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Randomized Controlled Trial
. 2019 Sep 4;2(9):e1910319.
doi: 10.1001/jamanetworkopen.2019.10319.

Alcohol Consumption and Risk of Dementia and Cognitive Decline Among Older Adults With or Without Mild Cognitive Impairment

Affiliations
Randomized Controlled Trial

Alcohol Consumption and Risk of Dementia and Cognitive Decline Among Older Adults With or Without Mild Cognitive Impairment

Manja Koch et al. JAMA Netw Open. .

Abstract

Importance: Substantial heterogeneity and uncertainty exist in the observed associations between alcohol consumption and dementia.

Objective: To assess the association between alcohol consumption and dementia and the roles of mild cognitive impairment (MCI) and apolipoprotein E ε4 (APOE E4) genotype in modifying this association.

Design, setting, and participants: This cohort study used data from the Ginkgo Evaluation of Memory Study, conducted from 2000 to 2008 among US community-dwelling participants. This study analyzed 3021 participants aged 72 years and older who were free of dementia. Data analysis was performed from 2017 to 2018.

Exposures: Self-reported alcohol consumption, drinking frequency, and quantity.

Main outcomes and measures: Using multivariable proportional hazards regression and linear mixed models, the risk of dementia and the rate of change over time in the Modified Mini-Mental State Examination were estimated.

Results: Among 3021 participants, the median (interquartile range) age was 78 (76-80) years; 1395 (46.2%) were female. During a median (interquartile range) follow-up of 6.0 (4.9-6.5) years, 512 cases of dementia occurred. For 7.1 to 14.0 drinks per week compared with less than 1.0 drink per week, the hazard ratios for dementia were 0.63 (95% CI, 0.38-1.06) among 2548 participants without MCI and 0.93 (95% CI, 0.47-1.84) among 473 participants with MCI. Among participants with MCI, the hazard ratio for dementia was 1.72 (95% CI, 0.87-3.40) for more than 14.0 drinks per week compared with less than 1.0 drink per week. The association of alcohol intake with dementia differed for participants with and without baseline MCI (P for interaction = .03). Among participants without MCI, daily low-quantity drinking was associated with lower dementia risk than infrequent higher-quantity drinking (hazard ratio, 0.45; 95% CI, 0.23-0.89; P = .02). Findings were consistent when stratified by sex, age, and APOE E4 genotype. Compared with drinking less than 1.0 drink per week, complete abstention (in participants without MCI) and the consumption of more than 14.0 drinks per week (in participants with MCI) were associated with lower Modified Mini-Mental State Examination scores (mean difference at follow-up compared with baseline, -0.46 point [95% CI, -0.87 to -0.04 point] and -3.51 points [95% CI, -5.75 to -1.27 points], respectively).

Conclusions and relevance: In this study, complete abstention and consuming more than 14.0 drinks per week (compared with drinking <1.0 drink per week) were associated with lower cognitive scores among participants aged 72 years and older. Particular caution is needed among individuals with MCI who continue to drink alcohol.

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Conflict of interest statement

Conflict of Interest Disclosures: Dr Fitzpatrick reported receiving grants from the University of Washington during the conduct of the study. Dr Williamson reported receiving grants from the National Institutes of Health (NIH) during the conduct of the study. Dr Lopez reported receiving personal fees from Grifols, Inc, outside the submitted work. Dr DeKosky reported receiving grants from the National Institute on Aging during the conduct of the study, personal fees from Amgen and Biogen, and royalties from Up To Date outside the submitted work. Dr Mukamal reported receiving grants from the NIH outside the submitted work. Dr Sink reported receiving grants from the NIH during the conduct of the study and reported that she was at the Wake Forest University School of Medicine and an NIH-funded investigator in the Ginkgo Evaluation of Memory Study when the data were collected and the first draft of the manuscript was generated. At the time of publication, Dr Sink is a full-time employee of Genentech, a member of the Roche Group. Genentech made no contribution to the Ginkgo Evaluation of Memory Study. No other disclosures were reported.

Figures

Figure.
Figure.. Risk of Dementia in Participants With and Without Mild Cognitive Impairment (MCI) at Baseline by Self-reported Weekly Number of Drinks
Plots show log hazard ratios (solid lines) and 95% confidence intervals (dashed lines) for risk of dementia by self-reported weekly number of drinks among 2548 participants without MCI at baseline (A) and 473 participants with MCI at baseline (B). Log hazard ratios were obtained from a generalized additive proportional hazards model with 3 df adjusted for age, sex, race/ethnicity, clinic site, educational level, social activity, smoking status, body mass index, lipid-lowering medication use, history of cardiovascular disease, diabetes, Center for Epidemiologic Studies Depression Scale score, treatment group assignment, and APOE genotype.

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