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Does Side of Onset Influence the Pattern of Cerebral Atrophy in Parkinson’s Disease?
BACKGROUND: Imaging studies have revealed widespread neurodegeneration in Parkinson’s disease (PD), but only a few considered the issue of asymmetrical clinical presentations. OBJECTIVE: To investigate if the side of onset influences the pattern of gray matter (GM) atrophy in PD. METHODS: Sixty pati...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018632/ https://www.ncbi.nlm.nih.gov/pubmed/27672378 http://dx.doi.org/10.3389/fneur.2016.00145 |
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author | Santos, Maria C. A. Campos, Lidiane S. Guimarães, Rachel P. Piccinin, Camila C. Azevedo, Paula C. Piovesana, Luiza G. De Campos, Brunno Machado Scarparo Amato-Filho, Augusto C. Cendes, Fernando D’Abreu, Anelyssa |
author_facet | Santos, Maria C. A. Campos, Lidiane S. Guimarães, Rachel P. Piccinin, Camila C. Azevedo, Paula C. Piovesana, Luiza G. De Campos, Brunno Machado Scarparo Amato-Filho, Augusto C. Cendes, Fernando D’Abreu, Anelyssa |
author_sort | Santos, Maria C. A. |
collection | PubMed |
description | BACKGROUND: Imaging studies have revealed widespread neurodegeneration in Parkinson’s disease (PD), but only a few considered the issue of asymmetrical clinical presentations. OBJECTIVE: To investigate if the side of onset influences the pattern of gray matter (GM) atrophy in PD. METHODS: Sixty patients (57.87 ± 10.27 years) diagnosed with idiopathic PD according to the U.K. Brain Bank criteria, 26 with right-sided disease onset (RDO) and 34 with left-sided disease onset (LDO), were compared to 80 healthy controls (HC) (57.1 ± 9.47 years). We acquired T1-weighted images on a 3 T scanner. Images were processed and analyzed with VBM8 (SPM8/Dartel) on Matlab R2012b platform. Statistic assessments included a two-sample test (family-wise error p < 0.05) with extent threshold of 20 voxels. RESULTS: Compared to HC, LDO patients had GM atrophy in the insula, putamen, anterior cingulate, frontotemporal cortex, and right caudate, while the RDO group showed atrophy at the anterior cingulate, insula, frontotemporal, and occipital cortex. CONCLUSION: This study revealed widespread GM atrophy in PD, predominantly in the left hemisphere, regardless of the side of onset. Future investigations should also consider handedness and side of onset to better characterize cerebral involvement and its progression in PD. |
format | Online Article Text |
id | pubmed-5018632 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50186322016-09-26 Does Side of Onset Influence the Pattern of Cerebral Atrophy in Parkinson’s Disease? Santos, Maria C. A. Campos, Lidiane S. Guimarães, Rachel P. Piccinin, Camila C. Azevedo, Paula C. Piovesana, Luiza G. De Campos, Brunno Machado Scarparo Amato-Filho, Augusto C. Cendes, Fernando D’Abreu, Anelyssa Front Neurol Neuroscience BACKGROUND: Imaging studies have revealed widespread neurodegeneration in Parkinson’s disease (PD), but only a few considered the issue of asymmetrical clinical presentations. OBJECTIVE: To investigate if the side of onset influences the pattern of gray matter (GM) atrophy in PD. METHODS: Sixty patients (57.87 ± 10.27 years) diagnosed with idiopathic PD according to the U.K. Brain Bank criteria, 26 with right-sided disease onset (RDO) and 34 with left-sided disease onset (LDO), were compared to 80 healthy controls (HC) (57.1 ± 9.47 years). We acquired T1-weighted images on a 3 T scanner. Images were processed and analyzed with VBM8 (SPM8/Dartel) on Matlab R2012b platform. Statistic assessments included a two-sample test (family-wise error p < 0.05) with extent threshold of 20 voxels. RESULTS: Compared to HC, LDO patients had GM atrophy in the insula, putamen, anterior cingulate, frontotemporal cortex, and right caudate, while the RDO group showed atrophy at the anterior cingulate, insula, frontotemporal, and occipital cortex. CONCLUSION: This study revealed widespread GM atrophy in PD, predominantly in the left hemisphere, regardless of the side of onset. Future investigations should also consider handedness and side of onset to better characterize cerebral involvement and its progression in PD. Frontiers Media S.A. 2016-09-12 /pmc/articles/PMC5018632/ /pubmed/27672378 http://dx.doi.org/10.3389/fneur.2016.00145 Text en Copyright © 2016 Santos, Campos, Guimarães, Piccinin, Azevedo, Piovesana, De Campos, Scarparo Amato-Filho, Cendes and D’Abreu. http://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) or licensor 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 Santos, Maria C. A. Campos, Lidiane S. Guimarães, Rachel P. Piccinin, Camila C. Azevedo, Paula C. Piovesana, Luiza G. De Campos, Brunno Machado Scarparo Amato-Filho, Augusto C. Cendes, Fernando D’Abreu, Anelyssa Does Side of Onset Influence the Pattern of Cerebral Atrophy in Parkinson’s Disease? |
title | Does Side of Onset Influence the Pattern of Cerebral Atrophy in Parkinson’s Disease? |
title_full | Does Side of Onset Influence the Pattern of Cerebral Atrophy in Parkinson’s Disease? |
title_fullStr | Does Side of Onset Influence the Pattern of Cerebral Atrophy in Parkinson’s Disease? |
title_full_unstemmed | Does Side of Onset Influence the Pattern of Cerebral Atrophy in Parkinson’s Disease? |
title_short | Does Side of Onset Influence the Pattern of Cerebral Atrophy in Parkinson’s Disease? |
title_sort | does side of onset influence the pattern of cerebral atrophy in parkinson’s disease? |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018632/ https://www.ncbi.nlm.nih.gov/pubmed/27672378 http://dx.doi.org/10.3389/fneur.2016.00145 |
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