Evidence map›Paper›PMID 21968928›Full record

SynthesisMolecular psychiatry2012

ADH1B is associated with alcohol dependence and alcohol consumption in populations of European and African ancestry.

L J Bierut, A M Goate, N Breslau, E O Johnson, S Bertelsen, L Fox, A Agrawal, K K Bucholz, R Grucza, V Hesselbrock and 11 more

Open access · greenAbstract readMeta-Analysis
In one paragraph

Synthesis in Molecular psychiatry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 134 papers, 13 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
134citing papers in PubMed, 13 pooled it
10.3field-weighted citation impact, top 1% 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

134 citing papers in PubMed, 13 syntheses or guidelines pooled it, 222 citations in OpenAlex.

  1. Genome-wide meta-analysis of alcohol use disorder in East Asians.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
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  7. KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference.Proceedings of the National Academy of Sciences of the United States of America · 2016
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  18. Effect ofBJPsych open · 2026
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74 more citing papers are in PubMed but not listed here.

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

21 authors at 10 institutions in 1 country.

L J BierutDepartment of Psychiatry, Washington University School of Medicine, St Louis, MO 63110, USA. laura@wustl.edu
A M Goate
N Breslau
E O Johnson
S Bertelsen
L Fox
A Agrawal
K K Bucholz
R Grucza
V Hesselbrock
J Kramer
S Kuperman
J Nurnberger
B Porjesz
N L Saccone
M Schuckit
J Tischfield
J C Wang
T Foroud
J P Rice
H J Edenberg
Washington University in St. Louis · USIndiana University School of MedicineMichigan State University · USRTI International · USRutgers, The State University of New Jersey · USState University of New York · USUniversity of California, San Diego · USUniversity of Connecticut · USUniversity of Iowa · USUniversity of Iowa Hospitals and Clinics · US

Funding

Subject CollectionU10AA008401 · NIAAA · SUNY DOWNSTATE MEDICAL CENTER · PI Yunlong Liu · 1989 to 2026
$162.7M
The Collaborative Genetic Study of Nicotine DependenceP01CA089392 · NCI · WASHINGTON UNIVERSITY · PI BIERUT, LAURA J. · 2001 to 2012
$17.3M
FAMILY STUDY OF COCAINE DEPENDENCER01DA013423 · NIDA · WASHINGTON UNIVERSITY · PI BIERUT, LAURA JEAN · 2000 to 2004
$2.2M
Case Control Candidate Gene Study of AddictionR01DA019963 · NIDA · WASHINGTON UNIVERSITY · PI BIERUT, LAURA J. · 2007 to 2009
$1.2M
Human Genetics of Addiction: A Study of Common and Specific FactorsK02DA021237 · NIDA · WASHINGTON UNIVERSITY · PI BIERUT, LAURA J. · 2007 to 2011
$567k
NCI NIH HHS P01 CA089392NIAAA NIH HHS U10 AA008401NIDA NIH HHS K02 DA021237NIDA NIH HHS R01 DA013423NIDA NIH HHS R01 DA019963
6 · The paper itself

Abstract

A coding variant in alcohol dehydrogenase 1B (ADH1B) (rs1229984) that leads to the replacement of Arg48 with His48 is common in Asian populations and reduces their risk for alcoholism, but because of very low allele frequencies the effects in European or African populations have been difficult to detect. We genotyped and analyzed this variant in three large European and African-American case-control studies in which alcohol dependence was defined by the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) criteria, and demonstrated a strong protective effect of the His48 variant (odds ratio (OR) 0.34, 95% confidence interval (CI) 0.24, 0.48) on alcohol dependence, with genome-wide significance (6.6 × 10(-10)). The hypothesized mechanism of action involves an increased aversive reaction to alcohol; in keeping with this hypothesis, the same allele is strongly associated with a lower maximum number of drinks in a 24-hour period (lifetime), with P=3 × 10(-13). We also tested the effects of this allele on the development of alcoholism in adolescents and young adults, and demonstrated a significantly protective effect. This variant has the strongest effect on risk for alcohol dependence compared with any other tested variant in European populations.

Indexed as

AdolescentAdultAgedAlcohol DehydrogenaseAlcohol DrinkingAlcoholismAllelesBlack or African AmericanBlack PeopleCase-Control StudiesFemaleGenotypeHumansMaleMiddle AgedPolymorphism, Single NucleotideADH1B protein, humanAlcohol Dehydrogenase

Identifiers

PMID21968928
PMCPMC3252425
OpenAlexW2137516476

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.