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T162. THICKER PREFRONTAL CORTEX IS ASSOCIATED WITH SUBCLINICAL NEGATIVE SYMPTOMS IN SCHIZOTYPY - AN ENIGMA CONSORTIUM META-ANALYSIS

BACKGROUND: Negative symptoms can be seen to represent a continuum from subclinical manifestations in the general population to severe symptoms in schizophrenia. Neuroanatomical studies show evidence of fronto-striatal structural abnormalities linked to negative symptoms in patients with schizophren...

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Autores principales: Kirschner, Matthias, Hodzic-Santor, Benazir, Kircher, Tilo, Nenadic, Igor, Fornito, Alex, Green, Melissa, Quide, Yann, Pantelis, Christos, Dannlowski, Udo, DeRosse, Pamela, Chan, Raymond, Debbané, Martin, Rössler, Wulf, Lebedeva, Irina, Park, Haeme, Marsman, Jan-Bernard, Gilleen, James, Fett, Anne-Kathrin, van Erp, Theo, Turner, Jessica, Thompson, Paul, Aleman, Andre, Modinos, Gemma, Kaiser, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7234734/
http://dx.doi.org/10.1093/schbul/sbaa029.722
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author Kirschner, Matthias
Hodzic-Santor, Benazir
Kircher, Tilo
Nenadic, Igor
Fornito, Alex
Green, Melissa
Quide, Yann
Pantelis, Christos
Dannlowski, Udo
DeRosse, Pamela
Chan, Raymond
Debbané, Martin
Rössler, Wulf
Lebedeva, Irina
Park, Haeme
Marsman, Jan-Bernard
Gilleen, James
Fett, Anne-Kathrin
van Erp, Theo
Turner, Jessica
Thompson, Paul
Aleman, Andre
Modinos, Gemma
Kaiser, Stefan
author_facet Kirschner, Matthias
Hodzic-Santor, Benazir
Kircher, Tilo
Nenadic, Igor
Fornito, Alex
Green, Melissa
Quide, Yann
Pantelis, Christos
Dannlowski, Udo
DeRosse, Pamela
Chan, Raymond
Debbané, Martin
Rössler, Wulf
Lebedeva, Irina
Park, Haeme
Marsman, Jan-Bernard
Gilleen, James
Fett, Anne-Kathrin
van Erp, Theo
Turner, Jessica
Thompson, Paul
Aleman, Andre
Modinos, Gemma
Kaiser, Stefan
author_sort Kirschner, Matthias
collection PubMed
description BACKGROUND: Negative symptoms can be seen to represent a continuum from subclinical manifestations in the general population to severe symptoms in schizophrenia. Neuroanatomical studies show evidence of fronto-striatal structural abnormalities linked to negative symptoms in patients with schizophrenia (Walton et al. 2018). However, it remains an open question whether these structural associations are also observed in ostensibly healthy individuals reporting subclinical negative symptoms. The present study used structural T1-weighted brain imaging data from the ENIGMA Schizotypy Working Group to investigate the relationship between subclinical negative symptoms and fronto-striatal structural measures. METHODS: We included 2,235 healthy unmedicated individuals with varying levels of schizotypy from 17 centers around the world. The complete sample had a weighted mean (range) age of 29.2 (15.9–39.6) and 59.4% (51–100) were male. Subclinical negative symptoms were assessed at each site separately using factor scores from self-report schizotypy questionnaires (i.e., the Community Assessment of Psychic Experiences, the Oxford-Liverpool Inventory of Feelings and Experiences, or the Schizotypal Personality Questionnaire). Based on prior studies in schizophrenia, we obtained cortical thickness from 22 frontal regions-of-interest (ROIs) and subcortical volumes from 6 striatal ROIs using FreeSurfer. We performed meta-analyses of effect sizes (standardized regression coefficients) from a model predicting mean cortical thickness by subclinical negative symptom scores, adjusting for age, sex, and site. The same analysis was repeated for subcortical volumes including intracranial volume as additional covariate. RESULTS: Meta-analyses revealed significant positive associations between subclinical negative symptoms and cortical thickness of the left frontal pole (βstd=0.091; pFDR=0.009), right medial orbitofrontal cortex (βstd=0.083; pFDR=0.009) and right anterior cingulate cortex (βstd=0.07; pFDR=0.011). DISCUSSION: Using a large sample of healthy unmedicated individuals with varying levels of schizotypal personality traits, this ENIGMA meta-analysis showed that subclinical negative symptoms are associated with thicker prefrontal cortex. The present data are contrary to previous findings in schizophrenia, which demonstrates a relationship between negative symptoms and lower prefrontal cortical thickness (Walton et al. 2018). These divergent neural correlates suggest that thicker cortex could be a potential compensatory mechanism preventing individuals with schizotypy from the clinical manifestation of severe negative symptoms. Alternatively, greater prefrontal cortical thickness could also be associated with pathological processes along the negative symptom continuum prior to clinical manifestation.
