Luppa P, Müller B, Jacob K, Kimmig R, Strowitzki T, Höss C, Weber M M, Engelhardt D, Lobo R A
Institut für Klinische Chemie und Pathobiochemie, Klinikum rechts der Isar, Technical University Munich, Germany.
J Clin Endocrinol Metab. 1995 Jan;80(1):280-8. doi: 10.1210/jcem.80.1.7829627.
To evaluate the clinical relevance of testing pituitary-ovarian responses in patients suffering from polycystic ovary syndrome (PCOS) with the GnRH agonist nafarelin, a 1.2-mg dose of nafarelin was given intranasally to 19 women with PCOS and 15 healthy premenopausal women. The subsequent analysis of steroids in both serum and urine during the test was carried out at several time points for up to 24 h. Serum levels of 17 alpha-hydroxyprogesterone were elevated at all time points of the test in PCOS patients vs. controls [at baseline, 3.5 +/- 0.2 vs. 1.8 +/- 0.1 nmol/L (P < 0.001); at 24 h, 9.9 +/- 0.9 vs. 4.9 +/- 0.3 nmol/L (P < 0.001)]. Basal levels of androstenedione were higher in the patient group, but there was no significant change during the test in either group. Serum testosterone levels were also found to differ in PCOS patients compared with the control values at baseline (2.2 +/- 0.2 vs. 1.5 +/- 0.1 nmol/L; P < 0.05) and after nafarelin treatment (at 24 h, 3.2 +/- 0.4 vs. 1.8 +/- 0.2 nmol/L; P < 0.05). Serum estradiol levels rose significantly in both groups during the test; the posttest levels were significantly higher in PCOS than in controls. The PCOS patients displayed a significant increase in androgen and gestagen metabolites as well as in glucocorticoid metabolites excreted in the urine during the 24 h. In the control subjects, except for 17 alpha-hydroxypregnanolone, which rose significantly, none of the urinary steroids investigated showed relevant changes during the nafarelin test. The posttest excretion of allo-tetrahydrocortisol (1.4 +/- 0.2 vs. 0.3 +/- 0.1 mumol/g creatinine; P < 0.001) and the increase in 17 alpha-hydroxypregnanolone excretion (1.4 +/- 0.2 vs. 0.3 +/- 0.1 mumol/g creatinine; P < 0.001) were distinctly higher in PCOS patients than in the controls; the diagnostic sensitivity of the combination of both parameters was 89% at a 93% specificity. Thus, measurements of 17 alpha-hydroxyprogesterone levels in serum and of urinary allo-tetrahydrocortisol and 17 alpha-hydroxypregnanolone after nafarelin treatment make this stimulation test a valuable diagnostic tool for identifying PCOS patients. The significant changes in the excretion of urinary androgen and gestagen metabolites, unmasked by GnRH agonist stimulation, suggest a functional alteration of the pituitary-ovarian axis. The reason for the increased excretion of glucocorticoid metabolites after nafarelin stimulation remains to be clarified.
为了评估使用促性腺激素释放激素(GnRH)激动剂那法瑞林检测多囊卵巢综合征(PCOS)患者垂体 - 卵巢反应的临床相关性,对19名PCOS女性和15名健康绝经前女性经鼻给予1.2mg剂量的那法瑞林。在长达24小时的测试期间,在几个时间点对血清和尿液中的类固醇进行后续分析。与对照组相比,PCOS患者在测试的所有时间点血清17α - 羟孕酮水平均升高[基线时,3.5±0.2 vs. 1.8±0.1 nmol/L(P <0.001);24小时时,9.9±0.9 vs. 4.9±0.3 nmol/L(P <0.001)]。患者组雄烯二酮的基础水平较高,但两组在测试期间均无显著变化。还发现PCOS患者的血清睾酮水平与基线时的对照值相比存在差异(2.2±0.2 vs. 1.5±0.1 nmol/L;P <0.05)以及那法瑞林治疗后(24小时时,3.2±0.4 vs. 1.8±0.2 nmol/L;P <0.05)。测试期间两组血清雌二醇水平均显著升高;PCOS患者测试后的水平显著高于对照组。PCOS患者在24小时内尿液中排泄的雄激素、孕激素代谢物以及糖皮质激素代谢物显著增加。在对照受试者中,除了17α - 羟孕烷醇酮显著升高外,所研究的尿类固醇在那法瑞林测试期间均未显示出相关变化。PCOS患者那法瑞林测试后尿中别 - 四氢皮质醇的排泄量(1.4±0.2 vs. 0.3±0.1 μmol/g肌酐;P <0.001)和17α - 羟孕烷醇酮排泄量的增加(1.4±0.2 vs. 0.3±0.1 μmol/g肌酐;P <0.001)明显高于对照组;这两个参数组合的诊断敏感性在特异性为93%时为89%。因此,测定血清中17α - 羟孕酮水平以及那法瑞林治疗后尿中别 - 四氢皮质醇和17α - 羟孕烷醇酮水平,使该刺激试验成为识别PCOS患者的有价值的诊断工具。GnRH激动剂刺激后尿雄激素和孕激素代谢物排泄的显著变化表明垂体 - 卵巢轴存在功能改变。那法瑞林刺激后糖皮质激素代谢物排泄增加的原因尚待阐明。