The Diagnostic Value of Mir-133a in ST Elevation and Non-ST Elevation Myocardial Infarction: A Meta-Analysis

Yehuda Wexler1, Udi Nussinovitch2

  • 1Rappaport Faculty of Medicine and Research Institute, Technion - Israel Institute of Technology, Haifa, Israel, POB 9649, Haifa 3109601, Israel.

Cells
|March 29, 2020
PubMed

Insights

MicroRNA-133a (Mir-133a) shows limited diagnostic value for acute myocardial infarction (AMI) due to inconsistent study results. Its utility may be better suited for risk stratification in specific non-ST elevation myocardial infarction (NSTEMI) cases.

Area of Science:

  • Biomarkers
  • Cardiovascular Disease Research
  • Molecular Diagnostics

Background:

  • Plasma microRNA signatures are increasingly studied for cardiovascular disease (CVD) correlations.
  • MicroRNA-133a (Mir-133a) has been extensively investigated as a potential biomarker for acute myocardial infarction (AMI).
  • Conflicting reports challenge the clinical utility and diagnostic accuracy of Mir-133a in AMI detection.

Purpose of the Study:

  • To systematically analyze the diagnostic performance of Mir-133a for AMI.
  • To investigate factors influencing Mir-133a's diagnostic accuracy, including control group characteristics.
  • To evaluate the potential of Mir-133a as a biomarker in specific cardiovascular conditions.

Main Methods:

  • Systematic literature search of Medline, Embase, and Web of Science for studies on Mir-133a and cardiovascular disease.
  • Quantitative analysis of 9 selected studies using receiver operating characteristic (ROC) curve analysis.
  • Assessment of diagnostic performance metrics, including pooled area under the curve (AUC), and subgroup analyses based on control type, age, and sex.

Main Results:

  • The overall pooled AUC for Mir-133a in diagnosing AMI was 0.73.
  • Studies using healthy controls showed a higher pooled AUC (0.89) compared to those using symptomatic controls (0.68).
  • Age and sex did not significantly impact the diagnostic performance of Mir-133a.

Conclusions:

  • Inconsistent results regarding Mir-133a's diagnostic utility are likely due to variations in control group selection and methodological differences.
  • Mir-133a demonstrates limited effectiveness in differentiating symptomatic patients from those with AMI.
  • Mir-133a may hold potential as a risk stratification biomarker for specific subsets of non-ST elevation myocardial infarction (NSTEMI).

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