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Therapies for Parkinson’s disease and the gut microbiome: evidence for bidirectional connection

The gut brain axis (GBA), a bidirectional communication pathway has often been linked to health and disease, and gut microbiota (GM), a key component of this pathway shown to be altered in Parkinson’s disease (PD), are suggested to contribute to the pathogenesis of PD. There are few studies that rep...

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Autores principales: Hey, Grace, Nair, Navya, Klann, Emily, Gurrala, Anjela, Safarpour, Delaram, Mai, Volker, Ramirez-Zamora, Adolfo, Vedam-Mai, Vinata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10261989/
https://www.ncbi.nlm.nih.gov/pubmed/37323145
http://dx.doi.org/10.3389/fnagi.2023.1151850
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author Hey, Grace
Nair, Navya
Klann, Emily
Gurrala, Anjela
Safarpour, Delaram
Mai, Volker
Ramirez-Zamora, Adolfo
Vedam-Mai, Vinata
author_facet Hey, Grace
Nair, Navya
Klann, Emily
Gurrala, Anjela
Safarpour, Delaram
Mai, Volker
Ramirez-Zamora, Adolfo
Vedam-Mai, Vinata
author_sort Hey, Grace
collection PubMed
description The gut brain axis (GBA), a bidirectional communication pathway has often been linked to health and disease, and gut microbiota (GM), a key component of this pathway shown to be altered in Parkinson’s disease (PD), are suggested to contribute to the pathogenesis of PD. There are few studies that report the impact of oral medication therapy on GM, however, there are even fewer studies that discuss the impact of other treatments such as device assisted therapies (DAT) including deep brain stimulation (DBS), levodopa-carbidopa intestinal gel infusion (LCIG) and photobiomodulation (PBM) and how these might impact GM. Here, we review the literature and summarize findings of the potential contributions of GM to the heterogenous clinical response to pharmaceutical therapies among individuals with PD. We also discuss the potential interactions between the GM and DATs such as DBS and LCIG and present evidence for alterations in GM in response to DATs. Given the complexity and highly individual nature of the GM of patients with PD and the potential influence that other external factors such as diet, lifestyle, medications, stage of the disease and other comorbidities, further investigations into the response of GM to therapies are worthy of future study in prospective, controlled trials as well as medication naïve individuals. Such detailed studies will help us further comprehend the relationship between GM in PD patients, and will help investigate the potential of targeting GM associated changes as a treatment avenue for PD.
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spelling pubmed-102619892023-06-15 Therapies for Parkinson’s disease and the gut microbiome: evidence for bidirectional connection Hey, Grace Nair, Navya Klann, Emily Gurrala, Anjela Safarpour, Delaram Mai, Volker Ramirez-Zamora, Adolfo Vedam-Mai, Vinata Front Aging Neurosci Aging Neuroscience The gut brain axis (GBA), a bidirectional communication pathway has often been linked to health and disease, and gut microbiota (GM), a key component of this pathway shown to be altered in Parkinson’s disease (PD), are suggested to contribute to the pathogenesis of PD. There are few studies that report the impact of oral medication therapy on GM, however, there are even fewer studies that discuss the impact of other treatments such as device assisted therapies (DAT) including deep brain stimulation (DBS), levodopa-carbidopa intestinal gel infusion (LCIG) and photobiomodulation (PBM) and how these might impact GM. Here, we review the literature and summarize findings of the potential contributions of GM to the heterogenous clinical response to pharmaceutical therapies among individuals with PD. We also discuss the potential interactions between the GM and DATs such as DBS and LCIG and present evidence for alterations in GM in response to DATs. Given the complexity and highly individual nature of the GM of patients with PD and the potential influence that other external factors such as diet, lifestyle, medications, stage of the disease and other comorbidities, further investigations into the response of GM to therapies are worthy of future study in prospective, controlled trials as well as medication naïve individuals. Such detailed studies will help us further comprehend the relationship between GM in PD patients, and will help investigate the potential of targeting GM associated changes as a treatment avenue for PD. Frontiers Media S.A. 2023-05-30 /pmc/articles/PMC10261989/ /pubmed/37323145 http://dx.doi.org/10.3389/fnagi.2023.1151850 Text en Copyright © 2023 Hey, Nair, Klann, Gurrala, Safarpour, Mai, Ramirez-Zamora and Vedam-Mai. 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 Aging Neuroscience
Hey, Grace
Nair, Navya
Klann, Emily
Gurrala, Anjela
Safarpour, Delaram
Mai, Volker
Ramirez-Zamora, Adolfo
Vedam-Mai, Vinata
Therapies for Parkinson’s disease and the gut microbiome: evidence for bidirectional connection
title Therapies for Parkinson’s disease and the gut microbiome: evidence for bidirectional connection
title_full Therapies for Parkinson’s disease and the gut microbiome: evidence for bidirectional connection
title_fullStr Therapies for Parkinson’s disease and the gut microbiome: evidence for bidirectional connection
title_full_unstemmed Therapies for Parkinson’s disease and the gut microbiome: evidence for bidirectional connection
title_short Therapies for Parkinson’s disease and the gut microbiome: evidence for bidirectional connection
title_sort therapies for parkinson’s disease and the gut microbiome: evidence for bidirectional connection
topic Aging Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10261989/
https://www.ncbi.nlm.nih.gov/pubmed/37323145
http://dx.doi.org/10.3389/fnagi.2023.1151850
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