Key result
Strenuous exercise during a marathon upregulated MI-associated microRNAs miR-133a-3p (p=0.03) and miR-142-5p (p=0.01) alongside elevated cTnT, suggesting limited diagnostic specificity for MI.
Why the study?
Cardiac troponin lacks diagnostic specificity for myocardial infarction, prompting evaluation of the MI-specificity of candidate circulating microRNAs during strenuous exercise-induced myocardial stress.
Does strenuous exercise alter the levels of MI-associated microRNAs similarly to cardiac troponin T in marathon runners?
Observational (n=210)
Does strenuous exercise alter the levels of MI-associated microRNAs similarly to cardiac troponin T in marathon runners?
p-value: p=0.03 and 0.01
Some MI-associated microRNAs show similar release kinetics to cTnT during strenuous exercise, limiting their diagnostic specificity, while others show different behavior and could improve diagnostic accuracy in a multi-marker strategy.
Background: The current gold standard biomarker for myocardial infarction (MI), cardiac troponin (cTn), is recognized for its high sensitivity and organ specificity; however, it lacks diagnostic specificity. Numerous studies have introduced circulating microRNAs as potential biomarkers for MI. This study investigates the MI-specificity of these serum microRNAs by investigating myocardial stress/injury due to strenuous exercise. Methods: MicroRNA biomarkers were retrieved by comprehensive review of 109 publications on diagnostic serum microRNAs for MI. MicroRNA levels were first measured by next-generation sequencing in pooled sera from runners (n = 46) before and after conducting a full competitive marathon. Hereafter, reverse transcription quantitative real-time PCR (qPCR) of 10 selected serum microRNAs in 210 marathon runners was performed (>10,000 qPCR measurements). Results: 27 potential diagnostic microRNA for MI were retrieved by the literature review. Eight microRNAs (miR-1-3p, miR-21-5p, miR-26a-5p, miR-122-5p, miR-133a-3p, miR-142-5p, miR-191-5p, miR-486-3p) showed positive correlations with cTnT in marathon runners, whereas two miRNAs (miR-134-5p and miR-499a-5p) showed no correlations. Upregulation of miR-133a-3p (p = 0.03) and miR-142-5p (p = 0.01) went along with elevated cTnT after marathon. Conclusion: Some MI-associated microRNAs (e.g., miR-133a-3p and miR-142-5p) have similar kinetics under strenuous exercise and MI as compared to cTnT, which suggests that their diagnostic specificity could be limited. In contrast, several MI-associated microRNAs (miR-26a-5p, miR-134-5p, miR-191-5p) showed different release behavior; hence, combining cTnT with these microRNAs within a multi-marker strategy may add diagnostic accuracy in MI.
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Samani et al. (2021) conducted an observational in Myocardial stress/injury (n=210). Strenuous exercise (full competitive marathon) vs. Baseline (before marathon) was evaluated on Upregulation of MI-associated microRNAs and correlation with cTnT (p=0.03 and 0.01). Strenuous exercise during a marathon upregulated MI-associated microRNAs miR-133a-3p (p=0.03) and miR-142-5p (p=0.01) alongside elevated cTnT, suggesting limited diagnostic specificity for MI.
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