社会化与社区老年人心血管疾病风险的性别差异:利用机器学习算法和传统方法进行的前瞻性队列研究

Achamyeleh Birhanu Teshale, Htet Lin Htun, Alice J. Owen, Joanne Ryan, JR Baker, Mor Vered, Christopher M Reid, Robyn L. Woods, Michael Berk, Andrew Tonkin, Johannes T Neumann, Monique F Kilkenny, Aung Zaw Zaw Phyo, Mark R Nelson, Nigel Stocks, Carlene Britt, Rosanne Freak-Poli
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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. 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引用次数: 0

摘要

背景 性别通过规范、社会关系、角色和行为影响心血管疾病(CVD)。本研究确定了与心血管疾病相关的社会化的性别特异性方面。方法 进行了一项纵向研究,涉及9936名(5231名女性和4705名男性)最初健康的、居住在社区的70岁或70岁以上的澳大利亚人,他们来自 "ASPirin in Reducing Events in the Elderly (ASPREE) "研究和 "ASPREE Longitudinal Study of Older Persons "研究,中位随访时间为6.4年。按照二元性别分别采用变量分类、变量选择(使用机器学习(ML)模型;弹性网和极度梯度提升)和 Cox 回归来识别与心血管疾病相关的社会化因素(25 个考虑因素)。结果 使用 ML 模型确定了不同的社会化因素。在 Cox 模型中,男女已婚/有伴侣与心血管疾病风险降低有关(男性:HR 0.76,95% CI 0.60 至 0.96;女性:HR 0.67,95% CI 0.58 至 0.95)。对于男性而言,有 3-8 名亲属与他们关系密切并可向他们求助(HR 0.76,95% CI 0.58 至 0.99;参考值)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gender-specific aspects of socialisation and risk of cardiovascular disease among community-dwelling older adults: a prospective cohort study using machine learning algorithms and a conventional method
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. Data may be obtained from a third party and are not publicly available. The ASPREE and ALSOP are not publicly available since they are ongoing. However, they are available to partnering and external researchers for projects of appropriate scientific merit and expressions of interest to analyse data from these datasets are co-ordinated through the ASPREE Access Management Site (AMS) ().
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