Evidence map›Paper›PMID 25319752›Full record

ArticleBrain structure & function2016

Oppositional COMT Val158Met effects on resting state functional connectivity in adolescents and adults.

Bernhard M Meyer, Julia Huemer, Ulrich Rabl, Roland N Boubela, Klaudius Kalcher, Andreas Berger, Tobias Banaschewski, Gareth Barker, Arun Bokde, Christian Büchel and 28 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Brain structure & function, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
3.1field-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, 2 syntheses or guidelines pooled it, 39 citations in OpenAlex.

  1. International journal of molecular sciences · 2022
    Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. Making Sense of Connectivity.The international journal of neuropsychopharmacology · 2019
    Review
  7. No association ofPeerJ · 2019
    Article
  8. Article
  9. [Key-topics in Austrian Child and Adolescent Psychiatry 2007-2017].Neuropsychiatrie : Klinik, Diagnostik, Therapie und Rehabilitation : Organ der Gesellschaft Osterreichischer Nervenarzte und Psychiater · 2017
    Article
  10. Article
  11. Article
  12. Article
  13. COMT ValFrontiers in human neuroscience · 2017
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
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

38 authors at 15 institutions in 7 countries.

Bernhard M MeyerDepartment of Psychiatry and Psychotherapy, Medical University of Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria.
Julia HuemerDepartment of Child and Adolescent Psychiatry, Medical University of Vienna, Vienna, Austria.
Ulrich RablDepartment of Psychiatry and Psychotherapy, Medical University of Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria.
Roland N BoubelaMR Centre of Excellence, Center for Medical Physics and Biomedical Engineering, Medical University of Vienna, Vienna, Austria.
Klaudius KalcherMR Centre of Excellence, Center for Medical Physics and Biomedical Engineering, Medical University of Vienna, Vienna, Austria.
Andreas BergerDepartment of Psychiatry and Psychotherapy, Medical University of Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria.
Tobias BanaschewskiCentral Institute of Mental Health, Faculty of Clinical Medicine Mannheim, Heidelberg University, Mannheim, Germany.
Gareth BarkerInstitute of Psychiatry, King's College, London, UK.
Arun BokdeInstitute of Neuroscience, Trinity College, Dublin, Ireland.
Christian BüchelUniversity Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Patricia ConrodDepartment of Psychiatry, Université de Montreal, CHU St. Justine Hospital, Montreal, Canada.
Sylvane DesrivièresInstitute of Psychiatry, King's College, London, UK.
Herta FlorCentral Institute of Mental Health, Faculty of Clinical Medicine Mannheim, Heidelberg University, Mannheim, Germany.
Vincent FrouinNeurospin, Commissariat à l'Energie Atomique, CEA-Saclay Center, Paris, France.
Jurgen GallinatDepartment of Psychiatry and Psychotherapy, Campus Charité Mitte, Berlin, Germany.
Hugh GaravanDepartment of Psychiatry and Psychology, University of Vermont, Burlington, USA.
Andreas HeinzDepartment of Psychiatry and Psychotherapy, Campus Charité Mitte, Berlin, Germany.
Bernd IttermannPhysikalisch-Technische Bundesanstalt, Berlin, Germany.
Tianye JiaInstitute of Psychiatry, King's College, London, UK.
Mark LathropMcGill University and Génome Québec Innovation Centre, Montreal, Canada.
Jean-Luc MartinotInstitut National de la Santé et de la Recherche Médicale, INSERM CEA Unit 1000 "Imaging and Psychiatry", Orsay, France.
Frauke NeesCentral Institute of Mental Health, Faculty of Clinical Medicine Mannheim, Heidelberg University, Mannheim, Germany.
Marcella RietschelCentral Institute of Mental Health, Faculty of Clinical Medicine Mannheim, Heidelberg University, Mannheim, Germany.
Michael N SmolkaDepartment of Psychiatry and Neuroimaging Center, Technische Universität Dresden, Dresden, Germany.
Lucie BartovaDepartment of Psychiatry and Psychotherapy, Medical University of Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria.
Ana PopovicDepartment of Psychiatry and Psychotherapy, Medical University of Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria.
Christian ScharingerDepartment of Psychiatry and Psychotherapy, Medical University of Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria.
Harald H SitteCenter for Biomolecular Medicine and Pharmacology, Medical University of Vienna, Vienna, Austria.
Hans SteinerDepartment of Psychiatry and Behavioral Sciences, Division of Child and Adolescent Psychiatry and Child Development, Stanford University School of Medicine, Stanford, USA.
Max H FriedrichDepartment of Child and Adolescent Psychiatry, Medical University of Vienna, Vienna, Austria.
Siegfried KasperDepartment of Psychiatry and Psychotherapy, Medical University of Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria.
Thomas PerkmannDepartment of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
Nicole Praschak-RiederDepartment of Psychiatry and Psychotherapy, Medical University of Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria.
Helmuth HaslacherDepartment of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
Harald EsterbauerDepartment of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
Ewald MoserMR Centre of Excellence, Center for Medical Physics and Biomedical Engineering, Medical University of Vienna, Vienna, Austria.
Gunter SchumannInstitute of Psychiatry, King's College, London, UK.
Lukas PezawasDepartment of Psychiatry and Psychotherapy, Medical University of Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria. lukas.pezawas@meduniwien.ac.at.
Medical University of Vienna · ATKing's College London · GBCentral Institute of Mental Health · DECharité - Universitätsmedizin Berlin · DECEA Paris-Saclay · FRHeidelberg University · DEInstitut d'Imagerie Biomédicale · FRMcGill University and Génome Québec Innovation Centre · CAPhysikalisch-Technische Bundesanstalt · DEStanford University · USTechnische Universität Dresden · DETrinity College Dublin · IEUniversität Hamburg · DEUniversité de Montréal · CAUniversity of Vermont · US

