Arosio M, Macchelli S, Rossi C M, Casati G, Biella O, Faglia G
Institute of Endocrine Sciences, University of Milan, Ospedale Maggiore IRCCS, Italy.
Eur J Endocrinol. 1995 Oct;133(4):430-9. doi: 10.1530/eje.0.1330430.
Treatment of acromegaly is effective in reversing the reduced life-span of patients only when serum growth hormone (GH) concentrations are lowered to less than 2.5 micrograms/l. Usual treatments achieve this goal in no more than 50-60% of patients. The effects of octreotide were studied in a prospective, open label study with 68 acromegalic patients enrolled in 10 Italian centers. Octreotide was administered sc at a dose of 100 micrograms t.i.d. for 1 year. After 3 months of therapy, octreotide was effective in decreasing serum GH levels below 2.5 micrograms/l in 16 out of 64 acromegalic patients (25%). Fifteen of them had pretreatment GH levels below 25 micrograms/l. Insulin-like growth factor I (IGF-I) levels normalized in about 40% of patients. No further GH reduction was observed after 1 year of treatment. The presence of abnormal GH responses to thyrotropin-releasing hormone (TRH) and gonadotropin-releasing hormone was reduced from 54 to 24% and from 16 to 12%, respectively. Tumor shrinkage was observed in 50% of 26 non-irradiated patients after 12 months of treatment. Both basal and TRH-stimulated serum prolactin levels significantly decreased in the 11 hyperprolactinemic patients. Although serum thyrotropin, free triiodothyronine and free thyroxine concentrations were not modified, a significant reduction of thyrotropin response to TRH was observed in the 9th month of therapy. In non-diabetic patients, an increase of mean blood glucose levels without modifications of fasting morning concentrations was found. About one-quarter of the patients with overt diabetes mellitus had an impairment of their metabolic control. Main clinical symptoms of acromegaly improved in 70-80% of patients.(ABSTRACT TRUNCATED AT 250 WORDS)
仅当血清生长激素(GH)浓度降至低于2.5微克/升时,肢端肥大症的治疗才能够有效逆转患者缩短的寿命。常规治疗在不超过50 - 60%的患者中实现这一目标。在一项前瞻性、开放标签研究中,对意大利10个中心招募的68例肢端肥大症患者研究了奥曲肽的疗效。奥曲肽以100微克的剂量皮下注射,每日三次,持续1年。治疗3个月后,奥曲肽在64例肢端肥大症患者中有16例(25%)有效降低血清GH水平至低于2.5微克/升。其中15例患者治疗前GH水平低于25微克/升。约40%的患者胰岛素样生长因子I(IGF - I)水平恢复正常。治疗1年后未观察到GH进一步降低。对促甲状腺激素释放激素(TRH)和促性腺激素释放激素的异常GH反应的发生率分别从54%降至24%和从16%降至12%。在26例未接受放疗的患者中,12个月治疗后50%观察到肿瘤缩小。11例高催乳素血症患者的基础和TRH刺激的血清催乳素水平均显著降低。尽管血清促甲状腺激素、游离三碘甲状腺原氨酸和游离甲状腺素浓度未改变,但在治疗第9个月观察到促甲状腺激素对TRH反应显著降低。在非糖尿病患者中,发现平均血糖水平升高,但空腹晨起血糖浓度未改变。约四分之一的显性糖尿病患者代谢控制受损。70 - 80%的患者肢端肥大症的主要临床症状得到改善。(摘要截短于250字)