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JAMA Psychiatry. 2016 Aug 1;73(8):852-61. doi: 10.1001/jamapsychiatry.2016.1135.

Polygenic Risk of Psychosis and Ventral Striatal Activation During Reward Processing in Healthy Adolescents.

Author information

1
Neuroscience and Mental Health Research Institute, Cardiff University, Cardiff, United Kingdom2Cardiff University Brain Imaging Research Centre, Cardiff University, Cardiff, United Kingdom.
2
Neuroscience and Mental Health Research Institute, Cardiff University, Cardiff, United Kingdom2Cardiff University Brain Imaging Research Centre, Cardiff University, Cardiff, United Kingdom3MRC Centre for Neuropsychiatric Genetics and Genomics, Institute o.
3
MRC Integrative Epidemiology Unit, School of Social and Community Medicine, Faculty of Medicine and Dentistry, University of Bristol, Bristol, United Kingdom.
4
Department of Child and Adolescent Psychiatry and Psychotherapy, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.
5
Discipline of Psychiatry, School of Medicine and Trinity College Institute of Neuroscience, Trinity College Dublin, Dublin, Ireland.
6
University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
7
MRC Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology, and Neuroscience, King's College, London, United Kingdom.
8
Department of Psychiatry, Universite de Montreal, CHU Ste Justine Hospital, Montreal, Quebec, Canada10Department of Psychological Medicine and Psychiatry, Institute of Psychiatry, Psychology, and Neuroscience, King's College, London, United Kingdom.
9
Department of Cognitive and Clinical Neuroscience, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.
10
Neurospin, Commissariat à l'Energie Atomique, Paris, France.
11
Department of Psychiatry and Psychotherapy, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
12
Departments of Psychiatry and Psychology, University of Vermont, Burlington.
13
Sir Peter Mansfield Imaging Centre School of Physics and Astronomy, University of Nottingham, Nottingham, United Kingdom.
14
Department of Psychiatry and Psychotherapy, Universitätsmedizin Berlin, Berlin, Germany.
15
Physikalisch-Technische Bundesanstalt, Berlin, Germany.
16
Institut National de la Santé et de la Recherche Médicale (INSERM), UMR 1000, Neuroimaging and Psychiatry Research Unit, University Paris-Sud, Orsay, France19University Paris Descartes, Sorbonne Paris Cité, Paris, France.
17
Institut National de la Santé et de la Recherche Médicale (INSERM), UMR 1000, Neuroimaging and Psychiatry Research Unit, University Paris-Sud, Orsay, France19University Paris Descartes, Sorbonne Paris Cité, Paris, France20Assistance Publique-Hôpitaux de P.
18
Institut National de la Santé et de la Recherche Médicale (INSERM), UMR 1000, Neuroimaging and Psychiatry Research Unit, University Paris-Sud, Orsay, France21Orsay Hospital, Orsay, France.
19
Rotman Research Institute, Baycrest Health Sciences, and Departments of Psychology and Psychiatry, University of Toronto, Toronto, Ontario, Canada.
20
Department of Child and Adolescent Psychiatry and Psychotherapy, Medical University of Vienna, Vienna, Austria.
21
Department of Psychiatry and Neuroimaging Center, Technische Universität Dresden, Dresden, Germany.
22
Department of Psychology, University College Dublin, Dublin, Ireland.

Erratum in

Abstract

IMPORTANCE:

Psychotic disorders are characterized by attenuated activity in the brain's valuation system in key reward processing areas, such as the ventral striatum (VS), as measured with functional magnetic resonance imaging.

OBJECTIVE:

To examine whether common risk variants for psychosis are associated with individual variation in the VS.

DESIGN, SETTING, AND PARTICIPANTS:

A cross-sectional study of a large cohort of adolescents from the IMAGEN study (a European multicenter study of reinforcement sensitivity in adolescents) was performed from March 1, 2008, through December 31, 2011. Data analysis was conducted from October 1, 2015, to January 9, 2016. Polygenic risk profile scores (RPSs) for psychosis were generated for 1841 healthy adolescents. Sample size and characteristics varied across regression analyses, depending on mutual information available (N = 1524-1836).

MAIN OUTCOMES AND MEASURES:

Reward-related brain function was assessed with blood oxygen level dependency (BOLD) in the VS using the monetary incentive delay (MID) task, distinguishing reward anticipation and receipt. Behavioral impulsivity, IQ, MID task performance, and VS BOLD were regressed against psychosis RPS at 4 progressive P thresholds (P < .01, P < .05, P < .10, and P < .50 for RPS models 1-4, respectively).

RESULTS:

In a sample of 1841 healthy adolescents (mean age, 14.5 years; 906 boys and 935 girls), we replicated an association between increasing psychosis RPS and reduced IQ (matrix reasoning: corrected P = .003 for RPS model 2, 0.4% variance explained), supporting the validity of the psychosis RPS models. We also found a nominally significant association between increased psychosis RPS and reduced MID task performance (uncorrected P = .03 for RPS model 4, 0.2% variance explained). Our main finding was a positive association between psychosis RPS and VS BOLD during reward anticipation at all 4 psychosis RPS models and for 2 P thresholds for reward receipt (RPS models 1 and 3), correcting for the familywise error rate (0.8%-1.9% variance explained).

CONCLUSIONS AND RELEVANCE:

These findings support an association between psychosis RPS and VS BOLD in adolescents. Genetic risk for psychosis may shape an individual's response to rewarding stimuli.

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