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
[1]   Cabergoline in the treatment of acromegaly: A study in 64 patients [J].
Abs, R ;
Verhelst, J ;
Maiter, D ;
Van Acker, K ;
Nobels, F ;
Coolens, JL ;
Mahler, C ;
Beckers, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (02) :374-378
[2]   Does bromocriptine improve glycemic control of obese type-2 diabetics? [J].
Aminorroaya, A ;
Janghorbani, M ;
Ramezani, M ;
Haghighi, S ;
Amini, M .
HORMONE RESEARCH, 2004, 62 (02) :55-59
[3]   Pituitary irradiation is ineffective in normalizing plasma insulin-like growth factor I in patients with acromegaly [J].
Barkan, AL ;
Halasz, I ;
Dornfeld, KJ ;
Jaffe, CA ;
Friberg, RD ;
Chandler, WF ;
Sandler, HM .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (10) :3187-3191
[4]   THE INTERNATIONAL REFERENCE REAGENT FOR INSULIN-LIKE GROWTH FACTOR-I [J].
BRISTOW, AF ;
GOODING, RP ;
DAS, REG .
JOURNAL OF ENDOCRINOLOGY, 1990, 125 (02) :191-197
[5]   Bromocriptine (Ergoset) reduces body weight and improves glucose tolerance in obese subjects [J].
Cincotta, AH ;
Meier, AH .
DIABETES CARE, 1996, 19 (06) :667-670
[6]  
Colao A, 2000, Expert Opin Pharmacother, V1, P555, DOI 10.1517/14656566.1.3.555
[7]   Cabergoline addition to depot somatostatin analogues in resistant acromegalic patients: efficacy and lack of predictive value of prolactin status [J].
Cozzi, R ;
Attanasio, R ;
Lodrini, S ;
Lasio, G .
CLINICAL ENDOCRINOLOGY, 2004, 61 (02) :209-215
[8]   Cabergoline in acromegaly: a renewed role for dopamine agonist treatment? [J].
Cozzi, R ;
Attanasio, R ;
Barausse, M ;
Dallabonzana, D ;
Orlandi, P ;
Da Re, N ;
Branca, V ;
Oppizzi, G ;
Gelli, G .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 1998, 139 (05) :516-521
[9]   Clinical pharmacokinetics of cabergoline [J].
Del Dotto, P ;
Bonuccelli, U .
CLINICAL PHARMACOKINETICS, 2003, 42 (07) :633-645
[10]   Reference ranges for two automated chemiluminescent assays for serum insulin-like growth factor I (IGF-I) and IGF-binding protein 3 (IGFBP-3) [J].
Elmlinger, MW ;
Kühnel, W ;
Weber, MM ;
Ranke, MB .
CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2004, 42 (06) :654-664