Salivary microR-153 and microR-223 Levels as Potential Diagnostic Biomarkers of Idiopathic Parkinson's Disease

Marisa Cressatti1,2, Lamin Juwara1,3, Julia M Galindez1,2

  • 1Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, Quebec, Canada.

Abstract

Insights

Saliva contains microRNAs (miRNAs) miR-153 and miR-223 that may diagnose Parkinson's disease (PD). These specific miRNAs are significantly decreased in PD patients, offering a potential non-invasive biomarker for early detection.

Area of Science:

  • Neuroscience
  • Biomarker Discovery
  • Molecular Biology

Background:

  • Parkinson's disease (PD) is a prevalent neurodegenerative disorder affecting millions worldwide.
  • Currently, no definitive diagnostic biomarker exists for routine clinical use in PD diagnosis.
  • MicroRNA (miRNA) dysregulation is implicated in neurodegeneration, with specific miRNAs like miR-153 and miR-223 potentially regulating alpha-synuclein in PD.

Purpose of the Study:

  • To investigate if salivary miR-153 and miR-223 levels are reduced in idiopathic PD patients.
  • To determine the potential of these salivary miRNAs as diagnostic biomarkers for PD.

Main Methods:

  • Saliva samples from 83 PD patients and 77 controls were analyzed for miR-153 and miR-223 levels using quantitative polymerase chain reaction.
  • Alpha-synuclein and heme oxygenase-1 protein levels were quantified using enzyme-linked immunosorbent assay.
  • Statistical analyses were adjusted for potential confounding factors like age, sex, and disease duration.

Main Results:

  • Significantly lower levels of miR-153 and miR-223 were observed in the saliva of PD patients compared to controls.
  • MiRNA levels did not correlate with PD progression (Hoehn and Yahr staging).
  • Receiver operating characteristic analysis showed good diagnostic accuracy for both miR-153 (79%) and miR-223 (77%).

Conclusions:

  • Salivary miR-153 and miR-223 demonstrate potential as valuable, non-invasive, and cost-effective diagnostic biomarkers for idiopathic Parkinson's disease.
  • These findings open avenues for simpler PD diagnostic approaches.