Valea Ana, Ghervan Cristina, Carsote Mara, Morar Andra, Iacob Iulia, Tomesc Florica, Pop Dan Dumitru, Georgescu Carmen
Department of Endocrinology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Department of Endocrinology, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Clujul Med. 2015;88(3):310-3. doi: 10.15386/cjmed-435. Epub 2015 Jul 1.
Acromegaly is a complex endocrine disorder caused by excessive secretion of GH, secondary to a GH secreting pituitary adenoma or a mixed pituitary adenoma secreting GH and PRL.
The aim of this study was to evaluate the effects of combination therapy: dopamine agonist and somatostatin analogue on GH and IGF1 levels in a group of 30 patients with acromegaly. Cabergoline in a dose of 2 mg/week and 4 mg/week respectively was associated with Sandostatin LAR in a dose of 20 mg/month and 30 mg/months respectively. Eight patients were treated with Lanreotide 30 mg/week and Cabergoline 2 mg/week and 3 patients were treated with Bromocriptine 10 mg/day and Sandostatin LAR 30 mg/month.
Combination therapy: Cabergoline and Sandostatin achieved normal levels of IGF1 in 32% of the patients, better results being obtained after 12 months of treatment in the group treated with 4 mg Cabergoline/week. In 37% of cases the levels of IGF1 decreased by 50% after 12 months of treatment. In the group treated with Cabergoline and Somatuline a normal level of IGF1 was achieved in 25% of patients after 12 months of treatment. The outcome for the group treated with Sandostatin and Bromocriptine was similar to that obtained under Cabergoline 2 mg/week. There was no significant correlation between the level of GH and the type or dose of dopamine agonist used.
In conclusion, combination therapy consisting of dopamine agonist and somatostatin analogue achieves a significant reduction of IGF1 levels in patients with mixed adenomas secreting GH and PRL. A decrease in IGF1 levels is directly correlated with the dose of Cabergoline used.
肢端肥大症是一种复杂的内分泌疾病,由生长激素(GH)分泌过多引起,继发于分泌GH的垂体腺瘤或分泌GH和催乳素(PRL)的混合性垂体腺瘤。
本研究旨在评估联合治疗(多巴胺激动剂和生长抑素类似物)对一组30例肢端肥大症患者GH和胰岛素样生长因子1(IGF1)水平的影响。分别给予剂量为2mg/周和4mg/周的卡麦角林,联合剂量分别为20mg/月和30mg/月的长效奥曲肽。8例患者接受30mg/周的兰瑞肽和2mg/周的卡麦角林治疗,3例患者接受10mg/天的溴隐亭和30mg/月的长效奥曲肽治疗。
联合治疗(卡麦角林和长效奥曲肽)使32%的患者IGF1水平恢复正常,在接受4mg卡麦角林/周治疗的组中,治疗12个月后效果更佳。在37%的病例中,治疗12个月后IGF1水平下降了50%。在接受卡麦角林和索马杜林治疗的组中,12个月治疗后25%的患者IGF1水平恢复正常。接受长效奥曲肽和溴隐亭治疗组的结果与接受2mg/周卡麦角林治疗组相似。GH水平与所用多巴胺激动剂的类型或剂量之间无显著相关性。
总之,多巴胺激动剂和生长抑素类似物组成的联合治疗可使分泌GH和PRL的混合性腺瘤患者的IGF1水平显著降低。IGF1水平的降低与所用卡麦角林的剂量直接相关。