Department of Endocrinology and Metabolic Diseases, Pôle Cardio-vasculaire et Métabolique, CHU Rangueil-Larrey, 24 Chemin de Pourvouville, TSA 30030, 31059 Toulouse Cedex 9, France.
Pituitary. 2012 Dec;15(4):518-25. doi: 10.1007/s11102-011-0361-9.
To describe glucose status changes in patients with acromegaly receiving somatostatin analog lanreotide as primary treatment. This retrospective, single-center study conducted during 1996-2008, included acromegalic patients receiving primary lanreotide treatment. Baseline and last follow-up visit assessments included glucose status (according to American Diabetes Association criteria), growth hormone (GH), and insulin-like growth factor-1 (IGF-1) levels. Glucose control was considered improved when fasting plasma glucose or antidiabetic treatments were reduced, and deteriorated if fasting glucose was the same/higher but with increased antidiabetic treatments. 42 patients (median age 50 years; range 29-75 years) were included. At baseline, 26 (62%) were normoglycemic, eight (19%) had impaired glucose tolerance/fasting glycemia, and eight (19%) had diabetes mellitus; family history of diabetes mellitus was significantly associated with abnormal glucose status. At final visit, the mean (SE) lanreotide dose was 108 (21) mg/month. Median treatment duration was 23 months, range 3-138 months, and 74% of patients received the 120-mg dose. Median GH levels decreased significantly (baseline, 12 [5-20] μg/l; final visit, 2.1 [1.0-4.7] μg/l; P < 0.0001); IGF-1 levels were age- and sex-normalized in 33% of patients. Glucose control deteriorated in seven patients (17%) and improved from abnormal levels in 10 (24%). Deterioration was associated with smaller GH decreases (median change, -3.4 μg/l vs. -10.7 μg/l, P = 0.014) and improvement with trend to lower BMI and younger age. During primary lanreotide treated acromegalic patients 60% had no change, 24% had an improvement and 17% had a worsening of glucose status. Deterioration was significantly associated with smaller GH decreases during primary lanreotide treatment.
描述接受生长抑素类似物兰瑞肽作为初始治疗的肢端肥大症患者的葡萄糖状态变化。这项回顾性、单中心研究于 1996-2008 年进行,纳入了接受初始兰瑞肽治疗的肢端肥大症患者。基线和最后一次随访评估包括葡萄糖状态(根据美国糖尿病协会标准)、生长激素(GH)和胰岛素样生长因子-1(IGF-1)水平。如果空腹血糖或降糖治疗减少,且葡萄糖控制改善;如果空腹血糖相同/更高但降糖治疗增加,则葡萄糖控制恶化。纳入 42 例患者(中位年龄 50 岁;范围 29-75 岁)。基线时,26 例(62%)血糖正常,8 例(19%)葡萄糖耐量受损/空腹血糖异常,8 例(19%)患有糖尿病;糖尿病家族史与异常葡萄糖状态显著相关。最后一次随访时,兰瑞肽的平均(SE)剂量为 108(21)mg/月。中位治疗时间为 23 个月,范围 3-138 个月,74%的患者接受 120mg 剂量。中位 GH 水平显著降低(基线时,12[5-20]μg/l;最后一次随访时,2.1[1.0-4.7]μg/l;P<0.0001);33%的患者 IGF-1 水平达到年龄和性别正常化。7 例患者(17%)葡萄糖控制恶化,10 例(24%)异常水平改善。恶化与 GH 降低幅度较小相关(中位数变化,-3.4μg/l 与-10.7μg/l,P=0.014),改善与 BMI 较低和年龄较小有关。在接受初始兰瑞肽治疗的肢端肥大症患者中,60%无变化,24%改善,17%恶化。恶化与初始兰瑞肽治疗期间 GH 降低幅度较小显著相关。