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认知正常志愿者中潜在 ADRD 血浆生物标志物的相关性。

Associations of potential ADRD plasma biomarkers in cognitively normal volunteers.

机构信息

Sanders-Brown Center on Aging and Alzheimer's Disease Center, University of Kentucky, Lexington, Kentucky, USA.

College of Public Health, Department of Epidemiology, University of Kentucky, Lexington, Kentucky, USA.

出版信息

Alzheimers Dement. 2023 Aug;19(8):3593-3601. doi: 10.1002/alz.13000. Epub 2023 Feb 25.

Abstract

INTRODUCTION

This study examined the relationships between 13 novel blood-plasma biomarkers and dementia-related demographic and health factors in a cohort of 237 cognitively normal research volunteers whose average age was ≈82 years and who were 63% female.

METHODS

We regressed each biomarker on selected covariates to explore the associations between the biomarkers and selected factors to assess whether they may contribute to biomarker values. Post hoc sensitivity analyses were done with updated data and consistent variable sets for robustness and batch effects.

RESULTS

Biomarker concentrations were largely not associated with demographics or health conditions, but some expected associations (e.g., apolipoprotein E [APOE] status with amyloid beta [Aβ]42/Aβ40) were observed. Post hoc results remained similar to those of the main analysis.

DISCUSSION

The absence of strong associations between the biomarkers with age, gender, or medical conditions suggests that changes in these biomarkers, when observed, may be attributable to neuropathological changes.

HIGHLIGHTS

Among N = 237 cognitively normal adults, we studied candidate Alzheimer's disease and related dementia (ADRD) plasma biomarkers. Biomarkers were largely not associated with demographic or health factors. Apolipoprotein E (APOE) status was associated with amyloid beta (Aβ)42/Aβ40 ratio. These results support hypotheses that plasma biomarkers are informative for ADRD.

摘要

简介

本研究在一个平均年龄约为 82 岁且 63%为女性的 237 名认知正常的研究志愿者队列中,考察了 13 种新型血浆生物标志物与痴呆相关的人口统计学和健康因素之间的关系。

方法

我们将每个生物标志物回归到选定的协变量上,以探索生物标志物与选定因素之间的关系,以评估它们是否可能影响生物标志物的值。为了稳健性和批次效应,我们使用更新的数据和一致的变量集进行了事后敏感性分析。

结果

生物标志物浓度与人口统计学或健康状况基本没有关联,但观察到了一些预期的关联(例如载脂蛋白 E [APOE]状态与淀粉样蛋白 β [Aβ]42/Aβ40)。事后结果与主要分析的结果相似。

讨论

生物标志物与年龄、性别或医疗条件之间没有强烈的关联表明,这些生物标志物的变化可能归因于神经病理学变化。

要点

在 N = 237 名认知正常的成年人中,我们研究了候选阿尔茨海默病和相关痴呆症(ADRD)的血浆生物标志物。生物标志物与人口统计学或健康因素基本没有关联。载脂蛋白 E (APOE) 状态与淀粉样蛋白 β (Aβ)42/Aβ40 比值有关。这些结果支持了血浆生物标志物对 ADRD 有信息价值的假说。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27ac/10440211/50e5f4de6bfd/nihms-1872774-f0001.jpg

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