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Sex, myelin, and clinical characteristics of Parkinson’s disease
OBJECTIVE: To determine if there are sex differences in myelin in Parkinson’s disease, and whether these explain some of the previously-described sex differences in clinical presentation. METHODS: Thirty-three subjects (23 males, 10 females) with Parkinson’s disease underwent myelin water fraction (...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10535348/ https://www.ncbi.nlm.nih.gov/pubmed/37781247 http://dx.doi.org/10.3389/fnins.2023.1235524 |
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author | Cai, Jiayue Kim, Jowon L. Wang, Yuheng Baumeister, Tobias R. Zhu, Maria Liu, Aiping Lee, Soojin McKeown, Martin J. |
author_facet | Cai, Jiayue Kim, Jowon L. Wang, Yuheng Baumeister, Tobias R. Zhu, Maria Liu, Aiping Lee, Soojin McKeown, Martin J. |
author_sort | Cai, Jiayue |
collection | PubMed |
description | OBJECTIVE: To determine if there are sex differences in myelin in Parkinson’s disease, and whether these explain some of the previously-described sex differences in clinical presentation. METHODS: Thirty-three subjects (23 males, 10 females) with Parkinson’s disease underwent myelin water fraction (MWF) imaging, an MRI scanning technique of in vivo myelin content. MWF of 20 white matter regions of interest (ROIs) were assessed. Motor symptoms were assessed using the Unified Parkinson’s Disease Rating Scale (UPDRS). Principal component analysis, logistic and multiple linear regressions, and t-tests were used to determine which white matter ROIs differed between sexes, the clinical features associated with these myelin changes, and if overall MWF and MWF laterality differed between males and females. RESULTS: Consistent with prior reports, tremor and bradykinesia were more likely seen in females, whereas rigidity and axial symptoms were more likely seen in males in our cohort. MWF of the thalamic radiation, cingulum, cingulum hippocampus, inferior fronto-occipital fasciculi, inferior longitudinal fasciculi, and uncinate were significant in predicting sex. Overall MWF and asymmetry of MWF was greater in males. MWF differences between sexes were associated with tremor symptomatology and asymmetry of motor performance. CONCLUSION: Sex differences in myelin are associated with tremor and asymmetry of motor presentation. While preliminary, our results suggest that further investigation of the role of biological sex in myelin pathology and clinical presentation in Parkinson’s disease is warranted. |
format | Online Article Text |
id | pubmed-10535348 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105353482023-09-29 Sex, myelin, and clinical characteristics of Parkinson’s disease Cai, Jiayue Kim, Jowon L. Wang, Yuheng Baumeister, Tobias R. Zhu, Maria Liu, Aiping Lee, Soojin McKeown, Martin J. Front Neurosci Neuroscience OBJECTIVE: To determine if there are sex differences in myelin in Parkinson’s disease, and whether these explain some of the previously-described sex differences in clinical presentation. METHODS: Thirty-three subjects (23 males, 10 females) with Parkinson’s disease underwent myelin water fraction (MWF) imaging, an MRI scanning technique of in vivo myelin content. MWF of 20 white matter regions of interest (ROIs) were assessed. Motor symptoms were assessed using the Unified Parkinson’s Disease Rating Scale (UPDRS). Principal component analysis, logistic and multiple linear regressions, and t-tests were used to determine which white matter ROIs differed between sexes, the clinical features associated with these myelin changes, and if overall MWF and MWF laterality differed between males and females. RESULTS: Consistent with prior reports, tremor and bradykinesia were more likely seen in females, whereas rigidity and axial symptoms were more likely seen in males in our cohort. MWF of the thalamic radiation, cingulum, cingulum hippocampus, inferior fronto-occipital fasciculi, inferior longitudinal fasciculi, and uncinate were significant in predicting sex. Overall MWF and asymmetry of MWF was greater in males. MWF differences between sexes were associated with tremor symptomatology and asymmetry of motor performance. CONCLUSION: Sex differences in myelin are associated with tremor and asymmetry of motor presentation. While preliminary, our results suggest that further investigation of the role of biological sex in myelin pathology and clinical presentation in Parkinson’s disease is warranted. Frontiers Media S.A. 2023-09-13 /pmc/articles/PMC10535348/ /pubmed/37781247 http://dx.doi.org/10.3389/fnins.2023.1235524 Text en Copyright © 2023 Cai, Kim, Wang, Baumeister, Zhu, Liu, Lee and McKeown. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Cai, Jiayue Kim, Jowon L. Wang, Yuheng Baumeister, Tobias R. Zhu, Maria Liu, Aiping Lee, Soojin McKeown, Martin J. Sex, myelin, and clinical characteristics of Parkinson’s disease |
title | Sex, myelin, and clinical characteristics of Parkinson’s disease |
title_full | Sex, myelin, and clinical characteristics of Parkinson’s disease |
title_fullStr | Sex, myelin, and clinical characteristics of Parkinson’s disease |
title_full_unstemmed | Sex, myelin, and clinical characteristics of Parkinson’s disease |
title_short | Sex, myelin, and clinical characteristics of Parkinson’s disease |
title_sort | sex, myelin, and clinical characteristics of parkinson’s disease |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10535348/ https://www.ncbi.nlm.nih.gov/pubmed/37781247 http://dx.doi.org/10.3389/fnins.2023.1235524 |
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