Sex-dependent associations of plasma high-density lipoprotein cholesterol and mortality risk in healthy older men and women: two prospective cohort studies

被引:1
作者
Hussain, Sultana Monira [1 ,2 ]
Tonkin, Andrew M. [1 ]
Watts, Gerald F. [3 ]
Lacaze, Paul [1 ]
Yu, Chenglong [1 ]
Beilin, Lawrence J. [3 ]
Zhou, Zhen [1 ,4 ]
Newman, Anne B. [5 ]
Neumann, Johannes T. [6 ,7 ]
Tran, Cammie [1 ]
Mcneil, John J. [1 ]
机构
[1] Monash Univ, Sch Publ Hlth & Prevent Med, Melbourne, Vic, Australia
[2] Univ Melbourne, Melbourne Med Sch, Dept Med Educ, Parkville, Vic, Australia
[3] Univ Western Australia, Sch Med, Perth, Australia
[4] Univ Tasmania, Menzies Inst Med Res, Hobart, Australia
[5] Univ Pittsburgh, Ctr Aging & Populat Hlth, Pittsburgh, PA USA
[6] Univ Heart & Vasc Ctr UHZ, Dept Cardiol, Hamburg, Germany
[7] German Ctr Cardiovasc Res DZHK, Partner Site Hamburg Kiel Lubeck, Hamburg, Germany
基金
美国国家卫生研究院; 英国医学研究理事会;
关键词
High-density lipoprotein cholesterol; All-cause mortality; Cardiovascular disease mortality; Cancer mortality; Non-cancer non-cardiovascular" mortality; Older adults; ALL-CAUSE; Y-CHROMOSOME; LIPIDS;
D O I
10.1007/s11357-023-00904-4
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The relationship between high plasma high-density lipoprotein cholesterol (HDL-C) and cause and mortality are not well established in healthy older people. This study examined the associations between HDL-C levels and mortality in initially healthy older men and women. This analysis included participants from the Aspirin in Reducing Events in the Elderly (ASPREE; n=18,668) trial and a matched cohort from the UK Biobank (UKB; n=62,849 =65 years). Cox regression was used to examine hazard ratios between HDL-C categories <1.03 mmol/L, 1.03-1.55 mmol/L (referent category), 1.55-2.07 mmol/L, and >2.07 mmol/L and all-cause, cancer, cardiovascular disease (CVD), and "non-cancer nonCVD" mortality. Genetic contributions were assessed using a polygenic score for HDL-C. Among ASPREE participants (aged 75 +/- 5 years), 1836 deaths occurred over a mean follow-up of 6.3 +/- 1.8 years. In men, the highest category of HDL-C levels was associated with increased risk of all-cause (HR 1.60, 95% CI 1.26-2.03), cancer (HR 1.37, 95% CI 0.96-2.00), and "non-cancer non-CVD" mortality (HR 2.35, 95% CI 1.41-3.42) but not CVD mortality (HR 1.08, 95% CI 0.60-1.94). The associations were replicated among UKB participants (aged 66.9 +/- 1.5 years), including 8739 deaths over a mean follow-up of 12.7 +/- 0.8 years. There was a non-linear association between HDL-C levels and all-cause and cause-specific mortality. The association between HDL-C levels and mortality was unrelated to variations in the HDL-C polygenic score. No significant association was found between HDL-C levels and mortality in women. Higher HDL-C levels are associated with increased risk from cancer and "non-cancer non-CVD" mortality in healthy older men but no such relationship was observed in women.
引用
收藏
页码:1461 / 1475
页数:15
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