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基于血液的多变量甲基化风险评分用于认知障碍和痴呆。

Blood-based multivariate methylation risk score for cognitive impairment and dementia.

机构信息

Department of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience (MHeNs), Faculty of Health, Medicine and Life Sciences (FHML), Maastricht University, Maastricht, The Netherlands.

Department of Biochemistry, Cardiovascular Research Institute Maastricht (CARIM), Faculty of Health, Medicine and Life Sciences (FHML), Maastricht University, Maastricht, The Netherlands.

出版信息

Alzheimers Dement. 2024 Oct;20(10):6682-6698. doi: 10.1002/alz.14061. Epub 2024 Aug 28.

Abstract

INTRODUCTION

The established link between DNA methylation and pathophysiology of dementia, along with its potential role as a molecular mediator of lifestyle and environmental influences, positions blood-derived DNA methylation as a promising tool for early dementia risk detection.

METHODS

In conjunction with an extensive array of machine learning techniques, we employed whole blood genome-wide DNA methylation data as a surrogate for 14 modifiable and non-modifiable factors in the assessment of dementia risk in independent dementia cohorts.

RESULTS

We established a multivariate methylation risk score (MMRS) for identifying mild cognitive impairment cross-sectionally, independent of age and sex (P = 2.0 × 10). This score significantly predicted the prospective development of cognitive impairments in independent studies of Alzheimer's disease (hazard ratio for Rey's Auditory Verbal Learning Test (RAVLT)-Learning = 2.47) and Parkinson's disease (hazard ratio for MCI/dementia= 2.59).

DISCUSSION

Our work shows the potential of employing blood-derived DNA methylation data in the assessment of dementia risk.

HIGHLIGHTS

We used whole blood DNA methylation as a surrogate for 14 dementia risk factors. Created a multivariate methylation risk score for predicting cognitive impairment. Emphasized the role of machine learning and omics data in predicting dementia. The score predicts cognitive impairment development at the population level.

摘要

简介

DNA 甲基化与痴呆病理生理学之间的既定联系,以及其作为生活方式和环境影响的分子介质的潜在作用,使血液衍生的 DNA 甲基化为早期痴呆风险检测提供了一种很有前途的工具。

方法

我们结合了广泛的机器学习技术,将全血基因组范围的 DNA 甲基化数据作为评估独立痴呆队列中痴呆风险的 14 个可改变和不可改变因素的替代物。

结果

我们建立了一个多变量甲基化风险评分(MMRS),用于在独立的认知障碍研究中,在不考虑年龄和性别的情况下,对轻度认知障碍进行横断面识别(P=2.0×10)。该评分显著预测了阿尔茨海默病(Rey 的听觉言语学习测试(RAVLT)学习的危险比为 2.47)和帕金森病(MCI/痴呆的危险比为 2.59)中认知障碍的前瞻性发展。

讨论

我们的工作表明,在评估痴呆风险时,利用血液衍生的 DNA 甲基化数据具有潜力。

要点

我们使用全血 DNA 甲基化作为 14 个痴呆风险因素的替代物。创建了一个多变量甲基化风险评分,用于预测认知障碍。强调了机器学习和组学数据在预测痴呆中的作用。该评分可预测人群水平的认知障碍发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0827/11633365/5b58a5883e6f/ALZ-20-6682-g005.jpg

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