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Multiple N-of-1 trials to investigate hypoxia therapy in Parkinson’s disease: study rationale and protocol

BACKGROUND: Parkinson’s disease (PD) is a neurodegenerative disease, for which no disease-modifying therapies exist. Preclinical and clinical evidence suggest that hypoxia-based therapy might have short- and long-term benefits in PD. We present the contours of the first study to assess the safety, f...

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Autores principales: Janssen Daalen, Jules M., Meinders, Marjan J., Giardina, Federica, Roes, Kit C. B., Stunnenberg, Bas C., Mathur, Soania, Ainslie, Philip N., Thijssen, Dick H. J., Bloem, Bastiaan R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9281145/
https://www.ncbi.nlm.nih.gov/pubmed/35836147
http://dx.doi.org/10.1186/s12883-022-02770-7
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author Janssen Daalen, Jules M.
Meinders, Marjan J.
Giardina, Federica
Roes, Kit C. B.
Stunnenberg, Bas C.
Mathur, Soania
Ainslie, Philip N.
Thijssen, Dick H. J.
Bloem, Bastiaan R.
author_facet Janssen Daalen, Jules M.
Meinders, Marjan J.
Giardina, Federica
Roes, Kit C. B.
Stunnenberg, Bas C.
Mathur, Soania
Ainslie, Philip N.
Thijssen, Dick H. J.
Bloem, Bastiaan R.
author_sort Janssen Daalen, Jules M.
collection PubMed
description BACKGROUND: Parkinson’s disease (PD) is a neurodegenerative disease, for which no disease-modifying therapies exist. Preclinical and clinical evidence suggest that hypoxia-based therapy might have short- and long-term benefits in PD. We present the contours of the first study to assess the safety, feasibility and physiological and symptomatic impact of hypoxia-based therapy in individuals with PD. METHODS/DESIGN: In 20 individuals with PD, we will investigate the safety, tolerability and short-term symptomatic efficacy of continuous and intermittent hypoxia using individual, double-blind, randomized placebo-controlled N-of-1 trials. This design allows for dose finding and for including more individualized outcomes, as each individual serves as its own control. A wide range of exploratory outcomes is deployed, including the Movement Disorders Society Unified Parkinson’s Disease Rating scale (MDS-UPDRS) part III, Timed Up & Go Test, Mini Balance Evaluation Systems (MiniBES) test and wrist accelerometry. Also, self-reported impression of overall symptoms, motor and non-motor symptoms and urge to take dopaminergic medication will be assessed on a 10-point Likert scale. As part of a hypothesis-generating part of the study, we also deploy several exploratory outcomes to probe possible underlying mechanisms of action, including cortisol, erythropoietin and platelet-derived growth factor β. Efficacy will be assessed primarily by a Bayesian analysis. DISCUSSION: This evaluation of hypoxia therapy could provide insight in novel pathways that may be pursued for PD treatment. This trial also serves as a proof of concept for deploying an N-of-1 design and for including individualized outcomes in PD research, as a basis for personalized treatment approaches. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT05214287 (registered January 28, 2022). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12883-022-02770-7.
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spelling pubmed-92811452022-07-15 Multiple N-of-1 trials to investigate hypoxia therapy in Parkinson’s disease: study rationale and protocol Janssen Daalen, Jules M. Meinders, Marjan J. Giardina, Federica Roes, Kit C. B. Stunnenberg, Bas C. Mathur, Soania Ainslie, Philip N. Thijssen, Dick H. J. Bloem, Bastiaan R. BMC Neurol Study Protocol BACKGROUND: Parkinson’s disease (PD) is a neurodegenerative disease, for which no disease-modifying therapies exist. Preclinical and clinical evidence suggest that hypoxia-based therapy might have short- and long-term benefits in PD. We present the contours of the first study to assess the safety, feasibility and physiological and symptomatic impact of hypoxia-based therapy in individuals with PD. METHODS/DESIGN: In 20 individuals with PD, we will investigate the safety, tolerability and short-term symptomatic efficacy of continuous and intermittent hypoxia using individual, double-blind, randomized placebo-controlled N-of-1 trials. This design allows for dose finding and for including more individualized outcomes, as each individual serves as its own control. A wide range of exploratory outcomes is deployed, including the Movement Disorders Society Unified Parkinson’s Disease Rating scale (MDS-UPDRS) part III, Timed Up & Go Test, Mini Balance Evaluation Systems (MiniBES) test and wrist accelerometry. Also, self-reported impression of overall symptoms, motor and non-motor symptoms and urge to take dopaminergic medication will be assessed on a 10-point Likert scale. As part of a hypothesis-generating part of the study, we also deploy several exploratory outcomes to probe possible underlying mechanisms of action, including cortisol, erythropoietin and platelet-derived growth factor β. Efficacy will be assessed primarily by a Bayesian analysis. DISCUSSION: This evaluation of hypoxia therapy could provide insight in novel pathways that may be pursued for PD treatment. This trial also serves as a proof of concept for deploying an N-of-1 design and for including individualized outcomes in PD research, as a basis for personalized treatment approaches. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT05214287 (registered January 28, 2022). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12883-022-02770-7. BioMed Central 2022-07-14 /pmc/articles/PMC9281145/ /pubmed/35836147 http://dx.doi.org/10.1186/s12883-022-02770-7 Text en © The Author(s) 2022 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Study Protocol
Janssen Daalen, Jules M.
Meinders, Marjan J.
Giardina, Federica
Roes, Kit C. B.
Stunnenberg, Bas C.
Mathur, Soania
Ainslie, Philip N.
Thijssen, Dick H. J.
Bloem, Bastiaan R.
Multiple N-of-1 trials to investigate hypoxia therapy in Parkinson’s disease: study rationale and protocol
title Multiple N-of-1 trials to investigate hypoxia therapy in Parkinson’s disease: study rationale and protocol
title_full Multiple N-of-1 trials to investigate hypoxia therapy in Parkinson’s disease: study rationale and protocol
title_fullStr Multiple N-of-1 trials to investigate hypoxia therapy in Parkinson’s disease: study rationale and protocol
title_full_unstemmed Multiple N-of-1 trials to investigate hypoxia therapy in Parkinson’s disease: study rationale and protocol
title_short Multiple N-of-1 trials to investigate hypoxia therapy in Parkinson’s disease: study rationale and protocol
title_sort multiple n-of-1 trials to investigate hypoxia therapy in parkinson’s disease: study rationale and protocol
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9281145/
https://www.ncbi.nlm.nih.gov/pubmed/35836147
http://dx.doi.org/10.1186/s12883-022-02770-7
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