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一种用于检测儿童促性腺激素的临床实用方法:通过超灵敏时间分辨免疫荧光分析法评估尿中的黄体生成素和卵泡刺激素作为血清检测的替代方法。

A clinically useful method for detecting gonadotropins in children: assessment of luteinizing hormone and follicle-stimulating hormone from urine as an alternative to serum by ultrasensitive time-resolved immunofluorometric assays.

作者信息

Demir A, Alfthan H, Stenman U H, Voutilainen R

机构信息

Department of Pediatrics, Helsinki University Central Hospital, Finland.

出版信息

Pediatr Res. 1994 Aug;36(2):221-6. doi: 10.1203/00006450-199408000-00014.

Abstract

To study the feasibility of noninvasive sampling in pediatric patients, we examined the concentrations of LH and FSH in paired serum and urine samples from 65 children (age 0-15 y) with highly sensitive time-resolved immunofluorometric assays. The detection limits of the assays were 0.015 IU/L for LH and 0.018 IU/L for FSH. These sensitivity levels allowed quantification of the low prepubertal LH and FSH concentrations. The correlation between serum and urine gonadotropin values was very good (r = 0.751, p < 0.001 for FSH; and r = 0.720, p < 0.001 for LH), and the urine and serum concentrations were very similar. Correction of urinary gonadotropin concentrations for changes in urinary flow by standard methods using density [concentration x (0.02/density-1)] or creatinine (concentration/creatinine) did not improve the correlation. Therefore, measurement of urinary gonadotropins without correction can simply be used in the pediatric outpatient setting as a noninvasive alternative to serum determinations.

摘要

为研究儿科患者无创采样的可行性,我们采用高灵敏度时间分辨免疫荧光分析法检测了65名0至15岁儿童配对的血清和尿液样本中促黄体生成素(LH)和促卵泡生成素(FSH)的浓度。该检测方法对LH的检测限为0.015 IU/L,对FSH的检测限为0.018 IU/L。这些灵敏度水平能够对青春期前较低的LH和FSH浓度进行定量分析。血清和尿液中促性腺激素值之间的相关性非常好(FSH:r = 0.751,p < 0.001;LH:r = 0.720,p < 0.001),且尿液和血清浓度非常相似。使用密度[浓度×(0.02/密度 - 1)]或肌酐(浓度/肌酐)的标准方法对尿流量变化进行校正后,并未改善促性腺激素浓度的相关性。因此,在儿科门诊环境中,无需校正即可测量尿促性腺激素,作为血清检测的无创替代方法。

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