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The influence of white matter hyperintensity on cognitive impairment in Parkinson's disease

The aim of this meta‐analysis was to review systematically and to identify the relationship between the severity and location of white matter hyperintensities (WMHs) and the degree of cognitive decline in patients with Parkinson’s disease (PD). We searched the PubMed, EMBASE, Web of Science, Ovid, a...

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Autores principales: Liu, Hailing, Deng, Bin, Xie, Fen, Yang, Xiaohua, Xie, Zhenchao, Chen, Yonghua, Yang, Zhi, Huang, Xiyan, Zhu, Shuzhen, Wang, Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419402/
https://www.ncbi.nlm.nih.gov/pubmed/34310081
http://dx.doi.org/10.1002/acn3.51429
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author Liu, Hailing
Deng, Bin
Xie, Fen
Yang, Xiaohua
Xie, Zhenchao
Chen, Yonghua
Yang, Zhi
Huang, Xiyan
Zhu, Shuzhen
Wang, Qing
author_facet Liu, Hailing
Deng, Bin
Xie, Fen
Yang, Xiaohua
Xie, Zhenchao
Chen, Yonghua
Yang, Zhi
Huang, Xiyan
Zhu, Shuzhen
Wang, Qing
author_sort Liu, Hailing
collection PubMed
description The aim of this meta‐analysis was to review systematically and to identify the relationship between the severity and location of white matter hyperintensities (WMHs) and the degree of cognitive decline in patients with Parkinson’s disease (PD). We searched the PubMed, EMBASE, Web of Science, Ovid, and Cochrane Library databases for clinical trials of the severity and location of WMHs on the degree of cognitive impairment in PD through October 2020. We conducted the survey to compare the association of WMH burden in patients with PD with mild cognitive impairment (PD‐MCI) versus those with normal cognition (PD‐NC) and in patients with PD with dementia (PDD) versus those with PD without dementia (PD‐ND). Nine studies with PD‐MCI versus PD‐NC and 10 studies with PDD versus PD‐ND comparisons were included. The WMH burden in PD‐MCI patients was significantly different compared to that in PD‐NC patients (standard mean difference, SMD = 0.39, 95% CI: 0.12 to 0.66, p = 0.005), while there was no correlation shown in the age‐matched subgroup of the comparison. In addition, PDD patients had a significantly higher burden of WMHs (SMD = 0.8, 95% CI: 0.44 to 1.71, p < 0.0001), especially deep white matter hyperintensities (SMD = 0.54, 95% CI: 0.36 to 0.73, p < 0.00001) and periventricular hyperintensities (SMD = 0.70, 95% CI: 0.36 to 1.04, p < 0.0001), than PD‐NC patients, regardless of the adjustment of age. WMHs might be imaging markers for cognitive impairment in PDD but not in PD‐MCI, regardless of age, vascular risk factors, or race. Further prospective studies are needed to validate the conclusions.
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spelling pubmed-84194022021-09-08 The influence of white matter hyperintensity on cognitive impairment in Parkinson's disease Liu, Hailing Deng, Bin Xie, Fen Yang, Xiaohua Xie, Zhenchao Chen, Yonghua Yang, Zhi Huang, Xiyan Zhu, Shuzhen Wang, Qing Ann Clin Transl Neurol Review The aim of this meta‐analysis was to review systematically and to identify the relationship between the severity and location of white matter hyperintensities (WMHs) and the degree of cognitive decline in patients with Parkinson’s disease (PD). We searched the PubMed, EMBASE, Web of Science, Ovid, and Cochrane Library databases for clinical trials of the severity and location of WMHs on the degree of cognitive impairment in PD through October 2020. We conducted the survey to compare the association of WMH burden in patients with PD with mild cognitive impairment (PD‐MCI) versus those with normal cognition (PD‐NC) and in patients with PD with dementia (PDD) versus those with PD without dementia (PD‐ND). Nine studies with PD‐MCI versus PD‐NC and 10 studies with PDD versus PD‐ND comparisons were included. The WMH burden in PD‐MCI patients was significantly different compared to that in PD‐NC patients (standard mean difference, SMD = 0.39, 95% CI: 0.12 to 0.66, p = 0.005), while there was no correlation shown in the age‐matched subgroup of the comparison. In addition, PDD patients had a significantly higher burden of WMHs (SMD = 0.8, 95% CI: 0.44 to 1.71, p < 0.0001), especially deep white matter hyperintensities (SMD = 0.54, 95% CI: 0.36 to 0.73, p < 0.00001) and periventricular hyperintensities (SMD = 0.70, 95% CI: 0.36 to 1.04, p < 0.0001), than PD‐NC patients, regardless of the adjustment of age. WMHs might be imaging markers for cognitive impairment in PDD but not in PD‐MCI, regardless of age, vascular risk factors, or race. Further prospective studies are needed to validate the conclusions. John Wiley and Sons Inc. 2021-07-26 /pmc/articles/PMC8419402/ /pubmed/34310081 http://dx.doi.org/10.1002/acn3.51429 Text en © 2021 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Review
Liu, Hailing
Deng, Bin
Xie, Fen
Yang, Xiaohua
Xie, Zhenchao
Chen, Yonghua
Yang, Zhi
Huang, Xiyan
Zhu, Shuzhen
Wang, Qing
The influence of white matter hyperintensity on cognitive impairment in Parkinson's disease
title The influence of white matter hyperintensity on cognitive impairment in Parkinson's disease
title_full The influence of white matter hyperintensity on cognitive impairment in Parkinson's disease
title_fullStr The influence of white matter hyperintensity on cognitive impairment in Parkinson's disease
title_full_unstemmed The influence of white matter hyperintensity on cognitive impairment in Parkinson's disease
title_short The influence of white matter hyperintensity on cognitive impairment in Parkinson's disease
title_sort influence of white matter hyperintensity on cognitive impairment in parkinson's disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419402/
https://www.ncbi.nlm.nih.gov/pubmed/34310081
http://dx.doi.org/10.1002/acn3.51429
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