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Clinical features of minor hallucinations in different phenotypes of Parkinson’s disease: A cross-sectional study

BACKGROUND: Minor hallucinations (MHs) are the most common psychiatric symptom associated with Parkinson’s disease (PDPsy), but little is known about their characteristics in different motor phenotypes, especially postural instability gait difficulty (PIGD). The aim of this study was to explore the...

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Autores principales: Wang, Yaxi, Li, Dongfeng, Chen, Yaning, Zhu, Sha, Jiang, Xu, Jiang, Yinyin, Gu, Ruxin, Shen, Bo, Zhu, Jun, Pan, Yang, Yan, Jun, Zhang, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10079986/
https://www.ncbi.nlm.nih.gov/pubmed/37034082
http://dx.doi.org/10.3389/fneur.2023.1158188
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author Wang, Yaxi
Li, Dongfeng
Chen, Yaning
Zhu, Sha
Jiang, Xu
Jiang, Yinyin
Gu, Ruxin
Shen, Bo
Zhu, Jun
Pan, Yang
Yan, Jun
Zhang, Li
author_facet Wang, Yaxi
Li, Dongfeng
Chen, Yaning
Zhu, Sha
Jiang, Xu
Jiang, Yinyin
Gu, Ruxin
Shen, Bo
Zhu, Jun
Pan, Yang
Yan, Jun
Zhang, Li
author_sort Wang, Yaxi
collection PubMed
description BACKGROUND: Minor hallucinations (MHs) are the most common psychiatric symptom associated with Parkinson’s disease (PDPsy), but little is known about their characteristics in different motor phenotypes, especially postural instability gait difficulty (PIGD). The aim of this study was to explore the clinical features of MHs in different subtypes of PD. METHODS: In this cross-sectional study, 213 patients with Parkinson’s disease (PD) were recruited, and the data obtained included comprehensive demographics, motor subtypes, clinical scale scores, and MH contents. Motor subtypes were classified as tremor-dominant (TD), PIGD or indeterminate according to Stebbins’ method. RESULTS: A total of 213 PD patients were included: 90 (42.3%) TD patients, 98 (46.0%) PIGD patients and 25 (11.7%) indeterminate. In total, 70 (32.9%) patients experienced MHs. Compared to patients with the TD phenotype, we found that patients with the PIGD phenotype had more severe motor and nonmotor symptoms. They also had a higher incidence of visual illusions (VIs) and a shorter MH latency. CONCLUSION: Our study demonstrated that compared to patients with the TD phenotype, patients with the PIGD phenotype had a higher incidence of MHs, especially VIs, which may lead to a higher incidence of visual hallucinations (VHs). They also had a shorter latency of MHs than patients with the TD phenotype, suggesting an earlier onset of MHs and a worse prognosis.
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spelling pubmed-100799862023-04-08 Clinical features of minor hallucinations in different phenotypes of Parkinson’s disease: A cross-sectional study Wang, Yaxi Li, Dongfeng Chen, Yaning Zhu, Sha Jiang, Xu Jiang, Yinyin Gu, Ruxin Shen, Bo Zhu, Jun Pan, Yang Yan, Jun Zhang, Li Front Neurol Neurology BACKGROUND: Minor hallucinations (MHs) are the most common psychiatric symptom associated with Parkinson’s disease (PDPsy), but little is known about their characteristics in different motor phenotypes, especially postural instability gait difficulty (PIGD). The aim of this study was to explore the clinical features of MHs in different subtypes of PD. METHODS: In this cross-sectional study, 213 patients with Parkinson’s disease (PD) were recruited, and the data obtained included comprehensive demographics, motor subtypes, clinical scale scores, and MH contents. Motor subtypes were classified as tremor-dominant (TD), PIGD or indeterminate according to Stebbins’ method. RESULTS: A total of 213 PD patients were included: 90 (42.3%) TD patients, 98 (46.0%) PIGD patients and 25 (11.7%) indeterminate. In total, 70 (32.9%) patients experienced MHs. Compared to patients with the TD phenotype, we found that patients with the PIGD phenotype had more severe motor and nonmotor symptoms. They also had a higher incidence of visual illusions (VIs) and a shorter MH latency. CONCLUSION: Our study demonstrated that compared to patients with the TD phenotype, patients with the PIGD phenotype had a higher incidence of MHs, especially VIs, which may lead to a higher incidence of visual hallucinations (VHs). They also had a shorter latency of MHs than patients with the TD phenotype, suggesting an earlier onset of MHs and a worse prognosis. Frontiers Media S.A. 2023-03-24 /pmc/articles/PMC10079986/ /pubmed/37034082 http://dx.doi.org/10.3389/fneur.2023.1158188 Text en Copyright © 2023 Wang, Li, Chen, Zhu, Jiang, Jiang, Gu, Shen, Zhu, Pan, Yan and Zhang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Wang, Yaxi
Li, Dongfeng
Chen, Yaning
Zhu, Sha
Jiang, Xu
Jiang, Yinyin
Gu, Ruxin
Shen, Bo
Zhu, Jun
Pan, Yang
Yan, Jun
Zhang, Li
Clinical features of minor hallucinations in different phenotypes of Parkinson’s disease: A cross-sectional study
title Clinical features of minor hallucinations in different phenotypes of Parkinson’s disease: A cross-sectional study
title_full Clinical features of minor hallucinations in different phenotypes of Parkinson’s disease: A cross-sectional study
title_fullStr Clinical features of minor hallucinations in different phenotypes of Parkinson’s disease: A cross-sectional study
title_full_unstemmed Clinical features of minor hallucinations in different phenotypes of Parkinson’s disease: A cross-sectional study
title_short Clinical features of minor hallucinations in different phenotypes of Parkinson’s disease: A cross-sectional study
title_sort clinical features of minor hallucinations in different phenotypes of parkinson’s disease: a cross-sectional study
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10079986/
https://www.ncbi.nlm.nih.gov/pubmed/37034082
http://dx.doi.org/10.3389/fneur.2023.1158188
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