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在一例特发性下丘脑性性腺功能减退患者中,促性腺激素治疗继发产生抗人绒毛膜促性腺激素抗体相关的甲状腺功能减退。

Hypothyroidism associated with anti-human chorionic gonadotropin antibodies secondarily produced by gonadotropin therapy in a case of idiopathic hypothalamic hypogonadism.

作者信息

Ogura T, Mimura Y, Otsuka F, Kishida M, Yokota K, Suzuki J, Nagai A, Hirakawa S, Makino H, Tobe K

机构信息

Health and Medical Center, Okayama University Graduate School of Medicine and Dentistry, Okayama 700-8558, Japan.

出版信息

J Endocrinol Invest. 2003 Nov;26(11):1128-35. doi: 10.1007/BF03345263.

Abstract

We report a 22-yr-old male patient with idiopathic hypothalamic hypogonadism who showed secondary resistance to gonadotropin (Gn) therapy over 3 yr after successful treatment with hCG combined with human menopausal Gn. The patient simultaneously developed subclinical hypothyroidism. Endocrine examination revealed low levels of testosterone (0.3 ng/ml), free T4 (0.91 ng/dl), and increased levels of TSH (31.1 microU/ml) in the serum. Serum autoantibodies to thyroid gland were all negative. Interestingly, thyroid function was improved after discontinuation of Gn therapy. In vitro assays by immunoprecipitation using 125I-hCG or 125I-TSH elucidated the presence of anti-hCG antibody in the serum 13 months after commencement of Gn therapy but anti-TSH antibody was not detected in the serum. Furthermore, the anti-hCG antibody specifically bound to hCG but not to other glycoproteins including TSH and FSH based on a competitive displacement assay. Bioassays using porcine thyroid cells revealed that the serum gamma-globulin fraction enables the suppression of cyclic AMP (cAMP) synthesis stimulated by TSH. Our findings suggest that anti-hCG and/or anti-idiotypic hCG antibodies induced by hCG therapy impaired TSH-dependent cAMP production through interfering with binding of TSH to its receptor, and this resulted in subclinical hypothyroidism in this patient.

摘要

我们报告一例22岁患有特发性下丘脑性性腺功能减退的男性患者,该患者在接受人绒毛膜促性腺激素(hCG)联合人绝经期促性腺激素(Gn)成功治疗3年后,对促性腺激素(Gn)治疗出现继发性抵抗。该患者同时发生了亚临床甲状腺功能减退。内分泌检查显示血清中睾酮水平低(0.3 ng/ml)、游离T4水平低(0.91 ng/dl),促甲状腺激素(TSH)水平升高(31.1 μU/ml)。甲状腺自身抗体均为阴性。有趣的是,停用Gn治疗后甲状腺功能得到改善。在Gn治疗开始13个月后,通过使用125I-hCG或125I-TSH进行免疫沉淀的体外试验,在血清中发现了抗hCG抗体,但在血清中未检测到抗TSH抗体。此外,基于竞争性置换试验,抗hCG抗体特异性结合hCG,但不结合包括TSH和FSH在内的其他糖蛋白。使用猪甲状腺细胞的生物测定显示,血清γ球蛋白组分能够抑制TSH刺激的环磷酸腺苷(cAMP)合成。我们的研究结果表明,hCG治疗诱导的抗hCG和/或抗独特型hCG抗体通过干扰TSH与其受体的结合,损害了TSH依赖性cAMP的产生,这导致了该患者的亚临床甲状腺功能减退。

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