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Journal of Clinical Endocrinology & Metabolism , doi:10.1210/jc.2005-2076
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The Journal of Clinical Endocrinology & Metabolism Vol. 91, No. 3 941-945
Copyright © 2006 by The Endocrine Society

Serum Anti-Müllerian Hormone as a Surrogate for Antral Follicle Count for Definition of the Polycystic Ovary Syndrome

P. Pigny, S. Jonard, Y. Robert and D. Dewailly

Laboratoire de Biochimie et Hormonologie (P.P.), Parc Eurasanté; Service de Gynécologie Endocrinienne et de Médecine de la Reproduction (S.J., D.D.), Hôpital Jeanne de Flandre; and Service de Radiologie, Hôpital Jeanne de Flandre (Y.R.), Centre Hospitalier Régional Universitaire de Lille, F-59037 Lille, France

Address all correspondence and requests for reprints to: P. Pigny, Laboratoire de Biochimie et Hormonologie, Parc Eurasanté, Centre Hospitalier Régional Universitaire, 59037 Lille cedex, France. E-mail: p-pigny{at}chru-lille.fr

Context: Despite its frequency, the polycystic ovary syndrome (PCOS) is still a difficult diagnosis in endocrinology, gynecology, and reproductive medicine. To help solve this issue, the Rotterdam consensus conference proposed to include the ultrasonographic follicle count as a new diagnostic criterion, in addition to hyperandrogenism and oligo-anovulation. Unfortunately, its assessment does not offer sufficient reliability worldwide.

Objective: The aim of our study was to check whether anti-Müllerian hormone (AMH) measurement in the serum could be a surrogate for antral follicle count in the diagnostic criteria of PCOS.

Design, Setting, and Patients: Serum AMH was measured with a second-generation immunoassay in a cohort of 73 PCOS patients and 96 controls, and its diagnostic power was evaluated by receiver operating characteristic curves. PCOS was diagnosed according to the Rotterdam definition.

Results: Serum AMH levels were 3-fold higher in PCOS patients than in controls (81.6 vs. 33.5 pmol/liter; P < 0.001) and were significantly related to the follicle number in the two groups. The area under the receiver operating characteristic curve for the AMH assay was 0.851, indicating a good diagnostic potency. Setting the threshold at 60 pmol/liter offered the best compromise between specificity (92%) and sensitivity (67%).

Conclusions: The serum AMH level is an accurate marker of the ovarian early antral follicle number and offers a good diagnostic potency. In situations where accurate ultrasonographic data are not available, AMH could thus be used instead of the follicle count as a diagnostic criterion and incorporated as such in the Rotterdam definition of PCOS.




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