Evidence map›Paper›PMID 29947313›Full record

ArticleThe British journal of psychiatry : the journal of mental science2018

Significant concordance of genetic variation that increases both the risk for obsessive-compulsive disorder and the volumes of the nucleus accumbens and putamen.

Derrek P Hibar, Joshua W Cheung, Sarah E Medland, Mary S Mufford, Neda Jahanshad, Shareefa Dalvie, Raj Ramesar, Evelyn Stewart, Odile A van den Heuvel, David L Pauls and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in The British journal of psychiatry : the journal of mental science, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 3 pooled it
6.6field-weighted citation impact, top 3% 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

25 citing papers in PubMed, 3 syntheses or guidelines pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Genetic meta-analysis of obsessive-compulsive disorder and self-report compulsive symptoms.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2020
    Pooled it
  3. Pooled it
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  10. Phenome-wide association studies betweenFrontiers in psychiatry · 2024
    Article
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  15. Observational
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  18. Targeting presynaptic H3 heteroreceptor in nucleus accumbens to improve anxiety and obsessive-compulsive-like behaviors.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  19. Review
  20. Brain Imaging Genomics: Integrated Analysis and Machine Learning.Proceedings of the IEEE. Institute of Electrical and Electronics Engineers · 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

14 authors at 8 institutions in 5 countries.

Derrek P HibarImaging Genetics Center,Keck School of Medicine of the University of Southern California,Marina del Rey,USA.
Joshua W CheungImaging Genetics Center,Keck School of Medicine of the University of Southern California,Marina del Rey,USA.
Sarah E MedlandQIMR Berghofer Medical Research Institute,Brisbane,Australia.
Mary S MuffordUniversity of Cape Town/Medical Research Council Human Genetics Research Unit,Division of Human Genetics,Department of Pathology,Institute of Infectious Disease and Molecular Medicine, Faculty of Health Sciences,University of Cape Town,South Africa.
Neda JahanshadImaging Genetics Center,Keck School of Medicine of the University of Southern California,Marina del Rey,USA.
Shareefa DalvieDepartment of Psychiatry and Mental Health,Groote Schuur Hospital,Cape Town,South Africa.
Raj RamesarUniversity of Cape Town/Medical Research Council Human Genetics Research Unit, Division of Human Genetics,Department of Pathology,Institute of Infectious Disease and Molecular Medicine, Faculty of Health Sciences, University of Cape Town,South Africa.
Evelyn StewartPsychiatric and Neurodevelopmental Genetics Unit,Center for Human Genetics Research,Harvard Medical School,Boston,USA,Department of Psychiatry,Massachusetts General Hospital,Boston,USAand British Columbia Mental Health and Addictions Research Institute,University of British Columbia,Vancouver,Canada.
Odile A van den HeuvelDepartment of Psychiatry, Neuroscience Campus Amsterdam and Department of Anatomy and Neurosciences,VU University Medical Center,Amsterdam,The Netherlands.
David L PaulsPsychiatric and Neurodevelopmental Genetics Unit,Center for Human Genetics Research,Harvard Medical Schooland Department of Psychiatry,Massachusetts General Hospital,Boston,USA.
James A KnowlesDepartment of Cell Biology,State University of New York Downstate Medical Center,Brooklyn,USA.
Dan J SteinDepartment of Psychiatry and Mental Health,Groote Schuur Hospital and Medical Research Council Unit on Risk and Resilience,Faculty of Health Sciences,University of Cape Town,South Africa.
Paul M ThompsonImaging Genetics Center,Keck School of Medicine of the University of Southern California,Marina del Rey,USA.
Enhancing Neuro Imaging Genetics through Meta Analysis (ENIGMA) Consortium and International Obsessive Compulsive Disorder Foundation Genetics Collaborative (IOCDF-GC)
University of Southern California · USUniversity of Cape Town · ZAAmsterdam Neuroscience · NLCenter for Human Genetics · USGroote Schuur Hospital · ZAMassachusetts General Hospital · USQIMR Berghofer Medical Research Institute · AUState University of New York · US

Funding

Training U54EB020403 · NIBIB · UNIVERSITY OF SOUTHERN CALIFORNIA · PI THOMPSON, PAUL M · 2014 to 2018
$10.1M
NIBIB NIH HHS U54 EB020403
6 · The paper itself

Abstract

backgroundMany studies have identified changes in the brain associated with obsessive-compulsive disorder (OCD), but few have examined the relationship between genetic determinants of OCD and brain variation.AimsWe present the first genome-wide investigation of overlapping genetic risk for OCD and genetic influences on subcortical brain structures.

methodUsing single nucleotide polymorphism effect concordance analysis, we measured genetic overlap between the first genome-wide association study (GWAS) of OCD (1465 participants with OCD, 5557 controls) and recent GWASs of eight subcortical brain volumes (13 171 participants).

resultsWe found evidence of significant positive concordance between OCD risk variants and variants associated with greater nucleus accumbens and putamen volumes. When conditioning OCD risk variants on brain volume, variants influencing putamen, amygdala and thalamus volumes were associated with risk for OCD.

conclusionsThese results are consistent with current OCD neurocircuitry models. Further evidence will clarify the relationship between putamen volume and OCD risk, and the roles of the detected variants in this disorder.Declaration of interestThe authors have declared that no competing interests exist.

Indexed as

Genetic VariationCase-Control StudiesFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMagnetic Resonance ImagingMaleNucleus AccumbensObsessive-Compulsive DisorderOrgan SizePolymorphism, Single NucleotidePutamenGenetic overlapneuroimagingobsessive–compulsive disorder

Identifiers

PMID29947313
PMCPMC6053271
OpenAlexW2810106332

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.