Altered Cortico-Striatal Connectivity in Offspring of Schizophrenia Patients Relative to Offspring of Bipolar Patients and Controls

Schizophrenia (SZ) and bipolar disorder (BD) share clinical features, genetic risk factors and neuroimaging abnormalities. There is evidence of disrupted connectivity in resting state networks in patients with SZ and BD and their unaffected relatives. Resting state networks are known to undergo reor...

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Veröffentlicht in:PloS one 2016-02, Vol.11 (2), p.e0148045-e0148045
Hauptverfasser: Solé-Padullés, Cristina, Castro-Fornieles, Josefina, de la Serna, Elena, Romero, Soledad, Calvo, Anna, Sánchez-Gistau, Vanessa, Padrós-Fornieles, Marta, Baeza, Inmaculada, Bargalló, Núria, Frangou, Sophia, Sugranyes, Gisela
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container_start_page e0148045
container_title PloS one
container_volume 11
creator Solé-Padullés, Cristina
Castro-Fornieles, Josefina
de la Serna, Elena
Romero, Soledad
Calvo, Anna
Sánchez-Gistau, Vanessa
Padrós-Fornieles, Marta
Baeza, Inmaculada
Bargalló, Núria
Frangou, Sophia
Sugranyes, Gisela
description Schizophrenia (SZ) and bipolar disorder (BD) share clinical features, genetic risk factors and neuroimaging abnormalities. There is evidence of disrupted connectivity in resting state networks in patients with SZ and BD and their unaffected relatives. Resting state networks are known to undergo reorganization during youth coinciding with the period of increased incidence for both disorders. We therefore focused on characterizing resting state network connectivity in youth at familial risk for SZ or BD to identify alterations arising during this period. We measured resting-state functional connectivity in a sample of 106 youth, aged 7-19 years, comprising offspring of patients with SZ (N = 27), offspring of patients with BD (N = 39) and offspring of community control parents (N = 40). We used Independent Component Analysis to assess functional connectivity within the default mode, executive control, salience and basal ganglia networks and define their relationship to grey matter volume, clinical and cognitive measures. There was no difference in connectivity within any of the networks examined between offspring of patients with BD and offspring of community controls. In contrast, offspring of patients with SZ showed reduced connectivity within the left basal ganglia network compared to control offspring, and they showed a positive correlation between connectivity in this network and grey matter volume in the left caudate. Our findings suggest that dysconnectivity in the basal ganglia network is a robust correlate of familial risk for SZ and can be detected during childhood and adolescence.
doi_str_mv 10.1371/journal.pone.0148045
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There is evidence of disrupted connectivity in resting state networks in patients with SZ and BD and their unaffected relatives. Resting state networks are known to undergo reorganization during youth coinciding with the period of increased incidence for both disorders. We therefore focused on characterizing resting state network connectivity in youth at familial risk for SZ or BD to identify alterations arising during this period. We measured resting-state functional connectivity in a sample of 106 youth, aged 7-19 years, comprising offspring of patients with SZ (N = 27), offspring of patients with BD (N = 39) and offspring of community control parents (N = 40). We used Independent Component Analysis to assess functional connectivity within the default mode, executive control, salience and basal ganglia networks and define their relationship to grey matter volume, clinical and cognitive measures. There was no difference in connectivity within any of the networks examined between offspring of patients with BD and offspring of community controls. In contrast, offspring of patients with SZ showed reduced connectivity within the left basal ganglia network compared to control offspring, and they showed a positive correlation between connectivity in this network and grey matter volume in the left caudate. 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There is evidence of disrupted connectivity in resting state networks in patients with SZ and BD and their unaffected relatives. Resting state networks are known to undergo reorganization during youth coinciding with the period of increased incidence for both disorders. We therefore focused on characterizing resting state network connectivity in youth at familial risk for SZ or BD to identify alterations arising during this period. We measured resting-state functional connectivity in a sample of 106 youth, aged 7-19 years, comprising offspring of patients with SZ (N = 27), offspring of patients with BD (N = 39) and offspring of community control parents (N = 40). We used Independent Component Analysis to assess functional connectivity within the default mode, executive control, salience and basal ganglia networks and define their relationship to grey matter volume, clinical and cognitive measures. 