Anti-Mullarian hormone versus day three follicular stimulating hormone and antral follicular count as a predictor for ovarian response to stimulation
DOI:
https://doi.org/10.61841/n0ycxg75Keywords:
Anti Mullarian hormone, follicular stimulating hormone, antral follicular count, ovarian reserveAbstract
Back ground: Recently, a new marker, the anti-mullarian hormone (AMH), has been evaluated as a marker of ovarian response. Since the number of ovarian follicles decline with increasing age, AMH level might be used as a marker for ovarian aging, and serum AMH can be measured at frequent time-points during menstrual cycle, suggesting the complete absence of fluctuation. Aim of study: To evaluate wither anti-Mullarian hormone is a better predictor of ovarian response to stimulation in comparism to day 3 follicular stimulating hormone (FSH) and antral follicular count (AFC).
Subjects and methods: This study was carried out at Bint AL-Huda teaching hospital in Thi-qar and Basrah IVF center during the period from 1st January 2012-1st January 2013 including 60 women with infertility caused by anovulation, and they were assesd by doing day 3 FSH, AMH and AFC, then they were subjected to ovulation induction treatment using clomiphene citrate 50 mg three times daily from day 2-6 of menstrual cycle and then assess at day 7 with transvaginal u/s and serum oestradiol level for the size and numbers of mature graffian follicle, if they were not responding to clomiphene citrate tablet they were given 3 ampules of follicular stimulating hormone ( follitropin beta ) (50iu/0.5ml) at day 7, 8, and 9 of menstrual cycle, on day 10-11 of menstrual cycle the MGF was assessed for the numbers and size and serum sample obtained for measurement of oestradiol level. The data were analyzed by using t test, pearson correlation, regression coefficient and area under receiver operating curve (ROC) was calculating as measure of predictive accuracy.
Result: From total (60) women. (11) patients have no ovarian response and (49) patients have normal ovarian response, the non responders group have significantly lower day 3 antral follicular count (AFC) <5 compare to normal responders >5 with p value=0.004, and also the non responders group had significantly low anti-Mullarian hormone level (AMH) (0.1±0.1) compare with normal responders the AMH level (1.2±0.6) with p value=0.001, follicular stimulating hormone level (FSH) was significantly higher in non responders (7.6±4.2) compare to normal responders the FSH level was (4.7±1.5) with p value=0.001,and the mean day 11 MGF count and E2 was higher in normal responders group compared with non responders group with p value=0.001. There was a ppositive correlation between AMH and AFC with MGF count while the correlation between FSH and MGF was negative. Multivariate analysis of the variables that predict good ovarian response to ovulation induction treatment demonstrate that the biochemical variable AMH was the most significant predictor as (R2=64. 9%).The AMH level was addressed as the only significant variable in determination of MGF numbers as AMH with a cut-off value >0.37ng/ml has area under the curve (accuracy)(0.96%) with p value <0.001 which was higher than that for AFC and FSH (73.3% and69.8%) respectively.
Conclusion: the present study concludes that AMH is a promising biochemical marker and it was better than day 3 AFC and FSH for the prediction of ovarian response, and the ability to predict poor response may be a valuable tool for patient counseling, since the poor responders have a lower probability of pregnancy and to estimate the starting dose of gonadotrophins (higher doses are required for poor responders).
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References
1. Sigman, M., Lipshultz, L.I., & Howards, S.S. (1997). Evaluation of the subfertile female. In Infertility in the Female (3rd ed., p. 174). St. Louis: Mosby–Year Book.
2. Gnoth, C., Godehardt, E., Frank-Herrmann, P., et al. (2005). Definition and prevalence of subfertility and infertility. Human Reproduction, 20, 1144–1147.
3. Boomsma, C.M., Keay, S.D., & Macklon, N.S. (2007). Peri-implantation glucocorticoid administration for assisted reproductive technology cycles. Cochrane Database of Systematic Reviews, (1), CD005996.
