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miR-30d Levels Predict Re-Hospitalization in Patients with Acute Cardiogenic Pulmonary Edema: A Preliminary Study
Giordano Bianchi1, Barbara Vizio2, Ornella Bosco2
1Division of Emergency Medicine and High Dependency Unit, Città della Salute e della Scienza di Torino, Molinette Hospital, 10126 Turin, Italy.
Abstract:
Acute cardiogenic pulmonary edema (ACPE) is a common and serious manifestation of heart failure (HF), representing 10-20% of all acute HF admissions. It is associated with elevated in-hospital mortality and high rates of re-hospitalization. MicroRs, like miR-30d, are of particular interest in heart failure due to their regulatory role in gene expression and potential as biomarkers for diagnosing and predicting patient outcomes, especially in high-risk cases such as ACPE. We conducted a cohort study on patients diagnosed with ACPE in the Emergency Department (ED). The circulating levels of miR-30d were analyzed at the time of hospital admission and at one-month follow-up along with other biomarkers. We enrolled 24 ACPE patients and 10 control subjects. Median age was 80.8 years (interquartile range, IQR, 8.2) in ACPE cases, and 78.5 years (IQR 9.8) in controls with a male/female ratio of 2 and 0.66, respectively. In ACPE patients, median cardiac ejection fraction was 42.5%, creatinine 1.63 mg/dL (IQR 1.24), troponin 63.5 ng/dL (58), and NT-proBNP 4243.5 pg/mL (IQR 5846) at ED evaluation. Median concentration of miR30d was 0.81 in controls, and 3.67 and 7.28 in ACPE patients at enrollment time and one month later, respectively. Re-hospitalization occurred in 7 ACPE patients in the following 3 months, and in 9 during the following year. miR-30d had a significant predictive value in assessing the risk of re-hospitalization at both 3 months and 1 year following the initial diagnosis of ACPE, while it did not in assessing the risk of death at 1 year. When compared with the other biomarkers, none of them showed a better accuracy than miR-30d. Our findings suggest that elevated levels of miR-30d are associated with an increased rate of hospital readmission at both 3 months and 1 year after discharge. Larger, multicenter studies will be needed to confirm the validity of circulating miR-30d levels as a potential biomarker useful for risk prediction in ACPE patients and its utility in improving individualized patient care.
Insights
Elevated miR-30d levels in acute cardiogenic pulmonary edema (ACPE) patients predict hospital readmission risk at 3 months and 1 year. This microRNA shows promise as a biomarker for ACPE patient outcomes.
Area of Science:
- Cardiology
- Biomarkers
- Genetics
Background:
- Acute cardiogenic pulmonary edema (ACPE) is a severe heart failure manifestation with high mortality and readmission rates.
- MicroRNAs (miRNAs), such as miR-30d, regulate gene expression and are potential biomarkers for heart failure, especially in high-risk ACPE cases.
Purpose of the Study:
- To investigate the role of circulating miR-30d levels in predicting re-hospitalization and mortality in patients with ACPE.
- To compare the predictive accuracy of miR-30d with other established biomarkers in ACPE patients.
Main Methods:
- A cohort study involving 24 ACPE patients diagnosed in the Emergency Department (ED) and 10 control subjects.
- Circulating miR-30d levels were measured at hospital admission and one-month follow-up.
- Analysis included comparison with other biomarkers (troponin, NT-proBNP) for predictive value of re-hospitalization and death.
Main Results:
- Median miR-30d concentrations were significantly higher in ACPE patients (3.67 at enrollment, 7.28 at 1 month) compared to controls (0.81).
- Elevated miR-30d levels significantly predicted re-hospitalization risk at both 3 months and 1 year post-discharge.
- miR-30d demonstrated superior accuracy in predicting re-hospitalization compared to other tested biomarkers; it did not predict 1-year mortality.
Conclusions:
- Circulating miR-30d levels are associated with increased hospital readmission rates in ACPE patients.
- miR-30d shows potential as a valuable biomarker for risk stratification and predicting re-hospitalization in ACPE.
- Further multicenter studies are warranted to validate miR-30d's utility in personalized patient care for ACPE.
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