Response to Letter Regarding Article, “Circulating MicroRNA-30d Is Associated With Response to Cardiac Resynchronization Therapy in Heart Failure and Regulates Cardiomyocyte Apoptosis: A Translational Pilot Study”
Author(s) -
Yonathan F. Melman,
Ravi V. Shah,
Kirsty Danielson,
Junjie Xiao,
Bridget Simonson,
Andreas S. Barth,
Khalid Chakir,
Gregory D. Lewis,
Zachary Lavender,
Quynh A. Truong,
André G. Kléber,
Ranendra Das,
Anthony Rosenzweig,
YaoYu Wang,
David A. Kass,
Jagmeet P. Singh,
Saumya Das
Publication year - 2016
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.115.019228
Subject(s) - medicine , heart failure , cardiac resynchronization therapy , cardiology , microrna , apoptosis , biochemistry , chemistry , ejection fraction , gene
We thank Sardu and colleagues for their comments. Our report demonstrates that baseline levels of microRNA-30d (miR-30d) are correlated with response to cardiac resynchronization therapy and that miR-30d was dynamically regulated by mechanical stress.1 Moreover, miR-30d appeared to be an adaptive response and was cardioprotective against tumor necrosis factor-α–mediated apoptosis. Similar to our study, Marfella et al2 noted differential expression of several plasma miRNAs in cardiac resynchronization therapy responders versus nonresponders 1 year after cardiac resynchronization therapy. The lack of significant overlap between the sets of extracellular miRNAs reflects some of the ongoing issues in extracellular RNA research. The first issue is differences in patient populations and small sample sizes. The second is variances in methodology. Several groups, including …
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