Ghizzoni L, Virdis R, Vottero A, Cappa M, Street M E, Zampolli M, Ibañez L, Bernasconi S
Department of Pediatrics, University of Parma, Italy.
J Clin Endocrinol Metab. 1996 Feb;81(2):601-6. doi: 10.1210/jcem.81.2.8636275.
To assess whether patients with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency exhibit a steroidogenic response to GnRH agonist consistent with functional ovarian hyperandrogenism (FOH) and elucidate the relationship between adrenal and ovarian hyperandrogenism, the LH, FSH, estradiol, 17-hydroxyprogesterone (17-OHP), androstenedione, total testosterone, dehydroepiandrosterone, and 17-hydroxypregnenolone responses to a sc dose of leuprolide acetate (500 micrograms) were evaluated in 10 patients with classic CAH (mean age, 18.4 +/- 0.95 yr), 7 of whom had oligomenorrhea, pretreated with dexamethasone (2 mg/day for 5 days, including the day of the test). The results were compared with those obtained in 11 patients with FOH (mean age, 18.7 +/- 0.46 yr) and 17 normal women (mean age, 19.68 +/- 0.59 yr) not pretreated with dexamethasone. Leuprolide acetate stimulation caused a significant augmentation of plasma E2, 17-OHP, androstenedione, testosterone, and 17-hydroxypregnenolone concentrations in all CAH patients. However, in only 6 (60%) of them, all with oligomenorrhea, was the 17-OHP response (posttest minus pretest value) similar to that of FOH patients and significantly higher than that in controls. In this subset of CAH patients, LH plasma levels after stimulation were significantly higher than those of CAH subjects with 17-OHP responses in the normal range, controls, and FOH patients, whereas FSH levels were similar to those of controls. In this latter group, plasma FSH concentrations after stimulation were significantly higher than those in FOH. In conclusion, the results of the present study indicate that LH-dependent functional ovarian hyperandrogenism is frequent in patients with classic CAH. As ovarian hyperandrogenism might be partially responsible for the menstrual irregularities that are common complications in such patients, all classic CAH patients with oligomenorrhea should undergo short term stimulation with GnRH agonists to ascertain the presence of ovarian hyperandrogenism and receive appropriate treatment.
为评估因21-羟化酶缺乏所致先天性肾上腺皮质增生症(CAH)患者是否表现出与功能性卵巢雄激素过多症(FOH)一致的对促性腺激素释放激素(GnRH)激动剂的类固醇生成反应,并阐明肾上腺与卵巢雄激素过多症之间的关系,对10例典型CAH患者(平均年龄18.4±0.95岁)进行了评估,其中7例有月经过少,在试验当天前用氟氢可的松预处理(2mg/天,共5天),评估皮下注射醋酸亮丙瑞林(500微克)后促黄体生成素(LH)、促卵泡生成素(FSH)、雌二醇、17-羟孕酮(17-OHP)、雄烯二酮、总睾酮、脱氢表雄酮和17-羟孕烯醇酮的反应。将结果与11例FOH患者(平均年龄18.7±0.46岁)和17例未用氟氢可的松预处理的正常女性(平均年龄19.68±0.59岁)的结果进行比较。醋酸亮丙瑞林刺激使所有CAH患者的血浆雌二醇、17-OHP、雄烯二酮、睾酮和17-羟孕烯醇酮浓度显著升高。然而,其中仅6例(60%),均有月经过少,其17-OHP反应(试验后减去试验前值)与FOH患者相似,且显著高于对照组。在这一CAH患者亚组中,刺激后LH血浆水平显著高于17-OHP反应在正常范围内的CAH受试者、对照组和FOH患者,而FSH水平与对照组相似。在后者组中,刺激后血浆FSH浓度显著高于FOH患者。总之,本研究结果表明,LH依赖性功能性卵巢雄激素过多症在典型CAH患者中很常见。由于卵巢雄激素过多症可能部分导致此类患者常见并发症月经不规律,所有有月经过少的典型CAH患者均应接受GnRH激动剂短期刺激以确定是否存在卵巢雄激素过多症并接受适当治疗。