School of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.
Department of Medical Education, Melbourne Medical School, The University of Melbourne, Parkville, Victoria, Australia.
Geroscience. 2024 Apr;46(2):1461-1475. doi: 10.1007/s11357-023-00904-4. Epub 2023 Aug 23.
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.
在健康的老年人中,高血浆高密度脂蛋白胆固醇(HDL-C)与病因和死亡率之间的关系尚未得到很好的确定。本研究旨在探讨 HDL-C 水平与最初健康的老年男性和女性死亡率之间的关系。该分析包括来自阿司匹林减少老年人事件(ASPREE;n=18668)试验的参与者和来自英国生物银行(UKB;n=62849≥65 岁)的匹配队列。使用 Cox 回归来检验 HDL-C 类别<1.03mmol/L、1.03-1.55mmol/L(参考类别)、1.55-2.07mmol/L 和>2.07mmol/L 与全因、癌症、心血管疾病(CVD)和“非癌症非 CVD”死亡率之间的危险比。使用 HDL-C 的多基因评分评估遗传贡献。在 ASPREE 参与者(年龄 75±5 岁)中,平均随访 6.3±1.8 年后发生了 1836 例死亡。在男性中,最高 HDL-C 水平类别与全因(HR 1.60,95%CI 1.26-2.03)、癌症(HR 1.37,95%CI 0.96-2.00)和“非癌症非 CVD”死亡率(HR 2.35,95%CI 1.41-3.42)的风险增加相关,但与 CVD 死亡率(HR 1.08,95%CI 0.60-1.94)无关。该关联在 UKB 参与者(年龄 66.9±1.5 岁)中得到了复制,包括平均随访 12.7±0.8 年后的 8739 例死亡。HDL-C 水平与全因和病因特异性死亡率之间存在非线性关系。HDL-C 水平与死亡率之间的关联与 HDL-C 多基因评分的变化无关。在女性中,未发现 HDL-C 水平与死亡率之间存在显著关联。在健康的老年男性中,较高的 HDL-C 水平与癌症和“非癌症非 CVD”死亡率增加相关,但在女性中未观察到这种关系。