Abstract

BackgroundThe manual Generation II (Gen II) ELISA method used to measure Anti-Müllerian Hormone (AMH) from Beckman Coulter has recently been superseded by a fully automated AMH immunoassay. The aim of this study was to evaluate the performance of the Access AMH assay and directly compare it to the modified Gen II ELISA method. A secondary aim was to verify that the fertile age-related AMH range previously established using the Gen II ELISA could be used to interpret results from the new automated Access assay.MethodsThe precision, stability, linearity, measurement range and detection limits were determined using recombinant AMH and patient serum samples. Different diluents and their effects on AMH concentration were compared. A correlation study was performed on patient samples to compare the Access AMH assay to the ELISA method on the Access2 and DxI800 analysers. The fertile AMH range was verified by comparing the 10th, 50th and 90th percentile values from both methods obtained from 489 natural conception pregnant women.ResultsThe Access AMH assay showed good performance across the measuring range for both intra-assay (CV 1.41–3.30 %) and inter-assay (CV 3.04–5.76 %) precision and acceptable sample stability. Dilution of the high concentration samples with the recommended diluent resulted in a small but significant downward shift in values. The assay was linear over the range of values recommended by the manufacturer, allowing for accurate reporting within the reported range. The two assay types were highly correlated (R2 = 0.9822 and 0.9832 for Access2 and DxI800, respectively), and the differences observed between the Access2 and DxI800 analysers were within clinically acceptable ranges, indicating that the methods are interchangeable. Furthermore, we demonstrated that results from the published reference range for the Gen II ELISA correlate with those from the automated Access AMH assay.ConclusionHere, we verified the published performance of the Access AMH assay and showed excellent correlation with the Gen II ELISA method. Moreover, we validated this correlation by confirming that the results from a fertile AMH reference range established using the preceding Gen II ELISA are interchangeable with the new automated Access AMH assay.Electronic supplementary materialThe online version of this article (doi:10.1186/s12958-016-0143-3) contains supplementary material, which is available to authorized users.

Highlights

  • The manual Generation II (Gen II) enzyme-linked immunosorbent assay (ELISA) method used to measure Anti-Müllerian Hormone (AMH) from Beckman Coulter has recently been superseded by a fully automated AMH immunoassay

  • Assay precision was evaluated for both intra- and inter-run precision using AMH quality control (QC) material consisting of human recombinant AMH (Beckman Coulter) at three known concentrations

  • Precision The Access assay showed good performance across the measuring range for the Access AMH Assay on both the Access2 and DxI800 instruments (Table 1)

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Summary

Introduction

The manual Generation II (Gen II) ELISA method used to measure Anti-Müllerian Hormone (AMH) from Beckman Coulter has recently been superseded by a fully automated AMH immunoassay. Anti-Müllerian hormone (AMH) is expressed by the ovarian granulosa cells of the female ovary where it has important autocrine and paracrine regulator functions in follicle development It is predominantly produced by the pre-antral and small antral follicles, and production declines during the final maturation process and luteal phase [1]. AMH serum concentration has emerged as a unique biological marker for the size of the residual follicular pool that exhibits high correlation with ovarian reserve [10]. This single blood test can assist in the prediction of ovarian response to stimulation, aid in the diagnosis of polycystic ovary syndrome (PCOS) and predict premature ovarian failure, among other uses [11,12,13,14]

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