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Gray Matter Microstructural Abnormalities and Working Memory Deficits in Individuals with Schizophrenia
OBJECTIVE: Working memory impairments serve as prognostic factors for patients with schizophrenia. Working memory deficits are mainly associated with gray matter (GM) thickness and volume. We investigated the association between GM diffusivity and working memory in controls and individuals with schi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Neuropsychiatric Association
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6444097/ https://www.ncbi.nlm.nih.gov/pubmed/30934191 http://dx.doi.org/10.30773/pi.2018.10.14.1 |
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author | Kim, HyunJung Shon, Seung-Hyun Joo, Sung Woo Yoon, Woon Lee, Jang-Han Hur, Ji-Won Lee, JungSun |
author_facet | Kim, HyunJung Shon, Seung-Hyun Joo, Sung Woo Yoon, Woon Lee, Jang-Han Hur, Ji-Won Lee, JungSun |
author_sort | Kim, HyunJung |
collection | PubMed |
description | OBJECTIVE: Working memory impairments serve as prognostic factors for patients with schizophrenia. Working memory deficits are mainly associated with gray matter (GM) thickness and volume. We investigated the association between GM diffusivity and working memory in controls and individuals with schizophrenia. METHODS: T1 and diffusion tensor images of the brain, working memory task (letter number sequencing) scores, and the demographic data of 90 individuals with schizophrenia and 97 controls were collected from the SchizConnect database. T1 images were parcellated into the 68 GM Regions of Interest (ROI). Axial Diffusivity (AD), Fractional Anisotropy (FA), Radial Diffusivity (RD), and Trace (TR) were calculated for each of the ROIs. RESULTS: Compared to the controls, schizophrenia group showed significantly increased AD, RD, and TR in specific regions on the frontal, temporal, and anterior cingulate area. Moreover, working memory was negatively correlated with AD, RD, and TR in the lateral orbitofrontal, superior temporal, inferior temporal, and rostral anterior cingulate area on left hemisphere in the individuals with schizophrenia. CONCLUSION: These results demonstrated GM microstructural abnormalities in the frontal, temporal, and anterior cingulate regions of individuals with schizophrenia. Furthermore, these regional GM microstructural abnormalities suggest a neuropathological basis for the working memory deficits observed clinically in individuals with schizophrenia. |
format | Online Article Text |
id | pubmed-6444097 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Korean Neuropsychiatric Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-64440972019-04-03 Gray Matter Microstructural Abnormalities and Working Memory Deficits in Individuals with Schizophrenia Kim, HyunJung Shon, Seung-Hyun Joo, Sung Woo Yoon, Woon Lee, Jang-Han Hur, Ji-Won Lee, JungSun Psychiatry Investig Original Article OBJECTIVE: Working memory impairments serve as prognostic factors for patients with schizophrenia. Working memory deficits are mainly associated with gray matter (GM) thickness and volume. We investigated the association between GM diffusivity and working memory in controls and individuals with schizophrenia. METHODS: T1 and diffusion tensor images of the brain, working memory task (letter number sequencing) scores, and the demographic data of 90 individuals with schizophrenia and 97 controls were collected from the SchizConnect database. T1 images were parcellated into the 68 GM Regions of Interest (ROI). Axial Diffusivity (AD), Fractional Anisotropy (FA), Radial Diffusivity (RD), and Trace (TR) were calculated for each of the ROIs. RESULTS: Compared to the controls, schizophrenia group showed significantly increased AD, RD, and TR in specific regions on the frontal, temporal, and anterior cingulate area. Moreover, working memory was negatively correlated with AD, RD, and TR in the lateral orbitofrontal, superior temporal, inferior temporal, and rostral anterior cingulate area on left hemisphere in the individuals with schizophrenia. CONCLUSION: These results demonstrated GM microstructural abnormalities in the frontal, temporal, and anterior cingulate regions of individuals with schizophrenia. Furthermore, these regional GM microstructural abnormalities suggest a neuropathological basis for the working memory deficits observed clinically in individuals with schizophrenia. Korean Neuropsychiatric Association 2019-03 2019-03-21 /pmc/articles/PMC6444097/ /pubmed/30934191 http://dx.doi.org/10.30773/pi.2018.10.14.1 Text en Copyright © 2019 Korean Neuropsychiatric Association 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 unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kim, HyunJung Shon, Seung-Hyun Joo, Sung Woo Yoon, Woon Lee, Jang-Han Hur, Ji-Won Lee, JungSun Gray Matter Microstructural Abnormalities and Working Memory Deficits in Individuals with Schizophrenia |
title | Gray Matter Microstructural Abnormalities and Working Memory Deficits in Individuals with Schizophrenia |
title_full | Gray Matter Microstructural Abnormalities and Working Memory Deficits in Individuals with Schizophrenia |
title_fullStr | Gray Matter Microstructural Abnormalities and Working Memory Deficits in Individuals with Schizophrenia |
title_full_unstemmed | Gray Matter Microstructural Abnormalities and Working Memory Deficits in Individuals with Schizophrenia |
title_short | Gray Matter Microstructural Abnormalities and Working Memory Deficits in Individuals with Schizophrenia |
title_sort | gray matter microstructural abnormalities and working memory deficits in individuals with schizophrenia |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6444097/ https://www.ncbi.nlm.nih.gov/pubmed/30934191 http://dx.doi.org/10.30773/pi.2018.10.14.1 |
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