Characteristics of autonomic dysfunction in neuronal intranuclear inclusion disease.

SCOPA-AUT assessment autonomic dysfunction autonomic symptoms neuronal intranuclear inclusion disease

Journal

Frontiers in neurology
ISSN: 1664-2295
Titre abrégé: Front Neurol
Pays: Switzerland
ID NLM: 101546899

Informations de publication

Date de publication:
2023
Historique:
received: 20 02 2023
accepted: 22 05 2023
medline: 30 6 2023
pubmed: 30 6 2023
entrez: 30 6 2023
Statut: epublish

Résumé

This study aimed to investigate the features of autonomic dysfunction (AutD) in a large cohort of patients with neuronal intranuclear inclusion disease (NIID). A total of 122 patients with NIID and 122 controls were enrolled. All participants completed the Scales for Outcomes in Parkinson's Disease-Autonomic Questionnaire (SCOPA-AUT) and genetic screening for GGC expanded repeats within the 94.26% of patients had AutD. Compared with controls, patients had more severe AutD in total SCOPA-AUT, gastrointestinal, urinary, cardiovascular, thermoregulatory, pupillomotor and sexual domains (all SCOPA-AUT can be used as a diagnostic and quantitative tool for autonomic dysfunction in NIID. The high prevalence of AutD in patients suggests that NIID diagnosis should be considered in patients with AutD, especially in those with unexplained AutD alone. AutD in patients is related to age, disease duration, impairment of daily living ability, and psychiatric symptoms.

Sections du résumé

Background UNASSIGNED
This study aimed to investigate the features of autonomic dysfunction (AutD) in a large cohort of patients with neuronal intranuclear inclusion disease (NIID).
Methods UNASSIGNED
A total of 122 patients with NIID and 122 controls were enrolled. All participants completed the Scales for Outcomes in Parkinson's Disease-Autonomic Questionnaire (SCOPA-AUT) and genetic screening for GGC expanded repeats within the
Results UNASSIGNED
94.26% of patients had AutD. Compared with controls, patients had more severe AutD in total SCOPA-AUT, gastrointestinal, urinary, cardiovascular, thermoregulatory, pupillomotor and sexual domains (all
Conclusion UNASSIGNED
SCOPA-AUT can be used as a diagnostic and quantitative tool for autonomic dysfunction in NIID. The high prevalence of AutD in patients suggests that NIID diagnosis should be considered in patients with AutD, especially in those with unexplained AutD alone. AutD in patients is related to age, disease duration, impairment of daily living ability, and psychiatric symptoms.

Identifiants

pubmed: 37388545
doi: 10.3389/fneur.2023.1168904
pmc: PMC10300412
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1168904

Informations de copyright

Copyright © 2023 Zhou, Tian, Zhang, Jiao, Liao, Zhou, Xiao, Xue, Duan, 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

Lu Zhou (L)

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

Yun Tian (Y)

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

Sizhe Zhang (S)

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

Bin Jiao (B)

Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
National Clinical Research Center for Geriatric Disorders, Central South University, Changsha, Hunan, China.
Engineering Research Center of Hunan Province in Cognitive Impairment Disorders, Central South University, Changsha, Hunan, China.

Xinxin Liao (X)

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

Yafang Zhou (Y)

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

Qiao Xiao (Q)

School of Life Sciences, Central South University, Changsha, Hunan, China.

Jin Xue (J)

School of Life Sciences, Central South University, Changsha, Hunan, China.

Ranhui Duan (R)

School of Life Sciences, Central South University, Changsha, Hunan, China.

Beisha Tang (B)

Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
National Clinical Research Center for Geriatric Disorders, Central South University, Changsha, Hunan, China.
Engineering Research Center of Hunan Province in Cognitive Impairment Disorders, Central South University, Changsha, Hunan, China.
Key Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha, Hunan, China.

Lu Shen (L)

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

Classifications MeSH