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

被引:0
作者
Sultana Monira Hussain
Andrew M Tonkin
Gerald F Watts
Paul Lacaze
Chenglong Yu
Lawrence J Beilin
Zhen Zhou
Anne B Newman
Johannes T Neumann
Cammie Tran
John J McNeil
机构
[1] Monash University,School of Public Health and Preventive Medicine
[2] The University of Melbourne,Department of Medical Education, Melbourne Medical School
[3] University of Western Australia,School of Medicine
[4] University of Tasmania,Menzies Institute for Medical Research
[5] University of Pittsburgh,Center for Aging and Population Health
[6] University Heart & Vascular Center (UHZ),Department of Cardiology
[7] Partner Site Hamburg/Kiel/Lübeck,German Center for Cardiovascular Research (DZHK)
来源
GeroScience | 2024年 / 46卷
关键词
High-density lipoprotein cholesterol; All-cause mortality; Cardiovascular disease mortality; Cancer mortality; “Non-cancer non-cardiovascular” mortality; Older adults;
D O I
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学科分类号
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 non-CVD” 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.
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页码:1461 / 1475
页数:14
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