Evidence map›Paper›PMID 22591209›Full record

ArticleAlcoholism, clinical and experimental research2013

Association of the ALDH1A1*2 promoter polymorphism with alcohol phenotypes in young adults with or without ALDH2*2.

Jacqueline M Otto, Christian S Hendershot, Susan E Collins, Tiebing Liang, Tamara L Wall

Open access · greenAbstract read
In one paragraph

Article in Alcoholism, clinical and experimental research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

3 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
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

5 authors at 4 institutions in 2 countries.

Jacqueline M OttoDepartment of Psychology, University of Washington, Seattle, WA 98195, USA. jmo5@u.washington.edu
Christian S Hendershot
Susan E Collins
Tiebing Liang
Tamara L Wall
University of Washington · USCentre for Addiction and Mental Health · CAIndiana University – Purdue University Indianapolis · USVA San Diego Healthcare System · US

Funding

Translational Research and Science Education (OUT)P60AA007611 · NIAAA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI Marian Lee Logrip · 2003 to 2026
$45.5M
Alcohol Involvement in Asian American Men and WomenR01AA011257 · NIAAA · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI WALL, TAMARA L · 2001 to 2010
$3.0M
ALCOHOL RESEARCH--RISK AND PROTECTION IN ETHNIC GROUPSK02AA000269 · NIAAA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI WALL, TAMARA L · 1998 to 2008
$1.0M
ALDH2, ADH1B and Alcohol Expectancies in Asian AmericansF31AA016440 · NIAAA · UNIVERSITY OF WASHINGTON · PI HENDERSHOT, CHRISTIAN S · 2006 to 2008
$98k
Alcohol and HIV risk: Genetic and endophenotype approachesF32AA018629 · NIAAA · UNIVERSITY OF NEW MEXICO · PI HENDERSHOT, CHRISTIAN S · 2009 to 2010
$80k
NIAAA NIH HHS F31 AA016440NIAAA NIH HHS F31AA016440NIAAA NIH HHS F32 AA018629NIAAA NIH HHS K02 AA000269NIAAA NIH HHS K02AA00269NIAAA NIH HHS P60 AA007611NIAAA NIH HHS P60AA07611-20NIAAA NIH HHS R01 AA011257NIAAA NIH HHS R01AA11257
6 · The paper itself

Abstract

backgroundPrior studies suggest a possible association of a promoter polymorphism in the ALDH1A1 gene ( ALDH1A1*2 ) with alcohol use or dependence. The aim of this study was to examine the association of ALDH1A1*2 with drinking behaviors in Asian young adults and to examine ALDH2 genotype as a potential moderator of these associations.

methodsAsian young adults (n = 951) were recruited from 2 college sites for studies of genetic associations with alcohol use behavior. Participants completed comprehensive background questionnaires on demographics and drinking behavior. Fingertip blood samples were obtained for DNA extraction and analysis.

resultsParticipants with the ALDH2*1/*2 genotype reported significantly lower levels (frequency and quantity) of drinking within the last 90 days, fewer numbers of heavy drinking episodes within the last 90 days, and lower lifetime maximum consumption levels compared with ALDH2*1/*1 participants. There were no significant main effects of ALDH1A1*2 on any drinking variables, nor was there a significant interaction between ALDH2 and ALDH1A1 genotypes on drinking outcomes.

conclusionsThe association of ALDH2*2 with reduced alcohol consumption replicates previous findings across numerous studies. Although ALDH1A1*2 was not associated with drinking levels, the lack of an ALDH1A1*2 effect in ALDH2*2 individuals is consistent with the only other study that has examined these associations in East Asian populations.

Indexed as

Promoter Regions, GeneticAdolescentAdultAlcohol DrinkingAldehyde DehydrogenaseAldehyde Dehydrogenase 1 FamilyAldehyde Dehydrogenase, MitochondrialAsian PeopleCaliforniaFemaleHumansMalePhenotypePolymorphism, GeneticRetinal DehydrogenaseWashingtonAldehyde DehydrogenaseAldehyde Dehydrogenase 1 FamilyAldehyde Dehydrogenase, MitochondrialALDH1A1 protein, humanALDH2 protein, humanRetinal Dehydrogenase

Identifiers

PMID22591209
PMCPMC3440549
OpenAlexW2114147284

What OpenQuestion holds

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LicenceTDM
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Registered trials

None linked

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.