考虑到APOE基因型,体育活动、认知活动和饮食模式对老年人认知障碍的综合影响:一项队列研究

IF 7.6 1区 医学 Q1 CLINICAL NEUROLOGY
Wen-Fang Zhong, Xiao-Meng Wang, Huan Chen, Wei-Qi Song, Jian Gao, Pei-Liang Chen, Qiao-Qiao Shen, Fang-Fei You, Chuan Li, Yue-Bin Lv, Zhi-Hao Li, Xiao-Ming Shi, Chen Mao
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引用次数: 0

摘要

背景:本研究旨在评估身体活动(PA)、认知活动(CA)和饮食模式对老年人认知障碍的影响,以及这些关联是否因载脂蛋白E (APOE)基因型而异。方法:从1998年到2014年,共有18909名65岁及以上的成年人入组。PA和CA使用反映参与各种活动的分数来评估,总活动(TA)分数计算为PA和CA分数的总和。采用she指数评价饮食质量。参与者根据活动水平和she指数的组合被分为生活方式组。APOE基因型分为APOEε4携带者和非携带者。在基线和随访时使用简易精神状态检查评估认知功能。采用调整后的Cox比例风险模型来评估生活方式与APOE基因型对认知障碍风险的相关性和相互作用。结果:在平均5.27±3.67年的随访期间,5713名参与者出现认知障碍。TA、PA或CA水平较高的参与者,结合健康饮食,始终表现出最低的认知障碍风险,TA的风险比(HR)为0.65[95%置信区间(CI): 0.60-0.71], PA的风险比(HR)为0.72 (95% CI: 0.66-0.78), PA的风险比(HR)为0.73 (95% CI: 0.73)。这种保护作用在APOEε4基因型组中保持一致,高TA、PA或CA结合健康饮食的非携带者的hr范围为0.54 - 0.67,非携带者的hr范围为0.63 - 0.69。此外,APOEε4携带者的hr为0.46 (95% CI: 0.28-0.76),非携带者的hr为0.47 (95% CI: 0.37-0.58),同时从事高PA、高CA和健康饮食的参与者对认知障碍的保护作用最大。结论:中国老年人在坚持高运动水平和健康饮食的情况下,认知功能障碍的下降幅度最大,当同时保持高运动、高认知活动和健康饮食时,其保护作用更强,且无论APOEε4状态如何,这种趋势都是一致的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Combined effects of physical activity, cognitive activity, and dietary patterns on cognitive impairment in older adults with consideration of APOE genotype: a cohort study.

Background: This study aims to evaluate the combination effects of physical activity (PA), cognitive activity (CA), and dietary patterns impacts cognitive impairment among older adults, and whether these associations differ by apolipoprotein E (APOE) genotype.

Methods: A total of 18,909 adults aged 65 years or older at baseline were enrolled from 1998 to 2014 years. PA and CA was assessed using scores that reflected participation in various activities, and a total activity (TA) score was calculated as the sum of PA and CA scores. Diet quality was assessed with the SHE-index. Participants were categorized into lifestyle groups based on combinations of activity levels and SHE-index. The APOE genotype was categorized as APOEε4 carriers versus non-carriers. Cognitive function was evaluated using the Mini-Mental State Examination at baseline and follow-up. Adjusted Cox proportional hazards models was used to estimate the association and interaction between lifestyle and APOE genotype on the risk of cognitive impairment.

Results: During a mean follow-up time of 5.27 ± 3.67 years, 5713 participants developed cognitive impairment. Participants with higher levels of TA, PA, or CA, combined with a healthy diet, consistently exhibited the lowest risk of cognitive impairment, with hazard ratios (HR) of 0.65 [95% confidence intervals (CIs): 0.60-0.71] for TA, 0.72 (95% CI: 0.66-0.78) for PA, and 0.73 (95% CI: 0.67-0.79) for CA. This protective effect remained consistent across APOEε4 genotype groups, with HRs ranging from 0.54 to 0.67 in carriers and 0.63 to 0.69 in non-carriers for higher TA, PA, or CA combined with a healthy diet. In addition, participants engaging in high PA, high CA, and a healthy diet simultaneously showed the greatest protection against cognitive impairment, with HRs of 0.46 (95% CI: 0.28-0.76) in APOEε4 carriers and 0.47 (95% CI: 0.37-0.58) in non-carriers.

Conclusions: The greatest decrease in cognitive impairment was observed among older Chinese adults adhering to both high activity levels and healthy diet, The protective effect was even stronger when high physical activity, high cognitive activity, and a healthy diet were maintained simultaneously, and this trend was consistent regardless of APOEε4 status.

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来源期刊
Alzheimer's Research & Therapy
Alzheimer's Research & Therapy 医学-神经病学
CiteScore
13.10
自引率
3.30%
发文量
172
审稿时长
>12 weeks
期刊介绍: Alzheimer's Research & Therapy is an international peer-reviewed journal that focuses on translational research into Alzheimer's disease and other neurodegenerative diseases. It publishes open-access basic research, clinical trials, drug discovery and development studies, and epidemiologic studies. The journal also includes reviews, viewpoints, commentaries, debates, and reports. All articles published in Alzheimer's Research & Therapy are included in several reputable databases such as CAS, Current contents, DOAJ, Embase, Journal Citation Reports/Science Edition, MEDLINE, PubMed, PubMed Central, Science Citation Index Expanded (Web of Science) and Scopus.
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