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特发性低促性腺激素性性腺功能减退男性促性腺激素释放激素分泌异常模式谱:临床与实验室相关性

The spectrum of abnormal patterns of gonadotropin-releasing hormone secretion in men with idiopathic hypogonadotropic hypogonadism: clinical and laboratory correlations.

作者信息

Spratt D I, Carr D B, Merriam G R, Scully R E, Rao P N, Crowley W F

出版信息

J Clin Endocrinol Metab. 1987 Feb;64(2):283-91. doi: 10.1210/jcem-64-2-283.

Abstract

Several lines of evidence indicate that hypothalamic-pituitary-gonadal activity varies among men with idiopathic hypogonadotropic hypogonadism (IHH). To test the hypothesis that a spectrum of abnormalities of GnRH secretion underlies the syndrome of IHH, we characterized the patterns of GnRH-induced gonadotropin secretion during periods of frequent sampling in 50 consecutive men with IHH and contrasted them with those in 20 normal men. The largest group of IHH patients (n = 42) had no detectable LH or FSH pulsations and could be categorized into 2 subsets according to the presence or absence of evidence of spontaneous puberty. The most severely affected subset (n = 32), who recalled no history of puberty, had testes with a mean volume of 3.3 +/- 0.5 (+/- SEM) ml, with a prepubertal appearance on biopsy, and often were anosmic (n = 17). The second subset of apulsatile IHH men (n = 10) had histories of partial or complete spontaneous sexual development with subsequent isolated loss of sexual function, testes with a mean volume of 13.3 +/- 1.9 ml (P less than 0.01 compared to the first subset), a pubertal or adult appearance of the testes on biopsy, and an intact sense of smell. In a second group of IHH patients (n = 3), LH was secreted predominantly in a nighttime pattern similar to that of normal children during early puberty. These men were aged 18-24 yr, had a mean testicular volume of 10.5 +/- 2.3 ml, pubertal changes on testicular biopsy, and an intact sense of smell. A third group of IHH men (n = 4) had LH pulses of abnormally low amplitude. Only one patient in this group had a history of spontaneous sexual development. The mean testicular volume of these patients was 5.6 +/- 1.9 ml, and the testes appeared prepubertal (n = 3) or pubertal (n = 1) on biopsy. In addition to these groups, another patient had apparent LH pulsations and nearly normal amplitude, but the LH was bioinactive and appeared to consist chiefly of alpha-subunit. Testing of other anterior pituitary hormone functions did not distinguish IHH men from normal men. However, those IHH patients with some evidence of endogenous GnRH secretion had higher basal and stimulated serum PRL levels than IHH men without such evidence (P less than 0.05), suggesting an influence of GnRH on PRL secretion.

摘要

多项证据表明,特发性低促性腺激素性性腺功能减退(IHH)男性的下丘脑 - 垂体 - 性腺活动存在差异。为了验证GnRH分泌异常谱是IHH综合征基础这一假设,我们对50例连续的IHH男性在频繁采样期间GnRH诱导的促性腺激素分泌模式进行了特征描述,并将其与20例正常男性的模式进行对比。最大的一组IHH患者(n = 42)未检测到LH或FSH脉冲,可根据是否有自发青春期的证据分为2个亚组。受影响最严重的亚组(n = 32),回忆不起青春期病史,睾丸平均体积为3.3±0.5(±SEM)ml,活检显示为青春期前外观,且常为嗅觉缺失(n = 17)。无脉冲性IHH男性的第二个亚组(n = 10)有部分或完全自发的性发育史,随后出现性功能孤立丧失,睾丸平均体积为13.3±1.9 ml(与第一个亚组相比,P < 0.01),活检显示睾丸为青春期或成人外观,且嗅觉正常。在第二组IHH患者(n = 3)中,LH主要以夜间模式分泌,类似于青春期早期正常儿童的模式。这些男性年龄在18 - 24岁,睾丸平均体积为10.5±2.3 ml,睾丸活检有青春期变化,且嗅觉正常。第三组IHH男性(n = 4)LH脉冲幅度异常低。该组中只有1例患者有自发的性发育史。这些患者的睾丸平均体积为5.6±1.9 ml,活检显示睾丸为青春期前(n = 3)或青春期(n = 1)外观。除了这些组外,另1例患者有明显的LH脉冲且幅度接近正常,但LH无生物活性,似乎主要由α亚基组成。对其他垂体前叶激素功能的检测并未区分IHH男性与正常男性。然而,那些有内源性GnRH分泌证据的IHH患者,其基础和刺激后的血清PRL水平高于无此类证据的IHH男性(P < 0.05),提示GnRH对PRL分泌有影响。

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