THE VALUE OF ANTI-MÜLLERIAN HORMONE IN THE DIAGNOSIS OF POLYCYSTIC OVARY SYNDROME


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Abstract

Objective. To estimate the value of anti-Müllerian hormone (AMH) for the diagnosis of polycystic ovary syndrome (PCOS) and the possible characteristics of its secretion in various phenotypes of the syndrome. Subjects and methods. The investigation enrolled 502 reproductive-aged women, including 250 patients aged 25.4±4.2 years (body mass index (BMI), 24.2±5.6 kg/m2) with PCOS and 252 women (aged 25,2±3,8years; BMI, 24.2±5.6 kg/m2) without reproductive dysfunction. Four phenotypes of the syndrome were identified using the Rotterdam criteria. Phenotypes A, B, C, and D were detected in 58, 10.4, 6.4, and 25.2% of the women, respectively. The investigators made complex clinical and laboratory examinations, including small pelvic ultrasound and a study of the androgen profile, AMH, luteinizing hormone, follicle-stimulating hormone, prolactin, and thyroid-stimulating hormone. Results. The mean serum AMH level in the healthy women and women with PCOS was 3.3±1.9 and15.8±10.2ng/ml, respectively (p < 0.05). The highest AMH level (17.9±11.6 ng/ml) was found in the women with phenotype A as compared with other phenotypes of the syndrome (p < 0.05). ROC analysis revealed that the threshold level of AMH for the diagnosis of PCOS was 5.2 ng/ml (an AUC of 0.97, a sensitivity of 95%, a specificity of 92%, and a confidence interval (CI)) of 95%). Conclusion. The AMH level exceeding 5.2 ng/ml can be considered as a threshold in the diagnosis of PCOS regardless of the phenotype of the syndrome. The elevated serum level of AMH is a more specific and sensitive diagnostic criterion for PCOS than enlarged ovaries.

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About the authors

A. A NAIDUKOVA

Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health of Russia

Email: aleeshka@mail.ru
post-graduate, department of gynecological endocrinology Moscow 117997, Ac. Oparina str. 4, Russia

E. K KAPRINA

Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health of Russia

post-graduate department of gynecological endocrinology Moscow 117997, Ac. Oparina str. 4, Russia

T. Yu IVANETS

Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health of Russia

Email: t_ivanetz@oparina4.ru
PhD, Head of Research and diagnostic laboratory Moscow 117997, Ac. Oparina str. 4, Russia

G. E CHERNUKHA

Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health of Russia

Email: g_chernukha@oparina4.ru
a doctor of medical sciences, professor, head of department of Gynecological Endocrinology Moscow 117997, Ac. Oparina str. 4, Russia

