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晚年肥胖是前驱期阿尔茨海默病的保护因素:一项纵向研究。

Late-life obesity is a protective factor for prodromal Alzheimer's disease: a longitudinal study.

机构信息

Department of Neurology, Qingdao Municipal Hospital, Nanjing Medical University, Nanjing, China.

College of Medicine and Pharmaceutics, Ocean University of China, Qingdao, China.

出版信息

Aging (Albany NY). 2020 Jan 25;12(2):2005-2017. doi: 10.18632/aging.102738.

Abstract

Higher body mass index (BMI) in late-life has recently been considered as a possible protective factor for Alzheimer's disease (AD), which yet remains conflicting. To test this hypothesis, we have evaluated the cross-sectional and longitudinal associations of BMI categories with CSF biomarkers, brain β-amyloid (Aβ) load, brain structure, and cognition and have assessed the effect of late-life BMI on AD risk in a large sample (n = 1,212) of non-demented elderly from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database. At baseline, higher late-life BMI categories were associated with higher levels of CSF Aβ42 (p=0.037), lower levels of CSF total-tau (t-tau, p=0.026) and CSF t-tau/Aβ42 (p=0.008), lower load of Aβ in the right hippocampus (p=0.030), as well as larger volumes of hippocampus (p<0.0001), entorhinal cortex (p=0.009) and middle temporal lobe (p=0.040). But no association was found with CSF phosphorylated-tau (p-tau) or CSF p-tau/Aβ42. Longitudinal studies showed that higher BMI individuals experienced a slower decline in cognitive function. In addition, Kaplan-Meier survival analysis revealed that higher late-life BMI had a reduced risk of progression to AD over time (p = 0.009). Higher BMI in late-life decreased the risk of AD, and this process may be driven by AD-related biomarkers.

摘要

晚年较高的体重指数(BMI)最近被认为是阿尔茨海默病(AD)的一个可能的保护因素,但这仍然存在争议。为了检验这一假设,我们评估了 BMI 类别与 CSF 生物标志物、脑β-淀粉样蛋白(Aβ)负荷、脑结构和认知的横断面和纵向关联,并评估了晚年 BMI 对来自阿尔茨海默病神经影像学倡议(ADNI)数据库的大量(n=1212)非痴呆老年人 AD 风险的影响。在基线时,较高的晚年 BMI 类别与 CSF Aβ42 水平较高相关(p=0.037),CSF 总 tau(t-tau)水平较低(p=0.026)和 CSF t-tau/Aβ42 水平较低(p=0.008),右侧海马体的 Aβ负荷较低(p=0.030),以及海马体(p<0.0001)、内嗅皮层(p=0.009)和中颞叶(p=0.040)的体积较大。但与 CSF 磷酸化 tau(p-tau)或 CSF p-tau/Aβ42 无相关性。纵向研究表明,BMI 较高的个体认知功能下降速度较慢。此外,Kaplan-Meier 生存分析显示,晚年较高的 BMI 随着时间的推移,AD 进展的风险降低(p=0.009)。晚年较高的 BMI 降低了 AD 的风险,这一过程可能是由 AD 相关的生物标志物驱动的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fad/7053604/5a4756173136/aging-12-102738-g001.jpg

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