Vierhapper H
Clinical Division of Endocrinology and Metabolism, University Clinic for Internal Medicine III, Vienna, Austria.
Growth Horm IGF Res. 1998 Feb;8 Suppl A:37-40. doi: 10.1016/s1096-6374(98)80007-5.
This study was conducted to evaluate whether stimulated concentrations of growth hormone (GH) are of practical use in establishing the diagnosis of acquired GH deficiency. The secretion of GH as stimulated by GH releasing hormone (GHRH; 100 microg i.v.) was studied in 33 patients with non-functioning pituitary macroadenomas prior to and after trans-sphenoidal adenomectomy, as well as in 25 non-selected subjects who had been referred for evaluation of various suspected non-pituitary diseases. Patients with pituitary macroadenomas, who needed substitution therapy for at least one additional pituitary hormone, presented with lower (P<0.05) GHRH-stimulated GH secretion (3.2 +/- 4.3 ng/ml) than the remaining patients with pituitary tumours (7.2 +/- 6.6 mg/ml). Both groups showed a marked overlap with the control group (7.1 +/- 5.5 ng/ml). Although GH stimulation tests are superior to other biochemical criteria of GH deficiency, they are still an inadequate method to reliably diagnose GH deficiency in an individual patient. In clinical practice GH replacement therapy should, therefore, only be considered if, in addition to impaired GH secretion, the patients present with additional defects in anterior pituitary function and clinical symptoms are compatible with a lack of GH.
本研究旨在评估刺激状态下生长激素(GH)的浓度在后天性GH缺乏症诊断中是否具有实际应用价值。对33例无功能性垂体大腺瘤患者经蝶窦腺瘤切除术前、后的GH释放激素(GHRH;静脉注射100微克)刺激的GH分泌情况进行了研究,并对25例因各种疑似非垂体疾病而转诊接受评估的未筛选受试者进行了研究。需要至少一种额外垂体激素替代治疗的垂体大腺瘤患者,其GHRH刺激的GH分泌(3.2±4.3纳克/毫升)低于其余垂体肿瘤患者(7.2±6.6微克/毫升)(P<0.05)。两组与对照组(7.1±5.5纳克/毫升)均有明显重叠。尽管GH刺激试验优于其他GH缺乏的生化标准,但在个体患者中,它仍然是一种不可靠的诊断GH缺乏的方法。因此,在临床实践中,只有当患者除了GH分泌受损外,还存在垂体前叶功能的其他缺陷且临床症状与GH缺乏相符时,才应考虑进行GH替代治疗。