References

  1. Diamanti-Kandarakis E., Dunaif A. Insulin resistance and the polycystic ovary syndrome revisited: an update on mechanisms and implications. Endocr. Rev. 2012; 33(6): 981-1030.
  2. Fauser B.C.J.M., Tarlatzis B.C., Rebar R.W., Legro R.S., Balen A.H., Lobo R. et al. Consensus on women’s health aspects of polycystic ovary syndrome (PCOS): the Amsterdam ESHRE/ASRM-Sponsored 3rd PCOS Consensus Workshop Group. Fertil. Steril. 2012; 97(28-38): e25.
  3. Dewailly D., Andersen C.Y., Balen A., Broekmans F., Dilaver N., Fanchin R. et al. The physiology and clinical utility of anti-Müllerian hormone in women. Hum. Reprod. Update. 2014; 20(3): 370-85.
  4. Pellatt L., Rice S., Dilaver N., Heshri A., Galea R., Brincat M. et al. Anti-Müllerian hormone reduces follicle sensitivity to folliclestimulating hormone in human granulosa cells. Fertil. Steril. 2011; 96(5): 1246-51. e1241.
  5. Попова П.В., Рязанцева Е.М., Рулёва О.Е., Зазерская И.Е., Гринёва Е.Н. Антимюллеров гормон как предиктор менструального ответа при лечении женщин с синдромом поликистозных яичников с помощью изменения образа жизни и терапии метформином. Вестник репродуктивного здоровья. 2010; 3-4: 24-9.
  6. Стрельченко Д.А., Перминова С.Г., Донников А.Е. Предикторы синдрома гиперстимуляции яичников в программе ЭКО. Акушерство и гинекология. 2015; 10: 19-26
  7. Pigny P., Merlen E., Robert Y., Cortet-Rudelli C., Decanter C., Jonard S., Dewailly D. Elevated serum level of anti-mullerian hormone in patients with polycystic ovary syndrome: relationship to the ovarian follicle excess and to the follicular arrest. J. Clin. Endocrinol. Metab. 2003; 88(12): 5957-62.
  8. Apridonidze T., Essah P.A., Luorno M.J., Nestler J.E. Prevalence and characteristics of the metabolic syndrome in women with polycystic ovary syndrome. J. Clin. Endocrinol. Metab. 2005; 90(4): 1929-35.
  9. Боярский К.Ю., Гайдуков С.Н., Машкова Е.А. Роль антимюллерова гормона (АМГ) в норме и при различных гинекологических заболеваниях. Журнал акушерства и женских болезней. 2009; 58(3): 75-85.
  10. Rosenfield R.L., Wroblewski K., Padmanabhan V., Littlejohn E., Mortensen M., Ehrmann D.A. Anti-Müllerian hormone levels are independently related to ovarian hyperandrogenism and polycystic ovaries. Fertil. Steril. 2012; 98(1): 242-9.
  11. Piouka A., Farmakiotis D., Katsikis I., Macut D., Gerou S., Panidis D. Anti-Müllerian hormone levels reflect severity of PCOS but are negatively influenced by obesity: relationship with increased luteinizing hormone levels. Am. J. Physiol. Endocrinol. Metab. 2009; 296(2): E238-43.
  12. Sahmay S., Atakul N., Oncul M., Tuten A., Aydogan B., Seyisoglu H. Serum anti-Müllerian hormone levels in the main phenotypes of polycystic ovary syndrome. Eur. J. Obstet. Gynecol. Reprod. Biol. 2013; 170(1): 157-61.
  13. Romualdi D., Di Florio C., Tagliaferri V., De Cicco S., Gagliano D., Immediata V. et al. The role of anti-Müllerian hormone in the characterization of the different polycystic ovary syndrome phenotypes. Reprod. Sci. 2016; 23(5): 655-61.
  14. Goodman N.F., Cobin R.H., Futterweit W., Glueck J.S., Legro R.S., Carmina E. American Association of Clinical Endocrinologists, American College of Endocrinology, and androgen excess and PCOS society disease state clinical review: guide to the best practices in the evaluation and treatment of polycystic ovary syndrome - part 1. Endocr. Pract. 2015; 21(11): 1291-300.
  15. Laven J.S., Mulders A.G., Visser J.A., Themmen A.P., De Jong F.H., Fauser B.C. Anti-Müllerian hormone serum concentrations in normoovulatory and anovulatory women of reproductive age. J. Clin. Endocrinol. Metab. 2004; 89(1): 318-23.
  16. Dewailly D., Gronier H., Poncelet E., Robin G., Leroy M., Pigny P. et al. Diagnosis of polycystic ovary syndrome (PCOS): revisiting the threshold values of follicle count on ultrasound and of the serum AMH level for the definition of polycystic ovaries. Hum. Reprod. 2011; 26(11): 3123-9.
  17. Li H.W., Anderson R.A., Yeung W.S., Ho P.C., Ng E.H.Y. Evaluation of serum anti-Miillerian hormone and inhibin В concentrations in the differential diagnosis of secondary oligoamenorrhea. Fertil. Steril. 2011; 96(3): 774-9.
  18. Eilertsen T.B., Vanky E., Carlsen S.M. Anti-Müllerian hormone in the diagnosis of polycystic ovarian syndrome: can morphologic description be replaced? Hum. Reprod. 2012; 27(8): 2494-502.
  19. Pigny P., Jonard S., Robert Y., Dewailly D. Serum anti-Müllerian hormone as a surrogate for antral follicle count for definition of the polycystic ovary syndrome. J. Clin. Endocrinol. Metab. 2006; 91(3): 941-5.
  20. Carmina E., Campagna A.M., Eruzzetti E., Lobo R.A. АМН measurement versus ovarian ultrasound the diagnosis of polycystic ovary syndrome (PCOS) in different phenotypes. Endocr. Pract. 2016; 22(3): 287-93.
  21. Lauritsen M.P., Bentzen J.G., Pinborg A., Loft A., Forman J.L., Thuesen L.L. et al. The prevalence of polycystic ovary syndrome in a normal population according to the Rotterdam criteria versus revised criteria including anti-Müllerian hormone. Hum. Reprod. 2014; 29(4): 791-801.
  22. Lujan M.E., Jarrett B.Y., Brooks E.D., Reines J.K., Peppin A.K., Muhn N. et al. Updated ultrasound criteria for polycystic ovary syndrome: reliable thresholds for elevated follicle population and ovarian volume. Hum. Reprod. 2013; 28(5): 1361-8.
  23. Kelsey T.W., Wright P., Nelson S.М., Anderson R.A., Wallace W.H. A validated model of serum anti-mullerian hormone from conception to menopause. PLoS One. 2011; 6(7): e22024.
  24. Nelson S.M., Messow M.C., Wallace A.M., Fleming R., McConnachie A. Nomogram for the decline in serum antimüllerian hormone: a population study of 9,601 infertility patients. Fertil. Steril. 2011; 95(2): 736-41. el-3.
  25. Nelson S.M., Messow M.C., McConnachie A., Wallace H., Kelsey T., Fleming R. et al. External validation of nomogram for the decline in serum anti-Müllerian hormone in women: a population study of 15,834 infertility patients. Reprod. Biomed. Online. 2011; 23(2): 204-6.
  26. Almog B., Shehata E, Suissa S., Holzer H., Shalom-Paz E., La Marca A. et al. Age-related normograms of serum antimüllerian hormone levels in a population of infertile women: a multicenter study. Fertil. Steril. 2011; 95(7): 2359-63.
  27. Nardo L.G., Yates A.P., Roberts S.A., Pemberton P., Laing I. The relationships between АМН, androgens, insulin resistance and basal ovarian follicular status in non-obese subfertile women with and without polycystic ovary syndrome. Hum Reprod. 2009;24:2917-2923.
  28. Lin Y.H., Chiu W.C., Wu C.H., Tzeng C.R., Hsu C.S., Hsu M.J. Antimüllerian hormone and polycystic ovary syndrome. Fertil. Steril. 2011; 96(1): 230-5

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