The association of sarcopenia, telomere length, and mortality: data from the NHANES 1999-2002

被引:23
作者
Rippberger, Peter L. [1 ]
Emeny, Rebecca T. [2 ,3 ,4 ]
Mackenzie, Todd A. [2 ,3 ,4 ]
Bartels, Stephen J. [3 ,4 ,5 ,6 ]
Batsis, John A. [3 ,4 ,5 ,6 ,7 ,8 ]
机构
[1] Univ New England, Coll Osteopath Med, Biddeford, ME USA
[2] Dartmouth, Dept Biomed Data Sci, Geisel Sch Med, Hanover, NH USA
[3] Dartmouth, Geisel Sch Med, Hanover, NH 03755 USA
[4] Dartmouth Inst Hlth Policy & Clin Practice, Lebanon, NH 03766 USA
[5] Dartmouth Coll, Dartmouth Ctr Hlth & Aging, Hanover, NH 03755 USA
[6] Dartmouth, Hlth Promot Res Ctr, Lebanon, NH 03755 USA
[7] Dartmouth Hitchcock Med Ctr, Sect Gen Internal Med, Lebanon, NH 03766 USA
[8] Dartmouth Weight & Wellness Ctr, Lebanon, NH 03766 USA
基金
美国国家卫生研究院;
关键词
NUTRITION EXAMINATION SURVEY; NATIONAL-HEALTH; OLDER-ADULTS; INFLAMMATION; STRENGTH; FRAILTY; AGE; DEFINITION; MECHANISMS; DISEASE;
D O I
10.1038/s41430-017-0011-z
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background/objectives Sarcopenia is defined as the loss of muscle mass or function with aging and is associated with adverse outcomes. Telomere shortening is associated with mortality, yet its relationship with sarcopenia is unknown. Subjects/methods Adults >= 60 years from the 1999-2002 NHANES with body composition measures were identified. Sarcopenia was defined using the two Foundation for the National Institute of Health definitions: appendicular lean mass (ALM) (men <19.75; women <15.02 kg); or ALM divided by body mass index (BMI) (ALM: BMI, men <0.789; women <0.512). Telomere length was assessed using quantitative PCR. Regression models predicted telomere length with sarcopenia (referent = no sarcopenia). Results We identified 2672 subjects. Mean age was 70.9 years (55.5% female). Prevalence of ALM and ALM: BMI sarcopenia was 29.2 and 22.1%. Deaths were higher in persons with sarcopenia as compared to those without sarcopenia (ALM: 46.4 vs. 33.4%, p < 0.001; ALM: BMI: 46.7 vs. 33.2%, p < 0.001). No adjusted differences were observed in telomere length in those with/without sarcopenia (ALM: 0.90 vs. 0.92, p = 0.74, ALM: BMI 0.89 vs. 0.92, p = 0.24). In men with ALM: BMI-defined sarcopenia, adjusted telomere length was significantly lower compared to men without sarcopenia (0.85 vs. 0.91, p = 0.013). With sarcopenia, we did not observe a significant association between telomere length and mortality (ALM: HR 1.11 [0.64,1.82], p = 0.68; ALM: BMI: HR 0.97 [0.53,1.77], p = 0.91), but noted significance in those without sarcopenia with mortality (ALM: HR 0.59 [0.40,0.86], p = 0.007; ALM: BMI: HR 0.62 [0.42,0.91]; p = 0.01). Conclusions We observed a potentially inverse relationship between telomere length and mortality in those without sarcopenia but did not observe a significant relationship between telomere length and mortality in the presence of sarcopenia.
引用
收藏
页码:255 / 263
页数:9
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