Evidence map›Paper›PMID 25079289›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2015

Shared genetic factors influence amygdala volumes and risk for alcoholism.

Alecia D Dager, D Reese McKay, Jack W Kent, Joanne E Curran, Emma Knowles, Emma Sprooten, Harald H H Göring, Thomas D Dyer, Godfrey D Pearlson, Rene L Olvera and 6 more

Abstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

30 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
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  6. Article
  7. Phenome-wide association studies betweenFrontiers in psychiatry · 2024
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  16. Validity and utility of Hierarchical Taxonomy of Psychopathology (HiTOP): II. Externalizing superspectrum.World psychiatry : official journal of the World Psychiatric Association (WPA) · 2021
    Article
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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

16 authors.

Alecia D Dager1] Olin Neuropsychiatry Research Center, Institute of Living, Hartford Hospital, Hartford, CT, USA [2] Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
D Reese McKay1] Olin Neuropsychiatry Research Center, Institute of Living, Hartford Hospital, Hartford, CT, USA [2] Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
Jack W KentDepartment of Genetics, Texas Biomedical Research Institute, San Antonio, TX, USA.
Joanne E CurranDepartment of Genetics, Texas Biomedical Research Institute, San Antonio, TX, USA.
Emma Knowles1] Olin Neuropsychiatry Research Center, Institute of Living, Hartford Hospital, Hartford, CT, USA [2] Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
Emma Sprooten1] Olin Neuropsychiatry Research Center, Institute of Living, Hartford Hospital, Hartford, CT, USA [2] Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
Harald H H GöringDepartment of Genetics, Texas Biomedical Research Institute, San Antonio, TX, USA.
Thomas D DyerDepartment of Genetics, Texas Biomedical Research Institute, San Antonio, TX, USA.
Godfrey D Pearlson1] Olin Neuropsychiatry Research Center, Institute of Living, Hartford Hospital, Hartford, CT, USA [2] Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
Rene L OlveraDepartment of Psychiatry, University of Texas Health Science Center San Antonio, San Antonio, TX, USA.
Peter T Fox1] Research Imaging Institute, University of Texas Health Science Center San Antonio, San Antonio, TX, USA [2] South Texas Veterans Health System, San Antonio, TX, USA.
William R LovalloDepartment of Psychiatry, Oklahoma University Heath Science Center and Veterans Administration Medical Center, Oklahoma City, OK, USA.
Ravi DuggiralaDepartment of Genetics, Texas Biomedical Research Institute, San Antonio, TX, USA.
Laura AlmasyDepartment of Genetics, Texas Biomedical Research Institute, San Antonio, TX, USA.
John BlangeroDepartment of Genetics, Texas Biomedical Research Institute, San Antonio, TX, USA.
David C Glahn1] Olin Neuropsychiatry Research Center, Institute of Living, Hartford Hospital, Hartford, CT, USA [2] Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.

Funding

Training U54EB020403 · NIBIB · UNIVERSITY OF SOUTHERN CALIFORNIA · PI THOMPSON, PAUL M · 2014 to 2018
$10.1M
Psychophysiological Precursors of AlcoholismR01AA012207 · NIAAA · UNIV OF ARKANSAS FOR MED SCIS · PI ACHESON, ASHLEY, KOCHUNOV, PETER V. · 2001 to 2025
$9.0M
Quantitative Trait Locus Mapping in Human PedigreesR37MH059490 · NIMH · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI BLANGERO, JOHN · 2001 to 2010
$6.8M
SOLAR-Eclipse Computational Tools for Imaging GeneticsR01EB015611 · NIBIB · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KOCHUNOV, PETER V. · 2012 to 2024
$5.0M
Genetics of Brain Structure and FunctionR01MH078111 · NIMH · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI BLANGERO, JOHN · 2006 to 2014
$4.5M
Genetics of Brain Structure and FunctionR01MH078143 · NIMH · YALE UNIVERSITY · PI GLAHN, DAVID C · 2006 to 2014
$4.3M
Genetics of Brain Structure and Function: Genome-Wide AssociationR01MH083824 · NIMH · YALE UNIVERSITY · PI GLAHN, DAVID C · 2008 to 2013
$3.3M
High Performance Computing System for Human GenomicsS10RR029392 · NCRR · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI BLANGERO, JOHN · 2010 to 2010
$2.1M
QUANTITATIVE TRAIT LOCUS MAPPING IN HUMAN PEDIGREESR01MH059490 · NIMH · SOUTHWEST FOUNDATION FOR BIOMEDICAL RES · PI BLANGERO, JOHN · 1998 to 2000
$426k
NCRR NIH HHS S10 RR029392NIAAA NIH HHS R01 AA012207NIBIB NIH HHS R01 EB015611NIBIB NIH HHS U54 EB020403NIMH NIH HHS MH0708143NIMH NIH HHS MH078111NIMH NIH HHS MH083824NIMH NIH HHS MH59490NIMH NIH HHS R01 MH059490NIMH NIH HHS R01 MH078111NIMH NIH HHS R01 MH078143NIMH NIH HHS R01 MH083824NIMH NIH HHS R37 MH059490
6 · The paper itself

Abstract

Alcohol abuse and dependence (alcohol use disorders, AUDs) are associated with brain shrinkage. Subcortical structures including the amygdala, hippocampus, ventral striatum, dorsal striatum, and thalamus subserve reward functioning and may be particularly vulnerable to alcohol-related damage. These structures may also show pre-existing deficits impacting the development and maintenance of AUD. It remains unclear whether there are common genetic features underlying both subcortical volumes and AUD. In this study, structural brain images were acquired from 872 Mexican-American individuals from extended pedigrees. Subcortical volumes were obtained using FreeSurfer, and quantitative genetic analyses were performed in SOLAR. We hypothesized the following: (1) reduced subcortical volumes in individuals with lifetime AUD relative to unrelated controls; (2) reduced subcortical volumes in individuals with current relative to past AUD; (3) in non-AUD individuals, reduced subcortical volumes in those with a family history of AUD compared to those without; and (4) evidence for common genetic underpinnings (pleiotropy) between AUD risk and subcortical volumes. Results showed that individuals with lifetime AUD showed larger ventricular and smaller amygdala volumes compared to non-AUD individuals. For the amygdala, there were no differences in volume between current vs past AUD, and non-AUD individuals with a family history of AUD demonstrated reductions compared to those with no such family history. Finally, amygdala volume was genetically correlated with the risk for AUD. Together, these results suggest that reduced amygdala volume reflects a pre-existing difference rather than alcohol-induced neurotoxic damage. Our genetic correlation analysis provides evidence for a common genetic factor underlying both reduced amygdala volumes and AUD risk.

Indexed as

Genetic PleiotropyGenetic Predisposition to DiseaseAdolescentAdultAgedAged, 80 and overAlcohol-Related DisordersAmygdalaFamilyFemaleHumansMagnetic Resonance ImagingMaleMexican AmericansMiddle AgedOrgan Size

Identifiers

PMID25079289
PMCPMC4443955

What OpenQuestion holds

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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.