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首页> 外文期刊>Human Reproduction >FSH, LH, inhibin B and estradiol levels in Turner syndrome depend on age and karyotype: longitudinal study of 70 Turner girls with or without spontaneous puberty.
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FSH, LH, inhibin B and estradiol levels in Turner syndrome depend on age and karyotype: longitudinal study of 70 Turner girls with or without spontaneous puberty.

机译:特纳综合征中的FSH,LH,抑制素B和雌二醇水平取决于年龄和核型:对70名具有或没有自发青春期的特纳女孩的纵向研究。

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摘要

BACKGROUND: Ovarian function in Turner syndrome (TS) patients depends on the specific karyotype. This retrospective clinical study evaluates the pituitary-gonadal axis during infancy, childhood and adolescence in TS patients according to karyotype and ovarian function. METHODS: A cohort of 70 TS patients (0-16 years) followed at a tertiary referral centre for paediatric endocrinology were included. Longitudinal measurements of reproductive hormones (FSH, LH, inhibin B and estradiol) prior to hormonal replacement treatment in 66 patients related to karyotype (A, 45,X; or B, miscellaneous karyotypes) and ovarian function (spontaneous puberty or absent spontaneous puberty) were compared with an age-matched reference range of 2406 healthy Danish females. RESULTS: The prevalence of spontaneous puberty was 6% for 45,X and 54% for miscellaneous karyotypes, P = 0.001. In all TS patients, gonadotrophins were higher during infancy and at expected puberty compared with levels at mid-childhood, where 21/25 and 23/27 had FSH and LH levels, respectively, within the reference range. In patients with absent spontaneous puberty, 10/12 had FSH in the reference range during the mid-childhood nadir. 45,X-TS patients had undetectable inhibin B at 0-16 years. Ovarian failure was predicted in 20/20 patients with exclusively undetectable inhibin B, while 9/10 with detectable inhibin B entered puberty spontaneously. Estradiol levels were elevated from 4 to 8 years. CONCLUSIONS: Ovarian function in TS patients is associated with the specific karyotype, and multiple undetectable inhibin B values during mid-childhood may predict absence of spontaneous puberty, although the specificity of the test is low. The biphasic age pattern of gonadotrophins was preserved in all patients, and spontaneous gonadotrophins are not useful as a diagnostic marker for TS in girls aged 6-10 years.
机译:背景:特纳综合征(TS)患者的卵巢功能取决于特定的核型。这项回顾性临床研究根据核型和卵巢功能评估了TS患者在婴儿期,儿童期和青春期的垂体-性腺轴。方法:包括70例TS患者(0-16岁),其后在三级转诊中心进行儿科内分泌学检查。在激素替代治疗之前,对66名与核型(A,45,X或B,其他核型)和卵巢功能(自发青春期或自发性青春期不相关)的患者进行激素替代治疗之前生殖激素(FSH,LH,抑制素B和雌二醇)的纵向测量与年龄相匹配的2406名丹麦健康女性的参考范围进行了比较。结果:45,X的自发青春期患病率为6%,其他核型的自发青春期患病率为54%,P = 0.001。在所有TS患者中,与儿童中期时的水平相比,婴儿期和预期青春期的促性腺激素水平更高,其中21/25和23/27的FSH和LH水平分别在参考范围内。在没有自发青春期的患者中,在儿童中期最低点时10/12的FSH在参考范围内。 45,X-TS患者在0-16岁时检测不到抑制素B。预测有20/20抑制素B完全检测不到的卵巢衰竭,而抑制素B可检测到的9/10则自发进入青春期。雌二醇水平从4年提高到8年。结论:TS患者的卵巢功能与特定的核型有关,尽管测试的特异性较低,但在儿童中期,多个无法检测到的抑制素B值可能预示着自发青春期的消失。所有患者均保留了促性腺激素的双相年龄模式,并且自发性促性腺激素不能用作6-10岁女孩的TS诊断标志。

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