Evidence map›Paper›PMID 30994927›Full record

ArticleAlcoholism, clinical and experimental research2019

The Genetic Relationship Between Alcohol Consumption and Aspects of Problem Drinking in an Ascertained Sample.

Emma C Johnson, Celine L St Pierre, Jacquelyn L Meyers, Fazil Aliev, Vivia V McCutcheon, Dongbing Lai, Danielle M Dick, Alison M Goate, John Kramer, Samuel Kuperman and 6 more

Open access · greenAbstract read
In one paragraph

Article in Alcoholism, clinical and experimental research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
1.8field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 2 syntheses or guidelines pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Genetic Architecture of Alcohol Use Disorder in Nepal.medRxiv : the preprint server for health sciences · 2025
    Article
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  13. High-Intensity Drinking in Adult Australian Twins.Alcoholism, clinical and experimental research · 2020
    Article
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

16 authors at 8 institutions in 2 countries.

Emma C JohnsonDepartment of Psychiatry, Washington University School of Medicine, St Louis, Missouri.ORCID 0000-0003-0394-777X
Celine L St PierreDivision of Biological and Biomedical Sciences, Washington University School of Medicine, Saint Louis, Missouri.
Jacquelyn L MeyersHenri Begleiter Neurodynamics Laboratory, Department of Psychiatry and Behavioral Sciences, SUNY Downstate Medical Center, Brooklyn, New York.
Fazil AlievDepartment of Psychiatry, Virginia Commonwealth University, Richmond, Virginia.
Vivia V McCutcheonDepartment of Psychiatry, Washington University School of Medicine, St Louis, Missouri.
Dongbing LaiDepartment of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana.
Danielle M DickDepartment of Psychology and Human and Molecular Genetics, Virginia Commonwealth University, Richmond, Virginia.ORCID 0000-0002-1636-893X
Alison M GoateDepartment of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, New York.
John KramerDepartment of Psychiatry, Roy J and Lucille A Carver College of Medicine, University of Iowa, Iowa City, Iowa.ORCID 0000-0002-1321-7087
Samuel KupermanDepartment of Psychiatry, Roy J and Lucille A Carver College of Medicine, University of Iowa, Iowa City, Iowa.
John I NurnbergerDepartment of Psychiatry, Indiana University School of Medicine, Indianapolis, Indiana.
Marc A SchuckitDepartment of Psychiatry, University of California San Diego, San Diego, California.ORCID 0000-0002-2323-7858
Bernice PorjeszHenri Begleiter Neurodynamics Laboratory, Department of Psychiatry and Behavioral Sciences, SUNY Downstate Medical Center, Brooklyn, New York.
Howard J EdenbergDepartment of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana.ORCID 0000-0003-0344-9690
Kathleen K BucholzDepartment of Psychiatry, Washington University School of Medicine, St Louis, Missouri.
Arpana AgrawalDepartment of Psychiatry, Washington University School of Medicine, St Louis, Missouri.
Washington University in St. Louis · USIndiana University School of MedicineSUNY Downstate Health Sciences University · USUniversity of Iowa · USIcahn School of Medicine at Mount Sinai · USKarabük University · TRUniversity of California San Diego · USVirginia Commonwealth University · US

Funding

Subject CollectionU10AA008401 · NIAAA · SUNY DOWNSTATE MEDICAL CENTER · PI JAY Arnold TISCHFIELD · 1989 to 2026
$162.7M
National Centralized Repository for Alzheimer's Disease and Related Dementias (NCRAD)U24AG021886 · NIA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI TATIANA M. FOROUD · 2002 to 2026
$119.8M
7/7 Psychiatric Genomics Consortium: Finding actionable variationU01MH109532 · NIMH · WASHINGTON UNIVERSITY · PI AGRAWAL, ARPANA, EDENBERG, HOWARD J · 2016 to 2020
$3.1M
3/7 Psychiatric Genomics Consortium: Finding actionable variationU01MH109536 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CHARNEY, ALEXANDER W, HUCKINS, LAURA MARIANNE · 2016 to 2020
$2.7M
Identifying Contributions to the Genetic Correlation Between Alcohol Use Disorders and SchizophreniaF32AA027435 · NIAAA · WASHINGTON UNIVERSITY · PI JOHNSON, EMMA COVEY · 2018 to 2020
$133k
NIAAA NIH HHS F32 AA027435NIAAA NIH HHS U10 AA008401NIA NIH HHS U24 AG021886NIMH NIH HHS U01 MH109532NIMH NIH HHS U01 MH109536
6 · The paper itself

Abstract

backgroundGenomewide association studies (GWAS) have begun to identify loci related to alcohol consumption, but little is known about whether this genetic propensity overlaps with specific indices of problem drinking in ascertained samples.

methodsIn 6,731 European Americans who had been exposed to alcohol, we examined whether polygenic risk scores (PRS) from a GWAS of weekly alcohol consumption in the UK Biobank predicted variance in 6 alcohol-related phenotypes: alcohol use, maximum drinks within 24 hours (MAXD), total score on the Self-Rating of the Effects of Ethanol Questionnaire (SRE-T), DSM-IV alcohol dependence (DSM4AD), DSM-5 alcohol use disorder symptom counts (DSM5AUDSX), and reduction/cessation of problematic drinking. We also examined the extent to which an single nucleotide polymorphism (rs1229984) in ADH1B, which is strongly associated with both alcohol consumption and dependence, contributed to the polygenic association with these phenotypes and whether PRS interacted with sex, age, or family history of alcoholism to predict alcohol-related outcomes. We performed mixed-effect regression analyses, with family membership and recruitment site included as random effects, as well as survival modeling of age of onset of DSM4AD.

resultsPRS for alcohol consumption significantly predicted variance in 5 of the 6 outcomes: alcohol use (Δmarginal R

conclusionsGenetic propensity for typical alcohol consumption was associated with alcohol use and was also associated with 4 of the additional 5 outcomes, though the variance explained in this sample was modest. Future GWAS that focus on the multifaceted nature of AUD, which goes beyond consumption, might reveal additional information regarding the polygenic underpinnings of problem drinking.

Indexed as

AdultAgedAged, 80 and overAlcohol-Related DisordersCentral Nervous System DepressantsEthanolFemaleGenome-Wide Association StudyHumansMaleMiddle AgedMultifactorial InheritanceCentral Nervous System DepressantsEthanolADH1BAlcohol ConsumptionAlcohol DependencePolygenic Risk

Identifiers

PMID30994927
PMCPMC6560626
OpenAlexW2940258811

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.