4. Edmonds, D.K. (2007). Dewhurst’s Textbook of Obstetrics & Gynaecology (7th ed., Chapter 45, pp. 459–460).
5. Büchter, D., Behre, H.M., Kliesch, S., & Nieschlag, E. (1998). Pulsatile GnRH or hCG/hMG as effective treatment for men with hypogonadotropic hypogonadism: A review of 42 cases. European Journal of Endocrinology, 139, 298–303.
6. Mahmood, T.A., & Templeton, A. (1991). Prevalence and genesis of endometriosis. Human Reproduction, 6, 544–549.
7. Barnhart, K.T., Dunsmoor, S.R., & Coutifaris, C. (2002). Effect of endometriosis on in vitro fertilization. Fertility and Sterility, 77, 1148–1155.
8. Brosens, I. (2004). Endometriosis and the outcome of in-vitro fertilization. Fertility and Sterility, 81, 1198–1200.
9. Giudice, L.C., & Kao, L.C. (2004). Endometriosis. The Lancet, 364, 1789–1799.
10. Rao, M., & Rao, D. (1977). Cytogenetic studies in primary infertility. Fertility and Sterility, 28, 209.
11. Goldenberg, R.L., & White, R. (1975). The effect of vaginal lubricants on sperm motility in vitro. Fertility and Sterility, 26, 872.
12. Hull, M.G., et al. (2000). Delayed conception and active and passive smoking. Fertility and Sterility, 74, 725–733.
13. ACOG Committee Opinion No. 316. (2005). Smoking cessation during pregnancy. Obstetrics & Gynecology, 106, 883.
14. Chavarro, J.M., et al. (2009). Caffeinated and alcoholic beverage intake in relation to ovulatory disorder infertility. Epidemiology.
15. Crosignani, P.G., et al. (2003). Overweight and obese anovulatory patients with polycystic ovary: Improvements induced by diet. Human Reproduction, 18, 1928–1932.
16. Florack, E.I., Zielhuis, G.A., & Rolland, R. (1994). Cigarette smoking, alcohol consumption, caffeine intake, and fecundability. Preventive Medicine, 23, 175–180.
17. Klonoff-Cohen, H. (2005). Female and male lifestyle habits and IVF: What is known and unknown. Human Reproduction Update, 11, 179–203.
18. Greene, M.F., Hare, J.W., Cloherty, J.P., Benacerraf, B.R., & Soeldner, J.S. (1989). First-trimester hemoglobin A1 and risk for major malformation and spontaneous abortion in diabetic pregnancy. Teratology, 39, 225–235.
19. Practice Committee of the American Society for Reproductive Medicine. (2008). Definitions of infertility and recurrent pregnancy loss. Fertility and Sterility, 90 (Suppl. 3).
20. Lim, S.A.T., & Rajan, R. (2002). Applied physiology and endocrinology of ovulation. In Postgraduate Obstetrics, Gynecology and Infertility (pp. 38–44).
21. Gleicher, N., & Barad, D. (2006). Ovarian age-based stimulation of young women with diminished ovarian reserve. Fertility and Sterility. https://doi.org/10.1016/j.fertnstert.2006.04.046
22. Lucely, D.M., & Baker, P.N. (2010). Evidence-Based Text for MRCOG in Gynecology and Obstetrics (Chapter 52, pp. 602–603).
23. The Rotterdam ESHRE/ASRM-Sponsored PCOS Consensus Workshop Group. (2004). Revised consensus on diagnostic criteria and long-term health risks related to polycystic ovary syndrome. Human Reproduction, 19, 41–47.
24. Adams, J., Polson, D.W., & Franks, S. (1986). Prevalence of polycystic ovaries in women with anovulation and idiopathic hirsutism. British Medical Journal, 293, 355–359.
25. Freundl, G., Godehardt, E., Kern, P.A., Frank-Herrmann, P., Koubenec, H.J., & Gnoth, C. (2003). Estimated maximum failure rates of cycle monitors using daily conception probabilities in the menstrual cycle. Human Reproduction, 18(12), 2628–2633.
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