Funding

Austrian Science Fund FWF F 3506
6 · The paper itself

Abstract

Prefrontal dopamine levels are relatively increased in adolescence compared to adulthood. Genetic variation of COMT (COMT Val158Met) results in lower enzymatic activity and higher dopamine availability in Met carriers. Given the dramatic changes of synaptic dopamine during adolescence, it has been suggested that effects of COMT Val158Met genotypes might have oppositional effects in adolescents and adults. The present study aims to identify such oppositional COMT Val158Met effects in adolescents and adults in prefrontal brain networks at rest. Resting state functional connectivity data were collected from cross-sectional and multicenter study sites involving 106 healthy young adults (mean age 24 ± 2.6 years), gender matched to 106 randomly chosen 14-year-olds. We selected the anterior medial prefrontal cortex (amPFC) as seed due to its important role as nexus of the executive control and default mode network. We observed a significant age-dependent reversal of COMT Val158Met effects on resting state functional connectivity between amPFC and ventrolateral as well as dorsolateral prefrontal cortex, and parahippocampal gyrus. Val homozygous adults exhibited increased and adolescents decreased connectivity compared to Met homozygotes for all reported regions. Network analyses underscored the importance of the parahippocampal gyrus as mediator of observed effects. Results of this study demonstrate that adolescent and adult resting state networks are dose-dependently and diametrically affected by COMT genotypes following a hypothetical model of dopamine function that follows an inverted U-shaped curve. This study might provide cues for the understanding of disease onset or dopaminergic treatment mechanisms in major neuropsychiatric disorders such as schizophrenia and attention deficit hyperactivity disorder.

Indexed as

Polymorphism, Single NucleotideAdolescentAdultBrainBrain MappingCatechol O-MethyltransferaseCross-Sectional StudiesFemaleGenotypeHumansMagnetic Resonance ImagingMaleNeural PathwaysPrefrontal CortexYoung AdultCatechol O-MethyltransferaseCOMT protein, humanAdolescentsCatechol-O-methyltransferaseCognitionDopamineFunctional neuroimagingMagnetic resonance imaging

Identifiers

PMID25319752
PMCPMC4667398
OpenAlexW2033890993

What OpenQuestion holds

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LicenceCC BY
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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.