Mahajan T, Lightman S L
University of Bristol, Division of Medicine, Bristol Royal Infirmary, United Kingdom.
J Clin Endocrinol Metab. 2000 Apr;85(4):1473-6. doi: 10.1210/jcem.85.4.6545.
GH deficiency (GHD) in adults is a well recognized clinical syndrome that results in significant metabolic and psychological morbidity. GH replacement therapy not only reverses these changes but improves the quality of life and results in a significant improvement in well being. There is no single simple and safe test to assess GHD. GHD in adults is diagnosed biochemically by provocative testing of GH secretion, and the insulin tolerance test (ITT) is accepted to be the test of choice. However, the ITT has many contraindications, needs multiple blood samples, and is potentially dangerous, requiring regular monitoring of patients in a specialized investigation unit. The aim of our study was to evaluate the GH-releasing effect of a combination of the hypothalamic secretagogue GHRH with a small dose of the synthetic peptide GHRP-2, to diagnose GHD. We have compared the GH response to ITT and GHRH/GHRP in a large group of adults with hypothalamic/pituitary disease (n = 36; 22 males and 14 females; age, 18 -59 yr) and in healthy volunteers (n = 30; 15 males and 15 females; age, 22-66 yr). The GHRH/GHRP test produces a measurable GH secretory response in normal, hypopituitary and GH-deficient patients. The test has no side effects. Using the ITT as our 'gold standard' with a GH response of 9 mU/L as our cut-off to define GHD, we compared the clinical efficacy of these two tests. Choosing an arbitrary cut-off of 17 mU/L to define GHD in the GHRH/GHRP test, this new test proved to have 78.6% sensitivity and 100% specificity even when we only used the 30-min datum point.
成人生长激素缺乏症(GHD)是一种公认的临床综合征,会导致明显的代谢和心理疾病。生长激素替代疗法不仅能逆转这些变化,还能提高生活质量,显著改善健康状况。目前尚无单一简单且安全的检测方法来评估生长激素缺乏症。成人生长激素缺乏症通过对生长激素分泌进行激发试验进行生化诊断,胰岛素耐量试验(ITT)被公认为是首选检测方法。然而,胰岛素耐量试验有许多禁忌症,需要采集多份血样,且存在潜在危险,需要在专门的检查科室对患者进行定期监测。我们研究的目的是评估下丘脑促分泌素生长激素释放激素(GHRH)与小剂量合成肽生长激素释放肽-2(GHRP-2)联合使用对生长激素的释放作用,以诊断生长激素缺乏症。我们比较了一大组患有下丘脑/垂体疾病的成年人(n = 36;22名男性和14名女性;年龄18 - 59岁)和健康志愿者(n = 30;15名男性和15名女性;年龄22 - 66岁)对胰岛素耐量试验和生长激素释放激素/生长激素释放肽-2试验的生长激素反应。生长激素释放激素/生长激素释放肽-2试验在正常、垂体功能减退和生长激素缺乏的患者中能产生可测量的生长激素分泌反应。该试验无副作用。以胰岛素耐量试验作为我们的“金标准”,将生长激素反应9 mU/L作为定义生长激素缺乏症的临界值,我们比较了这两种检测方法的临床疗效。在生长激素释放激素/生长激素释放肽-2试验中,选择任意17 mU/L的临界值来定义生长激素缺乏症,即使仅使用30分钟的数据点,这项新试验也被证明具有78.6%的敏感性和100%的特异性。