Growth hormone administration reduces circulating proinflammatory cytokines and soluble Fas/soluble Fas ligand system in patients with chronic heart failure secondary to idiopathic dilated cardiomyopathy

被引:38
作者
Adamopoulos, S [1 ]
Parissis, JT [1 ]
Georgiadis, M [1 ]
Karatzas, D [1 ]
Paraskevaidis, J [1 ]
Kroupis, C [1 ]
Karavolias, G [1 ]
Koniavitou, K [1 ]
Kremastinos, DT [1 ]
机构
[1] Onassis Cardiac Surg Ctr, Dept Cardiol 2, Athens, Greece
关键词
D O I
10.1067/mhj.2002.124052
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Recent studies have shown that an abnormal proinflammatory cytokine expression and apoptotic process contribute to adverse left ventricular remodeling and progress of chronic heart failure. This study investigates the effects of growth hormone (GH) administration on serum levels of representative proinflammatory cytokines and soluble apoptosis mediators in patients with chronic heart failure secondary to idiopathic dilated cardiomyopathy (IDC). Methods Serum levels of tumor necrosis factor-alpha (TNF-alpha), its soluble receptors (sTNF-RI, sTNF-RII), interleukin-6 (IL-6), soluble IL-6 receptor (sIL-6R), soluble Fas (sFas) and soluble Fas Ligand (sFasL) were determined (enzyme-linked immunosorbent assay method) in 10 patients with IDC (New York Heart Association class III, ejection fraction 24% -_ 2%) before and after a 3-month subcutaneous administration of 4 IU GH every other day (randomized crossover design). Peak oxygen consumption (Vo(2)max) was also used to evaluate the functional status of patients with IDC. Results Treatment with GH produced a significant reduction in serum levels of TNF-alpha. (8.2 +/- 1.2 vs 5.7 +/- 1.1 pg/mL, P < .05), sTNF-RI (3.9 +/- 0.4 vs 3.2 +/- 0.3 ng/mL, P < .05), sTNF-RII (2.6 +/- 0.3 vs 2.2 +/- 0.2 ng/mL, P < .05), IL-6 (5.5 +/- 0.6 vs 4.4 +/- 0.4 pg/mL, P = .05), sIL-6R (32.7 +/- 3.0 vs 28.2 +/- 3.0 ng/mL, P < .05), sFas (4.4 +/- 0.8 vs 3.1 +/- 0.6 ng/mL, P < .05), and sFasL (34.2 +/- 11.7 vs 18.8 +/- 7.3 pg/mL, P < .01). A significant improvement was also observed in Vo(2)max after the completion of 3 months' treatment with GH (15.0 +/- 0.8 vs 17.2 +/- 1.0 mL/kg/min, P < .05). Good correlations were found between GH-induced reduction in TNF-alpha levels and increase in Vo(2)max (r = -0.64, P < .05) as well as between GH-induced reduction in sFasL and increase in Vo(2)max (r = -0.56, P = .08). Conclusions GH administration reduces serum levels of proinflammatory cytokines and soluble Fas/FasL system in Conclusions GH administration reduces serum levels of proinflammatory cytokines and soluble Fas/FasL system in patients with IDC. These immunomodulatory effects may be associated with improvement in clinical performance and exercise capacity of patients with IDC.
引用
收藏
页码:359 / 364
页数:6
相关论文
共 29 条
[1]  
Adamopoulos S, 2000, CIRCULATION, V102, P522
[2]   Physical training reduces peripheral markers of inflammation in patients with chronic heart failure [J].
Adamopoulos, S ;
Parissis, J ;
Kroupis, C ;
Georgiadis, M ;
Karatzas, D ;
Karavolias, G ;
Koniavitou, K ;
Coats, AJS ;
Kremastinos, DT .
EUROPEAN HEART JOURNAL, 2001, 22 (09) :791-797
[3]  
Beranek JT, 1999, EUR HEART J, V20, P242
[4]   Efficacy and safety of calcium channel blockers in heart failure: Focus on recent trials with second-generation dihydropyridines [J].
de Vries, RJM ;
van Veldhuisen, DJ ;
Dunselman, PHJM .
AMERICAN HEART JOURNAL, 2000, 139 (02) :185-194
[5]   A preliminary study of growth hormone in the treatment of dilated cardiomyopathy [J].
Fazio, S ;
Sabatini, D ;
Capaldo, B ;
Vigorito, C ;
Giordano, A ;
Guida, R ;
Pardo, F ;
Biondi, B ;
Sacca, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (13) :809-814
[6]  
Fazio S, 1997, EUR HEART J, V18, P340
[7]   TUMOR-NECROSIS-FACTOR SOLUBLE RECEPTORS IN PATIENTS WITH VARIOUS DEGREES OF CONGESTIVE-HEART-FAILURE [J].
FERRARI, R ;
BACHETTI, T ;
CONFORTINI, R ;
OPASICH, C ;
FEBO, O ;
CORTI, A ;
CASSANI, G ;
VISIOLI, O .
CIRCULATION, 1995, 92 (06) :1479-1486
[8]  
FERRARI R, 1998, EUR HEART J, V19, P2
[9]   Effect of high- versus low-dose angiotensin converting enzyme inhibition on cytokine levels in chronic heart failure [J].
Gullestad, L ;
Aukrust, P ;
Ueland, T ;
Espevik, T ;
Yee, G ;
Vagelos, R ;
Froland, SS ;
Fowler, M .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1999, 34 (07) :2061-2067
[10]   2-PERIOD CROSSOVER CLINICAL-TRIAL [J].
HILLS, M ;
ARMITAGE, P .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1979, 8 (01) :7-20