Why the study?
Predicting post-MI left ventricular remodeling and HF remains challenging, and the clinical value of circulating microRNAs as remodeling predictors is controversial.
Do plasma levels of miR-101, miR-150, and miR-21 predict left ventricular remodeling after ST-elevation myocardial infarction?
Do plasma levels of miR-101, miR-150, and miR-21 predict left ventricular remodeling after ST-elevation myocardial infarction?
Plasma microRNAs (miR-101, miR-150, miR-21) do not predict post-MI ventricular remodeling, and their diagnostic value is confounded by clinical variables such as diabetes and hemoglobin levels.
May support miRNA-based post-MI remodeling prediction; leaves open clinical utility pending prospective validation.
Left ventricle remodeling (LVR) after acute myocardial infarction (MI) leads to impairment of both systolic and diastolic function, a significant contributor to heart failure (HF). Despite extensive research in the field, predicting post-MI LVR and HF is still a challenge. Several circulant microRNAs have been proposed as LVR predictors; however, their clinical value is controversial. Here, we used real-time quantitative PCR to quantify the plasma levels of hsa-miR-101, hsa-miR-150, and hsa-miR-21 on the first day of hospital admission of MI patients with ST-elevation (STEMI). We analyzed their correlation to the patient's clinical and paraclinical variables and evaluated their ability to discriminate between post-MI LVR and non-LVR. We show that, despite being excellent MI discriminators, none of these microRNAs can distinguish between LVR and non-LVR patients. Furthermore, we found that diabetes mellitus (DM), Hb level, and the number of erythrocytes significantly influence all three plasma microRNA levels. This suggests that plasma microRNAs' diagnostic and prognostic value in STEMI patients should be reevaluated and interpreted in the context of associated pathologies.
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Maries et al. (2023) studied this question.
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