Hosp Munich, Inst & Outpatient Clin Occupat Social & Environm, Inner Clin, Munich, Germany
[6] Helmholtz Zentrum Munchen, Inst Epidemiol, Neuherberg, Germany
[7] Comprehens Pneumol Ctr Munich CPC M, Neuherberg, Germany
[8] German Ctr Lung Res DZL, Neuherberg, Germany
[9] Helmholtz Zentrum Munchen, Res Unit Mol Epidemiol, Neuherberg, Germany
[10] Luxembourg Inst Hlth, Dept Infect & Immun, Esch Sur Alzette, Luxembourg
[11] Univ Southern Denmark, Odense Res Ctr Anaphylaxis, Dept Dermatol, Odense, Denmark
[12] Univ Southern Denmark, Allergy Ctr, Odense, Denmark
[13] Univ Kiel, Dept Genet Dermatol, Kiel, Germany
[14] Icahn Sch Med Mt Sinai, Dept Environm Med & Publ Hlth, New York, NY 10029 USA
[15] Columbia Univ, Mailman Sch Publ Hlth, Dept Environm Hlth Sci, New York, NY 10032 USA
[16] Univ Utah, Sch Med, Dept Populat Hlth Sci, Salt Lake City, UT 84132 USA
[17] Boston Univ, Sch Med, Vet Affairs Normat Aging Study, Vet Affairs Boston Healthcare Syst,Dept Med, Boston, MA 02118 USA
[18] Northwestern Univ, Feinberg Sch Med, Dept Prevent Med, Chicago, IL 60611 USA
[19] US EPA, Ctr Publ Hlth & Environm Assessment, Chapel Hill, NC 27709 USA
来源
AGING-US | 2020年 / 12卷 / 16期
关键词
DNA methylation age; COPD; lung function; accelerated aging; TELOMERE LENGTH; INFLAMMATION; STANDARDIZATION; ASTHMA; AGE;
D O I
10.18632/aging.103784
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Chronic obstructive pulmonary disease (COPD) is a frequent diagnosis in older individuals and contributor to global morbidity and mortality. Given the link between lung disease and aging, we need to understand how molecular indicators of aging relate to lung function and disease. Using data from the population-based KORA (Cooperative Health Research in the Region of Augsburg) surveys, we associated baseline epigenetic (DNA methylation) age acceleration with incident COPD and lung function. Models were adjusted for age, sex, smoking, height, weight, and baseline lung disease as appropriate. Associations were replicated in the Normative Aging Study. Of 770 KORA participants, 131 developed incident COPD over 7 years. Baseline accelerated epigenetic aging was significantly associated with incident COPD. The change in age acceleration (follow-up - baseline) was more strongly associated with COPD than baseline aging alone. The association between the change in age acceleration between baseline and follow-up and incident COPD replicated in the Normative Aging Study. Associations with spirometric lung function parameters were weaker than those with COPD, but a meta-analysis of both cohorts provide suggestive evidence of associations. Accelerated epigenetic aging, both baseline measures and changes over time, may be a risk factor for COPD and reduced lung function.
引用
收藏
页码:16539 / 16554
页数:16
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