Key result
Serum microRNA-423-5p linked to ~14% greater 6-month MACE risk in heart failure patients.
Why the study?
Heart failure patients remain at high risk of post-discharge cardiovascular events, and data evaluating serum microRNA-423-5p as a prognostic biomarker in Vietnamese populations are limited.
Does serum microRNA-423-5p level predict major adverse cardiovascular events at 6 months in patients with heart failure?
Cross-Sectional (n=250)
No
Does serum microRNA-423-5p level predict major adverse cardiovascular events at 6 months in patients with heart failure?
Odds Ratio: 1.14
Serum microRNA-423-5p levels independently predict 6-month major adverse cardiovascular events in patients with heart failure, offering a potential prognostic biomarker.
Serum miR-423-5p may refine post-discharge MACE risk stratification in Vietnamese HF patients; leaves open added value over established markers.
Background: Patients with heart failure remain at a relatively high risk of cardiovascular events after hospital discharge, adversely affecting survival and quality of life. Recent evidence suggests that serum microRNA-423-5p may serve as a prognostic biomarker; however, data in Vietnamese populations are limited. Objectives: To evaluate the prognostic value of serum microRNA-423-5p for major adverse cardiovascular events (MACE) in patients with heart failure. Materials and Methods: A cross-sectional study with a 6-month follow-up was conducted in 250 heart failure patients at Can Tho Central General Hospital from January 2024 to November 2025. Serum microRNA-423-5p levels were measured, and patients were followed for MACE, including rehospitalization for heart failure, non-fatal myocardial infarction, cardiovascular death, and all-cause mortality. Results: Males accounted for 56.0%. Patients with LVEF < 30% had higher NT-proBNP levels and smoking prevalence compared to those with LVEF ≥ 30% (p < 0.05). At 6 months, 29.6% experienced MACE, most commonly heart failure rehospitalization (23.2%), followed by all-cause mortality (7.6%), cardiovascular death (6.0%), and myocardial infarction (1.6%). Median microRNA-423-5p levels were higher in patients with MACE [4.23 (IQR: 1.82–17.63) vs. 2.50 (IQR: 0.96–5.46), (2−ΔCt); p < 0.05]. A cutoff value of 10.77 (2−ΔCt) demonstrated moderate prognostic performance (AUC = 0.652; 95% CI: 0.574–0.729; p < 0.05). Multivariable analysis identified LVEF <30% (OR = 1.94) and microRNA-423-5p (OR = 1.14) as independent predictors of MACE. Conclusions: Serum microRNA-423-5p is a useful biomarker for predicting 6-month cardiovascular events in patients with heart failure.
No takes yet. Share an insight, caveat, or question.
Huynh et al. (2026) conducted a cross-sectional in heart failure (n=250). Serum microRNA-423-5p was evaluated on major adverse cardiovascular events (MACE) (OR 1.14). Serum microRNA-423-5p was an independent predictor of 6-month major adverse cardiovascular events in patients with heart failure (OR 1.14; AUC 0.652, 95% CI 0.574-0.729, p<0.05).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: