[13.5-17岁青春期男性促性腺功能减退与青春期体质延迟的鉴别诊断新方法]。

Y L Skorodok, I Y Ioffe, E V Plotnikova, I I Nagornaya, L A Zhelenina, A V Kozhevnikova
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引用次数: 0

摘要

背景:促性腺功能减退(HH)和青春期体质延迟(CDP)的鉴别诊断是非常重要的,因为青春期的开始和结束没有任何医疗干预,在HH的情况下青春期没有发生或不完全。未能及时开始治疗导致患者的医疗和心理社会失调。目的:建立一种通过LH、FSH、睾酮和抑制素b水平评分来鉴别13.5-17岁男孩促性腺功能减退和体质性青春期延迟的方法。材料和方法:研究组由13.5-17岁的青春期延迟男性组成,包括所有观察结果。评估记忆、青春期分期、睾丸体积;化学发光法测定血清LH、FSH、睾酮(T)水平,ELISA法测定血清抑制素B、AMH水平。用雷普肾上腺素和人绒毛膜促性腺激素进行刺激试验(3天)。随访6 ~ 24个月。结果:本研究纳入年龄在13.5-17岁的青春期延迟男性青少年,其中56例为鉴别诊断方法,30例为对照组。我们已经创建了一种方法,可以区分HH和CDP。通过roc分析,确定了最敏感和特异的HH标记。LH、FSH、T和抑制素B的基础水平被选为门诊检测的最有效指标。根据我们自己的研究结果和科学数据,我们选择了数值范围,并根据它们对LH, FSH, T和抑制素B进行评分(分数)。然后我们为每种激素分配系数(k)。通过将分数乘以k来计算分数,然后将其求和并归一化为患者可以获得的最大分数。为了提高诊断的准确性,引入了年龄系数。计算结果为评分(S)的结果。CDP(10.65[3.13-14.91])与HH(76.46[57.79-83.74])的S差异有统计学意义(p<;0.001)。对照组有97%的病例经随访资料确诊为S (<;21.16和≥55.07)。本文提出了一种基于S的HH和CDP鉴别诊断算法。结论:LH、FSH、睾酮、抑制素B评分≥55.07可诊断促性腺功能减退症;21.16 -体质性青春期延迟的可能性很大。在得分≥21.16的情况下,但<;55.07,抑制素B/AMH比值的计算和/或刺激试验是必需的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

[A new way for the differential diagnosis of hypogonadotropic hypogonadism and constitutional delay of puberty in adolescent men aged 13.5-17 years].

[A new way for the differential diagnosis of hypogonadotropic hypogonadism and constitutional delay of puberty in adolescent men aged 13.5-17 years].

[A new way for the differential diagnosis of hypogonadotropic hypogonadism and constitutional delay of puberty in adolescent men aged 13.5-17 years].

[A new way for the differential diagnosis of hypogonadotropic hypogonadism and constitutional delay of puberty in adolescent men aged 13.5-17 years].

Background: Differential diagnosis of hypogonadotropic hypogonadism (HH) and constitutional delay of puberty (CDP) is extremely important since with the latter puberty begins and completes without any medical intervention and in the case of HH puberty does not occur or is incomplete. Failure to start treatment on time leads to medical and psychosocial maladjustment of the patient.

Aim: Development of a method for differential diagnosis of hypogonadotropic hypogonadism and constitutional delay of puberty in boys 13.5-17 years old by scoring the levels of LH, FSH, testosterone and inhibin B.

Materials and methods: The study group was formed by adolescent men 13.5-17 years old with delayed puberty including all observations. Anamnesis, stage of puberty, testicular volume were assessed; serum levels of LH, FSH, testosterone (T) were determined by chemiluminescent analysis and inhibin B, AMH by ELISA. Stimulation tests were performed with triptorelin and human chorionic gonadotropin (3 days). Patients were followed up for 6-24 months.

Results: The study included adolescent men at the age of 13.5-17 years with delayed puberty: 56 for the purpose of development a method of differential diagnosis, 30 for its control (control group). We`ve created a method that allows differentiate HH and CDP. Through the ROC-analysis the most sensitive and specific HH markers were identified. The basal levels of LH, FSH, T, and inhibin B were selected as most available for outpatient testing. Based on the results of our own research and scientific data we selected ranges of values and rated LH, FSH, T and inhibin B depending on them (marks). Then we assigned the coefficients (k) for each hormone. Scores were calculated by multiplying the marks by k then summed and normalized to the maximum amount the patient could get. To increase the accuracy of diagnosis an age coefficient was introduced. The result of the calculation was the result of the scoring (S). S for CDP (10.65 [3.13-14.91]) differed significantly from that for HH (76.46 [57.79-83.74]) (p< 0.001). Diagnoses based on S (<21.16 and ≥55.07) in the control group were confirmed by follow up data in 97% cases. An algorithm for the differential diagnosis of HH and CDP by using S has been developed.

Conclusion: The result of scoring of LH, FSH, testosterone, inhibin B levels ≥55.07 makes it possible to diagnose hypogonadotropic hypogonadism, < 21.16 - constitutional delay of puberty with a high probability. In the case of score ≥21.16 but < 55.07, calculation of the inhibin B/AMH ratio and/or stimulation tests are required.

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