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physiopathology</topic><topic>Neostriatum</topic><topic>Nerve Net - physiopathology</topic><topic>Nervous system</topic><topic>Networks</topic><topic>Neural networks</topic><topic>Neuroimaging</topic><topic>Neurology</topic><topic>Neurosciences</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Offspring</topic><topic>Parents</topic><topic>Patients</topic><topic>People and Places</topic><topic>Psychosis</topic><topic>Regression Analysis</topic><topic>Rest</topic><topic>Risk analysis</topic><topic>Risk factors</topic><topic>Schizophrenia</topic><topic>Schizophrenia - physiopathology</topic><topic>Sistema nerviós</topic><topic>Social Sciences</topic><topic>Studies</topic><topic>Substantia grisea</topic><topic>Teenagers</topic><topic>Trastorn bipolar</topic><topic>Young Adult</topic><topic>Young adults</topic><topic>Youth</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Solé-Padullés, Cristina</creatorcontrib><creatorcontrib>Castro-Fornieles, Josefina</creatorcontrib><creatorcontrib>de la Serna, Elena</creatorcontrib><creatorcontrib>Romero, Soledad</creatorcontrib><creatorcontrib>Calvo, Anna</creatorcontrib><creatorcontrib>Sánchez-Gistau, Vanessa</creatorcontrib><creatorcontrib>Padrós-Fornieles, Marta</creatorcontrib><creatorcontrib>Baeza, Inmaculada</creatorcontrib><creatorcontrib>Bargalló, Núria</creatorcontrib><creatorcontrib>Frangou, Sophia</creatorcontrib><creatorcontrib>Sugranyes, Gisela</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological &amp; Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies &amp; Aerospace Collection</collection><collection>Agricultural &amp; Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Meteorological &amp; Geoastrophysical Abstracts - 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Academic</collection><collection>Recercat</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Solé-Padullés, Cristina</au><au>Castro-Fornieles, Josefina</au><au>de la Serna, Elena</au><au>Romero, Soledad</au><au>Calvo, Anna</au><au>Sánchez-Gistau, Vanessa</au><au>Padrós-Fornieles, Marta</au><au>Baeza, Inmaculada</au><au>Bargalló, Núria</au><au>Frangou, Sophia</au><au>Sugranyes, Gisela</au><au>Abulseoud, Osama Ali</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Altered Cortico-Striatal Connectivity in Offspring of Schizophrenia Patients Relative to Offspring of Bipolar Patients and Controls</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2016-02-17</date><risdate>2016</risdate><volume>11</volume><issue>2</issue><spage>e0148045</spage><epage>e0148045</epage><pages>e0148045-e0148045</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Schizophrenia (SZ) and bipolar disorder (BD) share clinical features, genetic risk factors and neuroimaging abnormalities. There is evidence of disrupted connectivity in resting state networks in patients with SZ and BD and their unaffected relatives. Resting state networks are known to undergo reorganization during youth coinciding with the period of increased incidence for both disorders. We therefore focused on characterizing resting state network connectivity in youth at familial risk for SZ or BD to identify alterations arising during this period. We measured resting-state functional connectivity in a sample of 106 youth, aged 7-19 years, comprising offspring of patients with SZ (N = 27), offspring of patients with BD (N = 39) and offspring of community control parents (N = 40). We used Independent Component Analysis to assess functional connectivity within the default mode, executive control, salience and basal ganglia networks and define their relationship to grey matter volume, clinical and cognitive measures. There was no difference in connectivity within any of the networks examined between offspring of patients with BD and offspring of community controls. In contrast, offspring of patients with SZ showed reduced connectivity within the left basal ganglia network compared to control offspring, and they showed a positive correlation between connectivity in this network and grey matter volume in the left caudate. Our findings suggest that dysconnectivity in the basal ganglia network is a robust correlate of familial risk for SZ and can be detected during childhood and adolescence.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>26885824</pmid><doi>10.1371/journal.pone.0148045</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record>
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1932-6203
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subjects Abnormalities
Adolescence
Adolescent
Adolescents
Adult
Age
Analysis
Basal ganglia
Basal Ganglia - physiopathology
Biology and Life Sciences
Biomedical research
Bipolar disorder
Bipolar Disorder - physiopathology
Brain research
Care and treatment
Case-Control Studies
Child
Child & adolescent psychiatry
Child development
Children
Cluster Analysis
Cognition
Cognitive ability
Communities
Consortia
Corpus Striatum - physiopathology
Demography
Dopamine
Esquizofrènia
Executive function
Female
Ganglia
Genetic aspects
Gray Matter - pathology
Gray Matter - physiopathology
Humans
Independent component analysis
Male
Manic-depressive illness
Medical imaging
Medicine and Health Sciences
Mental disorders
Middle Aged
Neocortex - physiopathology
Neostriatum
Nerve Net - physiopathology
Nervous system
Networks
Neural networks
Neuroimaging
Neurology
Neurosciences
NMR
Nuclear magnetic resonance
Offspring
Parents
Patients
People and Places
Psychosis
Regression Analysis
Rest
Risk analysis
Risk factors
Schizophrenia
Schizophrenia - physiopathology
Sistema nerviós
Social Sciences
Studies
Substantia grisea
Teenagers
Trastorn bipolar
Young Adult
Young adults
Youth
title Altered Cortico-Striatal Connectivity in Offspring of Schizophrenia Patients Relative to Offspring of Bipolar Patients and Controls
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