体重和BMI变异与痴呆风险相关:一项荟萃分析。

0 MEDICINE, RESEARCH & EXPERIMENTAL
Sitian Fang, Lewei Guan, Huimin Jian, Xijian Dai, Lianggeng Gong
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引用次数: 0

摘要

新出现的证据表明,独立于平均水平的体重(BW)或体重指数(BMI)的波动可能会影响痴呆症的风险。然而,个体内体重或BMI变异与痴呆发生率之间的关系尚不清楚。本荟萃分析旨在澄清这一关系。到2025年3月25日,对PubMed、Embase和Web of Science进行了系统搜索,以确定报告痴呆结局与体重或体重指数变异性相关的纵向观察性研究。使用随机效应模型汇总比较最高和最低变异性类别的相对风险(rr)。进行亚组分析和敏感性分析以探索异质性并评估结果的稳健性。9项队列研究(10个数据集;共纳入4232666名参与者)。总体而言,高体重或BMI变异性与痴呆风险显著增加相关(RR = 1.36, 95% CI: 1.27-1.46;P < 0.001;I²= 84%)。体重(RR = 1.45)和BMI (RR = 1.34)变异性的相关性是一致的。亚组分析显示,前瞻性研究的相关性强于回顾性研究,未调整基线体重/体重指数的研究强于调整基线体重/体重指数的研究(亚组差异p < 0.05)。在敏感性分析和痴呆亚型(包括阿尔茨海默病和血管性痴呆)中,相关性仍然很强。未发现显著的发表偏倚(Egger检验,p = 0.22)。总之,体重或体重指数的个体差异可能与痴呆风险增加独立相关。这些发现强调了在中老年生活中保持体重稳定作为一种潜在的预防痴呆症策略的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Body weight and BMI variability linked to dementia risk: A meta-analysis.

Emerging evidence suggests that fluctuations in body weight (BW) or body mass index (BMI), independent of average levels, may influence dementia risk. However, the association  between  intra-individual variability in BW or BMI and incident dementia remains unclear. This meta-analysis aimed to clarify this relationship. A systematic search of PubMed, Embase, and Web of Science was conducted through March 25, 2025, to identify longitudinal observational studies reporting dementia outcomes in relation to BW or BMI variability. Relative risks (RRs) comparing the highest versus lowest variability categories were pooled using a random-effects model. Subgroup and sensitivity analyses were performed to explore heterogeneity and assess the robustness of the results. Nine cohort studies (10 datasets; 4,232,666 participants) were included. Overall, high BW or BMI variability was associated with a significantly increased risk of dementia (RR = 1.36, 95% CI: 1.27-1.46; p < 0.001; I² = 84%). The association was consistent for both BW (RR = 1.45) and BMI (RR = 1.34) variability. Subgroup analyses showed stronger associations in prospective studies than in retrospective ones, and in studies that did not adjust for baseline BW/BMI compared to those that did (p for subgroup difference < 0.05). Associations remained robust in sensitivity analyses and across dementia subtypes, including Alzheimer's disease and vascular dementia. No significant publication bias was detected (Egger's test, p = 0.22). In conclusion, greater intra-individual variability in BW or BMI may be independently associated with increased dementia risk. These findings underscore the importance of maintaining weight stability in mid-to-late life as a potential preventive strategy for dementia.

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