Relationship between alcohol consumption and dementia with Mendelian randomization approaches among older adults in the United States.

IF 4 Q1 CLINICAL NEUROLOGY Alzheimer''s and Dementia: Diagnosis, Assessment and Disease Monitoring Pub Date : 2024-06-20 eCollection Date: 2024-04-01 DOI:10.1002/dad2.12598
Kyle A Campbell, Mingzhou Fu, Elizabeth MacDonald, Matthew Zawistowski, Kelly M Bakulski, Erin B Ware
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Abstract

Introduction: In observational studies, the association between alcohol consumption and dementia is mixed.

Methods: We performed two-sample Mendelian randomization (MR) using summary statistics from genome-wide association studies of weekly alcohol consumption and late-onset Alzheimer's disease and one-sample MR in the Health and Retirement Study (HRS), wave 2012. Inverse variance weighted two-stage regression provided odds ratios of association between alcohol exposure and dementia or cognitively impaired, non-dementia relative to cognitively normal.

Results: Alcohol consumption was not associated with late-onset Alzheimer's disease using two-sample MR (odds ratio [OR] = 1.15, 95% confidence interval [CI]: [0.78, 1.72]). In HRS, doubling weekly alcohol consumption was not associated with dementia (African ancestries, n = 1,322, OR = 1.00, 95% CI [0.45, 2.25]; European ancestries, n = 7,160, OR = 1.37, 95% CI [0.53, 3.51]) or cognitively impaired, non-dementia (African ancestries, n = 1,322, OR = 1.17, 95% CI [0.69, 1.98]; European ancestries, n = 7,160, OR = 0.75, 95% CI [0.47, 1.22]).

Discussion: Alcohol consumption was not associated with cognitively impaired, non-dementia or dementia status.

Highlights: Cross-sectionally in a large, diverse sample, alcohol appears protective for dementia.We apply two- and one-sample Mendelian randomization to test inferred causality.Mendelian randomization approaches show no association with alcohol and dementia.We conclude that alcohol consumption should not be considered protective.

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用孟德尔随机方法研究美国老年人饮酒与痴呆症之间的关系。
简介:在观察性研究中,饮酒与痴呆症之间的关系喜忧参半:在观察性研究中,饮酒与痴呆之间的关系好坏参半:我们利用每周饮酒量与晚发性阿尔茨海默病的全基因组关联研究的汇总统计资料进行了两样本孟德尔随机化(MR),并在2012年波健康与退休研究(HRS)中进行了单样本MR。反方差加权两阶段回归提供了酒精暴露与痴呆或认知功能受损、非痴呆与认知功能正常之间的相关几率比:使用双样本 MR,饮酒与晚发性阿尔茨海默病无关(几率比 [OR] = 1.15,95% 置信区间 [CI]:[0.78, 1.72])。在 HRS 中,每周饮酒量增加一倍与痴呆症无关(非洲血统,n = 1 322,OR = 1.00,95% CI [0.45,2.25];欧洲血统,n = 7 160,OR = 1.37,95% CI [0.53,3.51])。53,3.51])或认知受损、非痴呆(非洲血统,n = 1 322,OR = 1.17,95% CI [0.69,1.98];欧洲血统,n = 7 160,OR = 0.75,95% CI [0.47,1.22]):讨论:饮酒与认知障碍、非痴呆或痴呆状态无关:我们采用双样本和单样本孟德尔随机法来检验推断的因果关系,结果显示酒精与痴呆症没有关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.80
自引率
7.50%
发文量
101
审稿时长
8 weeks
期刊介绍: Alzheimer''s & Dementia: Diagnosis, Assessment & Disease Monitoring (DADM) is an open access, peer-reviewed, journal from the Alzheimer''s Association® that will publish new research that reports the discovery, development and validation of instruments, technologies, algorithms, and innovative processes. Papers will cover a range of topics interested in the early and accurate detection of individuals with memory complaints and/or among asymptomatic individuals at elevated risk for various forms of memory disorders. The expectation for published papers will be to translate fundamental knowledge about the neurobiology of the disease into practical reports that describe both the conceptual and methodological aspects of the submitted scientific inquiry. Published topics will explore the development of biomarkers, surrogate markers, and conceptual/methodological challenges. Publication priority will be given to papers that 1) describe putative surrogate markers that accurately track disease progression, 2) biomarkers that fulfill international regulatory requirements, 3) reports from large, well-characterized population-based cohorts that comprise the heterogeneity and diversity of asymptomatic individuals and 4) algorithmic development that considers multi-marker arrays (e.g., integrated-omics, genetics, biofluids, imaging, etc.) and advanced computational analytics and technologies.
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