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High-Density Lipoprotein Cholesterol and All-Cause and Cause-Specific Mortality Among the Elderly

Authors :
Xiaoming Shi
Fu Rong Li
Zhi-Hao Li
Yue Bin Lv
Meng Chen Zou
Virginia B. Kraus
Xiang Gao
Jinqiu Yuan
Chen Mao
Xi Ru Zhang
Wen Fang Zhong
Xian Bo Wu
Source :
The Journal of Clinical Endocrinology & Metabolism. 104:3370-3378
Publication Year :
2019
Publisher :
The Endocrine Society, 2019.

Abstract

The patterns of the association between high-density lipoprotein cholesterol (HDL-C) concentrations and mortality among the elderly are still unclear.To examine the association of HDL-C concentrations with mortality and to identify the optimal HDL-C concentration range that predicts the lowest risk of all-cause mortality among the elderly.This was a nationwide, community-based, prospective cohort study.This study included 7766 elderly individuals (aged ≥65 years; mean age: 74.4 years) from the Health and Retirement Study. Cox proportional hazards models and Cox models with penalized smoothing splines were used to estimate hazard ratios (HRs) with 95% CI for all-cause and cause-specific mortality.During a median follow-up of 5.9 years, 1921 deaths occurred. After a full adjustment for covariates, a nonlinear (P0.001 for nonlinearity) association was found between HDL-C and all-cause mortality [minimum mortality risk at 71 mg/dL (1.84 mM)]; the risk for all-cause mortality was significantly higher in the groups with HDL-C concentration61 mg/dL (1.58 mM; HR: 1.18; 95% CI: 1.05 to 1.33) and with HDL-C concentration87 mg/dL (2.25 mM; HR: 1.56; 95% CI: 1.17 to 2.07) than in the group with HDL-C concentrations ranging from 61 to 87 mg/dL (1.58 to 2.25 mM). Nonlinear associations of HDL-C concentrations with both cardiovascular and noncardiovascular mortality were also observed (both P0.001 for nonlinearity).Among the elderly, nonlinear associations were found between HDL-C and all-cause and cardiovascular mortality. The single optimal HDL-C concentration and range were 71 mg/dL and 61 to 87 mg/dL, respectively.

Details

ISSN :
19457197 and 0021972X
Volume :
104
Database :
OpenAIRE
Journal :
The Journal of Clinical Endocrinology & Metabolism
Accession number :
edsair.doi.dedup.....c0b5460fe94ffb2f6218b6171cafd386
Full Text :
https://doi.org/10.1210/jc.2018-02511