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单次应用卡麦角林对接受培维索孟治疗的肢端肥大症患者内源性生长激素水平的急性影响。

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

作者信息

Roemmler J, Steffin B, Gutt B, Schneider H J, Sievers C, Bidlingmaier M, Schopohl J

机构信息

Medizinische Klinik, Innenstadt, University of Munich, Germany.

出版信息

Growth Horm IGF Res. 2010 Oct;20(5):338-44. doi: 10.1016/j.ghir.2010.05.004. Epub 2010 Jul 2.

Abstract

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 6h GH profile after pegvisomant alone (P) and a 9h profile in combination with oral cabergoline 0.5mg (PC) were performed. After 3 or 6h, 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 μg/l (range 3.2-36.6 μg/l), PC: 8.0 μg/l (1.6-48 μg/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 μg/l (0.4-27.1 μg/l, 100%) to 8.1 μg/l (0.2-24.7 μg/l, 66%) appeared in P at 300 min (p<0.01). Also in PC a decline from 7.8 μg/l (1.1-29.6 μg/l, 100%) to 5.2 μg/l (0.4-23.9 μg/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.

摘要

目的

生长激素(GH)受体拮抗剂培维索孟治疗会使GH水平呈剂量依赖性升高。卡麦角林可使约40%的肢端肥大症患者的GH分泌受到抑制。然而,尚未对接受培维索孟治疗的患者进行卡麦角林急性效应的研究。我们开展这项横断面研究以评估额外单次给予卡麦角林后的内源性GH水平。

设计

纳入9例接受培维索孟治疗的肢端肥大症患者。分别进行单独使用培维索孟(P)后的6小时GH谱分析以及联合口服0.5mg卡麦角林(PC)后的9小时谱分析。3或6小时后,所有患者均接受标准化清淡混合餐。采用特殊的内部检测方法测定内源性血清GH和培维索孟水平。GH检测显示不受培维索孟干扰。

结果

各谱分析中基线时的内源性GH水平无显著差异(P组:16.5μg/L(范围3.2 - 36.6μg/L),PC组:8.0μg/L(1.6 - 48μg/L),p>0.05)。在两种谱分析中,进餐前GH均有波动。PC组中GH下降更为明显,但这种下降无统计学意义。餐后,P组在300分钟时内源性GH水平从16.4μg/L(0.4 - 27.1μg/L,100%)显著降至8.1μg/L(0.2 - 24.7μg/L,66%)(p<0.01)。PC组在300分钟时也观察到从7.8μg/L(1.1 - 29.6μg/L,100%)降至5.2μg/L(0.4 - 23.9μg/L,75%),但不显著。

结论

肢端肥大症患者在培维索孟治疗期间单次口服卡麦角林后,内源性GH水平无显著降低。

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