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Abnormal cortical thickening and thinning in idiopathic normal-pressure hydrocephalus
We investigated differences in cortical thickness between idiopathic normal-pressure hydrocephalus (INPH) patients and healthy controls. We also explored whether a relationship exists between cortical thinning and gait disturbance in INPH patients. Forty-nine INPH patients and 26 healthy controls we...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7712876/ https://www.ncbi.nlm.nih.gov/pubmed/33273614 http://dx.doi.org/10.1038/s41598-020-78067-x |
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author | Kang, Kyunghun Han, Jaehwan Lee, Sang-Woo Jeong, Shin Young Lim, Yong-Hyun Lee, Jong-Min Yoon, Uicheul |
author_facet | Kang, Kyunghun Han, Jaehwan Lee, Sang-Woo Jeong, Shin Young Lim, Yong-Hyun Lee, Jong-Min Yoon, Uicheul |
author_sort | Kang, Kyunghun |
collection | PubMed |
description | We investigated differences in cortical thickness between idiopathic normal-pressure hydrocephalus (INPH) patients and healthy controls. We also explored whether a relationship exists between cortical thinning and gait disturbance in INPH patients. Forty-nine INPH patients and 26 healthy controls were imaged with MRI, including 3-dimensional volumetric images, for automated surface-based cortical thickness analysis across the entire brain. Compared with age- and gender-matched healthy controls, unexpectedly, INPH patients showed statistically significant cortical thickening mainly in areas located in the high convexity of the frontal, parietal, and occipital regions. Additionally, cortical thinning mainly in temporal and orbitofrontal regions was observed in the INPH group relative to the control group. The Gait Status Scale (GSS) scores were negatively correlated with cortical thickness in the medial orbital part of the superior frontal gyrus, gyrus rectus, superior temporal gyrus, temporal pole, and insula. A distinctive pattern of cortical thickness changes was found in INPH patients. We cautiously suggest that cortical thickening in INPH can result from reactive gliosis. Further, our results support the hypothesis that cortical thinning in INPH can result from neuronal degeneration. In addition, cortical thinning can play an important role in gait disturbances in INPH patients. |
format | Online Article Text |
id | pubmed-7712876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77128762020-12-03 Abnormal cortical thickening and thinning in idiopathic normal-pressure hydrocephalus Kang, Kyunghun Han, Jaehwan Lee, Sang-Woo Jeong, Shin Young Lim, Yong-Hyun Lee, Jong-Min Yoon, Uicheul Sci Rep Article We investigated differences in cortical thickness between idiopathic normal-pressure hydrocephalus (INPH) patients and healthy controls. We also explored whether a relationship exists between cortical thinning and gait disturbance in INPH patients. Forty-nine INPH patients and 26 healthy controls were imaged with MRI, including 3-dimensional volumetric images, for automated surface-based cortical thickness analysis across the entire brain. Compared with age- and gender-matched healthy controls, unexpectedly, INPH patients showed statistically significant cortical thickening mainly in areas located in the high convexity of the frontal, parietal, and occipital regions. Additionally, cortical thinning mainly in temporal and orbitofrontal regions was observed in the INPH group relative to the control group. The Gait Status Scale (GSS) scores were negatively correlated with cortical thickness in the medial orbital part of the superior frontal gyrus, gyrus rectus, superior temporal gyrus, temporal pole, and insula. A distinctive pattern of cortical thickness changes was found in INPH patients. We cautiously suggest that cortical thickening in INPH can result from reactive gliosis. Further, our results support the hypothesis that cortical thinning in INPH can result from neuronal degeneration. In addition, cortical thinning can play an important role in gait disturbances in INPH patients. Nature Publishing Group UK 2020-12-03 /pmc/articles/PMC7712876/ /pubmed/33273614 http://dx.doi.org/10.1038/s41598-020-78067-x Text en © The Author(s) 2020 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kang, Kyunghun Han, Jaehwan Lee, Sang-Woo Jeong, Shin Young Lim, Yong-Hyun Lee, Jong-Min Yoon, Uicheul Abnormal cortical thickening and thinning in idiopathic normal-pressure hydrocephalus |
title | Abnormal cortical thickening and thinning in idiopathic normal-pressure hydrocephalus |
title_full | Abnormal cortical thickening and thinning in idiopathic normal-pressure hydrocephalus |
title_fullStr | Abnormal cortical thickening and thinning in idiopathic normal-pressure hydrocephalus |
title_full_unstemmed | Abnormal cortical thickening and thinning in idiopathic normal-pressure hydrocephalus |
title_short | Abnormal cortical thickening and thinning in idiopathic normal-pressure hydrocephalus |
title_sort | abnormal cortical thickening and thinning in idiopathic normal-pressure hydrocephalus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7712876/ https://www.ncbi.nlm.nih.gov/pubmed/33273614 http://dx.doi.org/10.1038/s41598-020-78067-x |
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