童年不良经历和晚年肌肉减少症:来自加拿大老龄化纵向研究的基线数据。

IF 2.1 Q3 GERIATRICS & GERONTOLOGY
Menelaos M Dimitriadis, Kitty J E Kokkeler, Emiel O Hoogendijk, Radboud M Marijnissen, Ivan Aprahamian, Hans W Jeuring, Richard C Oude Voshaar
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引用次数: 0

摘要

背景:不良童年经历(ace)与早期和长期的心理健康问题和躯体多病有关。越来越多的证据表明,ace也可能加速老年人的身体衰弱。本研究探讨了ace与肌肉减少症之间的关系,肌肉减少症是一种与年龄相关的疾病,也是虚弱的核心组成部分。方法:分析来自加拿大纵向老龄化研究(CLSA)的基线数据,包括25,327名年龄在45-85岁之间的参与者(50.3%为女性)。肌少症的定义采用修订后的欧洲老年人肌少症工作组(EWGSOP2)指南。通过《童年暴力经历问卷》和《全国青少年至成人健康第三波纵向研究问卷》对ACE进行评估,涵盖8个ACE类别。多重逻辑回归模型检验了ACE计数与肌肉减少症之间的关系,并根据年龄、性别、教育程度、收入和种族进行了调整。结果:考虑到年龄与ACE之间存在显著的相互作用(p < 0.01),我们将分析分为4个年龄组(45-54岁、55-64岁、65-74岁和75-85岁)。显著相关性仅出现在年龄最大的组(75-85岁;OR = 0.93 [95% CI: 0.86-1.00], p = 0.043),但结果与我们假设的方向相反。敏感性分析证实了ACE和肌肉减少症不同手术方式的结果。结论:高ACE暴露与中老年人肌肉减少症无关。在年龄最大的亚组中出现的意想不到的保护性关联可能反映了生存偏差。需要年龄分层的纵向研究来澄清这种关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Adverse Childhood Experiences and Sarcopenia in Later Life: Baseline Data from the Canadian Longitudinal Study on Aging.

Adverse Childhood Experiences and Sarcopenia in Later Life: Baseline Data from the Canadian Longitudinal Study on Aging.

Backgrounds: Adverse Childhood Experiences (ACEs) are linked to early and long-lasting mental health issues and somatic multimorbidity. Emerging evidence suggests ACEs may also accelerate physical frailty in old age. This study examines the association between ACEs and sarcopenia, an ageing-related disease and core component of frailty.

Methods: Baseline data from the Canadian Longitudinal Study on Aging (CLSA), including 25,327 participants aged 45-85 years (50.3% female sex) were analyzed. Sarcopenia was defined using the revised European Working Group of Sarcopenia in Older People (EWGSOP2) guidelines. ACE were assessed via the Childhood Experiences of Violence Questionnaire and the National Longitudinal Study of Adolescent to Adult Health Wave III questionnaire, covering eight ACE categories. Multiple logistic regression models examined the association between the number of ACE count and sarcopenia, which were adjusted for age, sex, education, income, and ethnicity.

Results: Given a significant interaction between age and ACE (p < 0.01), analyses were stratified into four age groups (45-54, 55-64, 65-74, and 75-85 years). A significant association only emerged in the oldest group (75-85 years; OR = 0.93 [95% CI: 0.86-1.00], p = 0.043), but this result was in the opposite direction we hypothesized. Sensitivity analyses confirmed findings across different operationalisations of ACE and sarcopenia.

Conclusions: Higher ACE exposure was not associated with sarcopenia in middle aged and older adults. The unexpected protective association in the oldest-old subgroup may reflect survival bias. Age-stratified longitudinal studies are needed to clarify this relationship.

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来源期刊
Geriatrics
Geriatrics 医学-老年医学
CiteScore
3.30
自引率
0.00%
发文量
115
审稿时长
20.03 days
期刊介绍: • Geriatric biology • Geriatric health services research • Geriatric medicine research • Geriatric neurology, stroke, cognition and oncology • Geriatric surgery • Geriatric physical functioning, physical health and activity • Geriatric psychiatry and psychology • Geriatric nutrition • Geriatric epidemiology • Geriatric rehabilitation
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