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虚弱对非痴呆认知轨迹的影响受性别和阿尔茨海默病遗传风险的调节。

Frailty effects on non-demented cognitive trajectories are moderated by sex and Alzheimer's genetic risk.

机构信息

Department of Psychology, University of Alberta, P217 Biological Sciences Building, Edmonton, AB, Canada.

Neuroscience and Mental Health Institute, University of Alberta, 4-120 Katz Group Centre, Edmonton, AB, Canada.

出版信息

Alzheimers Res Ther. 2019 Jun 21;11(1):55. doi: 10.1186/s13195-019-0509-9.

Abstract

BACKGROUND

Age-related frailty reflects cumulative multisystem physiological and health decline. Frailty increases the risk of adverse brain and cognitive outcomes, including differential decline and dementia. In a longitudinal sample of non-demented older adults, we examine whether (a) the level and/or change in frailty predicts trajectories across three cognitive domains (memory, speed, and executive function (EF)) and (b) prediction patterns are modified by sex or Alzheimer's genetic risk (Apolipoprotein E (APOE)).

METHODS

Participants (n = 632; M age = 70.7, range 53-95; 3 waves) were from the Victoria Longitudinal Study. After computing a frailty index, we used latent growth modeling and path analysis to test the frailty effects on level and change in three latent variables of cognition. We tested two potential moderators by stratifying by sex and APOE risk (ε4+, ε4-).

RESULTS

First, frailty levels predicted speed and EF performance (level) and differential memory change slopes. Second, change in frailty predicted the rate of decline for both speed and EF. Third, sex moderation analyses showed that females were selectively sensitive to (a) frailty effects on memory change and (b) frailty change effects on speed change. In contrast, the frailty effects on EF change were stronger in males. Fourth, genetic moderation analyses showed that APOE risk (e4+) carriers were selectively sensitive to frailty effects on memory change.

CONCLUSION

In non-demented older adults, increasing frailty is strongly associated with the differential decline in cognitive trajectories. For example, higher (worse) frailty was associated with more rapid memory decline than was lower (better) frailty. These effects, however, are moderated by both genetic risk and sex.

摘要

背景

与年龄相关的虚弱反映了多系统生理和健康衰退的累积。虚弱会增加不良大脑和认知结果的风险,包括认知能力的不同下降和痴呆。在一个非痴呆的老年纵向样本中,我们研究了(a)虚弱的水平和/或变化是否预测三个认知领域(记忆、速度和执行功能(EF))的轨迹,以及(b)预测模式是否会被性别或阿尔茨海默病遗传风险(载脂蛋白 E(APOE))改变。

方法

参与者(n=632;平均年龄 70.7,范围 53-95;3 个波次)来自维多利亚纵向研究。在计算了一个虚弱指数后,我们使用潜在增长建模和路径分析来测试虚弱对三个认知潜在变量的水平和变化的影响。我们通过性别和 APOE 风险(ε4+,ε4-)分层来测试两个潜在的调节因素。

结果

首先,虚弱水平预测了速度和 EF 表现(水平)以及记忆变化斜率的差异。其次,虚弱的变化预测了速度和 EF 的下降速度。第三,性别调节分析表明,女性对(a)虚弱对记忆变化的影响以及(b)虚弱对速度变化的影响更为敏感。相比之下,男性对 EF 变化的虚弱影响更强。第四,遗传调节分析表明,APOE 风险(e4+)携带者对虚弱对记忆变化的影响更为敏感。

结论

在非痴呆的老年人群中,虚弱程度的增加与认知轨迹的不同下降密切相关。例如,较高(较差)的虚弱与记忆下降速度较快有关,而较低(较好)的虚弱则与记忆下降速度较慢有关。然而,这些影响受到遗传风险和性别的调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0f9/6587247/1101840698db/13195_2019_509_Fig1_HTML.jpg

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