Title of article :
Cardiac Contractility Modulation Electrical Signals Improve Myocardial Gene Expression in Patients With Heart Failure Original Research Article
Author/Authors :
Christian Butter، نويسنده , , Sharad Rastogi، نويسنده , , Hans-Heinrich Minden، نويسنده , , Jürgen Meyh?fer، نويسنده , , Daniel Burkhoff، نويسنده , , Hani N. Sabbah، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Pages :
6
From page :
1784
To page :
1789
Abstract :
Objectives The objective of this study was to test whether cardiac contractility modulation (CCM) electric signals induce reverse molecular remodeling in myocardium of patients with heart failure. Background Heart failure is associated with up-regulation of myocardial fetal and stretch response genes and down-regulation of Ca2+ cycling genes. Treatment with CCM signals has been associated with improved symptoms and exercise tolerance in heart failure patients. We tested the impact of CCM signals on myocardial gene expression in 11 patients. Methods Endomyocardial biopsies were obtained at baseline and 3 and 6 months thereafter. The CCM signals were delivered in random order of ON for 3 months and OFF for 3 months. Messenger ribonucleic acid expression was analyzed in the core lab by investigators blinded to treatment sequence. Expression of A- and B-type natriuretic peptides and α-myosin heavy chain (MHC), the sarcoplasmic reticulum genes SERCA-2a, phospholamban and ryanodine receptors, and the stretch response genes p38 mitogen activated protein kinase and p21 Ras were measured using reverse transcription-polymerase chain reaction and bands quantified in densitometric units. Results The 3-month therapy OFF phase was associated with increased expression of A- and B-type natriuretic peptides, p38 mitogen activated protein kinase, and p21 Ras and decreased expression of α-MHC, SERCA-2a, phospholamban, and ryanodine receptors. In contrast, the 3-month ON therapy phase resulted in decreased expression of A- and B-type natriuretic peptides, p38 mitogen activated protein kinase and p21 Ras and increased expression of α-MHC, SERCA-2a, phospholamban, and ryanodine receptors. Conclusions The CCM signal treatment reverses the cardiac maladaptive fetal gene program and normalizes expression of key sarcoplasmic reticulum Ca2+ cycling and stretch response genes. These changes may contribute to the clinical effects of CCM.
Keywords :
RNA , MHC , DNA , deoxyribonucleic acid , heart failure , myosin heavy chain , CCM , Hf , ribonucleic acid , Minnesota Living With Heart Failure questionnaire , 6-min walk test , sarcoplasmic reticulum calcium adenosine triphosphatase , cardiac contractility modulation , MLHFQ , 6MW , SERCA-2a
Journal title :
JACC (Journal of the American College of Cardiology)
Serial Year :
2008
Journal title :
JACC (Journal of the American College of Cardiology)
Record number :
473294
Link To Document :
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