Key result
Circulating miR-221 expression significantly correlated with myocardial collagen volume fraction (r=0.454, P=0.002) and late gadolinium enhancement (r=0.630, P=0.004) in HOCM.
Why the study?
The association of microRNA expression between circulation and myocardium in hypertrophic cardiomyopathy remained unclear.
Is circulating miR-221 a reliable biomarker for myocardial hypertrophy and fibrosis in patients with hypertrophic obstructive cardiomyopathy?
Observational (n=42)
Is circulating miR-221 a reliable biomarker for myocardial hypertrophy and fibrosis in patients with hypertrophic obstructive cardiomyopathy?
Effect estimate: r = 0.454
p-value: p=0.002
Circulating miR-221 correlates with myocardial expression, fibrosis, and hypertrophy, suggesting its potential as a non-invasive biomarker in hypertrophic obstructive cardiomyopathy.
Hypothesis-generating for miR-221 as fibrosis biomarker in HOCM; prospective validation needed before clinical adoption.
AIM: Circulating microRNA expression has become a biomarker of cardiovascular disease; however, the association of microRNA expression between circulation and myocardium in hypertrophic cardiomyopathy remains unclear. The present study aimed to find a circulating biomarker correlated not only to myocardial expression, but also to cardiac hypertrophy and fibrosis. METHOD: Forty-two cases of hypertrophic obstructive cardiomyopathy (HOCM) diagnosed by echocardiography and magnetic resonance were analysed for microRNA expression in plasma and myocardial tissue. RESULTS: The results showed that myocardial miR-221 was significantly increased (z = -2.249, P = 0.024) and significantly correlated with collagen volume fraction (CVF) (r = 0.516, P < 0.001), late gadolinium enhancement (LGE) (r = 0.307, P = 0.048), and peripheral circulation (r = 0.434, P = 0.004). Moreover, circulating miR-221 expression was significantly correlated with CVF (r = 0.454, P = 0.002), LGE (r = 0.630, P = 0.004), maximum interventricular septal thickness (MIVST) of echocardiography (r = 0.318, P = 0.042), and MIVST of magnetic resonance (r = 0.342, P = 0.027). The area under the receiver operating characteristic curve of miR-221 was 0.764. CONCLUSIONS: Circulating miR-221 is consistent with that in myocardial tissue, and correlated with myocardial fibrosis and hypertrophy. It can be used as a biomarker for evaluating myocardial hypertrophy and fibrosis in HOCM.
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Huang et al. (2020) conducted an observational in Hypertrophic obstructive cardiomyopathy (HOCM) (n=42). Circulating microRNA-221 was evaluated on Correlation of circulating miR-221 with collagen volume fraction (CVF) (r = 0.454, p=0.002). Circulating miR-221 expression significantly correlated with myocardial collagen volume fraction (r=0.454, P=0.002) and late gadolinium enhancement (r=0.630, P=0.004) in HOCM.
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