TY - JOUR
T1 - Gender-specific aspects of socialisation and risk of cardiovascular disease among community-dwelling older adults
T2 - A prospective cohort study using machine learning algorithms and a conventional method
AU - Teshale, Achamyeleh Birhanu
AU - Htun, Htet Lin
AU - Owen, Alice J.
AU - Ryan, Joanne
AU - Baker, J. R.
AU - Vered, Mor
AU - Reid, Christopher M.
AU - Woods, Robyn L.
AU - Berk, Michael
AU - Tonkin, Andrew
AU - Neumann, Johannes T.
AU - Kilkenny, Monique F.
AU - Phyo, Aung Zaw Zaw
AU - Nelson, Mark R.
AU - Stocks, Nigel
AU - Britt, Carlene
AU - Freak-Poli, Rosanne
N1 - Funding Information:
ASPREE was supported by grants from the National Institute on Aging and the National Cancer Institute at the US National Institutes of Health (grant numbers:. U01AG029824 and U19AG062682); the National Health and Medical Research Council of Australia (NHMRC, grant numbers: 334047 and 1127060); Monash University (Australia) and the Victorian Cancer Agency (Australia). ALSOP was supported by funding from Monash University, ANZ Trustees, the Wicking Trust and the Mason Foundation. Other funding resources and collaborating organisations of the ASPREE study and ALSOP substudy are listed at http://www.aspree.org . AT and HLH are supported by Monash International Tuition Scholarship and Monash Graduate Scholarship. JR is supported by an NHMRC Investigator Grant Leadership Level 1 (2016438). MB is supported by an NHMRC Senior Principal Research Fellowship and Leadership 3 Investigator grant (1156072 and 2017131). MFK report receiving research fellowship support from the National Heart Foundation of Australia (105737).
Publisher Copyright:
© Author(s) (or their employer(s)) 2024. No commercial re-use. See rights and permissions. Published by BMJ.
PY - 2024
Y1 - 2024
N2 - Background: Gender influences cardiovascular disease (CVD) through norms, social relations, roles and behaviours. This study identified gender-specific aspects of socialisation associated with CVD. Methods: A longitudinal study was conducted, involving 9936 (5,231 women and 4705 men) initially healthy, community-dwelling Australians aged 70 years or more from the ASPirin in Reducing Events in the Elderly (ASPREE) study and ASPREE Longitudinal Study of Older Persons, with a median follow-up time of 6.4 years. Variable categorisation, variable selection (using machine learning (ML) models; Elastic Net and extreme gradient boosting) and Cox-regression were employed separately by binary gender to identity socialisation factors (n=25 considered) associated with CVD. Results: Different socialisation factors were identified using the ML models. In the Cox model, for both genders, being married/partnered was associated with a reduced risk of CVD (men: HR 0.76, 95% CI 0.60 to 0.96; women: HR 0.67, 95% CI 0.58 to 0.95). For men, having 3-8 relatives they felt close to and could call on for help (HR 0.76, 95% CI 0.58 to 0.99; reference <3 relatives), having 3-8 relatives they felt at ease talking with about private matters (HR 0.70, 95% CI 0.55 to 0.90; reference <3 relatives) or playing games such as chess or cards (HR 0.82, 95% CI 0.67 to 1.00) was associated with reduced risk of CVD. For women, living with others (HR 0.71, 95% CI 0.55 to 0.91) or having ≥3 friends they felt at ease talking with about private matters (HR 0.74, 95% CI 0.58 to 0.95; reference <3 friends) was associated with a lower risk of CVD. Conclusions: This study demonstrates the need to prioritise gender-specific social factors to improve cardiovascular health in older adults.
AB - Background: Gender influences cardiovascular disease (CVD) through norms, social relations, roles and behaviours. This study identified gender-specific aspects of socialisation associated with CVD. Methods: A longitudinal study was conducted, involving 9936 (5,231 women and 4705 men) initially healthy, community-dwelling Australians aged 70 years or more from the ASPirin in Reducing Events in the Elderly (ASPREE) study and ASPREE Longitudinal Study of Older Persons, with a median follow-up time of 6.4 years. Variable categorisation, variable selection (using machine learning (ML) models; Elastic Net and extreme gradient boosting) and Cox-regression were employed separately by binary gender to identity socialisation factors (n=25 considered) associated with CVD. Results: Different socialisation factors were identified using the ML models. In the Cox model, for both genders, being married/partnered was associated with a reduced risk of CVD (men: HR 0.76, 95% CI 0.60 to 0.96; women: HR 0.67, 95% CI 0.58 to 0.95). For men, having 3-8 relatives they felt close to and could call on for help (HR 0.76, 95% CI 0.58 to 0.99; reference <3 relatives), having 3-8 relatives they felt at ease talking with about private matters (HR 0.70, 95% CI 0.55 to 0.90; reference <3 relatives) or playing games such as chess or cards (HR 0.82, 95% CI 0.67 to 1.00) was associated with reduced risk of CVD. For women, living with others (HR 0.71, 95% CI 0.55 to 0.91) or having ≥3 friends they felt at ease talking with about private matters (HR 0.74, 95% CI 0.58 to 0.95; reference <3 friends) was associated with a lower risk of CVD. Conclusions: This study demonstrates the need to prioritise gender-specific social factors to improve cardiovascular health in older adults.
KW - CARDIOVASCULAR DISEASES
KW - GERIATRICS
KW - GERONTOLOGY
KW - PUBLIC HEALTH
KW - SOCIAL CAPITAL
UR - http://www.scopus.com/inward/record.url?scp=85196298661&partnerID=8YFLogxK
U2 - 10.1136/jech-2023-221860
DO - 10.1136/jech-2023-221860
M3 - Article
C2 - 38839108
AN - SCOPUS:85196298661
SN - 0143-005X
JO - Journal of Epidemiology and Community Health
JF - Journal of Epidemiology and Community Health
M1 - jech-2023-221860
ER -