The acute effect of a single application of cabergoline on endogenous GH levels in patients with acromegaly on pegvisomant treatment

被引:10
作者
Roemmler, J. [1 ]
Steffin, B.
Gutt, B. [2 ]
Schneider, H. J.
Sievers, C. [3 ]
Bidlingmaier, M.
Schopohl, J.
机构
[1] Univ Munich, Dept Internal Med, Med Klin, D-80336 Munich, Germany
[2] Tech Univ Munich, Acad Teaching Hosp Bogenhausen, Munich, Germany
[3] Max Planck Inst Psychiat, D-80804 Munich, Germany
关键词
Acromegaly; Growth hormone receptor antagonist; Dopamine agonist; Combined medical treatment; Acute effect; Endogenous GH; GROWTH-FACTOR-I; HORMONE-RECEPTOR ANTAGONIST; SOMATOSTATIN ANALOGS; BROMOCRIPTINE ERGOSET; PITUITARY IRRADIATION; GLUCOSE-TOLERANCE; HEALTHY WOMEN; INSULIN; PROLACTIN; BLOCKADE;
D O I
10.1016/j.ghir.2010.05.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objective: Treatment with pegvisomant, an antagonist of growth hormone (GH) receptors, increases GH levels in a dose dependent manner. Cabergoline can suppress GH secretion in approximately 40% of acromegalic patients. However, the acute effects of cabergoline have not been studied in patients treated with pegvisomant. We performed this cross-sectional study to evaluate endogenous GH after an additional single cabergoline administration. Design: 9 acromegalic patients on pegvisomant therapy were included. A 6 h GH profile after pegvisomant alone (P) and a 9 h profile in combination with oral cabergoline 0.5 mg (PC) were performed. After 3 or 6 h, all patients received a standardized light mixed meal. Endogenous serum GH and pegvisomant levels were measured by special in-house assays. The GH assay showed no interference with pegvisomant. Results: Endogenous GH levels at baseline did not differ significantly between the profiles (P: 16.5 mu g/l (range 3.2-36.6 mu g/l), PC: 8.0 mu g/l (1.6-48 mu g/l), p>0.05). In both profiles. GH fluctuated before meal. GH decreased more pronounced in PC but this decrease was not statistically significant. After meal, a significant decline in endogenous GH levels from 16.4 mu g/l (0.4-27.1 mu g/l, 100%) to 8.1 mu g/l (0.2-24.7 mu g/l, 66%) appeared in P at 300 min (p<0.01). Also in PC a decline from 7.8 mu g/l (1.1-29.6 mu g/l, 100%) to 5.2 mu g/l (0.4-23.9 mu g/l, 75%) at 300 min was observed but it was not significant. Conclusion: Endogenous GH is not significantly decreased after a single oral cabergoline application during pegvisomant treatment in acromegaly. (C) 2010 Growth Hormone Research Society. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:338 / 344
页数:7
相关论文
共 40 条
[21]   Effects of a quick-release form of bromocriptine (ergoset) on fasting and postprandial plasma glucose, insulin, lipid, and lipoprotein concentrations in obese nondiabetic hyperinsulinemic women [J].
Kamath, V ;
Jones, CN ;
Yip, JC ;
Varasteh, BB ;
Cincotta, AH ;
Reaven, GM ;
Chen, YDI .
DIABETES CARE, 1997, 20 (11) :1697-1701
[22]  
KAYATH MJ, 1992, BRAZ J MED BIOL RES, V25, P449
[23]   Growth hormone receptor antagonists: Discovery, development, and use in patients with acromegaly [J].
Kopchick, JJ ;
Parkinson, C ;
Stevens, EC ;
Trainer, PJ .
ENDOCRINE REVIEWS, 2002, 23 (05) :623-646
[24]   PROLACTIN - DIABETOGENIC HORMONE [J].
LANDGRAF, R ;
LANDGRAFLEURS, MMC ;
WEISSMANN, A ;
HORL, R ;
WERDER, KV ;
SCRIBA, PC .
DIABETOLOGIA, 1977, 13 (02) :99-104
[25]   Efficacy of Combined Treatment with Lanreotide and Cabergoline in Selected Therapy-Resistant Acromegalic Patients [J].
Marzullo P. ;
Ferone D. ;
Di Somma C. ;
Pivonello R. ;
Filippella M. ;
Lombardi G. ;
Colao A. .
Pituitary, 1999, 1 (2) :115-120
[26]   Consensus statement: medical management of acromegaly [J].
Melmed, S ;
Casanueva, F ;
Cavagnini, F ;
Chanson, P ;
Frohman, LA ;
Gaillard, R ;
Ghigo, E ;
Ho, K ;
Jaquet, P ;
Kleinberg, D ;
Lamberts, S ;
Laws, E ;
Lombardi, G ;
Sheppard, MC ;
Thorner, M ;
Vance, ML ;
Wass, JAH ;
Giustina, A .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2005, 153 (06) :737-740
[27]  
Minniti G, 1997, Clin Ter, V148, P601
[28]   Blockade of the growth hormone (GH) receptor unmasks rapid GH-releasing peptide-6-mediated tissue-specific insulin resistance [J].
Muller, AF ;
Janssen, JA ;
Hofland, LJ ;
Lamberts, SW ;
Bidlingmaier, M ;
Strasburger, CJ ;
van der Lely, AJ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (02) :590-593
[29]   Long-term efficacy and safety of combined treatment of somatostatin analogs and Pegvisomant in acromegaly [J].
Neggers, Sebastian J. C. M. M. ;
van Aken, Maarten O. ;
Janssen, Joop A. M. J. L. ;
Feelders, Richard A. ;
de Herder, Wouter W. ;
van der Lely, Aart-Jan .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2007, 92 (12) :4598-4601
[30]   Pegvisomant interference in GH assays results in underestimation of GH levels [J].
Paisley, A. N. ;
Hayden, K. ;
Ellis, A. ;
Anderson, J. ;
Wieringa, G. ;
Trainer, P. J. .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2007, 156 (03) :315-319