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Microstructural network alterations of olfactory dysfunction in newly diagnosed Parkinson’s disease

Olfactory dysfunction is a robust and early sign for Parkinson’s disease (PD). Previous studies have revealed its association with dementia and related neural changes in PD. Yet, how olfactory dysfunction affects white matter (WM) microstructure in newly diagnosed and untreated PD remains unclear. H...

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Autores principales: Wen, Ming-Ching, Xu, Zheyu, Lu, Zhonghao, Chan, Ling Ling, Tan, Eng King, Tan, Louis C. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5624890/
https://www.ncbi.nlm.nih.gov/pubmed/28970540
http://dx.doi.org/10.1038/s41598-017-12947-7
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author Wen, Ming-Ching
Xu, Zheyu
Lu, Zhonghao
Chan, Ling Ling
Tan, Eng King
Tan, Louis C. S.
author_facet Wen, Ming-Ching
Xu, Zheyu
Lu, Zhonghao
Chan, Ling Ling
Tan, Eng King
Tan, Louis C. S.
author_sort Wen, Ming-Ching
collection PubMed
description Olfactory dysfunction is a robust and early sign for Parkinson’s disease (PD). Previous studies have revealed its association with dementia and related neural changes in PD. Yet, how olfactory dysfunction affects white matter (WM) microstructure in newly diagnosed and untreated PD remains unclear. Here we comprehensively examined WM features using unbiased whole-brain analyses. 88 newly diagnosed PD patients without dementia (70 with hyposmia and 18 without hyposmia) and 33 healthy controls underwent clinical assessment and diffusion tensor imaging (DTI) scanning. Tract-based special statistics (TBSS), graph-theoretic methods and network-based statistics (NBS) were used to compare regional and network-related WM features between groups. TBSS analysis did not show any differences in fractional anisotropy and mean diffusivity between groups. Compared with controls, PD patients without hyposmia showed a significant decrease in global efficiency, whilst PD patients with hyposmia exhibited significantly reduced global and local efficiency and additionally a disrupted connection between the right medial orbitofrontal cortex and left rectus and had poorer frontal-related cognitive functioning. These results demonstrate that hyposmia-related WM changes in early PD only occur at the network level. The confined disconnectivity between the bilateral olfactory circuitry may serve as a biomarker for olfactory dysfunction in early PD.
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spelling pubmed-56248902017-10-12 Microstructural network alterations of olfactory dysfunction in newly diagnosed Parkinson’s disease Wen, Ming-Ching Xu, Zheyu Lu, Zhonghao Chan, Ling Ling Tan, Eng King Tan, Louis C. S. Sci Rep Article Olfactory dysfunction is a robust and early sign for Parkinson’s disease (PD). Previous studies have revealed its association with dementia and related neural changes in PD. Yet, how olfactory dysfunction affects white matter (WM) microstructure in newly diagnosed and untreated PD remains unclear. Here we comprehensively examined WM features using unbiased whole-brain analyses. 88 newly diagnosed PD patients without dementia (70 with hyposmia and 18 without hyposmia) and 33 healthy controls underwent clinical assessment and diffusion tensor imaging (DTI) scanning. Tract-based special statistics (TBSS), graph-theoretic methods and network-based statistics (NBS) were used to compare regional and network-related WM features between groups. TBSS analysis did not show any differences in fractional anisotropy and mean diffusivity between groups. Compared with controls, PD patients without hyposmia showed a significant decrease in global efficiency, whilst PD patients with hyposmia exhibited significantly reduced global and local efficiency and additionally a disrupted connection between the right medial orbitofrontal cortex and left rectus and had poorer frontal-related cognitive functioning. These results demonstrate that hyposmia-related WM changes in early PD only occur at the network level. The confined disconnectivity between the bilateral olfactory circuitry may serve as a biomarker for olfactory dysfunction in early PD. Nature Publishing Group UK 2017-10-02 /pmc/articles/PMC5624890/ /pubmed/28970540 http://dx.doi.org/10.1038/s41598-017-12947-7 Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Wen, Ming-Ching
Xu, Zheyu
Lu, Zhonghao
Chan, Ling Ling
Tan, Eng King
Tan, Louis C. S.
Microstructural network alterations of olfactory dysfunction in newly diagnosed Parkinson’s disease
title Microstructural network alterations of olfactory dysfunction in newly diagnosed Parkinson’s disease
title_full Microstructural network alterations of olfactory dysfunction in newly diagnosed Parkinson’s disease
title_fullStr Microstructural network alterations of olfactory dysfunction in newly diagnosed Parkinson’s disease
title_full_unstemmed Microstructural network alterations of olfactory dysfunction in newly diagnosed Parkinson’s disease
title_short Microstructural network alterations of olfactory dysfunction in newly diagnosed Parkinson’s disease
title_sort microstructural network alterations of olfactory dysfunction in newly diagnosed parkinson’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5624890/
https://www.ncbi.nlm.nih.gov/pubmed/28970540
http://dx.doi.org/10.1038/s41598-017-12947-7
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