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Glutathione as a Molecular Marker of Functional Impairment in Patients with At-Risk Mental State: 7-Tesla (1)H-MRS Study
A substantial number of individuals with clinical high-risk (CHR) mental state do not transition to psychosis. However, regardless of future diagnostic trajectories, many of these individuals develop poor social and occupational functional outcomes. The levels of glutathione, a crucial cortical anti...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8307096/ https://www.ncbi.nlm.nih.gov/pubmed/34356175 http://dx.doi.org/10.3390/brainsci11070941 |
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author | Jeon, Peter Limongi, Roberto Ford, Sabrina D. Branco, Cassandra Mackinley, Michael Gupta, Maya Powe, Laura Théberge, Jean Palaniyappan, Lena |
author_facet | Jeon, Peter Limongi, Roberto Ford, Sabrina D. Branco, Cassandra Mackinley, Michael Gupta, Maya Powe, Laura Théberge, Jean Palaniyappan, Lena |
author_sort | Jeon, Peter |
collection | PubMed |
description | A substantial number of individuals with clinical high-risk (CHR) mental state do not transition to psychosis. However, regardless of future diagnostic trajectories, many of these individuals develop poor social and occupational functional outcomes. The levels of glutathione, a crucial cortical antioxidant, may track variations in functional outcomes in early psychosis and prodromal states. Thirteen clinical high-risk and 30 healthy control volunteers were recruited for a 7-Tesla magnetic resonance spectroscopy scan with a voxel positioned within the dorsal anterior cingulate cortex (ACC). Clinical assessment scores were collected to determine if any association was observable with glutathione levels. The Bayesian Spearman’s test revealed a positive association between the Social and Occupational Functioning Assessment Scale (SOFAS) and the glutathione concentration in the clinical high-risk group but not in the healthy control group. After accounting for variations in the SOFAS scores, the CHR group had higher GSH levels than the healthy subjects. This study is the first to use 7-Tesla magnetic resonance spectroscopy to test whether ACC glutathione levels relate to social and occupational functioning in a clinically high-risk group and offers preliminary support for glutathione levels as a clinically actionable marker of prognosis in emerging adults presenting with risk features for various severe mental illnesses. |
format | Online Article Text |
id | pubmed-8307096 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83070962021-07-25 Glutathione as a Molecular Marker of Functional Impairment in Patients with At-Risk Mental State: 7-Tesla (1)H-MRS Study Jeon, Peter Limongi, Roberto Ford, Sabrina D. Branco, Cassandra Mackinley, Michael Gupta, Maya Powe, Laura Théberge, Jean Palaniyappan, Lena Brain Sci Article A substantial number of individuals with clinical high-risk (CHR) mental state do not transition to psychosis. However, regardless of future diagnostic trajectories, many of these individuals develop poor social and occupational functional outcomes. The levels of glutathione, a crucial cortical antioxidant, may track variations in functional outcomes in early psychosis and prodromal states. Thirteen clinical high-risk and 30 healthy control volunteers were recruited for a 7-Tesla magnetic resonance spectroscopy scan with a voxel positioned within the dorsal anterior cingulate cortex (ACC). Clinical assessment scores were collected to determine if any association was observable with glutathione levels. The Bayesian Spearman’s test revealed a positive association between the Social and Occupational Functioning Assessment Scale (SOFAS) and the glutathione concentration in the clinical high-risk group but not in the healthy control group. After accounting for variations in the SOFAS scores, the CHR group had higher GSH levels than the healthy subjects. This study is the first to use 7-Tesla magnetic resonance spectroscopy to test whether ACC glutathione levels relate to social and occupational functioning in a clinically high-risk group and offers preliminary support for glutathione levels as a clinically actionable marker of prognosis in emerging adults presenting with risk features for various severe mental illnesses. MDPI 2021-07-17 /pmc/articles/PMC8307096/ /pubmed/34356175 http://dx.doi.org/10.3390/brainsci11070941 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Jeon, Peter Limongi, Roberto Ford, Sabrina D. Branco, Cassandra Mackinley, Michael Gupta, Maya Powe, Laura Théberge, Jean Palaniyappan, Lena Glutathione as a Molecular Marker of Functional Impairment in Patients with At-Risk Mental State: 7-Tesla (1)H-MRS Study |
title | Glutathione as a Molecular Marker of Functional Impairment in Patients with At-Risk Mental State: 7-Tesla (1)H-MRS Study |
title_full | Glutathione as a Molecular Marker of Functional Impairment in Patients with At-Risk Mental State: 7-Tesla (1)H-MRS Study |
title_fullStr | Glutathione as a Molecular Marker of Functional Impairment in Patients with At-Risk Mental State: 7-Tesla (1)H-MRS Study |
title_full_unstemmed | Glutathione as a Molecular Marker of Functional Impairment in Patients with At-Risk Mental State: 7-Tesla (1)H-MRS Study |
title_short | Glutathione as a Molecular Marker of Functional Impairment in Patients with At-Risk Mental State: 7-Tesla (1)H-MRS Study |
title_sort | glutathione as a molecular marker of functional impairment in patients with at-risk mental state: 7-tesla (1)h-mrs study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8307096/ https://www.ncbi.nlm.nih.gov/pubmed/34356175 http://dx.doi.org/10.3390/brainsci11070941 |
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