Clinical features of progressive supranuclear palsy

BackgroundProgressive supranuclear palsy (PSP) is a clinically heterogenous atypical parkinsonian syndrome. Therefore, early recognition and correct diagnosis of PSP is challenging but essential. This study aims to characterize the clinical manifestations, magnetic resonance imaging (MRI), and longi...

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Main Authors: Yafei Wen, Qijie Yang, Bin Jiao, Weiwei Zhang, Jingyi Lin, Yuan Zhu, Qian Xu, Hui Zhou, Ling Weng, Xinxin Liao, Yafang Zhou, Junling Wang, Jifeng Guo, Xinxiang Yan, Hong Jiang, Beisha Tang, Lu Shen
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-08-01
Series:Frontiers in Aging Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fnagi.2023.1229491/full
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author Yafei Wen
Qijie Yang
Bin Jiao
Bin Jiao
Bin Jiao
Bin Jiao
Bin Jiao
Weiwei Zhang
Jingyi Lin
Yuan Zhu
Qian Xu
Qian Xu
Hui Zhou
Ling Weng
Ling Weng
Xinxin Liao
Yafang Zhou
Junling Wang
Jifeng Guo
Jifeng Guo
Jifeng Guo
Jifeng Guo
Xinxiang Yan
Xinxiang Yan
Xinxiang Yan
Xinxiang Yan
Hong Jiang
Beisha Tang
Beisha Tang
Beisha Tang
Beisha Tang
Lu Shen
Lu Shen
Lu Shen
Lu Shen
Lu Shen
Lu Shen
author_facet Yafei Wen
Qijie Yang
Bin Jiao
Bin Jiao
Bin Jiao
Bin Jiao
Bin Jiao
Weiwei Zhang
Jingyi Lin
Yuan Zhu
Qian Xu
Qian Xu
Hui Zhou
Ling Weng
Ling Weng
Xinxin Liao
Yafang Zhou
Junling Wang
Jifeng Guo
Jifeng Guo
Jifeng Guo
Jifeng Guo
Xinxiang Yan
Xinxiang Yan
Xinxiang Yan
Xinxiang Yan
Hong Jiang
Beisha Tang
Beisha Tang
Beisha Tang
Beisha Tang
Lu Shen
Lu Shen
Lu Shen
Lu Shen
Lu Shen
Lu Shen
author_sort Yafei Wen
collection DOAJ
description BackgroundProgressive supranuclear palsy (PSP) is a clinically heterogenous atypical parkinsonian syndrome. Therefore, early recognition and correct diagnosis of PSP is challenging but essential. This study aims to characterize the clinical manifestations, magnetic resonance imaging (MRI), and longitudinal MRI changes of PSP in China.MethodClinical and MRI presentations were compared among 150 cases with PSP. Then the longitudinal MRI changes among 20 patients with PSP were further explored. Additionally, a series of midbrain-based MRI parameters was compared between PSP-P and PD.ResultsThroughout the course of the disease, there were differences in the symptoms of the fall and hand tremor between the PSP-RS and PSP-P. There were significant differences in the six midbrain-based MRI parameters between the PSP-RS and the PSP-P, including hummingbird sign, midbrain diameter, midbrain to pons ratio (MTPR), midbrain area, midbrain area to pons area ratio (Ma/Pa), and midbrain tegmental length (MBTegm). Longitudinal MRI studies revealed that the annual rel.ΔMTPR and rel.Δ (Ma/Pa) for PSP were 5.55 and 6.52%, respectively; additionally, PSP-RS presented a higher decline rate than PSP-P. Moreover, MTPR ≤0.56, midbrain diameter ≤ 0.92, midbrain area ≤ 1.00, and third ventricle width ≤ 0.75 could identify PSP-P from PD.ConclusionPSP-P differs from PSP-RS regarding clinical manifestations, MRI, and longitudinal MRI changes. MRI parameters could be potential imaging markers to identify PSP-P from PD.
