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Animals : an open access journal from MDPI2021; 11(7); doi: 10.3390/ani11072004

Anti-Müllerian Hormone and OPU-ICSI Outcome in the Mare.

Abstract: Anti-Müllerian hormone (AMH) reflects the population of growing follicles and has been related to mammalian fertility. In the horse, clinical application of ovum pick-up and intracytoplasmic sperm injection (OPU-ICSI) is increasing, but results depend largely on the individuality of the mare. The aim of this study was to assess AMH as a predictor for the OPU-ICSI outcome in horses. Therefore, 103 mares with a total follicle count above 10 were included in a commercial OPU-ICSI session and serum AMH was determined using ELISA. Overall, the AMH level was significantly correlated with the number of aspirated follicles and the number of recovered oocytes (p < 0.001). Mares with a high AMH level (≥2.5 µg/L) yielded significantly greater numbers of follicles (22.9 ± 1.2), oocytes (13.5 ± 0.8), and blastocysts (2.1 ± 0.4) per OPU-ICSI session compared to mares with medium (1.5-2.5 µg/L) or low AMH levels (<1.5 µg/L), but no significant differences in blastocyst rates were observed. Yet, AMH levels were variable and 58% of the mares with low AMH also produced an embryo. In conclusion, measurement of serum AMH can be used to identify mares with higher chances of producing multiple in vitro embryos, but not as an independent predictor of successful OPU-ICSI in horses.
Publication Date: 2021-07-05 PubMed ID: 34359132PubMed Central: PMC8300260DOI: 10.3390/ani11072004Google Scholar: Lookup
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  • Journal Article

Summary

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The research article discusses a study that aimed to assess the Anti-Müllerian hormone (AMH) as a potential predictor for the outcomes of the ovum pick-up and intracytoplasmic sperm injection (OPU-ICSI) fertility treatment in horses. The findings suggest that while higher levels of AMH can identify mares more likely to produce multiple in vitro embryos, it cannot be used solely to predict successful OPU-ICSI outcomes.

Study Motivation and Objective

  • The researchers embarked on this study due to the increasing application of OPU-ICSI in horses, a method that extracts eggs directly from the mare’s ovaries and injects a single sperm into each egg.
  • The key objective of the research was to investigate whether AMH, a hormone reflecting the population of growing follicles within a mare’s ovaries, could be leveraged as a predictor for the outcome of OPU-ICSI in horses.

Research Methodology

  • The study included 103 mares that had more than 10 total follicles, an important preliminary criterion for inclusion given the hormone’s purported link to the ovarian follicle population.
  • Serum AMH levels in these mares were determined with a scientific method known as ELISA (Enzyme-Linked Immunosorbent Assay).
  • The researchers then conducted a commercial OPU-ICSI session on the mares, correlating the obtained results with the measured AMH levels.

Key Findings

  • The study found a significant correlation between AMH levels, the number of aspirated follicles, and the number of retrieved oocytes, establishing a connection between high AMH levels and a greater number of follicles and oocytes.
  • Mares with high AMH levels also yielded more blastocysts (precursors to embryos) per OPU-ICSI session compared to those with medium or low AMH levels.
  • No significant differences in blastocyst rates were found in relation to AMH levels, and surprisingly, 58% of the mares with low AMH levels still produced an embryo.

Conclusion

  • While the measurement of serum AMH levels can help identify mares likely to produce multiple in vitro embryos, it shouldn’t be used as the sole predictor of successful OPU-ICSI outcome in horses.
  • The findings imply that while AMH offers some predictive power, it’s an unreliable standalone predictor for fertility treatments, highlighting the need for additional factors in predicting OPU-ICSI outcomes.

Cite This Article

APA
Papas M, Govaere J, Peere S, Gerits I, Van de Velde M, Angel-Velez D, De Coster T, Van Soom A, Smits K. (2021). Anti-Müllerian Hormone and OPU-ICSI Outcome in the Mare. Animals (Basel), 11(7). https://doi.org/10.3390/ani11072004

Publication

ISSN: 2076-2615
NlmUniqueID: 101635614
Country: Switzerland
Language: English
Volume: 11
Issue: 7

Researcher Affiliations

Papas, Marion
  • Department of Reproduction, Obstetrics and Herd Health, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.
Govaere, Jan
  • Department of Reproduction, Obstetrics and Herd Health, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.
Peere, