Skip Navigation



Human Reproduction Update Advance Access published online on September 30, 2009

Human Reproduction Update, doi:10.1093/humupd/dmp036
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by La Marca, A.
Right arrow Articles by Volpe, A.
PubMed
Right arrow PubMed Citation
Right arrow Articles by La Marca, A.
Right arrow Articles by Volpe, A.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2009. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Anti-Müllerian hormone (AMH) as a predictive marker in assisted reproductive technology (ART)

A. La Marca1,3, G. Sighinolfi1, D. Radi1, C. Argento1, E. Baraldi1, A. Carducci Artenisio2, G. Stabile2 and A. Volpe1

1 Mother-Infant Department, Section of Obstetrics and Gynecology, University of Modena and Reggio Emilia, Policlinico of Modena, Via del Pozzo, 71, 41100 Modena, Italy 2 Department of Medicine and Pharmacology, University of Messina, Messina, Italy

To whom correspondence should be addressed at: 3 Correspondence address. Tel: +39-059-422-4379; Fax: +39-059-422-4394; E-mail: antlamarca{at}libero.it

BACKGROUND: In women, anti-Müllerian hormone (AMH) levels may represent the ovarian follicular pool and could be a useful marker of ovarian reserve. The clinical application of AMH measurement has been proposed in the prediction of quantitative and qualitative aspects in assisted reproductive technologies (ART). In men AMH is secreted in both the serum and seminal fluid. Its measurement may be useful in clinical evaluation of the infertile male.

METHODS: The PubMed database was systematically searched for studies published until the end of January 2009, search criteria relevant to AMH, ovarian reserve, ovarian response to gonadotrophin stimulation, spermatogenesis and azoospermia were used.

RESULTS: AMH seems to be a better marker in predicting ovarian response to controlled ovarian stimulation than age of the patient, FSH, estradiol and inhibin B. A similar performance for AMH and antral follicular count has been reported. In clinical practice, AMH measurement may be useful in the prediction of poor response and cycle cancellation and also of hyper-response and ovarian hyperstimulation syndrome. In the male, the wide overlap of AMH values between controls and infertile men precludes this hormone from being a useful marker of spermatogenesis.

CONCLUSIONS: As AMH may permit the identification of both the extremes of ovarian stimulation, a possible role for its measurement may be in the individualization of treatment strategies in order to reduce the clinical risk of ART along with optimized treatment burden. It is fundamental to clarify the cost/benefit of its use in ovarian reserve testing. Regarding the role of AMH in the evaluation of infertile men, AMH as single marker of spermatogenesis does not seem to reach a satisfactory clinical utility.

Key words: AMH / ART / COS / poor response / OHSS / azoospermia

Received on February 11, 2009; revised August 21, 2009; accepted on August 26, 2009


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.