Circulating microRNAs as potential biomarkers for the diagnosis of Parkinson's disease: A meta-analysis

W T Zhang1, Y J Wang2, Y F Yao2

  • 1Xi'an Daxing Hospital, Shaanxi, China; International Doctoral School, University of Seville, Seville, Spain.

Neurologia
|September 4, 2024
PubMed
Abstract

Insights

Circulating microRNAs (miRNAs) show promise for diagnosing Parkinson's disease (PD). This meta-analysis confirms their potential as non-invasive biomarkers, with pooled accuracy metrics indicating reliable diagnostic capability.

Area of Science:

  • Biomarkers
  • Neurodegenerative Diseases
  • Molecular Diagnostics

Background:

  • Parkinson's disease (PD) is a common neurodegenerative disorder.
  • Circulating microRNAs (miRNAs) are being investigated as potential diagnostic markers for PD.
  • Existing studies show inconsistent results, necessitating a comprehensive evaluation.

Purpose of the Study:

  • To systematically evaluate the diagnostic accuracy of circulating miRNAs for Parkinson's disease.
  • To synthesize evidence from multiple studies using meta-analysis.
  • To identify factors influencing diagnostic performance.

Main Methods:

  • A systematic literature search was conducted across major databases (PubMed, Embase, Web of Science, etc.) up to January 2022.
  • Meta-analysis was performed to calculate pooled sensitivity, specificity, positive and negative likelihood ratios, diagnostic odds ratio (DOR), and area under the curve (AUC).
  • Subgroup analyses and Deeks' funnel plot asymmetry test were used to assess heterogeneity and publication bias.

Main Results:

  • The meta-analysis included 44 studies with 3298 PD patients and 2529 controls.
  • Pooled diagnostic accuracy: sensitivity 0.79, specificity 0.82, AUC 0.87.
  • miRNA clusters demonstrated higher diagnostic accuracy than single miRNAs; no significant publication bias was found.

Conclusions:

  • Circulating miRNAs exhibit significant potential as novel, non-invasive biomarkers for Parkinson's disease diagnosis.
  • The findings support the use of circulating miRNAs in clinical settings for PD detection.
  • Further research may focus on optimizing miRNA panels for improved diagnostic precision.