Key result
Decreased cardiac miR-133 expression was associated with increased heart failure severity, including a 25% decrease in patients with NT-proBNP >1,800 pg/ml compared to <300 pg/ml (p=0.023).
Why the study?
Is cardiac miR-1 and miR-133 expression associated with signs of heart failure in patients undergoing coronary artery bypass grafting?
Observational (n=83)
Is cardiac miR-1 and miR-133 expression associated with signs of heart failure in patients undergoing coronary artery bypass grafting?
Effect estimate: 25% decrease
p-value: p=0.023
Decreased cardiac miR-133 expression is associated with clinical and hemodynamic signs of heart failure in patients with coronary artery disease undergoing CABG.
Supports miR-133 investigation in HF; should not change CABG practice pending prospective validation.
OBJECTIVES: Coronary artery disease (CAD)-associated ischemic heart failure is characterized by dysregulated gene expression which is partly mediated by microRNAs (miRNAs). While the muscle-specific miR-1 and miR-133 are involved in cardiac development and hypertrophy, their role in heart failure resulting from CAD is unknown. We, therefore, tested the hypothesis that cardiac miR-1 and miR-133 expression is associated with signs of heart failure in patients undergoing coronary artery bypass grafting. METHODS: 83 patients were included in this prospective study. Cardiac index and vascular pressures were measured under general anesthesia and the miRNA expression was quantified (RNase protection assay and real-time PCR) from samples of the right atrial myocardium. RESULTS: miR-133 expression decreased significantly with increased severity of heart failure, as indicated by a greater New York Heart Association (NYHA) functional class (p = 0.014) and increased pulmonary artery occlusion pressure (p = 0.045). Furthermore, patients with NT-proBNP concentrations >1,800 pg/ml showed a 25% decrease in miR-133 expression compared to patients with concentrations <300 pg/ml (p = 0.023). In contrast, no associations were detected for miR-1 expression. CONCLUSIONS: In surgical CAD patients, a decreased miR-133 expression is associated with variables characteristic of heart failure. This supports a role for miR-133 but not miR-1 in the adaption to and/or remodeling of the ischemic heart.
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Danowski et al. (2013) conducted an observational in Coronary artery disease-associated ischemic heart failure (n=83). Cardiac miR-133 and miR-1 expression vs. Patients with lower severity of heart failure was evaluated on Signs of heart failure (NYHA functional class, pulmonary artery occlusion pressure, NT-proBNP concentrations) (25% decrease, p=0.023). Decreased cardiac miR-133 expression was associated with increased heart failure severity, including a 25% decrease in patients with NT-proBNP >1,800 pg/ml compared to <300 pg/ml (p=0.023).
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