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Multi-Trajectories of Intrinsic Capacity Decline and Their Impact on Age-Related Outcomes: A 20-Year National Longitudinal Cohort Study

认知功能衰退 医学 老化 萧条(经济学) 人口学 逻辑回归 老年学 危险系数 比例危险模型 生活质量(医疗保健) 纵向研究 队列研究 队列 晚年抑郁症 认知 内科学 痴呆 疾病 置信区间 精神科 病理 护理部 社会学 经济 宏观经济学
作者
Lin-Chieh Meng,Hui-Min Chuang,Wan‐Hsuan Lu,Wei‐Ju Lee,Chih‐Kuang Liang,Ching‐Hui Loh,Fei‐Yuan Hsiao,Liang Kung Chen
出处
期刊:Aging and Disease [Aging and Disease]
标识
DOI:10.14336/ad.2023.1115-1
摘要

The existence of intrinsic capacity (IC) subtypes and their distinct impacts on age-related outcomes remain unexplored. This study sought to investigate IC impairment trajectories across domains and their associations with the risk of age-related outcomes, including falls, functional limitations, reduced quality of life (QoL) and mortality at 4- and 8-year follow-ups. The study sample comprised 1,782 older adults residing in the community from the Taiwan Longitudinal Study on Ageing (TLSA). Utilizing group-based multitrajectory modeling, distinct subtypes of IC decline trajectories across various domains were identified. Cox proportional hazard models and multivariable logistic regression analyses were employed to assess the associations between the identified subtypes and age-related outcomes. We identified four subtypes of IC decline: robust with mild decline (n=902), hearing loss with cognitive decline (n=197), physio-cognitive decline (PCD) with depression (n=373), and severe IC decline (n=310). Over the 4-year study period, compared to the robust with mild decline group, hearing loss with cognitive decline group exhibited a significantly higher risk of diminished QoL (OR=2.53 [1.66-3.86], p<0.01), whereas those in the PCD with depression group experienced an elevated risk of falls (OR=1.62 [1.18-2.23], p<0.01), as well as functional limitation (OR=2.61 [1.81-3.75], p<.01). Individuals in the severe IC decline group faced a substantially increased risk of all outcomes of interest. Distinct subtypes of IC decline across different domains have varying impacts on age-related outcomes, highlighting the need for a personalized approach to promote healthy ageing at the population level, while further investigation into specific pathophysiological mechanisms is warranted as well.
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