Affiliation:
1. Department of Pathophysiology Jagiellonian University, Collegium Medicum Kraków Poland
2. Department of Neurology, Medical College Jagiellonian University Kraków Poland
3. Department of Visceral Surgery and Medicine, Bern University Hospital University of Bern Bern Switzerland
4. Maurice Müller Laboratories, Department for Biomedical Research University of Bern Bern Switzerland
5. Department of Neurosurgery and Neurotraumatology, Medical College Jagiellonian University Kraków Poland
Abstract
AbstractBackgroundThe gut microbiota has been implicated in Parkinson's disease (PD), with alterations observed in microbial composition and reduced microbial species richness, which may influence gastrointestinal symptoms in PD patients. It remains to be determined whether the severity of gastrointestinal symptoms correlates with microbiota variations in PD patients treated pharmacologically or with subthalamic nucleus deep brain stimulation (STN‐DBS) therapy. This study aims to explore how these treatments affect gut microbiota and gastrointestinal symptoms in PD, identifying specific microbial differences associated with each treatment modality.MethodsA total of 42 individuals diagnosed with PD, along with 38 age‐matched household control participants, contributed stool samples for microbiota characterization. Differences in the gut microbiota across various groups of PD patients and their households were identified through comprehensive sequencing of the 16S rRNA gene amplicon sequencing.Key ResultsDifferences in microbial communities were observed between PD patients and controls, as well as between PD patients receiving pharmacological treatment and those with STN‐DBS. Pharmacologically treated advanced PD patients have higher gastrointestinal dysfunctions. Gut microbiota profile linked to STN‐DBS and reduced levodopa consumption, characterized by its anti‐inflammatory properties, might play a role in diminishing gastrointestinal dysfunction relative to only pharmacological treatments.Conclusions & InferencesAdvanced PD patients on medication exhibit more gastrointestinal issues, despite relatively stable microbial diversity, indicating a complex interaction between gut microbiota, PD progression, and treatment effects. An imbalanced gut–brain axis, particularly due to reduced butyrate production, may lead to constipation by affecting the enteric nervous system, which emphasizes the need to incorporate gut microbiome insights into treatment strategies.
Funder
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
Narodowe Centrum Nauki