美国和欧洲老年人痴呆前肌肉力量和身体表现的轨迹。

IF 7.8 Q2 BUSINESS
Youjin Jiang, Yi Ding, Qiuyu Cao, Xianglin Wu, Xiaoran Li, Yu Xu, Zhiyun Zhao, Min Xu, Jieli Lu, Tiange Wang, Guang Ning, Weiqing Wang, Yufang Bi, Yuchen Xu, Mian Li
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引用次数: 0

摘要

背景:肌肉功能与痴呆风险之间的关系仍然难以捉摸,因为研究表明,肌肉功能受损可能既是痴呆的危险因素,也是痴呆的后果,阻碍了因果推理。目的:我们旨在通过研究美国和欧洲老年人痴呆发病前几年肌肉功能的非线性轨迹,阐明肌肉功能与痴呆发病之间的时间关系。设计:病例对照研究。背景:数据来自英国老龄化纵向研究(ELSA, 2004-2018,波浪2-9)、健康与退休研究(HRS, 2004-2018,波浪7-14)和欧洲健康、老龄化和退休调查(SHARE, 2004-2017,波浪1-7)。参与者:对于握力分析,从ELSA、HRS和SHARE队列中纳入了18335名年龄在60岁及以上的参与者。对于步态速度分析,从ELSA和HRS队列中纳入了11,690名年龄在60岁及以上的参与者。测量方法:使用Smedley测力计通过握力评估肌肉力量,使用定时8英尺步行测试通过步态速度评估身体表现,评估每两年或每四年进行一次。痴呆的诊断采用自我报告的医师诊断和认知功能评估。在嵌套病例对照设计中,使用潜在过程混合模型在向后时间尺度上分析肌肉力量和身体表现的轨迹。结果:痴呆发病前12年和13年,患者和对照组的肌肉功能轨迹有显著差异(握力:系数[SE], -0.23 [0.05], P < 0.001;步态速度:系数[SE], -0.24 [0.08], P = 0.003)。在诊断前6年和8年,手部握力和步态速度的病理轨迹分别显示加速期。在调整痴呆前加速后,更大的握力(每增加1公斤)与痴呆风险的适度降低相关(风险比,0.98;95% CI, 0.97-0.99),而更快的步态速度(每1 m/s增量)显著降低风险(风险比,0.35;95% ci, 0.23-0.53)。结论:这些发现强调了肌肉功能是早期发现和动态监测痴呆风险的一种经济有效的工具,并将其确定为预防的可修改目标。肌肉功能也可以帮助识别高危人群,优先纳入痴呆症预防和治疗的临床试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Trajectories of muscle strength and physical performance preceding dementia in older US and European populations.

Background: The association between muscle function and dementia risk remains elusive, as studies suggest that impaired muscle function may act as both a risk factor for and a consequence of dementia, hindering causal inference.

Objectives: We aimed to clarify the temporal relationship between muscle function and incident dementia by investigating non-linear trajectories of muscle function in the years preceding dementia onset in older US and European populations.

Design: Case-control study.

Setting: Data were combined from the English Longitudinal Study of Ageing (ELSA, 2004-2018, waves 2-9), Health and Retirement Study (HRS, 2004-2018, waves 7-14), and Survey of Health, Ageing and Retirement in Europe (SHARE, 2004-2017, waves 1-7).

Participants: For handgrip strength analysis, 18,335 participants aged 60 and older were included from the ELSA, HRS, and SHARE cohorts. For gait speed analysis, 11,690 participants aged 60 and older were included from the ELSA and HRS cohorts.

Measurements: Muscle strength was assessed by handgrip strength using a Smedley dynamometer, and physical performance was evaluated by gait speed using the Timed 8-Foot Walk test, with assessments conducted biennially or quadrennially. Dementia was diagnosed using self-reported physician diagnosis and cognitive-functional assessments. Trajectories of muscle strength and physical performance were analyzed on a backward timescale using latent-process mixed models within a nested case-control design.

Results: Significant differences in muscle function trajectories were observed between cases and controls 12 and 13 years prior to dementia onset (handgrip strength: coefficient [SE], -0.23 [0.05], P < 0.001; gait speed: coefficient [SE], -0.24 [0.08], P = 0.003). The pathological trajectories of handgrip strength and gait speed revealed periods of acceleration beginning 6 and 8 years prior to diagnosis, respectively. After adjusting for pre-dementia acceleration, greater handgrip (per 1-kg increment) was associated with a modest reduction in dementia risk (hazard ratio, 0.98; 95 % CI, 0.97-0.99), while faster gait speed (per 1-m/s increment) markedly lowered risk (hazard ratio, 0.35; 95 % CI, 0.23-0.53).

Conclusions: These findings highlight muscle function as a cost-effective tool for early detection and dynamic monitoring of dementia risk and identify it as a modifiable target for prevention. Muscle function may also assist in identifying high-risk groups for preferential enrollment into clinical trials for dementia prevention and treatment.

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来源期刊
The Journal of Prevention of Alzheimer's Disease
The Journal of Prevention of Alzheimer's Disease Medicine-Psychiatry and Mental Health
CiteScore
9.20
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0.00%
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期刊介绍: The JPAD Journal of Prevention of Alzheimer’Disease will publish reviews, original research articles and short reports to improve our knowledge in the field of Alzheimer prevention including: neurosciences, biomarkers, imaging, epidemiology, public health, physical cognitive exercise, nutrition, risk and protective factors, drug development, trials design, and heath economic outcomes.JPAD will publish also the meeting abstracts from Clinical Trial on Alzheimer Disease (CTAD) and will be distributed both in paper and online version worldwide.We hope that JPAD with your contribution will play a role in the development of Alzheimer prevention.
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