Decreased Expression of miR-133a but Not of miR-1 is Associated with Signs of Heart Failure in Patients Undergoing Coronary Bypass Surgery

被引:44
作者
Danowski, Nina [1 ]
Manthey, Iris [1 ]
Jakob, Heinz Guenther [3 ]
Siffert, Winfried [1 ]
Peters, Juergen [2 ]
Frey, Ulrich H. [2 ]
机构
[1] Univ Duisburg Essen, Inst Pharmakogenet, Essen, Germany
[2] Univ Duisburg Essen, Klin Anasthesiol & Intensivmed, Essen, Germany
[3] Univ Duisburg Essen, Klin Thorax & Kardiovaskulare Chirurg, Essen, Germany
关键词
MicroRNAs; Coronary artery bypass grafting; Heart failure; MICRORNA EXPRESSION; GENE-EXPRESSION; MESSENGER-RNA; MUSCLE; PROLIFERATION; SIGNATURES; REVEALS;
D O I
10.1159/000348563
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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. Copyright (C) 2013 S. Karger AG, Basel
引用
收藏
页码:125 / 130
页数:6
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