Freda Pamela U, Nuruzzaman Abu T, Reyes Carlos M, Sundeen Robert E, Post Kalmon D
Department of Medicine, Columbia University College of Physicians and Surgeons, New York, New York 10032, USA.
J Clin Endocrinol Metab. 2004 Feb;89(2):495-500. doi: 10.1210/jc.2003-031316.
Our initial study in postoperative patients with acromegaly identified a group of patients in remission, as defined by normal IGF-I levels, but who had a subtle abnormality of GH suppression after oral glucose. To investigate the significance of this abnormality, we have undertaken further detailed testing of GH secretion and a longitudinal follow-up of some of these patients. Of the 110 postoperative patients with acromegaly evaluated by oral glucose tolerance test, 76 were in remission (i.e. normal IGF-I level), and of these subjects with acromegaly in remission, 50 had normal nadir GH (<0.14 microg/ml) (group I), and 26 had abnormal nadir GH (>0.14 microg/ml) (group II). Fourteen subjects in remission, seven from remission group I and seven from remission group II, underwent additional testing consisting of both hourly GH sampling over 8 h and, on a separate day, arginine stimulation testing. The mean of hourly GH was higher in group II (0.47 +/- 0.04 microg/liter) than in group I (0.19 +/- 0.07 microg/liter; P = 0.002). GH response to arginine was greater in group II than in group I (P < 0.01). Of those patients in remission from the initial cohort studied, 49 (30 subjects from group I and 19 from group II) underwent serial longitudinal oral glucose tolerance testing every 1-2 yr over a 1- to 6.5-yr period (mean follow-up, 3.2 yr). The initial pattern of GH suppression persisted in most patients. IGF-I levels remained normal in all patients in group II, but five subjects from group II developed an elevated IGF-I level and, thus, a biochemical recurrence. The rate of disease recurrence was greater in group II than in group I (P = 0.003). We have found that some postoperative subjects with acromegaly in remission with normal IGF-I levels have persistently abnormal nadir GH levels after oral glucose that may be accompanied by other evidence of greater GH secretion than postoperative patients with normal GH suppression. This abnormal pattern of GH suppression may be associated with increased risk of disease recurrence in some patients.
我们对肢端肥大症术后患者的初步研究确定了一组缓解期患者,其定义为胰岛素样生长因子-I(IGF-I)水平正常,但口服葡萄糖后生长激素(GH)抑制存在细微异常。为了研究这种异常的意义,我们对GH分泌进行了进一步的详细检测,并对其中一些患者进行了纵向随访。在通过口服葡萄糖耐量试验评估的110例肢端肥大症术后患者中,76例处于缓解期(即IGF-I水平正常),在这些处于缓解期的肢端肥大症患者中,50例的最低GH水平正常(<0.14μg/ml)(第一组),26例的最低GH水平异常(>0.14μg/ml)(第二组)。14例处于缓解期的患者,7例来自缓解期第一组,7例来自缓解期第二组,接受了额外检测,包括8小时内每小时采集GH样本,以及在另一天进行精氨酸刺激试验。第二组每小时GH的平均值(0.47±0.04μg/升)高于第一组(0.19±0.07μg/升;P = 0.002)。第二组对精氨酸的GH反应大于第一组(P < 0.01)。在最初研究队列中处于缓解期的患者中,49例(第一组30例,第二组19例)在1至6.5年期间(平均随访3.2年)每1至2年进行一次系列纵向口服葡萄糖耐量试验。大多数患者最初的GH抑制模式持续存在。第二组所有患者的IGF-I水平均保持正常,但第二组有5例患者的IGF-I水平升高,从而出现生化复发。第二组的疾病复发率高于第一组(P = 0.003)。我们发现,一些IGF-I水平正常的肢端肥大症术后缓解期患者口服葡萄糖后最低GH水平持续异常,可能伴有比GH抑制正常的术后患者更多的GH分泌证据。这种异常的GH抑制模式可能与一些患者疾病复发风险增加有关。