Jørgensen Jens Otto Lunde, Feldt-Rasmussen Ulla, Frystyk Jan, Chen Jian-Wen, Kristensen Lars Østergård, Hagen Claus, Ørskov Hans
Medical Department M, Aarhus University Hospital, Norrebrogade 44, DK-8000 C Aarhus, Denmark.
J Clin Endocrinol Metab. 2005 Oct;90(10):5627-31. doi: 10.1210/jc.2005-0531. Epub 2005 Jul 26.
Pegvisomant is a GH receptor antagonist that blocks the peripheral actions of GH in acromegaly. Pegvisomant, in contrast to somatostatin (SMS) analogs, does not suppress the activity of the GH-producing adenoma.
We assessed the effects of cotreatment with pegvisomant and SMS in acromegaly on GH secretion, IGF-I levels, and glucose tolerance.
DESIGN, PATIENTS, AND INTERVENTIONS: Eleven patients with persistent disease despite previous therapy underwent the following fixed treatment algorithm: 1) on SMS therapy, 2) off therapy for 2 months, 3) 6-wk treatment with 10 mg/d pegvisomant, 4) 6-wk treatment with 15 mg/d pegvisomant, and 5) 3-month treatment with 15 mg pegvisomant plus SMS. Blood was sampled in the fasting state and during an oral glucose tolerance test.
Total serum IGF-I levels (micrograms per liter) decreased after pegvisomant, but the lowest levels were obtained with cotreatment [458 +/- 67 (SMS), 562 +/- 78 (active), 376 +/- 51 (10 mg), 269 (15 mg), 195 +/- 24 (combined) (P < 0.0001)]. Free and bioactive IGF-I changed in a similar pattern. Steady-state pegvisomant levels (micrograms per liter) were obtained, but SMS cotreatment increased pegvisomant levels by 20% (P = 0.02) [2631 +/- 616 (10 mg), 6536 +/- 1413 (15 mg), 8030 +/- 1914 (combined)]. Pegvisomant increased endogenous GH levels (micrograms per liter), which was countered by SMS cotreatment [5.1 +/- 1.3 (SMS), 8.9 +/- 2.9 (active), 14.6 +/- 4.9 (10 mg), 19.7 +/- 6.5 (15 mg), 11.8 +/- 2.8 (combined) (P < 0.01)]. Plasma glucose levels (millimoles per liter) were highest during SMS and lowest during pegvisomant 15 mg [2-h oral glucose tolerance test: 10.3 +/- 0.7 (SMS), 8.9 +/- 0.7 (active), 7.2 +/- 0.7 (10 mg), 6.5 +/- 0.5 (15 mg), 8.0 +/- 0.8 (combined) (P = 0.02)].
Dual blockade of the GH axis with pegvisomant and a SMS analog is feasible in acromegaly.
培维索孟是一种生长激素(GH)受体拮抗剂,可阻断肢端肥大症患者体内GH的外周作用。与生长抑素(SMS)类似物不同,培维索孟不会抑制产生GH的腺瘤的活性。
我们评估了培维索孟与SMS联合治疗对肢端肥大症患者GH分泌、胰岛素样生长因子-I(IGF-I)水平和糖耐量的影响。
设计、患者和干预措施:11例尽管先前接受过治疗但仍患有持续性疾病的患者接受了以下固定治疗方案:1)接受SMS治疗;2)停药2个月;3)使用10mg/d培维索孟治疗6周;4)使用15mg/d培维索孟治疗6周;5)使用15mg培维索孟加SMS治疗3个月。在空腹状态和口服葡萄糖耐量试验期间采集血液样本。
培维索孟治疗后血清总IGF-I水平(微克/升)下降,但联合治疗时达到最低水平[458±67(SMS),562±78(未治疗),376±51(10mg),269(15mg),195±24(联合)(P<0.0001)]。游离和生物活性IGF-I的变化模式相似。获得了培维索孟的稳态水平(微克/升),但SMS联合治疗使培维索孟水平提高了20%(P=0.02)[2631±616(10mg),6536±1413(15mg),8030±1914(联合)]。培维索孟可提高内源性GH水平(微克/升),而SMS联合治疗可抵消这一作用[5.1±1.3(SMS),8.9±2.9(未治疗),14.6±4.9(10mg),19.7±6.5(15mg),11.8±2.8(联合)(P<0.01)]。血浆葡萄糖水平(毫摩尔/升)在SMS治疗期间最高,在培维索孟15mg治疗期间最低[2小时口服葡萄糖耐量试验:10.3±0.7(SMS),8.9±0.7(未治疗),7.2±0.7(10mg),6.5±0.5(15mg),8.0±0.8(联合)(P=0.02)]。
培维索孟与SMS类似物双重阻断GH轴在肢端肥大症治疗中是可行的。