Evidence map›Paper›PMID 37612092›Full record

ArticleJournal of atherosclerosis and thrombosis2024

Alcohol Consumption and Cerebral Small- and Large-Vessel Diseases: A Mendelian Randomization Analysis.

Takashi Hisamatsu, Yasuharu Tabara, Aya Kadota, Sayuki Torii, Keiko Kondo, Yuichiro Yano, Akihiko Shiino, Kazuhiko Nozaki, Tomonori Okamura, Hirotsugu Ueshima and 1 more

Open access · diamondAbstract read
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Article in Journal of atherosclerosis and thrombosis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
2.3field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 2 syntheses or guidelines pooled it, 9 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Takashi HisamatsuDepartment of Public Health, Shiga University of Medical Science.
Yasuharu TabaraDepartment of Public Health, Shiga University of Medical Science.
Aya KadotaDepartment of Public Health, Shiga University of Medical Science.
Sayuki ToriiDepartment of Public Health, Shiga University of Medical Science.
Keiko KondoDepartment of Public Health, Shiga University of Medical Science.
Yuichiro YanoDepartment of Public Health, Shiga University of Medical Science.
Akihiko ShiinoMolecular Neuroscience Research Center, Shiga University of Medical Science.
Kazuhiko NozakiDepartment of Neurosurgery, Shiga University of Medical Science.
Tomonori OkamuraDepartment of Public Health, Shiga University of Medical Science.
Hirotsugu UeshimaDepartment of Public Health, Shiga University of Medical Science.
Katsuyuki MiuraDepartment of Public Health, Shiga University of Medical Science.
Shiga University of Medical Science · JPKeio University · JPOkayama University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsIt remains inconclusive regarding alcohol intake and stroke risk because determining risk factors depends on the specific pathogenesis of stroke. We used the variant rs671 in the aldehyde dehydrogenase 2 gene (ALDH2) as an instrument to investigate the causal role of alcohol intake in cerebral small- and large-vessel diseases.

methodsWe studied 682 men (mean age, 70.0 years), without stroke, in a cross-sectional Mendelian randomization analysis. We assessed small-vessel diseases (SVDs), which comprised lacunar infarcts, white matter hyperintensities (WMHs), and cerebral microbleeds, and large intracranial artery stenosis (ICAS) on brain magnetic resonance imaging.

resultsThe median (25%tiles, 75%tiles) alcohol consumption by ALDH2-rs671 inactive A allele (n=313 [45.9%]) and non-A allele (n=369 [54.1%]) carriers was 3.5 (0.0, 16.0) and 32.0 (12.9, 50.0) g/day, respectively. Non-A allele carriers had higher prevalent hypertension and lower low-density lipoprotein cholesterol concentrations than A allele carriers. In age-adjusted ordinal logistic regression for graded burden, odds ratios (95% confidence intervals) for total SVDs, lacunar infarcts, WMHs, cerebral microbleeds, and ICAS in non-Aallele carriers were 1.46 (1.09-1.94), 1.41 (0.95-2.08), 1.39 (1.05-1.85), 1.69 (1.06-2.69), and 0.70 (0.50-0.98), respectively, compared with A allele carriers. These associations attenuated to statistical non-significance after considering covariates and amount of alcohol intake.

conclusionsOur findings suggest a positive association of alcohol consumption with risk of cerebral SVDs and its inverse association with risk of large-vessel disease through intermediaries, such as hypertension or low-density lipoprotein cholesterol. These findings provide insight into potential causal mechanisms linking alcohol consumption with stroke risk.

Indexed as

Cerebral Small Vessel DiseasesHypertensionStrokeStroke, LacunarAgedAlcohol DrinkingAldehyde Dehydrogenase, MitochondrialCerebral HemorrhageCholesterol, LDLCross-Sectional StudiesHumansMaleMendelian Randomization AnalysisAldehyde Dehydrogenase, MitochondrialALDH2 protein, humanCholesterol, LDLAlcoholAldehyde dehydrogenase 2Cerebral small-vessel diseaseIntracranial artery stenosisMendelian randomization

Identifiers

PMID37612092
PMCPMC10857837
OpenAlexW4386058572

What OpenQuestion holds

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LicenceCC BY-NC-SA
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Registered trials

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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 OpenQuestion graph.