TY - JOUR
T1 - Sex-dependent associations of plasma high-density lipoprotein cholesterol and mortality risk in healthy older men and women
T2 - two prospective cohort studies
AU - Hussain, Sultana Monira
AU - Tonkin, Andrew M.
AU - Watts, Gerald F.
AU - Lacaze, Paul
AU - Yu, Chenglong
AU - Beilin, Lawrence J.
AU - Zhou, Zhen
AU - Newman, Anne B.
AU - Neumann, Johannes T.
AU - Tran, Cammie
AU - McNeil, John J.
N1 - Funding Information:
Open Access funding enabled and organized by CAUL and its Member Institutions The Aspirin in Reducing Events in the Elderly (ASPREE) study was supported by grants from the National Institute on Aging and the National Cancer Institute at the National Institutes of Health (U01AG029824 and U19AG062682), the National Health and Medical Research Council of Australia (334037 and 1127060), Monash University (Melbourne, VIC, Australia), and the Victorian Cancer Agency (Australia).
Funding Information:
Dr. Hussain is the recipient of National Health and Medical Research Council (NHMRC) Early Career Fellowship (APP1142198). Professor McNeil is supported through an NHMRC Leadership Fellowship (IG 1173690). P.L. is supported by a National Heart Foundation Future Leader Fellowship (102604). No other disclosures are reported by the other authors.
Publisher Copyright:
© 2023, The Author(s).
PY - 2024/4
Y1 - 2024/4
N2 - 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.
AB - 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.
KW - All-cause mortality
KW - Cancer mortality
KW - Cardiovascular disease mortality
KW - High-density lipoprotein cholesterol
KW - Older adults
KW - “Non-cancer non-cardiovascular” mortality
UR - http://www.scopus.com/inward/record.url?scp=85168619124&partnerID=8YFLogxK
U2 - 10.1007/s11357-023-00904-4
DO - 10.1007/s11357-023-00904-4
M3 - Article
C2 - 37610595
AN - SCOPUS:85168619124
SN - 2509-2715
VL - 46
SP - 1461
EP - 1475
JO - GeroScience
JF - GeroScience
IS - 2
ER -