Adverse effects of hypertension, supine hypertension, and perivascular space on cognition and motor function in PD

Abstract Dilated perivascular space (dPVS) has recently been reported as a biomarker for cognitive impairment in Parkinson’s disease (PD). However, comprehensive interrelationships between various clinical risk factors, dPVS, white-matter hyperintensities (WMH), cognition, and motor function in PD h...

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Autores principales: Na-Young Shin, Yae Won Park, Sang-Won Yoo, Ji-Yeon Yoo, Yangsean Choi, Jinhee Jang, Kook-Jin Ahn, Bum-soo Kim, Joong-Seok Kim
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Publicado: Nature Portfolio 2021
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spelling oai:doaj.org-article:8d453d4304024b5ca63b154d40a1c23e2021-12-02T16:27:55ZAdverse effects of hypertension, supine hypertension, and perivascular space on cognition and motor function in PD10.1038/s41531-021-00214-62373-8057https://doaj.org/article/8d453d4304024b5ca63b154d40a1c23e2021-08-01T00:00:00Zhttps://doi.org/10.1038/s41531-021-00214-6https://doaj.org/toc/2373-8057Abstract Dilated perivascular space (dPVS) has recently been reported as a biomarker for cognitive impairment in Parkinson’s disease (PD). However, comprehensive interrelationships between various clinical risk factors, dPVS, white-matter hyperintensities (WMH), cognition, and motor function in PD have not been studied yet. The purpose of this study was to test whether dPVS might mediate the effect of clinical risk factors on WMH, cognition, and motor symptoms in PD patients. A total of 154 PD patients were assessed for vascular risk factors (hypertension, diabetes mellitus, and dyslipidemia), autonomic dysfunction (orthostatic hypotension and supine hypertension [SH]), APOE ε4 genotype, rapid eye movement sleep-behavior disorder, motor symptoms, and cognition status. The degree of dPVS was evaluated in the basal ganglia (BG) and white matter using a 5-point visual scale. Periventricular, deep, and total WMH severity was also assessed. Path analysis was performed to evaluate the associations of these clinical factors and imaging markers with cognitive status and motor symptoms. Hypertension and SH were significantly associated with more severe BGdPVS, which was further associated with higher total WMH, consequently leading to lower cognitive status. More severe BGdPVS was also associated with worse motor symptoms, but without mediation of total WMH. Similar associations were seen when using periventricular WMH as a variable, but not when using deep WMH as a variable. In conclusion, BGdPVS mediates the effect of hypertension and SH on cognitive impairment via total and periventricular WMH, while being directly associated with more severe motor symptoms.Na-Young ShinYae Won ParkSang-Won YooJi-Yeon YooYangsean ChoiJinhee JangKook-Jin AhnBum-soo KimJoong-Seok KimNature PortfolioarticleNeurology. Diseases of the nervous systemRC346-429ENnpj Parkinson's Disease, Vol 7, Iss 1, Pp 1-7 (2021)
institution DOAJ
collection DOAJ
language EN
topic Neurology. Diseases of the nervous system
RC346-429
spellingShingle Neurology. Diseases of the nervous system
RC346-429
Na-Young Shin
Yae Won Park
Sang-Won Yoo
Ji-Yeon Yoo
Yangsean Choi
Jinhee Jang
Kook-Jin Ahn
Bum-soo Kim
Joong-Seok Kim
Adverse effects of hypertension, supine hypertension, and perivascular space on cognition and motor function in PD
description Abstract Dilated perivascular space (dPVS) has recently been reported as a biomarker for cognitive impairment in Parkinson’s disease (PD). However, comprehensive interrelationships between various clinical risk factors, dPVS, white-matter hyperintensities (WMH), cognition, and motor function in PD have not been studied yet. The purpose of this study was to test whether dPVS might mediate the effect of clinical risk factors on WMH, cognition, and motor symptoms in PD patients. A total of 154 PD patients were assessed for vascular risk factors (hypertension, diabetes mellitus, and dyslipidemia), autonomic dysfunction (orthostatic hypotension and supine hypertension [SH]), APOE ε4 genotype, rapid eye movement sleep-behavior disorder, motor symptoms, and cognition status. The degree of dPVS was evaluated in the basal ganglia (BG) and white matter using a 5-point visual scale. Periventricular, deep, and total WMH severity was also assessed. Path analysis was performed to evaluate the associations of these clinical factors and imaging markers with cognitive status and motor symptoms. Hypertension and SH were significantly associated with more severe BGdPVS, which was further associated with higher total WMH, consequently leading to lower cognitive status. More severe BGdPVS was also associated with worse motor symptoms, but without mediation of total WMH. Similar associations were seen when using periventricular WMH as a variable, but not when using deep WMH as a variable. In conclusion, BGdPVS mediates the effect of hypertension and SH on cognitive impairment via total and periventricular WMH, while being directly associated with more severe motor symptoms.
format article
author Na-Young Shin
Yae Won Park
Sang-Won Yoo
Ji-Yeon Yoo
Yangsean Choi
Jinhee Jang
Kook-Jin Ahn
Bum-soo Kim
Joong-Seok Kim
author_facet Na-Young Shin
Yae Won Park
Sang-Won Yoo
Ji-Yeon Yoo
Yangsean Choi
Jinhee Jang
Kook-Jin Ahn
Bum-soo Kim
Joong-Seok Kim
author_sort Na-Young Shin
title Adverse effects of hypertension, supine hypertension, and perivascular space on cognition and motor function in PD
title_short Adverse effects of hypertension, supine hypertension, and perivascular space on cognition and motor function in PD
title_full Adverse effects of hypertension, supine hypertension, and perivascular space on cognition and motor function in PD
title_fullStr Adverse effects of hypertension, supine hypertension, and perivascular space on cognition and motor function in PD
title_full_unstemmed Adverse effects of hypertension, supine hypertension, and perivascular space on cognition and motor function in PD
title_sort adverse effects of hypertension, supine hypertension, and perivascular space on cognition and motor function in pd
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/8d453d4304024b5ca63b154d40a1c23e
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