A combination of 8 circulating miRNAs demonstrated high diagnostic value for detecting diffuse myocardial fibrosis in patients with hypertrophic cardiomyopathy, yielding an area under the curve of 0.87.
Observational (n=59)
No
Do circulating miRNAs serve as diagnostic biomarkers for diffuse myocardial fibrosis in patients with hypertrophic cardiomyopathy?
A panel of circulating miRNAs may serve as a novel, non-invasive biomarker for detecting diffuse myocardial fibrosis in patients with hypertrophic cardiomyopathy.
Effect estimate: AUC 0.87
BACKGROUND: Circulating microRNAs may represent novel markers for cardiovascular diseases. We evaluated whether circulating miRNAs served as potential biomarkers for diffuse myocardial fibrosis in patients with hypertrophic cardiomyopathy (HCM). METHODS: Cardiac magnetic resonance imaging with postcontrast T1 mapping was performed to non-invasively quantify diffuse myocardial fibrosis in HCM patients who were classified into two groups (T1 < 470 ms or T1 ≥ 470 ms, as likely or unlikely to have diffuse fibrosis, respectively). First, we screened 84 miRNAs using human serum/plasma miRNA array on plasma of 8 HCM patients (4/group based on T1 time) and 4 healthy controls. From the results of this initial array, 16 miRNAs were selected based on their fold changes and relevance to myocardial fibrosis for further validation by Taqman real-time PCR in 55 HCM patients. RESULTS: Among the 16 miRNAs, the expression of miR-96-5p and miR-373-3p was low. The remaining 14 (miR-18a-5p, miR-146a-5p, miR-30d-5p, miR-17-5p, miR-200a-3p, miR-19b-3p, miR-21-5p, miR-193-5p, miR-10b-5p, miR-15a-5p, miR-192-5p, miR-296-5p, miR-29a-3p, and miR-133a-3p) were upregulated in HCM patients with T1 < 470 ms compared with those with T1 ≥ 470 ms, and 11 (except miR-192-5p, miR-296-5p and miR-133a-3p) were significantly inversely correlated with postcontrast T1 values. Individual miRNA had moderate diagnostic value for diffuse myocardial fibrosis (AUC: 0.663-0.742), but the diagnostic value was greatly improved (AUC: 0.87) for a combination of 8 miRNAs. In comparison, circulating markers of collagen turnover did not have predictive values for diffuse myocardial fibrosis. CONCLUSIONS: These findings suggest that circulating miRNAs provide attractive candidates as putative biomarkers for diffuse myocardial fibrosis in HCM.
Lü et al. (Thu,) conducted a observational in Hypertrophic cardiomyopathy (n=59). Circulating microRNAs (biomarker panel) vs. Patients without diffuse myocardial fibrosis (T1 ≥ 470 ms) was evaluated on Diagnostic value (Area Under the Curve) of a combination of 8 circulating miRNAs for diffuse myocardial fibrosis (AUC 0.87). A combination of 8 circulating miRNAs demonstrated high diagnostic value for detecting diffuse myocardial fibrosis in patients with hypertrophic cardiomyopathy, yielding an area under the curve of 0.87.