Evidence map›Paper›PMID 24834916›Full record

ArticlePloS one2014

Dopamine genetic risk score predicts depressive symptoms in healthy adults and adults with depression.

Kristin M Pearson-Fuhrhop, Erin C Dunn, Sarah Mortero, William J Devan, Guido J Falcone, Phil Lee, Avram J Holmes, Marisa O Hollinshead, Joshua L Roffman, Jordan W Smoller and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
6.2field-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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 80 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. A randomized controlled trial of disclosing genetic risk information for Alzheimer disease via telephone.Genetics in medicine : official journal of the American College of Medical Genetics · 2018
    Trial
  4. Article
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  6. Polygenic Risks for Depression and Neural Responses to Reward and Punishment in Young Adults.Biological psychiatry. Cognitive neuroscience and neuroimaging · 2025
    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

12 authors at 5 institutions in 1 country.

Kristin M Pearson-FuhrhopDepartment of Anatomy and Neurobiology, University of California Irvine, Irvine, California, United States of America.
Erin C DunnCenter for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, United States of America; Department of Psychiatry, Massachusetts General Hospital/Harvard Medical School, Boston, Massachusetts, United States of America; Stanley Center for Psychiatric Research, The Broad Institute of Harvard and MIT, Cambridge, Massachusetts, United States of America.
Sarah MorteroDepartment of Anatomy and Neurobiology, University of California Irvine, Irvine, California, United States of America.
William J DevanCenter for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, United States of America.
Guido J FalconeCenter for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, United States of America.
Phil LeeCenter for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, United States of America; Department of Psychiatry, Massachusetts General Hospital/Harvard Medical School, Boston, Massachusetts, United States of America; Stanley Center for Psychiatric Research, The Broad Institute of Harvard and MIT, Cambridge, Massachusetts, United States of America.
Avram J HolmesDepartment of Psychiatry, Massachusetts General Hospital/Harvard Medical School, Boston, Massachusetts, United States of America; Department of Psychology, Yale University, New Haven, Connecticut, United States of America.
Marisa O HollinsheadDepartment of Psychology, Center for Brain Science, Harvard University, Cambridge, Massachusetts, United States of America.
Joshua L RoffmanDepartment of Psychiatry, Massachusetts General Hospital/Harvard Medical School, Boston, Massachusetts, United States of America.
Jordan W SmollerCenter for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, United States of America; Department of Psychiatry, Massachusetts General Hospital/Harvard Medical School, Boston, Massachusetts, United States of America; Stanley Center for Psychiatric Research, The Broad Institute of Harvard and MIT, Cambridge, Massachusetts, United States of America.
Jonathan RosandCenter for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, United States of America; Department of Neurology, Massachusetts General Hospital/Harvard Medical School, Boston, Massachusetts, United States of America; Program in Medical and Population Genetics, The Broad Institute of Harvard and MIT, Cambridge, Massachusetts, United States of America.
Steven C CramerDepartment of Anatomy and Neurobiology, University of California Irvine, Irvine, California, United States of America; Department of Neurology, University of California Irvine, Irvine, California, United States of America.
Massachusetts General Hospital · USHarvard University · USUniversity of California, Irvine · USBroad Institute · USCenter for Human Genetics · US

Funding

ZOVIRAX CREAM TO TREAT HERPES LABIALIS IN ADOLESCENTSM01RR000827 · NCRR · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HAAS, RICHARD H · 1985 to 2010
$74.3M
Institute for Clinical and Translational ScienceUL1TR000153 · NCATS · UNIVERSITY OF CALIFORNIA-IRVINE · PI COOPER, DAN M · 2012 to 2015
$12.1M
BDNF Genotype, Cortical Plasticity and Recovery From StrokeR01NS058755 · NINDS · UNIVERSITY OF FLORIDA · PI KLEIM, JEFFREY A · 2008 to 2011
$1.5M
Research and Mentoring on Integrating Psychiatric Genetics and NeuroscienceK24MH094614 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI SMOLLER, JORDAN W · 2012 to 2016
$925k
Dimensional Neurogenetic Markers of Limbic System Integrity & Psychiatric IllnessK01MH099232 · NIMH · YALE UNIVERSITY · PI HOLMES, AVRAM J · 2013 to 2017
$738k
Brain plasticity and rehabilitation after strokeK24HD074722 · NICHD · UNIVERSITY OF CALIFORNIA-IRVINE · PI CRAMER, STEVEN C. · 2013 to 2017
$588k
Neuroimaging genetics to study social cognitive deficits in ASD and schizophreniaK99MH101367 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI LEE, PHIL H. · 2014 to 2015
$237k
NCATS NIH HHS UL1 TR000153NCRR NIH HHS 5M011 RR-00827-29NCRR NIH HHS M01 RR000827NICHD NIH HHS K24 HD074722NIMH NIH HHS K01 MH099232NIMH NIH HHS K01MH099232NIMH NIH HHS K24 MH094614NIMH NIH HHS K99 MH101367NINDS NIH HHS R01 NS058755
6 · The paper itself

Abstract

backgroundDepression is a common source of human disability for which etiologic insights remain limited. Although abnormalities of monoamine neurotransmission, including dopamine, are theorized to contribute to the pathophysiology of depression, evidence linking dopamine-related genes to depression has been mixed. The current study sought to address this knowledge-gap by examining whether the combined effect of dopamine polymorphisms was associated with depressive symptomatology in both healthy individuals and individuals with depression.

methodsData were drawn from three independent samples: (1) a discovery sample of healthy adult participants (n = 273); (2) a replication sample of adults with depression (n = 1,267); and (3) a replication sample of healthy adult participants (n = 382). A genetic risk score was created by combining functional polymorphisms from five genes involved in synaptic dopamine availability (COMT and DAT) and dopamine receptor binding (DRD1, DRD2, DRD3).

resultsIn the discovery sample, the genetic risk score was associated with depressive symptomatology (β = -0.80, p = 0.003), with lower dopamine genetic risk scores (indicating lower dopaminergic neurotransmission) predicting higher levels of depression. This result was replicated with a similar genetic risk score based on imputed genetic data from adults with depression (β = -0.51, p = 0.04). Results were of similar magnitude and in the expected direction in a cohort of healthy adult participants (β = -0.86, p = 0.15).

conclusionsSequence variation in multiple genes regulating dopamine neurotransmission may influence depressive symptoms, in a manner that appears to be additive. Further studies are required to confirm the role of genetic variation in dopamine metabolism and depression.

Indexed as

Genetic VariationPhenotypeAdultCatechol O-MethyltransferaseDepressionDopamine Plasma Membrane Transport ProteinsGenotypeHumansLinear ModelsReceptors, DopamineRisk AssessmentCatechol O-MethyltransferaseCOMT protein, humanDopamine Plasma Membrane Transport ProteinsReceptors, Dopamine

Identifiers

PMID24834916
PMCPMC4023941
OpenAlexW2108656770

What OpenQuestion holds

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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.