Related Experiment Video
Updated: Oct 26, 2025

Controlling Parkinson's Disease With Adaptive Deep Brain Stimulation
Published on: July 16, 2014
MicroRNA expression changes in Parkinson's disease (PD) patients' leukocytes prior to and following deep brain
Soreq Lilach1, Bergman Hagai2, Israel Zvi2
1UCL Institute of Neurology London, UK.
Abstract:
The second most prevalent neurodegenerative disorder worldwide in the elderly is Parkinson's disease (PD). It is a major risk factor for aging. Objectives: Currently the involvement of miRNAs in the disease is mainly unclear. Additionally, the disease aetiology is complex and there are no available disease-modifying medications. Therefore, more evidence is required concerning its pathogenesis and developing new treatment modalities. Methods: Here, we studied the expression profiles of about 900 miRNAs in PD patients prior to and following deep brain stimulation (DBS) both on and following 1 hour off electrical stimulation and as compared with age and gender matched healthy control (HC) donor samples, using Affymetrix miRNA microarrays. We analysed statistically the data using Affymetrix expression console software. Results: We detected significantly altered miRNAs pre and post DBS treatment. Conclusions: Our findings indicate the involvement of miRNAs in PD. Future studies can enlarge the number of samples and use RNA sequencing platform to quantify further miRNAs in PD samples. We may also use the expression levels of miRNAs as biomarkers for PD in the blood.
Insights
MicroRNAs (miRNAs) show altered expression in Parkinson's disease (PD) patients, even after deep brain stimulation (DBS). These findings suggest miRNAs could serve as potential biomarkers for PD diagnosis and treatment.
Area of Science:
- Neuroscience
- Genetics
- Biomarkers
Background:
- Parkinson's disease (PD) is a leading neurodegenerative disorder in the elderly, with complex etiology and no current disease-modifying treatments.
- The role of microRNAs (miRNAs) in PD pathogenesis remains largely undetermined, necessitating further investigation into disease mechanisms and therapeutic strategies.
Purpose of the Study:
- To investigate the expression profiles of approximately 900 miRNAs in Parkinson's disease patients.
- To compare miRNA expression before and after deep brain stimulation (DBS) therapy, including on and off stimulation states.
- To identify potential miRNA biomarkers for PD by comparing patient samples with age and gender-matched healthy controls (HC).
Main Methods:
- Utilized Affymetrix miRNA microarrays to analyze miRNA expression profiles in PD patients and healthy controls.
- Collected samples from PD patients pre- and post-deep brain stimulation (DBS), both during and after electrical stimulation.
- Performed statistical analysis of the expression data using Affymetrix Expression Console software.
Main Results:
- Identified a significant number of differentially expressed miRNAs in Parkinson's disease patients.
- Detected significant alterations in miRNA expression profiles pre- and post-deep brain stimulation (DBS) treatment.
- Observed distinct miRNA expression patterns between PD patients and healthy controls.
Conclusions:
- The study provides evidence for the involvement of specific miRNAs in the pathophysiology of Parkinson's disease.
- Altered miRNA expression levels suggest their potential utility as blood-based biomarkers for PD diagnosis and monitoring.
- Future research should involve larger sample sizes and RNA sequencing for comprehensive miRNA quantification in PD.
More Related Videos
09:46Analysis of Gene Expression Changes in the Rat Hippocampus After Deep Brain Stimulation of the Anterior Thalamic Nucleus
Published on: March 8, 2015
07:14A Novel Approach to Assess Motor Outcome of Deep Brain Stimulation Effects in the Hemiparkinsonian Rat: Staircase and Cylinder Test
Published on: May 31, 2016
Related Concept Videos
Neural Regulation
Parkinson's Disease: Treatment
Parkinson's Disease is primarily a result of the loss of dopaminergic neurons in the substantia nigra pars compacta. The cornerstone of...