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Quantitative Macromolecular Proton Fraction Mapping Reveals Altered Cortical Myelin Profile in Schizophrenia Spectrum Disorders

Myelin abnormalities have been reported in schizophrenia spectrum disorders (SSD) in white matter. However, in vivo examinations of cortical myeloarchitecture in SSD, especially those using quantitative measures, are limited. Here, we employed macromolecular proton fraction (MPF) obtained from quant...

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Autores principales: Sui, Yu Veronica, Bertisch, Hilary, Lee, Hong-Hsi, Storey, Pippa, Babb, James S, Goff, Donald C, Samsonov, Alexey, Lazar, Mariana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8271044/
https://www.ncbi.nlm.nih.gov/pubmed/34296161
http://dx.doi.org/10.1093/texcom/tgab015
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author Sui, Yu Veronica
Bertisch, Hilary
Lee, Hong-Hsi
Storey, Pippa
Babb, James S
Goff, Donald C
Samsonov, Alexey
Lazar, Mariana
author_facet Sui, Yu Veronica
Bertisch, Hilary
Lee, Hong-Hsi
Storey, Pippa
Babb, James S
Goff, Donald C
Samsonov, Alexey
Lazar, Mariana
author_sort Sui, Yu Veronica
collection PubMed
description Myelin abnormalities have been reported in schizophrenia spectrum disorders (SSD) in white matter. However, in vivo examinations of cortical myeloarchitecture in SSD, especially those using quantitative measures, are limited. Here, we employed macromolecular proton fraction (MPF) obtained from quantitative magnetization transfer imaging to characterize intracortical myelin organization in 30 SSD patients versus 34 healthy control (HC) participants. We constructed cortical myelin profiles by extracting MPF values at various cortical depths and quantified their shape using a nonlinearity index (NLI). To delineate the association of illness duration with myelin changes, SSD patients were further divided into 3 duration groups. Between-group comparisons revealed reduced NLI in the SSD group with the longest illness duration (>5.5 years) compared with HC predominantly in bilateral prefrontal areas. Within the SSD group, cortical NLI decreased with disease duration and was positively associated with a measure of spatial working memory capacity as well as with cortical thickness (CT). Layer-specific analyses suggested that NLI decreases in the long-duration SSD group may arise in part from significantly increased MPF values in the midcortical layers. The current study reveals cortical myelin profile changes in SSD with illness progression, which may reflect an abnormal compensatory mechanism of the disorder.
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spelling pubmed-82710442021-07-21 Quantitative Macromolecular Proton Fraction Mapping Reveals Altered Cortical Myelin Profile in Schizophrenia Spectrum Disorders Sui, Yu Veronica Bertisch, Hilary Lee, Hong-Hsi Storey, Pippa Babb, James S Goff, Donald C Samsonov, Alexey Lazar, Mariana Cereb Cortex Commun Original Article Myelin abnormalities have been reported in schizophrenia spectrum disorders (SSD) in white matter. However, in vivo examinations of cortical myeloarchitecture in SSD, especially those using quantitative measures, are limited. Here, we employed macromolecular proton fraction (MPF) obtained from quantitative magnetization transfer imaging to characterize intracortical myelin organization in 30 SSD patients versus 34 healthy control (HC) participants. We constructed cortical myelin profiles by extracting MPF values at various cortical depths and quantified their shape using a nonlinearity index (NLI). To delineate the association of illness duration with myelin changes, SSD patients were further divided into 3 duration groups. Between-group comparisons revealed reduced NLI in the SSD group with the longest illness duration (>5.5 years) compared with HC predominantly in bilateral prefrontal areas. Within the SSD group, cortical NLI decreased with disease duration and was positively associated with a measure of spatial working memory capacity as well as with cortical thickness (CT). Layer-specific analyses suggested that NLI decreases in the long-duration SSD group may arise in part from significantly increased MPF values in the midcortical layers. The current study reveals cortical myelin profile changes in SSD with illness progression, which may reflect an abnormal compensatory mechanism of the disorder. Oxford University Press 2021-02-24 /pmc/articles/PMC8271044/ /pubmed/34296161 http://dx.doi.org/10.1093/texcom/tgab015 Text en © The Author(s) 2021. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Sui, Yu Veronica
Bertisch, Hilary
Lee, Hong-Hsi
Storey, Pippa
Babb, James S
Goff, Donald C
Samsonov, Alexey
Lazar, Mariana
Quantitative Macromolecular Proton Fraction Mapping Reveals Altered Cortical Myelin Profile in Schizophrenia Spectrum Disorders
title Quantitative Macromolecular Proton Fraction Mapping Reveals Altered Cortical Myelin Profile in Schizophrenia Spectrum Disorders
title_full Quantitative Macromolecular Proton Fraction Mapping Reveals Altered Cortical Myelin Profile in Schizophrenia Spectrum Disorders
title_fullStr Quantitative Macromolecular Proton Fraction Mapping Reveals Altered Cortical Myelin Profile in Schizophrenia Spectrum Disorders
title_full_unstemmed Quantitative Macromolecular Proton Fraction Mapping Reveals Altered Cortical Myelin Profile in Schizophrenia Spectrum Disorders
title_short Quantitative Macromolecular Proton Fraction Mapping Reveals Altered Cortical Myelin Profile in Schizophrenia Spectrum Disorders
title_sort quantitative macromolecular proton fraction mapping reveals altered cortical myelin profile in schizophrenia spectrum disorders
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8271044/
https://www.ncbi.nlm.nih.gov/pubmed/34296161
http://dx.doi.org/10.1093/texcom/tgab015
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