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spelling pubmed-72347342020-05-23 T162. THICKER PREFRONTAL CORTEX IS ASSOCIATED WITH SUBCLINICAL NEGATIVE SYMPTOMS IN SCHIZOTYPY - AN ENIGMA CONSORTIUM META-ANALYSIS Kirschner, Matthias Hodzic-Santor, Benazir Kircher, Tilo Nenadic, Igor Fornito, Alex Green, Melissa Quide, Yann Pantelis, Christos Dannlowski, Udo DeRosse, Pamela Chan, Raymond Debbané, Martin Rössler, Wulf Lebedeva, Irina Park, Haeme Marsman, Jan-Bernard Gilleen, James Fett, Anne-Kathrin van Erp, Theo Turner, Jessica Thompson, Paul Aleman, Andre Modinos, Gemma Kaiser, Stefan Schizophr Bull Poster Session III BACKGROUND: Negative symptoms can be seen to represent a continuum from subclinical manifestations in the general population to severe symptoms in schizophrenia. Neuroanatomical studies show evidence of fronto-striatal structural abnormalities linked to negative symptoms in patients with schizophrenia (Walton et al. 2018). However, it remains an open question whether these structural associations are also observed in ostensibly healthy individuals reporting subclinical negative symptoms. The present study used structural T1-weighted brain imaging data from the ENIGMA Schizotypy Working Group to investigate the relationship between subclinical negative symptoms and fronto-striatal structural measures. METHODS: We included 2,235 healthy unmedicated individuals with varying levels of schizotypy from 17 centers around the world. The complete sample had a weighted mean (range) age of 29.2 (15.9–39.6) and 59.4% (51–100) were male. Subclinical negative symptoms were assessed at each site separately using factor scores from self-report schizotypy questionnaires (i.e., the Community Assessment of Psychic Experiences, the Oxford-Liverpool Inventory of Feelings and Experiences, or the Schizotypal Personality Questionnaire). Based on prior studies in schizophrenia, we obtained cortical thickness from 22 frontal regions-of-interest (ROIs) and subcortical volumes from 6 striatal ROIs using FreeSurfer. We performed meta-analyses of effect sizes (standardized regression coefficients) from a model predicting mean cortical thickness by subclinical negative symptom scores, adjusting for age, sex, and site. The same analysis was repeated for subcortical volumes including intracranial volume as additional covariate. RESULTS: Meta-analyses revealed significant positive associations between subclinical negative symptoms and cortical thickness of the left frontal pole (βstd=0.091; pFDR=0.009), right medial orbitofrontal cortex (βstd=0.083; pFDR=0.009) and right anterior cingulate cortex (βstd=0.07; pFDR=0.011). DISCUSSION: Using a large sample of healthy unmedicated individuals with varying levels of schizotypal personality traits, this ENIGMA meta-analysis showed that subclinical negative symptoms are associated with thicker prefrontal cortex. The present data are contrary to previous findings in schizophrenia, which demonstrates a relationship between negative symptoms and lower prefrontal cortical thickness (Walton et al. 2018). These divergent neural correlates suggest that thicker cortex could be a potential compensatory mechanism preventing individuals with schizotypy from the clinical manifestation of severe negative symptoms. Alternatively, greater prefrontal cortical thickness could also be associated with pathological processes along the negative symptom continuum prior to clinical manifestation. Oxford University Press 2020-05 2020-05-18 /pmc/articles/PMC7234734/ http://dx.doi.org/10.1093/schbul/sbaa029.722 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Poster Session III
Kirschner, Matthias
Hodzic-Santor, Benazir
Kircher, Tilo
Nenadic, Igor
Fornito, Alex
Green, Melissa
Quide, Yann
Pantelis, Christos
Dannlowski, Udo
DeRosse, Pamela
Chan, Raymond
Debbané, Martin
Rössler, Wulf
Lebedeva, Irina
Park, Haeme
Marsman, Jan-Bernard
Gilleen, James
Fett, Anne-Kathrin
van Erp, Theo
Turner, Jessica
Thompson, Paul
Aleman, Andre
Modinos, Gemma
Kaiser, Stefan
T162. THICKER PREFRONTAL CORTEX IS ASSOCIATED WITH SUBCLINICAL NEGATIVE SYMPTOMS IN SCHIZOTYPY - AN ENIGMA CONSORTIUM META-ANALYSIS
title T162. THICKER PREFRONTAL CORTEX IS ASSOCIATED WITH SUBCLINICAL NEGATIVE SYMPTOMS IN SCHIZOTYPY - AN ENIGMA CONSORTIUM META-ANALYSIS
title_full T162. THICKER PREFRONTAL CORTEX IS ASSOCIATED WITH SUBCLINICAL NEGATIVE SYMPTOMS IN SCHIZOTYPY - AN ENIGMA CONSORTIUM META-ANALYSIS
title_fullStr T162. THICKER PREFRONTAL CORTEX IS ASSOCIATED WITH SUBCLINICAL NEGATIVE SYMPTOMS IN SCHIZOTYPY - AN ENIGMA CONSORTIUM META-ANALYSIS
title_full_unstemmed T162. THICKER PREFRONTAL CORTEX IS ASSOCIATED WITH SUBCLINICAL NEGATIVE SYMPTOMS IN SCHIZOTYPY - AN ENIGMA CONSORTIUM META-ANALYSIS
title_short T162. THICKER PREFRONTAL CORTEX IS ASSOCIATED WITH SUBCLINICAL NEGATIVE SYMPTOMS IN SCHIZOTYPY - AN ENIGMA CONSORTIUM META-ANALYSIS
title_sort t162. thicker prefrontal cortex is associated with subclinical negative symptoms in schizotypy - an enigma consortium meta-analysis
topic Poster Session III
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7234734/
http://dx.doi.org/10.1093/schbul/sbaa029.722
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