Evidence map›Paper›PMID 39401906›Full record

ArticleEnvironmental health and preventive medicine2024

Asian flush gene variant increases mild cognitive impairment risk: a cross-sectional study of the Yoshinogari Brain MRI Checkup Cohort.

Mikiko Tokiya, Manabu Hashimoto, Kenji Fukuda, Kazuhiro Kawamoto, Chiho Akao, Mariko Tsuji, Yusuke Yakushiji, Haruki Koike, Akiko Matsumoto

Abstract read
In one paragraph

Article in Environmental health and preventive medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Mikiko TokiyaDepartment of Environmental Medicine, Saga University.
Manabu HashimotoNational Hospital Organization Hizen Psychiatric Medical Center.
Kenji FukudaDepartment of Cerebrovascular Disease, St. Mary's Hospital.
Kazuhiro KawamotoDepartment of Environmental Medicine, Saga University.
Chiho AkaoDepartment of Environmental Medicine, Saga University.
Mariko TsujiNational Hospital Organization Hizen Psychiatric Medical Center.
Yusuke YakushijiDepartment of Neurology, Kansai Medical University.
Haruki KoikeDivision of Neurology, Department of Internal Medicine, Faculty of Medicine, Saga University.
Akiko MatsumotoDepartment of Environmental Medicine, Saga University.ORCID http://orcid.org/0000-0002-8445-4071

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe East Asian-specific genetic diversity, the rs671 variant of aldehyde dehydrogenase 2, causes the "Asian flush" phenomenon following alcohol consumption, resulting in an alcohol avoidance phenotype. The variant is suggested as a risk factor for Alzheimer's disease; however, its association with mild cognitive impairment (MCI), an effective target for secondary prevention of dementia, remains unclear.

methodThis cross-sectional study examined 430 individuals aged 60-80 years (251 women) without overt cognitive impairment in Yoshinogari, Japan. The effect of the rs671 variant on MCI, defined by scores <26 or <25 on the Japanese version of the Montreal Cognitive Assessment, was evaluated using multivariate logistic regression.

resultsThe models included APOEε4, sex, age, education, history of habitual drinking, Brinkman index, hypertension, diabetes, and subclinical magnetic resonance imaging findings and consistently estimated the risk of the rs671 variant. Subsequently, stratified analyses by history of habitual drinking were performed based on an interactive effect between rs671 and alcohol consumption, and the rs671 variant significantly influenced MCI in participants who did not drink habitually, with odds ratios ranging from 1.9 to 2.1 before and after adjusting for covariates, suggesting an association independent of hippocampal atrophy and small vessel dysfunction. Conversely, no such association with the rs671 variant was observed in participants with a history of habitual alcohol use. Instead, hippocampal atrophy and silent infarcts were associated with MCI.

conclusionsThis is the first study to demonstrate an association between the rs671 variant and MCI morbidity. The findings highlight the need for race-specific preventive strategies and suggest potential unrecognized mechanisms in dementia development.

Indexed as

Alcohol DrinkingAldehyde Dehydrogenase, MitochondrialCognitive DysfunctionFlushingAgedAged, 80 and overBrainCohort StudiesCross-Sectional StudiesEast Asian PeopleFemaleGenetic Predisposition to DiseaseHumansJapanMagnetic Resonance ImagingMaleAldehyde Dehydrogenase, MitochondrialALDH2 protein, humanAldehyde dehydrogenase 2DementiaMild cognitive impairment (MCI)PreventionRacers671

Identifiers

PMID39401906
PMCPMC11473384

What Socratic holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.