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从中年期开始的大脑淀粉样蛋白β和tau 与认知的关联。

Associations of cerebral amyloid beta and tau with cognition from midlife.

机构信息

Department of Neurology, Cedars Sinai Medical Center, Los Angeles, California, USA.

Glenn Biggs Institute for Alzheimer's & Neurodegenerative Diseases, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.

出版信息

Alzheimers Dement. 2024 Sep;20(9):5901-5911. doi: 10.1002/alz.14060. Epub 2024 Jul 22.

Abstract

INTRODUCTION

Understanding early neuropathological changes and their associations with cognition may aid dementia prevention. This study investigated associations of cerebral amyloid and tau positron emission tomography (PET) retention with cognition in a predominately middle-aged community-based cohort and examined factors that may modify these relationships.

METHODS

C-Pittsburgh compound B amyloid and F-flortaucipir tau PET imaging were performed. Associations of amyloid and tau PET with cognition were evaluated using linear regression. Interactions with age, apolipoprotein E (APOE) ε4 status, and education were examined.

RESULTS

Amyloid and tau PET were not associated with cognition in the overall sample (N = 423; mean: 57 ± 10 years; 50% female). However, younger age (< 55 years) and APOE ε4 were significant effect modifiers, worsening cognition in the presence of higher amyloid and tau.

DISCUSSION

Higher levels of Aβ and tau may have a pernicious effect on cognition among APOE ε4 carriers and younger adults, suggesting a potential role for targeted early interventions.

HIGHLIGHTS

Risk and resilience factors influenced cognitive vulnerability due to Aβ and tau. Higher fusiform tau associated with poorer visuospatial skills in younger adults. APOE ε4 interacted with Aβ and tau to worsen cognition across multiple domains.

摘要

简介

了解早期神经病理学变化及其与认知的关联可能有助于预防痴呆。本研究调查了在以中年为主的社区人群中,大脑淀粉样蛋白和 tau 正电子发射断层扫描(PET)保留与认知的关联,并研究了可能改变这些关联的因素。

方法

进行 C-Pittsburgh 复合 B 淀粉样蛋白和 F-flortaucipir tau PET 成像。使用线性回归评估淀粉样蛋白和 tau PET 与认知的关联。研究了年龄、载脂蛋白 E(APOE)ε4 状态和教育的交互作用。

结果

在整个样本(N=423;平均年龄:57±10 岁;50%为女性)中,淀粉样蛋白和 tau PET 与认知均无关联。然而,年龄较小(<55 岁)和 APOE ε4 是显著的效应修饰因子,在存在更高水平的淀粉样蛋白和 tau 的情况下会使认知恶化。

讨论

较高水平的 Aβ 和 tau 可能对 APOE ε4 携带者和年轻成年人的认知产生有害影响,这表明有针对性的早期干预可能发挥作用。

重点

风险和恢复力因素影响了由于 Aβ 和 tau 引起的认知脆弱性。年轻成年人的梭状回 tau 较高与较差的视觉空间技能相关。APOE ε4 与 Aβ 和 tau 相互作用,导致多个领域的认知恶化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a52/11497641/304d4e5caf0d/ALZ-20-5901-g002.jpg

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