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Diagnostic significance of salivary testosterone measurement revisited: using liquid chromatography/mass spectrometry and enzyme-linked immunosorbent assay

机译:唾液睾丸激素测定的诊断意义:液相色谱/质谱和酶联免疫吸附测定

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Background & Objectives: The use of saliva as a material for screening biomarkers has several advantages in the study of large research populations. Since testosterone is not bound to protein in saliva, salivary testosterone determination provides an excellent approach for the evaluation of serum bioavailable or free testosterone. Liquid chromatography/mass spectrometry (LC-MS) has been considered to be a gold standard for estimating serum total testosterone levels in male serum. Our objective was to evaluate the reliability of salivary testosterone levels as measured by LC-MS. We also investigated the association between salivary testosterone measured by LC-MS and that measured by enzyme-linked immunosorbent assay (ELISA) in order to evaluate the clinical application for ELISA measures.Methods: The study involved 51 healthy male volunteers (median age = 57 years old; range = 30-85 years) and 29 patients with late-onset hypogonadism (LOH) (median age = 65 years; range = 55-78 years) in order to include a wide range of testosterone levels (median age of all subjects = 65 years; range = 30-85 years). Serum total testosterone was measured using LC-MS, and sex hormone binding globulin (SHBG) by immunoradiometric assay. Serum free testosterone and bioavailable testosterone levels were calculated using an international formula. Salivary testosterone levels were measured using LC-MS and ELISA.Results: Salivary testosterone levels measured by LC-MS were in accordance with calculated serum free testosterone levels (r = 0.655, p < 0.001, y = 0.91x + 27.04; where x is the salivary testosterone measured by LC-MS and y is the calculated free testosterone). Salivary testosterone measured by LC-MS and ELISA showed a strong correlation (r = 0.808, p < 0.001).Conclusion: Salivary testosterone measured by LC-MS and ELISA is a non-invasive, reliable substitute for serum calculated free or bioavailable testosterone.
机译:背景与目的:在大量研究人群的研究中,使用唾液作为筛选生物标志物的材料具有多个优势。由于睾丸激素不与唾液中的蛋白质结合,因此唾液中睾丸激素的测定为评估血清生物利用度或游离睾丸激素提供了一种极好的方法。液相色谱/质谱法(LC-MS)被认为是估计男性血清中血清总睾丸激素水平的金标准。我们的目标是评估通过LC-MS测量的唾液睾丸激素水平的可靠性。我们还调查了LC-MS测定的唾液睾丸激素与酶联免疫吸附测定(ELISA)测定的唾液睾丸激素之间的联系,以评估ELISA措施的临床应用。方法:本研究涉及51名健康男性志愿者(中位年龄= 57岁)岁;范围= 30-85岁)和29例迟发性性腺功能减退(LOH)患者(中位年龄= 65岁;范围= 55-78岁),以包括广泛范围的睾丸激素水平(所有患者的中位年龄)受试者= 65岁;范围= 30-85岁)。使用LC-MS测定血清总睾丸激素,并通过免疫放射分析法测定性激素结合球蛋白(SHBG)。使用国际公式计算无血清睾丸激素和可利用的睾丸激素水平。结果:通过LC-MS测定的唾液睾丸激素水平符合计算的血清游离睾丸激素水平(r = 0.655,p <0.001,y = 0.91x + 27.04;其中x为(LC-MS测得的唾液睾丸激素,y为计算出的游离睾丸激素)。 LC-MS和ELISA测定的唾液睾丸激素呈强相关性(r = 0.808,p <0.001)。

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