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Cross-Sectional Associations of Sarcopenia and Its Components with Neuropsychological Performance among Memory Clinic Patients with Mild Cognitive Impairment and Alzheimer’s Disease

肌萎缩 医学 记忆广度 痴呆 认知 神经心理学 口语流利性测试 握力 情景记忆 试制试验 阿尔茨海默病 老年学 物理医学与康复 疾病 物理疗法 内科学 精神科 工作记忆
作者
Taiki Sugimoto,Yoko Kuroda,N. Matsumoto,Kazuhisa Uchida,Yoshinobu Kishino,Naoki Saji,Shumpei Niida,Takashi Sakurai
出处
期刊:The Journal of frailty & aging [SERDI]
被引量:4
标识
DOI:10.14283/jfa.2022.3
摘要

The association of sarcopenia with cognitive function in its specific domains remains poorly understood.To investigate the association of sarcopenia and its components with neuropsychological performance among patients with mild cognitive impairment (MCI) and Alzheimer's disease (AD).Cross-sectional design.A memory clinic in Japan.The study included 497 MCI/684 AD patients aged 65-89 years.Patients were assessed for muscle mass by bioelectrical impedance analysis, muscle strength by hand grip strength (HGS), and physical performance by timed up and go test (TUG). Sarcopenia was defined as presence of both low muscle strength and low muscle mass. The patients underwent neuropsychological tests, including logical memory, frontal lobe assessment battery, word fluency test, Raven's colored progressive matrices, digit span, and the Alzheimer's disease assessment scale-cognitive subscale (ADAS-cog).The prevalence of sarcopenia in men and women was 24.1% and 19.5%, respectively. In multiple regression analyses adjusting for confounders, unlike in men, sarcopenia was associated with memory function in women (ADAS-cog, memory domain, coefficient = 1.08, standard error (SE) = 0.36), which was thought likely due to the relationship between HGS and memory function (immediate recall of logical memory, coefficient = 0.07, SE = 0.03; ADAS-cog, memory domain, coefficient = -0.10, SE = 0.03). Of the components of sarcopenia in both sexes, HGS and TUG were associated with visuospatial function and frontal lobe function, respectively.The specific association of sarcopenia and its components with cognitive domains may provide the key to elucidating the muscle-brain interactions in AD.

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