Cortical Volume Differences in Subjects at Risk for Psychosis Are Driven by Surface Area
dc.contributor | Sistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP | |
dc.contributor.author | BUECHLER, Roman | |
dc.contributor.author | WOTRUBA, Diana | |
dc.contributor.author | MICHELS, Lars | |
dc.contributor.author | THEODORIDOU, Anastasia | |
dc.contributor.author | METZLER, Sibylle | |
dc.contributor.author | WALITZA, Susanne | |
dc.contributor.author | HANGGI, Jurgen | |
dc.contributor.author | KOLLIAS, Spyros | |
dc.contributor.author | ROSSLER, Wulf | |
dc.contributor.author | HEEKEREN, Karsten | |
dc.date.accessioned | 2021-02-18T13:59:36Z | |
dc.date.available | 2021-02-18T13:59:36Z | |
dc.date.issued | 2020 | |
dc.description.abstract | In subjects at risk for psychosis, the studies on gray matter volume (GMV) predominantly reported volume loss compared with healthy controls (CON). However, other important morphological measurements such as cortical surface area (CSA) and cortical thickness (CT) were not systematically compared. So far, samples mostly comprised subjects at genetic risk or at clinical risk fulfilling an ultra-high risk (UHR) criterion. No studies comparing UHR subjects with at-risk subjects showing only basic symptoms (BS) investigated the differences in CSA or CT. Therefore, we aimed to unravel the contribution of the 2 morphometrical measures constituting the cortical volume (CV) and to test whether these groups inhere different morphometric features. We conducted a surface-based morphometric analysis in 34 CON, 46 BS, and 39 UHR to examine between-group differences in CV, CSA, and CT vertex-wise across the whole cortex. Compared with BS and CON, UHR individuals presented increased CV in frontal and parietal regions, which was driven by larger CSA. These groups did not differ in CT. Yet, at-risk subjects who later developed schizophrenia showed thinning in the occipital cortex. Furthermore, BS presented increased CSA compared with CON. Our results suggest that volumetric differences in UHR subjects are driven by CSA while CV loss in converters seems to be based on cortical thinning. We attribute the larger CSA in UHR to aberrant pruning representing a vulnerability to develop psychotic symptoms reflected in different levels of vulnerability for BS and UHR, and cortical thinning to a presumably stress-related cortical decomposition. | eng |
dc.description.index | MEDLINE | eng |
dc.description.sponsorship | Zurich Program for Sustainable Development of Mental Health Services (ZInEP) | |
dc.identifier.citation | SCHIZOPHRENIA BULLETIN, v.46, n.6, p.1511-1519, 2020 | |
dc.identifier.doi | 10.1093/schbul/sbaa066 | |
dc.identifier.eissn | 1745-1701 | |
dc.identifier.issn | 0586-7614 | |
dc.identifier.uri | https://observatorio.fm.usp.br/handle/OPI/39603 | |
dc.language.iso | eng | |
dc.publisher | OXFORD UNIV PRESS | eng |
dc.relation.ispartof | Schizophrenia Bulletin | |
dc.rights | restrictedAccess | eng |
dc.rights.holder | Copyright OXFORD UNIV PRESS | eng |
dc.subject | schizophrenia | eng |
dc.subject | surface-based morphometry | eng |
dc.subject | cortical thickness | eng |
dc.subject | prodrome | eng |
dc.subject.other | ultra-high-risk | eng |
dc.subject.other | anterior cingulate cortex | eng |
dc.subject.other | clinical high-risk | eng |
dc.subject.other | mental state | eng |
dc.subject.other | schizophrenia | eng |
dc.subject.other | thickness | eng |
dc.subject.other | brain | eng |
dc.subject.other | abnormalities | eng |
dc.subject.other | individuals | eng |
dc.subject.other | transition | eng |
dc.subject.wos | Psychiatry | eng |
dc.title | Cortical Volume Differences in Subjects at Risk for Psychosis Are Driven by Surface Area | eng |
dc.type | article | eng |
dc.type.category | original article | eng |
dc.type.version | publishedVersion | eng |
dspace.entity.type | Publication | |
hcfmusp.affiliation.country | Alemanha | |
hcfmusp.affiliation.countryiso | ch | |
hcfmusp.affiliation.countryiso | de | |
hcfmusp.author.external | BUECHLER, Roman:Univ Hosp Psychiat Zurich, Zurich Program Sustainable Dev Mental Hlth Serv Z, Zurich, Switzerland; Univ Hosp Zurich, Dept Neuroradiol, Zurich, Switzerland | |
hcfmusp.author.external | WOTRUBA, Diana:Univ Hosp Psychiat Zurich, Zurich Program Sustainable Dev Mental Hlth Serv Z, Zurich, Switzerland; Univ Hosp Zurich, Dept Neuroradiol, Zurich, Switzerland | |
hcfmusp.author.external | MICHELS, Lars:Univ Hosp Zurich, Dept Neuroradiol, Zurich, Switzerland | |
hcfmusp.author.external | THEODORIDOU, Anastasia:Univ Hosp Psychiat Zurich, Zurich Program Sustainable Dev Mental Hlth Serv Z, Zurich, Switzerland; Univ Hosp Psychiat Zurich, Dept Psychiat Psychotherapy & Psychosomat, Zurich, Switzerland | |
hcfmusp.author.external | METZLER, Sibylle:Univ Hosp Psychiat Zurich, Zurich Program Sustainable Dev Mental Hlth Serv Z, Zurich, Switzerland | |
hcfmusp.author.external | WALITZA, Susanne:Univ Zurich, Dept Child & Adolescent Psychiat, Zurich, Switzerland | |
hcfmusp.author.external | HANGGI, Jurgen:Univ Zurich, Dept Psychol, Div Neuropsychol, Zurich, Switzerland | |
hcfmusp.author.external | KOLLIAS, Spyros:Univ Hosp Zurich, Dept Neuroradiol, Zurich, Switzerland | |
hcfmusp.author.external | HEEKEREN, Karsten:Univ Hosp Psychiat Zurich, Zurich Program Sustainable Dev Mental Hlth Serv Z, Zurich, Switzerland; Univ Hosp Psychiat Zurich, Dept Psychiat Psychotherapy & Psychosomat, Zurich, Switzerland; LVR Hosp, Dept Psychiat & Psychotherapy 1, Cologne, Germany | |
hcfmusp.citation.scopus | 14 | |
hcfmusp.description.beginpage | 1511 | |
hcfmusp.description.endpage | 1519 | |
hcfmusp.description.issue | 6 | |
hcfmusp.description.volume | 46 | |
hcfmusp.origem | WOS | |
hcfmusp.origem.pubmed | 32463880 | |
hcfmusp.origem.scopus | 2-s2.0-85097113421 | |
hcfmusp.origem.wos | WOS:000607041400021 | |
hcfmusp.publisher.city | OXFORD | eng |
hcfmusp.publisher.country | ENGLAND | eng |
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