Evidence map›Paper›PMID 36180423›Full record

ArticleTranslational psychiatry2022

Parsing genetically influenced risk pathways: genetic loci impact problematic alcohol use via externalizing and specific risk.

Peter B Barr, Travis T Mallard, Sandra Sanchez-Roige, Holly E Poore, Richard Karlsson Linnér, COGA Collaborators, Irwin D Waldman, Abraham A Palmer, K Paige Harden, Danielle M Dick

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
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  4. Growth Trajectories of Suicide Ideation and Attempt in a Population-Based Cohort from the United States.Archives of suicide research : official journal of the International Academy for Suicide Research · 2026
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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

10 authors at 15 institutions in 2 countries.

Peter B BarrDepartment of Psychiatry & Behavioral Sciences, SUNY Downstate Health Sciences University, Brooklyn, NY, USA. peter.barr@downstate.edu.ORCID 0000-0001-9321-657X
Travis T MallardPsychiatric and Neurodevelopmental Genetics Unit, Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
Sandra Sanchez-RoigeDepartment of Psychiatry, University of California San Diego, La Jolla, CA, USA.ORCID 0000-0001-6137-5699
Holly E PooreDepartment of Psychiatry, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, USA.
Richard Karlsson LinnérDepartment of Economics, Leiden University, Leiden, The Netherlands.
COGA Collaborators
Irwin D WaldmanDepartment of Psychology, Emory University, Atlanta, GA, USA.ORCID 0000-0002-6862-1837
Abraham A PalmerDepartment of Psychiatry, University of California San Diego, La Jolla, CA, USA.ORCID 0000-0003-3634-0747
K Paige HardenDepartment of Psychology, University of Texas at Austin, Austin, TX, USA.ORCID 0000-0002-1557-6737
Danielle M DickDepartment of Psychiatry, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, USA.
Rutgers, The State University of New Jersey · USState University of New York · USWashington University in St. Louis · USIndiana University School of MedicineUniversity of Iowa · USEmory University · USHoward University · USIcahn School of Medicine at Mount Sinai · USUniversity of California San Diego · USUniversity of Connecticut · USHarvard University · USLeiden University · NLLifespan · USNational Institute on Alcohol Abuse and Alcoholism · USSUNY Downstate Health Sciences University · US

Funding

Subject CollectionU10AA008401 · NIAAA · SUNY DOWNSTATE MEDICAL CENTER · PI JESSICA E SALVATORE · 1989 to 2026
$162.7M
Project 5 - Genetic architecture of alcohol use disorder using cross-trait genetic correlations and public next-generation sequencing studiesP50AA022537 · NIAAA · VIRGINIA COMMONWEALTH UNIVERSITY · PI JENNIFER T WOLSTENHOLME · 2014 to 2026
$19.6M
The development of alcohol misuse and related problems from adolescence to early midlifeR01AA015416 · NIAAA · WASHINGTON UNIVERSITY · PI DICK, DANIELLE M, SALVATORE, JESSICA E · 2005 to 2024
$7.6M
Using the Genetic Architecture of Substance Use Disorders to Advance Gene Identification and Understanding of Pathways of RiskR01DA050721 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI DANIELLE M DICK · 2020 to 2026
$3.9M
Building Bridges to Allow Cross-species Translational genetics for the Study of AddictionDP1DA054394 · NIDA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SANCHEZ ROIGE, SANDRA · 2021 to 2025
$2.4M
Molecular Neuroscience of Alcohol and Drug Abuse Research TrainingT32AA028254 · NIAAA · RUTGERS, THE STATE UNIV OF N.J. · PI ASTON-JONES, GARY S., SARKAR, DIPAK KUMAR · 2019 to 2023
$1.3M
Twin, molecular, and developmental approaches to understanding alcohol misuseK02AA018755 · NIAAA · VIRGINIA COMMONWEALTH UNIVERSITY · PI DICK, DANIELLE M · 2010 to 2019
$1.3M
Medical Research Council MC_PC_17228Medical Research Council MC_QA137853NIAAA NIH HHS K02 AA018755NIAAA NIH HHS P50 AA022537NIAAA NIH HHS P50AA022537NIAAA NIH HHS R01 AA015416NIAAA NIH HHS R01AA015416NIAAA NIH HHS T32 AA028254NIAAA NIH HHS U10 AA008401NIDA NIH HHS DP1 DA054394NIDA NIH HHS DP1DA054394NIDA NIH HHS R01 DA050721NIDA NIH HHS R01DA050721
6 · The paper itself

Abstract

Genome-wide association studies (GWAS) identify genetic variants associated with a trait, regardless of how those variants are associated with the outcome. Characterizing whether variants for psychiatric outcomes operate via specific versus general pathways provides more informative measures of genetic risk. In the current analysis, we used multivariate GWAS to tease apart variants associated with problematic alcohol use (ALCP-total) through either a shared risk for externalizing (EXT) or a problematic alcohol use-specific risk (ALCP-specific). SNPs associated with ALCP-specific were primarily related to alcohol metabolism. Genetic correlations showed ALCP-specific was predominantly associated with alcohol use and other forms of psychopathology, but not other forms of substance use. Polygenic scores for ALCP-total were associated with multiple forms of substance use, but polygenic scores for ALCP-specific were only associated with alcohol phenotypes. Polygenic scores for both ALCP-specific and EXT show different patterns of associations with alcohol misuse across development. Our results demonstrate that focusing on both shared and specific risk can better characterize pathways of risk for substance use disorders. Parsing risk pathways will become increasingly relevant as genetic information is incorporated into clinical practice.

Indexed as

Genome-Wide Association StudySubstance-Related DisordersAlcohol DrinkingGenetic LociGenetic Predisposition to DiseaseHumansMultifactorial Inheritance

Identifiers

PMID36180423
PMCPMC9525649
OpenAlexW4298138395

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.