Evidence map›Paper›PMID 24962325›Full record

ArticleDrug and alcohol dependence2014

Genome-wide survival analysis of age at onset of alcohol dependence in extended high-risk COGA families.

Manav Kapoor, Jen-Chyong Wang, Leah Wetherill, Nhung Le, Sarah Bertelsen, Anthony L Hinrichs, John Budde, Arpana Agrawal, Laura Almasy, Kathleen Bucholz and 14 more

Open access · greenAbstract read
In one paragraph

Article in Drug and alcohol dependence, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 3 pooled it
2.1field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 3 syntheses or guidelines pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Identification of novel genetic loci and candidate genes for progressive ethanol consumption in diversity outbred mice.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
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  11. Recent advances in genetic studies of alcohol use disorders.Current genetic medicine reports · 2020
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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

24 authors at 9 institutions in 1 country.

Manav KapoorWashington University School of Medicine, United States.
Jen-Chyong WangWashington University School of Medicine, United States.
Leah WetherillIndiana University School of Medicine, United States.
Nhung LeWashington University School of Medicine, United States.
Sarah BertelsenWashington University School of Medicine, United States.
Anthony L HinrichsWashington University School of Medicine, United States.
John BuddeWashington University School of Medicine, United States.
Arpana AgrawalWashington University School of Medicine, United States.
Laura AlmasySouthwest Foundation for Biomedical Research, United States.
Kathleen BucholzWashington University School of Medicine, United States.
Danielle M DickVirginia Commonwealth University, United States.
Oscar HarariWashington University School of Medicine, United States.
Xuei XiaolingIndiana University School of Medicine, United States.
Victor HesselbrockUniversity of Connecticut Health Center, United States.
John KramerUniversity of Iowa Carver College of Medicine, United States.
John I NurnbergerIndiana University School of Medicine, United States.
John RiceWashington University School of Medicine, United States.
Marc SchuckitUniversity of California, San Diego, United States.
Jay TischfieldRutgers University, United States.
Bernice PorjeszSUNY Health Sciences Center, United States.
Howard J EdenbergIndiana University School of Medicine, United States.
Laura BierutWashington University School of Medicine, United States.
Tatiana ForoudIndiana University School of Medicine, United States.
Alison GoateWashington University School of Medicine, United States. Electronic address: goate@wustl.edu.
Washington University in St. Louis · USUniversity School · USRutgers, The State University of New Jersey · USTexas Biomedical Research Institute · USUConn Health · USUniversity of California San Diego · USUniversity of Iowa · USUniversity of Washington · USVirginia Commonwealth University · US

Funding

Subject CollectionU10AA008401 · NIAAA · SUNY DOWNSTATE MEDICAL CENTER · PI JESSICA E SALVATORE · 1989 to 2026
$162.7M
Quality Assurance and Quality Control Project Management: Improving Submissions and Study Conduct in the Human Subjects Research Prior Approval ProcessUL1TR002529 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI MOE, SHARON M, WIEHE, SARAH ELIZABETH · 2018 to 2022
$27.2M
Indiana Clinical and Translational Sciences InstituteUL1TR001108 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI DENNE, SCOTT C., SHEKHAR, ANANTHA · 2013 to 2017
$23.3M
Twin, molecular, and developmental approaches to understanding alcohol misuseK02AA018755 · NIAAA · VIRGINIA COMMONWEALTH UNIVERSITY · PI DICK, DANIELLE M · 2010 to 2019
$1.3M
AGE AT FIRST DRINK AND ALCOHOLISM: INTERSECTION OF GENES AND ENVIRONMENTR21AA021235 · NIAAA · WASHINGTON UNIVERSITY · PI AGRAWAL, ARPANA · 2013 to 2014
$392k
NCATS NIH HHS UL1 TR001108NIAAA NIH HHS K02 AA018755NIAAA NIH HHS R21 AA021235NIAAA NIH HHS R21AA021235NIAAA NIH HHS U10 AA008401NIAAA NIH HHS U10AA008401
6 · The paper itself

Abstract

backgroundThe age at onset of alcohol dependence (AD) is a critical moderator of genetic associations for alcohol dependence. The present study evaluated whether single nucleotide polymorphisms (SNPs) can influence the age at onset of AD in large high-risk families from the Collaborative Study on the Genetics of Alcoholism (COGA).

methodsGenomewide SNP genotyping was performed in 1788 regular drinkers from 118 large European American families densely affected with alcoholism. We used a genome-wide Cox proportional hazards regression model to test for association between age at onset of AD and SNPs.

resultsThis family-based analysis identified an intergenic SNP, rs2168784 on chromosome 3 that showed strong evidence of association (P=5×10(-9)) with age at onset of AD among regular drinkers. Carriers of the minor allele of rs2168784 had 1.5 times the hazard of AD onset as compared with those homozygous for the major allele. By the age of 20 years, nearly 30% of subjects homozygous for the minor allele were alcohol dependent while only 19% of those homozygous for the major allele were. We also identified intronic SNPs in the ADP-ribosylation factor like 15 (ARL15) gene on chromosome 5 (P=1.11×10(-8)) and the UTP20 small subunit (UTP20) gene on chromosome 12 (P=4.32×10(-8)) that were associated with age at onset of AD.

conclusionsThis extended family based genome-wide cox-proportional hazards analysis identified several loci that might be associated with age at onset of AD.

Indexed as

Genetic Predisposition to DiseaseGenotypePolymorphism, Single NucleotideAdolescentAdultAge of OnsetAlcohol DrinkingAlcoholismAllelesFemaleGenome-Wide Association StudyHumansMaleMiddle AgedPhenotypeWhite PeopleAge at onsetAlcohol dependenceGWASSNPSurvival analysis

Identifiers

PMID24962325
PMCPMC4127128
OpenAlexW2018750223

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.