Comparison of automated methods for the determination of antimüllerian hormone in women.

Andreea Ion, Julie Brossaud, Jean-Benoît Corcuff, Cindy Lauro, Agnès Georges
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Abstract

Antimüllerian hormone (AMH), a protein secreted by granulosa cells, is a quantitative marker of the ovarian reserve. Due to its clinical value, the anti-müllerian hormone is a test highly prescribed by doctors, especially in the medically assisted procreation (MAP) department. The antral follicle count (AFC) and the result of the AMH test, are systematically evaluated during a fertility preservation consultation and also as part of the monitoring of ovarian function. Different methods for the measurement of AMH level exist, but none of them is currently available in our hormonology laboratory at Bordeaux University Hospital. The introduction of one of these technical assays in our laboratory could shorten the delay of reaching the result. According to our objectives, our study made it possible to observe the performance and analytical limits of the Biomerieux and Fujirebio technology, by comparing it with Roche technology, known as the reference, by analysing 50 AMH samples, on each of them and evaluating the results. In our study, despite a good agreement between the three assay methods, the importance of an international standard from a diagnostic point of view was once again noted. National medical commissions do strongly insist on the need of setting up an international standard in order to facilitate the development of reference values, decrease inter-laboratory variability and the cost due to repeated assays, as well as to improve patient safety by avoiding poor estimation of values.

妇女抗勒氏杆菌激素自动测定方法的比较。
勒氏激素(AMH)是一种由颗粒细胞分泌的蛋白质,是卵巢储备的定量标志。由于其临床价值,抗勒氏杆菌激素是医生经常开具的测试,特别是在医学辅助生殖(MAP)部门。输卵管卵泡计数(AFC)和AMH测试的结果,在生育保留咨询期间进行系统评估,也作为卵巢功能监测的一部分。测量AMH水平的方法不同,但目前在波尔多大学医院的激素实验室没有一种方法可用。在我们实验室引入其中一种技术分析方法可以缩短得出结果的延迟。根据我们的目标,我们的研究通过分析50个AMH样品并评估结果,将生物梅里埃和富士生物技术与罗氏技术(称为参考技术)进行比较,从而观察生物梅里埃和富士生物技术的性能和分析极限。在我们的研究中,尽管三种测定方法之间有很好的一致性,但从诊断的角度来看,再次注意到国际标准的重要性。国家医学委员会确实坚决坚持有必要制定一项国际标准,以促进参考值的制定,减少实验室间的差异和由于重复化验而造成的成本,并通过避免对值的错误估计来改善患者的安全。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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