Clinical features of progressive supranuclear palsy.

Richardson’s syndrome longitudinal MRI parkinsonism phenotype progressive supranuclear palsy

Journal

Frontiers in aging neuroscience
ISSN: 1663-4365
Titre abrégé: Front Aging Neurosci
Pays: Switzerland
ID NLM: 101525824

Informations de publication

Date de publication:
2023
Historique:
received: 26 05 2023
accepted: 18 08 2023
medline: 15 9 2023
pubmed: 15 9 2023
entrez: 15 9 2023
Statut: epublish

Résumé

Progressive 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. Clinical 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. Throughout 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. PSP-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.

Sections du résumé

Background UNASSIGNED
Progressive 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.
Method UNASSIGNED
Clinical 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.
Results UNASSIGNED
Throughout 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.
Conclusion UNASSIGNED
PSP-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.

Identifiants

pubmed: 37711994
doi: 10.3389/fnagi.2023.1229491
pmc: PMC10498458
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1229491

Informations de copyright

Copyright © 2023 Wen, Yang, Jiao, Zhang, Lin, Zhu, Xu, Zhou, Weng, Liao, Zhou, Wang, Guo, Yan, Jiang, Tang and Shen.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Yafei Wen (Y)

Department of Neurology, Xiangya Hospital, Central South University, Changsha, China.

Qijie Yang (Q)

Department of Neurology, Xiangya Hospital, Central South University, Changsha, China.

Bin Jiao (B)

Department of Neurology, Xiangya Hospital, Central South University, Changsha, China.
National Clinical Research Center for Geriatric Disorders, Central South University, Changsha, China.
Engineering Research Center of Hunan Province in Cognitive Impairment Disorders, Central South University, Changsha, China.
Hunan International Scientific and Technological Cooperation Base of Neurodegenerative and Neurogenetic Diseases, Changsha, China.
Key Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha, China.

Weiwei Zhang (W)

Department of Radiology, Xiangya Hospital, Central South University, Changsha, China.

Jingyi Lin (J)

Engineering Research Center of Hunan Province in Cognitive Impairment Disorders, Central South University, Changsha, China.

Yuan Zhu (Y)

Department of Neurology, Xiangya Hospital, Central South University, Changsha, China.

Qian Xu (Q)

Department of Neurology, Xiangya Hospital, Central South University, Changsha, China.
National Clinical Research Center for Geriatric Disorders, Central South University, Changsha, China.

Hui Zhou (H)

Department of Neurology, Xiangya Hospital, Central South University, Changsha, China.

Ling Weng (L)

Department of Neurology, Xiangya Hospital, Central South University, Changsha, China.
National Clinical Research Center for Geriatric Disorders, Central South University, Changsha, China.

Xinxin Liao (X)

Department of Geriatrics Neurology, Xiangya Hospital, Central South University, Changsha, China.

Yafang Zhou (Y)

Department of Geriatrics Neurology, Xiangya Hospital, Central South University, Changsha, China.

Junling Wang (J)

Department of Neurology, Xiangya Hospital, Central South University, Changsha, China.

Jifeng Guo (J)

Department of Neurology, Xiangya Hospital, Central South University, Changsha, China.
National Clinical Research Center for Geriatric Disorders, Central South University, Changsha, China.
Hunan International Scientific and Technological Cooperation Base of Neurodegenerative and Neurogenetic Diseases, Changsha, China.
Key Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha, China.

Xinxiang Yan (X)

Department of Neurology, Xiangya Hospital, Central South University, Changsha, China.
National Clinical Research Center for Geriatric Disorders, Central South University, Changsha, China.
Hunan International Scientific and Technological Cooperation Base of Neurodegenerative and Neurogenetic Diseases, Changsha, China.
Key Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha, China.

Hong Jiang (H)

Department of Neurology, Xiangya Hospital, Central South University, Changsha, China.

Beisha Tang (B)

Department of Neurology, Xiangya Hospital, Central South University, Changsha, China.
National Clinical Research Center for Geriatric Disorders, Central South University, Changsha, China.
Hunan International Scientific and Technological Cooperation Base of Neurodegenerative and Neurogenetic Diseases, Changsha, China.
Key Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha, China.

Lu Shen (L)

Department of Neurology, Xiangya Hospital, Central South University, Changsha, China.
National Clinical Research Center for Geriatric Disorders, Central South University, Changsha, China.
Engineering Research Center of Hunan Province in Cognitive Impairment Disorders, Central South University, Changsha, China.
Hunan International Scientific and Technological Cooperation Base of Neurodegenerative and Neurogenetic Diseases, Changsha, China.
Key Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha, China.
Key Laboratory of Organ Injury, Aging and Regenerative Medicine of Hunan Province, Changsha, China.

Classifications MeSH