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Performance characteristics of two immunoassays for the measurement of urinary luteinizing hormone

机译:两种测定尿中黄体生成素的免疫测定的性能特点

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摘要

Urine luteinizing hormone (LH) concentration is routinely measured in all anti-doping laboratories to exclude recoirfbinant LH abuse and to test any potential alteration of the hypophyseal-gonadal axis. Before establishing proper reference values among professional top level athletes, an extended validation of two commercial immunoassays for LH measurements was performed.Elecsys~R 1010 and Access~R are two automated immunoanalyzers for central laboratories. The limit of detection, the limit of quantification, intra-laboratory, inter-technique correlation, precision, accuracy were determined. Furthermore, reference urinary LH distribution values for male and female top level athletes were determined. Stability studies of LH in urine following freezing and thawing cycles (n = 3) as well as storage conditions at room temperature, 4 degC and -20 degC were performed.Male and female subjects showed important urinary corrected (specific gravity correction) LH distribution differences. Intra-assay precision for the Access~R analyzer was less than 8.0% whereas inter-assay was close to 11%. Intra and inter-assay precision for the Elecsys~R 1010 analyzer was slightly better. A good inter-technique correlation was obtained ([Elecsys~R 1010] = 1.0434[Access~R] + 1.146, R = 0.953). No urinary LH loss was observed after two freezing and thawing cycles. On the other hand, time and bad storage conditions such as elevated temperature can deteriorate rapidly urinary LH.In conclusion, both analyzers showed acceptable performances and are suitable for screening anti-doping analyses. Each anti-doping laboratory has to settle its own reference distribution values and then determine when to launch a confirmation procedure. This takes place then depending on the positivity criteria the anti-doping laboratory has established and validated. This study also clearly showed that the time delay between the urine collection and the analysis should be reduced as much as possible and urine samples should be transported in optimal conditions (low temperature and quickly) to decrease urinary LH deterioration.
机译:在所有反兴奋剂实验室中都常规测量尿液中的黄体生成激素(LH)浓度,以排除可再组合的LH滥用并检测下垂体-性腺轴的任何潜在变化。在建立专业顶级运动员的参考值之前,对两种用于LH测量的商业免疫分析方法进行了扩展验证。Elecsys〜R 1010和Access〜R是用于中央实验室的两种自动免疫分析仪。确定了检测限,定量限,实验室内,技术间的相关性,精度,准确性。此外,确定了男性和女性顶级运动员的参考尿LH分布值。进行冷冻和解冻(n = 3)循环后,尿液中LH的稳定性研究以及室温,4摄氏度和-20摄氏度下的储存条件进行了研究。男性和女性受试者显示出重要的尿液校正(比重校正)LH分布差异。 Access〜R分析仪的测定内精密度小于8.0%,而测定间精密度则接近11%。 Elecsys〜R 1010分析仪的批内和批间精密度略高。获得了良好的技术间相关性([Elecsys〜R 1010] = 1.0434 [Access〜R] + 1.146,R = 0.953)。在两个冷冻和解冻循环后,未观察到尿液LH损失。另一方面,时间和恶劣的储存条件(例如高温)会迅速使尿液中的LH恶化。总而言之,这两种分析仪均表现出可接受的性能,适用于筛选反掺杂分析。每个反兴奋剂实验室必须确定自己的参考分布值,然后确定何时启动确认程序。然后根据反兴奋剂实验室建立并验证的阳性标准进行检测。该研究还清楚地表明,应尽可能缩短尿液收集和分析之间的时间延迟,并应在最佳条件下(低温和快速)运输尿液样本,以减少尿液中LH的恶化。

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