Low Social Support Is Associated With Shorter Leukocyte Telomere Length in Late Life: Multi-Ethnic Study of Atherosclerosis

被引:72
作者
Carroll, Judith E. [2 ]
Roux, Ana V. Diez [3 ]
Fitzpatrick, Annette L. [4 ]
Seeman, Teresa [1 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Div Geriatr, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Semel Inst Neurosci & Human Behav, Cousins Ctr Psychoneuroimmunol, Los Angeles, CA 90095 USA
[3] Univ Michigan, Dept Epidemiol, Ctr Integrat Approaches Hlth Dispar, Ann Arbor, MI 48109 USA
[4] Univ Washington, Sch Publ Hlth, Dept Epidemiol, Seattle, WA 98195 USA
来源
PSYCHOSOMATIC MEDICINE | 2013年 / 75卷 / 02期
关键词
telomere length; social support; cellular aging; loneliness; isolation; older adults; CARDIOVASCULAR-DISEASE; CHRONIC STRESS; OXIDATIVE STRESS; SENESCENCE; MECHANISMS; HEALTH; LONELINESS; DYNAMICS; ADULTS; CELLS;
D O I
10.1097/PSY.0b013e31828233bf
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: The primary goal was to test the hypothesis that limited social support (SS) is related to shorter leukocyte telomere length (LTL), particularly in an older adult population. Methods: Cross-sectional analyses were performed on 948 participants aged 45 to 84 years at Examination 1 of the Multi-Ethnic Study of Atherosclerosis (18.4% white, 53.1% Hispanics, and 28.5% African American). LTL was determined by using quantitative polymerase chain reaction, and SS was measured with the Enhancing Recovery in Coronary Heart Disease SS inventory. Results: Across the entire sample, SS was not associated with LTL (p = .87) after adjusting for demographic (age, sex, race/ethnicity, socioeconomic status), age x sex, age x race, health (body mass index, diabetes, pulse pressure), and life-style factors (smoking, physical activity, diet); however, the interaction term age (dichotomized) x SS was significant (p = .001). Stratification by age group revealed a positive association between SS (score range, 5-25) and LTL in the older (65-84 years; B[SE] = .005[.002]; p = .007) but not younger participants (45-64 years; p = .12) after adjusting for covariates. Conclusions: These results from a racially/ethnically diverse community sample of men and women provide initial evidence that low SS is associated with shorter LTL in adults aged 65 years and older and is consistent with the hypothesis that social environment may contribute to rates of cellular aging, particularly in late life.
引用
收藏
页码:171 / 177
页数:7
相关论文
共 74 条
[1]  
[Anonymous], FALLS OLD AD OV
[2]   Telomeres and aging [J].
Aubert, Geraldine ;
Lansdorp, Peter M. .
PHYSIOLOGICAL REVIEWS, 2008, 88 (02) :557-579
[3]   Genetics of leukocyte telomere length and its role in atherosclerosis [J].
Aviv, Abraham .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2012, 730 (1-2) :68-74
[4]   Leukocyte telomere length: the telomere tale continues [J].
Aviv, Abraham .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2009, 89 (06) :1721-1722
[5]   Leukocyte Telomere Dynamics: Longitudinal Findings Among Young Adults in the Bogalusa Heart Study [J].
Aviv, Abraham ;
Chen, Wei ;
Gardner, Jeffrey P. ;
Kimura, Masayuki ;
Brimacombe, Michael ;
Cao, Xiaojian ;
Srinivasan, Sathanur R. ;
Berenson, Gerald S. .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2009, 169 (03) :323-329
[6]   Multi-ethnic study of atherosclerosis: Objectives and design [J].
Bild, DE ;
Bluemke, DA ;
Burke, GL ;
Detrano, R ;
Roux, AVD ;
Folsom, AR ;
Greenland, P ;
Jacobs, DR ;
Kronmal, R ;
Liu, K ;
Nelson, JC ;
O'Leary, D ;
Saad, MF ;
Shea, S ;
Szklo, M ;
Tracy, RP .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2002, 156 (09) :871-881
[7]   Stress, inflammation and cardiovascular disease [J].
Black, PH ;
Garbutt, LD .
JOURNAL OF PSYCHOSOMATIC RESEARCH, 2002, 52 (01) :1-23
[8]   Telomere states and cell fates [J].
Blackburn, EH .
NATURE, 2000, 408 (6808) :53-56
[9]   Telomeres and telomerase: their mechanisms of action and the effects of altering their functions [J].
Blackburn, EH .
FEBS LETTERS, 2005, 579 (04) :859-862
[10]   Cellular senescence, ageing and disease [J].
Burton, D. G. A. .
AGE, 2009, 31 (01) :1-9