Effect of clenbuterol on cardiac and skeletal muscle function during left ventricular assist device support

被引:38
作者
George, Isaac
Xydas, Steve
Mancini, Donna M.
Lamanca, John
DiTullio, Marco
Marboe, Charles C.
Shane, Elizabeth
Schulman, Allison R.
Colley, Patrick M.
Petrilli, Christopher M.
Naka, Yoshifumi
Oz, Mehmet C.
Maybaum, Simon
机构
[1] Columbia Univ, Coll Phys & Surg, Dept Surg, Div Cardiothorac Surg, New York, NY 10032 USA
[2] Columbia Univ, Coll Phys & Surg, Dept Med, Div Cardiol, New York, NY 10032 USA
[3] Columbia Univ, Coll Phys & Surg, Dept Pathol, New York, NY 10032 USA
[4] Columbia Univ, Coll Phys & Surg, Dept Med, Div Endocrinol, New York, NY 10032 USA
[5] Albert Einstein Coll Med, Div Cardiol, Dept Med, New York, NY USA
关键词
D O I
10.1016/j.healun.2006.06.017
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: High-dose clenbuterol (a selective beta(2)-adrenergic agonist) has been proposed to promote myocardial recovery during left ventricular assist device (LVAD) support, but its effects on cardiac and skeletal muscle are largely unknown. Methods: Seven subjects with heart failure (5 ischemic, 2 non-ischemic) were started on oral clenbuterol 5 to 46 weeks post-LVAD implantation and up-titrated to daily doses of 720 mu g. The following procedures were performed at baseline and after 3 months of therapy: echocardiography at reduced support (4 liters/min); cardiopulmonary exercise testing; body composition analysis; and quadriceps maximal voluntary contraction (MVC). Myocardial histologic analysis was measured at device implantation and explantation. Results: There were no serious adverse events or arrhythmias. Creatine phosphokinase (CPK) was elevated in 4 subjects, with no clinical sequelae. No change in ejection fraction was seen. End-diastolic dimension increased significantly (4.73 +/- 0.67 vs 5.24 +/- 0.66; p < 0.01), despite a trend toward increased IV mass. Body weight and lean mass increased significantly (75.5 +/- 17.9 vs 79.2 +/- 25.1 kg, 21.1 +/- 8.9 vs 23.6 +/- 9.7 kg, respectively; both p < 0.05). Exercise capacity did not change, but MVC improved significantly from 37.0 +/- 15.7 to 45.8 +/- 20.6 kg (P < 0.05). No significant change in myocyte size or collagen deposition was seen. Conclusions: Cardiac function did not improve in this cohort of LVAD patients treated with high-dose clenbuterol. However, clenbuterol therapy increased skeletal muscle mass and strength and prevented the expected decrease in myocyte size during LVAD support. Further study will clarify its potential for cardiac and skeletal muscle recovery.
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页码:1084 / 1090
页数:7
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