Prognostic value of leukocyte telomere length in patients with stable coronary artery disease - Data from the heart and soul study

被引:158
作者
Farzaneh-Far, Ramin [1 ]
Cawthon, Richard M. [2 ]
Na, Beeya [3 ]
Browner, Warren S. [4 ]
Schiller, Nelson B. [1 ,3 ]
Whooley, Mary A. [1 ,3 ]
机构
[1] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[2] Univ Utah, Eccles Inst Human Genet, Salt Lake City, UT USA
[3] Vet Affairs Med Ctr, San Francisco, CA 94121 USA
[4] Calif Pacific Med Ctr, Res Inst, San Francisco, CA USA
关键词
telomere; aging; leukocyte; prognosis; coronary;
D O I
10.1161/ATVBAHA.108.167049
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-Telomere shortening has been proposed as a marker of biological aging. Whether leukocyte telomere length is associated with mortality among patients with stable coronary artery disease (CAD) is unknown. Methods and Results-We measured leukocyte telomere length in 780 patients with stable CAD in a prospective cohort study. Participants were categorized by quartiles of telomere length. Hazard Ratios (HRs) and 95% confidence intervals were calculated for all-cause mortality, heart failure (HF) hospitalization, and cardiovascular (CV) events. After 4.4 years of follow-up there were 166 deaths. Compared with participants in the highest telomere length quartile, those in the lowest quartile were at increased risk of death (age-adjusted HR 1.8; 95% CI 1.2 to 2.9). After multivariate adjustment for clinical (HR 2.1; CI 1.3 to 3.3), inflammatory (HR 2.0; CI 1.2 to 3.2), and echocardiographic (HR 1.9; CI 1.0 to 3.5) risk factors, patients in the lowest quartile of telomere length remained at significantly increased risk of death compared to those in the highest quartile. Patients in the lowest quartile of telomere length were also at significantly increased risk of HF hospitalization (HR 2.6; CI 1.1 to 6.0) but not CV events (HR 1.7; CI 0.9 to 3.5). Conclusions-Reduced leukocyte telomere length is associated with all-cause mortality in patients with stable CAD. The prognostic value of short telomeres in predicting death is not completely captured by existing clinical, inflammatory, and echocardiographic markers of risk.
引用
收藏
页码:1379 / 1384
页数:6
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