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Nocebo effect in multiple system atrophy: systematic review and meta-analysis of placebo-controlled clinical trials

BACKGROUND: Nocebo effect is prevalent among neurological diseases, resulting in low adherence and treatment outcome. We sought to examine the nocebo effect in randomized controlled trials (RCTs) in multiple system atrophy (MSA). METHODS: We searched RCTs in MSA from Medline since September, 2021. R...

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Autores principales: Wang, Zi-Xuan, Zhang, Nan-Nan, Zhao, Hai-Xia, Song, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789733/
https://www.ncbi.nlm.nih.gov/pubmed/34973075
http://dx.doi.org/10.1007/s10072-021-05758-2
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author Wang, Zi-Xuan
Zhang, Nan-Nan
Zhao, Hai-Xia
Song, Jie
author_facet Wang, Zi-Xuan
Zhang, Nan-Nan
Zhao, Hai-Xia
Song, Jie
author_sort Wang, Zi-Xuan
collection PubMed
description BACKGROUND: Nocebo effect is prevalent among neurological diseases, resulting in low adherence and treatment outcome. We sought to examine the nocebo effect in randomized controlled trials (RCTs) in multiple system atrophy (MSA). METHODS: We searched RCTs in MSA from Medline since September, 2021. RCTs for drug treatment conducted in adult MSA patients with more than 5 cases in each treatment arm were included. We assessed the number of dropout due to placebo intolerance. We also did a symptomatic/disease-modifying subgroup analysis based on two different treatment purposes. The STATA software was used for statistical analysis. Overall heterogeneity was assessed using the Cochran Q and I(2). RESULTS: Data were extracted from 11 RCTs fulfilling our search criteria. Of 540 placebo-treated patients, 64.2% reported at least one adverse event (AE) and 7.5% reported dropout because of AEs. The chance of dropping out because of an AE and experiencing at least one AE did not differ between placebo and active drug treatment arms. Besides, the pooled nocebo dropout rate in the symptomatic subgroup was similar to that of the disease-modifying subgroup. CONCLUSION: In MSA RCTs, nocebo dropout rate was not at a low level among neurological disorders. Nocebo effect was an important reason of dropout because of AE in placebo and active drug treatment arms. Different treatment purposes may not influence nocebo effect.
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spelling pubmed-87897332022-02-02 Nocebo effect in multiple system atrophy: systematic review and meta-analysis of placebo-controlled clinical trials Wang, Zi-Xuan Zhang, Nan-Nan Zhao, Hai-Xia Song, Jie Neurol Sci Review Article BACKGROUND: Nocebo effect is prevalent among neurological diseases, resulting in low adherence and treatment outcome. We sought to examine the nocebo effect in randomized controlled trials (RCTs) in multiple system atrophy (MSA). METHODS: We searched RCTs in MSA from Medline since September, 2021. RCTs for drug treatment conducted in adult MSA patients with more than 5 cases in each treatment arm were included. We assessed the number of dropout due to placebo intolerance. We also did a symptomatic/disease-modifying subgroup analysis based on two different treatment purposes. The STATA software was used for statistical analysis. Overall heterogeneity was assessed using the Cochran Q and I(2). RESULTS: Data were extracted from 11 RCTs fulfilling our search criteria. Of 540 placebo-treated patients, 64.2% reported at least one adverse event (AE) and 7.5% reported dropout because of AEs. The chance of dropping out because of an AE and experiencing at least one AE did not differ between placebo and active drug treatment arms. Besides, the pooled nocebo dropout rate in the symptomatic subgroup was similar to that of the disease-modifying subgroup. CONCLUSION: In MSA RCTs, nocebo dropout rate was not at a low level among neurological disorders. Nocebo effect was an important reason of dropout because of AE in placebo and active drug treatment arms. Different treatment purposes may not influence nocebo effect. Springer International Publishing 2022-01-01 2022 /pmc/articles/PMC8789733/ /pubmed/34973075 http://dx.doi.org/10.1007/s10072-021-05758-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review Article
Wang, Zi-Xuan
Zhang, Nan-Nan
Zhao, Hai-Xia
Song, Jie
Nocebo effect in multiple system atrophy: systematic review and meta-analysis of placebo-controlled clinical trials
title Nocebo effect in multiple system atrophy: systematic review and meta-analysis of placebo-controlled clinical trials
title_full Nocebo effect in multiple system atrophy: systematic review and meta-analysis of placebo-controlled clinical trials
title_fullStr Nocebo effect in multiple system atrophy: systematic review and meta-analysis of placebo-controlled clinical trials
title_full_unstemmed Nocebo effect in multiple system atrophy: systematic review and meta-analysis of placebo-controlled clinical trials
title_short Nocebo effect in multiple system atrophy: systematic review and meta-analysis of placebo-controlled clinical trials
title_sort nocebo effect in multiple system atrophy: systematic review and meta-analysis of placebo-controlled clinical trials
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789733/
https://www.ncbi.nlm.nih.gov/pubmed/34973075
http://dx.doi.org/10.1007/s10072-021-05758-2
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