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Published on: January 28, 2020
Long-term prognostic value of myocardin expression levels in non-ischemic dilated cardiomyopathy
Maria E Marketou1, Joanna Kontaraki2, Alexandros Patrianakos3
1Cardiology Department, Heraklion University Hospital, Stavrakia, P.O. Box 1352, Heraklion, Crete, Greece. maryemarke@yahoo.gr.
Insights
Gene expression of myocardin in peripheral blood cells can predict long-term outcomes for non-ischemic dilated cardiomyopathy (NIDCM) patients. Lower myocardin levels indicate higher risks of congestive heart failure (CHF) mortality.
Area of Science:
- Cardiology
- Molecular Biology
- Genetics
Background:
- Non-ischemic dilated cardiomyopathy (NIDCM) is associated with substantial patient mortality.
- Effective prognostic biomarkers for long-term outcomes in NIDCM patients are needed for improved risk stratification.
Purpose of the Study:
- To evaluate the prognostic value of myocardin gene expression in peripheral blood cells for NIDCM patients.
- To assess the association between myocardin levels and mortality due to congestive heart failure (CHF) and all-cause mortality.
Main Methods:
- Retrospective analysis of 101 optimally treated NIDCM patients.
- Gene expression levels of myocardin were measured in peripheral blood cells.
- Long-term follow-up (median 8 years) including mortality data was collected.
Main Results:
- Patients with lower myocardin levels (<14.26) exhibited significantly higher CHF and all-cause mortality (p < 0.001).
- Myocardin expression level was an independent predictor of death from CHF (HR 14.5, 95% CI 5.3-39).
- Overall mortality was 61.4% and CHF mortality was 49.5% during follow-up.
Conclusions:
- Peripheral blood cell gene expression of myocardin, an early myocardial marker, can serve as a prognostic biomarker for NIDCM patients.
- Myocardin may aid in the risk stratification of NIDCM patients, potentially improving long-term management and outcomes.
Abstract:
The mortality of patients with non-ischemic dilated cardiomyopathy (NIDCM) remains substantial. We evaluated gene expression levels of myocardin, an early cardiac gene, in the peripheral blood cells of NIDCM patients as a prognostic biomarker in their long-term outcome and mortality from congestive HF (CHF). We retrospectively analyzed 101 consecutives optimally treated NIDCM patients of Cretan origin who were enrolled from the HF clinic of our hospital from November 2005 to December 2008. Our patient data were either taken from their medical files or recorded during visits to the HF unit or hospitalizations. Follow-up was carried out by telephone interview and by accessing information from general practitioners and cardiologists in private practice. The median follow-up period was 8 years (mean follow-up 7 ± 3.4 years). The overall mortality during follow-up was 61.4%, while mortality due to congestive heart failure (CHF) was 49.5%. Higher CHF and all-cause mortality were observed in patients with myocardin levels < 14.26 (p < 0.001 for both CHF and all-cause mortality). A multivariate Cox regression analysis showed that myocardin level of expression had independent significant prognostic value for the risk of death from CHF (HR 14.5, 95% confidence interval (CI) 5.3-39) in those patients. Peripheral blood cells gene expression of myocardin, an early myocardial marker, may serve as prognostic biomarkers of the long-term outcome of patients with NIDCM. Our findings open new prospects in the risk stratification of these patients.
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