Blood-based microRNA signatures differentiate various forms of cardiac hypertrophy. (1st October 2015)

• Record Type: Journal Article
• Authors: Derda, Anselm A.; Thum, Sabrina; Lorenzen, Johan M.; Bavendiek, Udo; Heineke, Joerg; Keyser, Britta; Stuhrmann, Manfred; Givens, Raymond C.; Kennel, Peter J.; Christian Schulze, P.; Widder, Julian D.; Bauersachs, Johann; Thum, Thomas
• Is Part Of: International journal of cardiology. Volume 196(2015)
• Page Start: 115
• Page End: 122
• Publication Date: 2015-10-01
• Subjects: MicroRNA -- Hypertrophic cardiomyopathies -- Aortic stenosis -- Amyloidosis -- Biomarker -- Diagnosis; Cardiology -- Periodicals; Electronic journals; 616.12
• DOI: 10.1016/j.ijcard.2015.05.185
• Languages: English
• ISSNs: 0167-5273

Abstract

Abstract: Background: Hypertrophic cardiomyopathy (HCM) is caused by mutations in different structural genes and induces pathological hypertrophy with sudden cardiac death as a possible consequence. HCM can be separated into hypertrophic non-obstructive and obstructive cardiomyopathy (HNCM/HOCM) with different clinical treatment approaches. We here distinguished between HNCM, HOCM, cardiac amyloidosis and aortic stenosis by using microRNA profiling and investigated potential interactions between circulating miRNA levels and the most common mutations in MYH7and MYBPC3 genes. Methods: Our study included 4 different groups: 23 patients with HNCM, 28 patients with HOCM, 47 patients with aortic stenosis and 22 healthy controls. Based on previous findings, 8 different cardiovascular known microRNAs (miR-1, miR-21, miR-29a, miR-29b, miR-29c, miR-133a, miR-155 and miR-499) were studied in serum of all patients and compared with clinically available patient data. Results: We found miR-29a levels to be increased in patients with HOCM and correlating markers of cardiac hypertrophy. This was not the case in HNCM patients. In contrast, we identified miR-29c to be upregulated in aortic stenosis but not the other patient groups. ROC curve analysis of miR-29a/c distinguished between HOCM patients and aortic stenosis patients. MiR-29a and miR-155 levels discriminated HNCM patients from patients with senile cardiac amyloidosis. MiR-29a increased mainly in HOCM patients with a mutation in MYH7, whereas miR-155 was decreased in hypertrophic cardiomyopathy patients with a mutation in MYBPC3. Conclusion: We demonstrated that miR-29a and miR-29c show a specific signature to distinguish between aortic stenosis, hypertrophic non-obstructive and obstructive cardiomyopathies and thus could be developed into clinically useful biomarkers.