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Regional Cerebral Cortical Atrophy is Related to Urinary Tract Symptoms in Parkinson's Disease

Authors
Roh, HaewonKang, JuneHwang, Soon-YoungKoh, Seong-BeomKim, Jong Hyun
Issue Date
3월-2021
Publisher
WILEY
Keywords
Cortical thinning; Parkinson& #8217; disease; nonmotor symptom; precuneus; urinary symptoms
Citation
JOURNAL OF NEUROIMAGING, v.31, no.2, pp.363 - 371
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF NEUROIMAGING
Volume
31
Number
2
Start Page
363
End Page
371
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/139028
DOI
10.1111/jon.12829
ISSN
1051-2284
Abstract
BACKGROUND AND PURPOSE Lower urinary tract symptoms (LUTS) are the most common nonmotor symptoms usually occurring mid-stage of Parkinson's disease (PD); however, its underlying mechanisms are unknown. We aimed to assess whether corticometry or volumetry can identify a pattern of cerebral cortical changes in PD patients with LUTS. METHODS We recruited 85 idiopathic PD patients and performed corticometry and volumetry on various cortical regions using each patient's magnetic resonance imaging. To identify a correlation between the cortical thickness/volume and nonmotor symptoms scale domain 7 scores, which represent the severity of LUTS, we performed general linear model and region of interest analyses. RESULTS Significant regional thinning of the left precuneus, left temporal pole, left precentral, right precuneus, and right pars opercularis was correlated with nonmotor symptoms scale domain 7 scores. We also found that cortical volumes of left precuneus and left frontal pole were inversely correlated with the severity of urinary symptoms. CONCLUSIONS This study showed that the thicknesses and volumes of several cortical regions were significantly correlated with the severity of LUTS in PD patients. The findings of regional atrophy and thinning of specific cortical regions in this study provide additional evidence that multiple cortical regions, especially the precuneus cortex, not only may be involved in urinary dysfunctions of PD patients but also may help to elucidate the exact underlying mechanisms for LUTS in PD patients.
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