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spelling doaj.art-1902f4e89ff04d718370cf8339183a042023-08-31T04:53:00ZengFrontiers Media S.A.Frontiers in Aging Neuroscience1663-43652023-08-011510.3389/fnagi.2023.12294911229491Clinical features of progressive supranuclear palsyYafei Wen0Qijie Yang1Bin Jiao2Bin Jiao3Bin Jiao4Bin Jiao5Bin Jiao6Weiwei Zhang7Jingyi Lin8Yuan Zhu9Qian Xu10Qian Xu11Hui Zhou12Ling Weng13Ling Weng14Xinxin Liao15Yafang Zhou16Junling Wang17Jifeng Guo18Jifeng Guo19Jifeng Guo20Jifeng Guo21Xinxiang Yan22Xinxiang Yan23Xinxiang Yan24Xinxiang Yan25Hong Jiang26Beisha Tang27Beisha Tang28Beisha Tang29Beisha Tang30Lu Shen31Lu Shen32Lu Shen33Lu Shen34Lu Shen35Lu Shen36Department of Neurology, Xiangya Hospital, Central South University, Changsha, ChinaDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, ChinaDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, ChinaNational Clinical Research Center for Geriatric Disorders, Central South University, Changsha, ChinaEngineering Research Center of Hunan Province in Cognitive Impairment Disorders, Central South University, Changsha, ChinaHunan International Scientific and Technological Cooperation Base of Neurodegenerative and Neurogenetic Diseases, Changsha, ChinaKey Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha, ChinaDepartment of Radiology, Xiangya Hospital, Central South University, Changsha, ChinaEngineering Research Center of Hunan Province in Cognitive Impairment Disorders, Central South University, Changsha, ChinaDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, ChinaDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, ChinaNational Clinical Research Center for Geriatric Disorders, Central South University, Changsha, ChinaDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, ChinaDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, ChinaNational Clinical Research Center for Geriatric Disorders, Central South University, Changsha, ChinaDepartment of Geriatrics Neurology, Xiangya Hospital, Central South University, Changsha, ChinaDepartment of Geriatrics Neurology, Xiangya Hospital, Central South University, Changsha, ChinaDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, ChinaDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, ChinaNational Clinical Research Center for Geriatric Disorders, Central South University, Changsha, ChinaHunan International Scientific and Technological Cooperation Base of Neurodegenerative and Neurogenetic Diseases, Changsha, ChinaKey Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha, ChinaDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, ChinaNational Clinical Research Center for Geriatric Disorders, Central South University, Changsha, ChinaHunan International Scientific and Technological Cooperation Base of Neurodegenerative and Neurogenetic Diseases, Changsha, ChinaKey Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha, ChinaDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, ChinaDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, ChinaNational Clinical Research Center for Geriatric Disorders, Central South University, Changsha, ChinaHunan International Scientific and Technological Cooperation Base of Neurodegenerative and Neurogenetic Diseases, Changsha, ChinaKey Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha, ChinaDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, ChinaNational Clinical Research Center for Geriatric Disorders, Central South University, Changsha, ChinaEngineering Research Center of Hunan Province in Cognitive Impairment Disorders, Central South University, Changsha, ChinaHunan International Scientific and Technological Cooperation Base of Neurodegenerative and Neurogenetic Diseases, Changsha, ChinaKey Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha, ChinaKey Laboratory of Organ Injury, Aging and Regenerative Medicine of Hunan Province, Changsha, ChinaBackgroundProgressive supranuclear palsy (PSP) is a clinically heterogenous atypical parkinsonian syndrome. Therefore, early recognition and correct diagnosis of PSP is challenging but essential. This study aims to characterize the clinical manifestations, magnetic resonance imaging (MRI), and longitudinal MRI changes of PSP in China.MethodClinical and MRI presentations were compared among 150 cases with PSP. Then the longitudinal MRI changes among 20 patients with PSP were further explored. Additionally, a series of midbrain-based MRI parameters was compared between PSP-P and PD.ResultsThroughout the course of the disease, there were differences in the symptoms of the fall and hand tremor between the PSP-RS and PSP-P. There were significant differences in the six midbrain-based MRI parameters between the PSP-RS and the PSP-P, including hummingbird sign, midbrain diameter, midbrain to pons ratio (MTPR), midbrain area, midbrain area to pons area ratio (Ma/Pa), and midbrain tegmental length (MBTegm). Longitudinal MRI studies revealed that the annual rel.ΔMTPR and rel.Δ (Ma/Pa) for PSP were 5.55 and 6.52%, respectively; additionally, PSP-RS presented a higher decline rate than PSP-P. Moreover, MTPR ≤0.56, midbrain diameter ≤ 0.92, midbrain area ≤ 1.00, and third ventricle width ≤ 0.75 could identify PSP-P from PD.ConclusionPSP-P differs from PSP-RS regarding clinical manifestations, MRI, and longitudinal MRI changes. MRI parameters could be potential imaging markers to identify PSP-P from PD.https://www.frontiersin.org/articles/10.3389/fnagi.2023.1229491/fullprogressive supranuclear palsyphenotypeRichardson’s syndromeparkinsonismlongitudinal MRI
spellingShingle Yafei Wen
Qijie Yang
Bin Jiao
Bin Jiao
Bin Jiao
Bin Jiao
Bin Jiao
Weiwei Zhang
Jingyi Lin
Yuan Zhu
Qian Xu
Qian Xu
Hui Zhou
Ling Weng
Ling Weng
Xinxin Liao
Yafang Zhou
Junling Wang
Jifeng Guo
Jifeng Guo
Jifeng Guo
Jifeng Guo
Xinxiang Yan
Xinxiang Yan
Xinxiang Yan
Xinxiang Yan
Hong Jiang
Beisha Tang
Beisha Tang
Beisha Tang
Beisha Tang
Lu Shen
Lu Shen
Lu Shen
Lu Shen
Lu Shen
Lu Shen
Clinical features of progressive supranuclear palsy
Frontiers in Aging Neuroscience
progressive supranuclear palsy
phenotype
Richardson’s syndrome
parkinsonism
longitudinal MRI
title Clinical features of progressive supranuclear palsy
title_full Clinical features of progressive supranuclear palsy
title_fullStr Clinical features of progressive supranuclear palsy
title_full_unstemmed Clinical features of progressive supranuclear palsy
title_short Clinical features of progressive supranuclear palsy
title_sort clinical features of progressive supranuclear palsy
topic progressive supranuclear palsy
phenotype
Richardson’s syndrome
parkinsonism
longitudinal MRI
url https://www.frontiersin.org/articles/10.3389/fnagi.2023.1229491/full
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