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手握力与无痴呆老年男性的学习和语言流畅性有关:来自 NHANES 的见解。

Handgrip strength is associated with learning and verbal fluency in older men without dementia: insights from the NHANES.

机构信息

Department of Musculoskeletal Biology, Institute of Life Course and Medical Sciences, University of Liverpool, Liverpool, UK.

Society of Meta-Research and Biomedical Innovation, London, UK.

出版信息

Geroscience. 2023 Apr;45(2):1049-1058. doi: 10.1007/s11357-022-00703-3. Epub 2022 Nov 30.

DOI:10.1007/s11357-022-00703-3
PMID:36449219
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9886698/
Abstract

Low handgrip strength, a hallmark measure of whole-body strength, has been linked with greater odds of cognitive decline and dementia; however, conflicting findings, which could be due to population characteristics and choice of tools, such for the assessment of handgrip strength and cognitive function domains, also exist. Therefore, we examined the relationship of handgrip strength with a comprehensive list of tests to assess domains of cognitive function using a representative sample of US older men and women without neurodegenerative disorders such as dementia. We analyzed cross-sectional data from the US National Health and Nutrition Examination Survey (NHANES) between 2011 and 2014, with a study cohort of 777 older adults (380 men and 397 women) above 60 years of age. Handgrip strength was assessed using a handgrip dynamometer, while cognitive function was assessed through the Consortium to Establish a Registry for Alzheimer's Disease (CERAD) Word List Learning Test (WLLT), Word List Recall Test (WLRT), Intrusion Word Count Test (WLLT-IC and WLRT-IC), the Animal Fluency Test (AFT), and the Digit Symbol Substitution Test (DSST). Sex-stratified multiple linear regression analyses were performed upon covariate adjustment for age, ethnicity, socio-economic status, education, medical history, body mass index, physical activity, energy, protein, and alcohol intake. Maximal handgrip strength was positively associated with cognitive function scores, including CERAD WLLT (P = 0.009, R = 0.146) and AFT (P = 0.022, R = 0.024) in older men, but not in women (CERAD WLLT: P = 0.253, AFT: P = 0.370). No significant associations with CERAD WLLRT (men: P = 0.057, women: P = 0.976), WLLT-IC (men: P = 0.671, women: P = 0.869), WLLRT-IC (men: P = 0.111, women: P = 0.861), and DSST (men: P = 0.108, women: P = 0.091) were observed. Dose-response curves exhibited a prominent linear relationship between all significant associations after covariate adjustment, with no indication of a plateau in these relationships. In conclusion, higher handgrip strength was independently associated with better learning ability for novel verbal information and verbal fluency in US men over the age of 60 and without dementia. Longitudinal studies are required to confirm whether muscle strength independently predicts cognitive function changes in older adults in a sex-specific manner, and whether this connection is affirmed to the possibility of reverse causation due to declines in physical activity levels in the preclinical phase of dementia.

摘要

握力低,这是全身力量的一个重要衡量标准,与认知能力下降和痴呆的几率增加有关;然而,也存在相互矛盾的发现,这可能是由于人群特征和评估握力和认知功能领域的工具选择不同所致。因此,我们使用没有神经退行性疾病(如痴呆)的美国老年男性和女性的代表性样本,检查了握力与评估认知功能领域的综合测试列表之间的关系。我们分析了 2011 年至 2014 年期间美国国家健康和营养检查调查(NHANES)的横断面数据,研究队列包括 777 名 60 岁以上的老年人(380 名男性和 397 名女性)。握力使用握力测力计进行评估,而认知功能则通过认知障碍建立登记册 Consortium (CERAD)单词列表学习测试(WLLT)、单词列表回忆测试(WLRT)、干扰单词计数测试(WLLT-IC 和 WLRT-IC)、动物流畅性测试(AFT)和数字符号替代测试(DSST)进行评估。在对年龄、种族、社会经济地位、教育、病史、体重指数、身体活动、能量、蛋白质和酒精摄入量进行协变量调整后,进行了按性别分层的多元线性回归分析。最大握力与认知功能评分呈正相关,包括 CERAD WLLT(P=0.009,R=0.146)和 AFT(P=0.022,R=0.024)在老年男性中,但在女性中没有(CERAD WLLT:P=0.253,AFT:P=0.370)。与 CERAD WLLRT(男性:P=0.057,女性:P=0.976)、WLLT-IC(男性:P=0.671,女性:P=0.869)、WLLRT-IC(男性:P=0.111,女性:P=0.861)和 DSST(男性:P=0.108,女性:P=0.091)均无显著相关性。在调整协变量后,所有显著关联的剂量-反应曲线显示出明显的线性关系,并且这些关系没有表现出平台期。总之,在没有痴呆的情况下,60 岁以上的美国男性握力越高,与新的口头信息学习能力和口头流畅性的关系越密切。需要进行纵向研究,以确认肌肉力量是否以性别特异性的方式独立预测老年人的认知功能变化,以及由于痴呆前阶段身体活动水平下降而导致的这种联系是否被逆转因果关系所证实。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a914/9886698/efb96dca63ed/11357_2022_703_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a914/9886698/efb96dca63ed/11357_2022_703_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a914/9886698/efb96dca63ed/11357_2022_703_Fig1_HTML.jpg

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