4.5 Article

MicroRNA profiling as a novel diagnostic tool for identification of patients with inflammatory and/or virally induced cardiomyopathies

期刊

ESC HEART FAILURE
卷 8, 期 1, 页码 408-422

出版社

WILEY PERIODICALS, INC
DOI: 10.1002/ehf2.13090

关键词

MiRNA; Virus; Inflammation; Myocarditis; DCM

资金

  1. ERA-Net on Cardiovascular Diseases (ERA-CV
  2. Berlin, Germany) [JTC2016-40-158]
  3. ERA-Net on Cardiovascular Diseases (ERA-CV
  4. Rome, Italy) [JTC2016-40-158]
  5. ERA-Net on Cardiovascular Diseases (ERA-CV
  6. Madrid, Spain) [JTC2016-40-158]
  7. ProFIT grant of the Investitionsbank Berlin/EFRE (Berlin, Germany) [10169028]
  8. German Research Foundation (DFG)', Transregional Collaborative Research Center 'Inflammatory Cardiomyopathy -Molecular Pathogenesis and Therapy' [CRC TR19]
  9. Federal Ministry of Education and Research (BMBF) [03WKP55D]

向作者/读者索取更多资源

This study identified and evaluated prognostic miRNAs in the serum of patients with inflammatory heart diseases. The expression of certain miRNAs allowed for differentiation between patients with virus and/or inflammation and healthy donors, as well as for sorting out patients with dilated cardiomyopathy from other study groups. This miRNA profile provides a non-invasive diagnostic perspective for identifying patients with intramyocardial inflammation and/or viral persistence.
Aims MicroRNAs (miRNAs) might be used as prospective biomarkers for the identification of unexplained heart failure caused by a viral and/or inflammatory process. The aim of this study was to identify and to evaluate prognostic miRNAs in serum of patients with inflammatory heart diseases diagnosed by endomyocardial biopsies. Methods and results After TaqMan (R) OpenArray (R) screening of 754 unique circulating miRNAs in serum of biopsy-proven patients [184 patients with inflammatory and/or virally induced myocardial diseases (DCMi), 25 patients with dilated cardiomyopathy (DCM), and 25 healthy donors], we identified seven miRNAs of interest (P < 0.05). These data have been verified by single qRT-PCR assays in other biopsy-proven patients (159 patients with viral and/or inflammatory myocardial diseases, 46 patients with DCM, and 60 healthy donors). The expression of let-7f, miR-197, miR-223, miR-93, and miR-379 allowed us to differentiate between patients with a virus and/or inflammation and healthy donors (P < 0.05) with the specificity over 93%. Based on the expression of miR-21 and miR-30a-5p, we could sort out patients with DCM from all other study groups (P < 0.05) with the specificity over 95%. Conclusions This miRNA profile provides for the first time a new non-invasive diagnostic perspective to identify patients with intramyocardial inflammation and/or viral persistence only from single serum sample, independently of prescribed therapy and time of symptoms onset. It allows the early finding of those patients relevant for myocardial biopsy for exact diagnosis and further proscription of causal aetiology-driven specific treatment.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据