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Bimodal distribution of tone-matching deficits indicates discrete pathophysiological entities within the syndrome of schizophrenia
To date, no measures are available that permit differentiation of discrete, clinically distinct subtypes of schizophrenia (SZ) with potential differential underlying pathophysiologies. Over recent years, there has been increasing recognition that SZ is heterogeneously associated with deficits in ear...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6731304/ https://www.ncbi.nlm.nih.gov/pubmed/31492832 http://dx.doi.org/10.1038/s41398-019-0557-8 |
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author | Dondé, Clément Martínez, Antigona Kantrowitz, Joshua T. Silipo, Gail Dias, Elisa C. Patel, Gaurav H. Sanchez-Peña, Juan Corcoran, Cheryl M. Medalia, Alice Saperstein, Alice Vail, Blair Javitt, Daniel C. |
author_facet | Dondé, Clément Martínez, Antigona Kantrowitz, Joshua T. Silipo, Gail Dias, Elisa C. Patel, Gaurav H. Sanchez-Peña, Juan Corcoran, Cheryl M. Medalia, Alice Saperstein, Alice Vail, Blair Javitt, Daniel C. |
author_sort | Dondé, Clément |
collection | PubMed |
description | To date, no measures are available that permit differentiation of discrete, clinically distinct subtypes of schizophrenia (SZ) with potential differential underlying pathophysiologies. Over recent years, there has been increasing recognition that SZ is heterogeneously associated with deficits in early auditory processing (EAP), as demonstrated using clinically applicable tasks such as tone-matching task (TMT). Here, we pooled TMT performances across 310 SZ individuals and 219 healthy controls (HC), along with clinical, cognitive, and resting-state functional-connectivity MRI (rsFC-MRI) measures. In addition, TMT was measured in a group of 24 patients at symptomatic clinical high risk (CHR) for SZ and 24 age-matched HC (age range 7–27 years). We provide the first demonstration that the EAP deficits are bimodally distributed across SZ subjects (P < 0.0001 vs. unimodal distribution), with one group showing entirely unimpaired TMT performance (SZ-EAP+), and a second showing an extremely large TMT impairment (SZ-EAP−), relative to both controls (d = 2.1) and SZ-EAP+ patients (d = 3.4). The SZ-EAP− group predominated among samples drawn from inpatient sites, showed higher levels of cognitive symptoms (PANSS), worse social cognition and a differential deficit in neurocognition (MATRICS battery), and reduced functional capacity. rsFC-MRI analyses showed significant reduction in SZ-EAP− relative to controls between subcortical and cortical auditory regions. As opposed to SZ, CHR patients showed intact EAP function. In HC age-matched to CHR, EAP ability was shown to increase across the age range of vulnerability preceding SZ onset. These results indicate that EAP measure segregates between discrete SZ subgroups. As TMT can be readily implemented within routine clinical settings, its use may be critical to account for the heterogeneity of clinical outcomes currently observed across SZ patients, as well as for pre-clinical detection and efficacious treatment selection. |
format | Online Article Text |
id | pubmed-6731304 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67313042019-09-10 Bimodal distribution of tone-matching deficits indicates discrete pathophysiological entities within the syndrome of schizophrenia Dondé, Clément Martínez, Antigona Kantrowitz, Joshua T. Silipo, Gail Dias, Elisa C. Patel, Gaurav H. Sanchez-Peña, Juan Corcoran, Cheryl M. Medalia, Alice Saperstein, Alice Vail, Blair Javitt, Daniel C. Transl Psychiatry Article To date, no measures are available that permit differentiation of discrete, clinically distinct subtypes of schizophrenia (SZ) with potential differential underlying pathophysiologies. Over recent years, there has been increasing recognition that SZ is heterogeneously associated with deficits in early auditory processing (EAP), as demonstrated using clinically applicable tasks such as tone-matching task (TMT). Here, we pooled TMT performances across 310 SZ individuals and 219 healthy controls (HC), along with clinical, cognitive, and resting-state functional-connectivity MRI (rsFC-MRI) measures. In addition, TMT was measured in a group of 24 patients at symptomatic clinical high risk (CHR) for SZ and 24 age-matched HC (age range 7–27 years). We provide the first demonstration that the EAP deficits are bimodally distributed across SZ subjects (P < 0.0001 vs. unimodal distribution), with one group showing entirely unimpaired TMT performance (SZ-EAP+), and a second showing an extremely large TMT impairment (SZ-EAP−), relative to both controls (d = 2.1) and SZ-EAP+ patients (d = 3.4). The SZ-EAP− group predominated among samples drawn from inpatient sites, showed higher levels of cognitive symptoms (PANSS), worse social cognition and a differential deficit in neurocognition (MATRICS battery), and reduced functional capacity. rsFC-MRI analyses showed significant reduction in SZ-EAP− relative to controls between subcortical and cortical auditory regions. As opposed to SZ, CHR patients showed intact EAP function. In HC age-matched to CHR, EAP ability was shown to increase across the age range of vulnerability preceding SZ onset. These results indicate that EAP measure segregates between discrete SZ subgroups. As TMT can be readily implemented within routine clinical settings, its use may be critical to account for the heterogeneity of clinical outcomes currently observed across SZ patients, as well as for pre-clinical detection and efficacious treatment selection. Nature Publishing Group UK 2019-09-06 /pmc/articles/PMC6731304/ /pubmed/31492832 http://dx.doi.org/10.1038/s41398-019-0557-8 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Dondé, Clément Martínez, Antigona Kantrowitz, Joshua T. Silipo, Gail Dias, Elisa C. Patel, Gaurav H. Sanchez-Peña, Juan Corcoran, Cheryl M. Medalia, Alice Saperstein, Alice Vail, Blair Javitt, Daniel C. Bimodal distribution of tone-matching deficits indicates discrete pathophysiological entities within the syndrome of schizophrenia |
title | Bimodal distribution of tone-matching deficits indicates discrete pathophysiological entities within the syndrome of schizophrenia |
title_full | Bimodal distribution of tone-matching deficits indicates discrete pathophysiological entities within the syndrome of schizophrenia |
title_fullStr | Bimodal distribution of tone-matching deficits indicates discrete pathophysiological entities within the syndrome of schizophrenia |
title_full_unstemmed | Bimodal distribution of tone-matching deficits indicates discrete pathophysiological entities within the syndrome of schizophrenia |
title_short | Bimodal distribution of tone-matching deficits indicates discrete pathophysiological entities within the syndrome of schizophrenia |
title_sort | bimodal distribution of tone-matching deficits indicates discrete pathophysiological entities within the syndrome of schizophrenia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6731304/ https://www.ncbi.nlm.nih.gov/pubmed/31492832 http://dx.doi.org/10.1038/s41398-019-0557-8 |
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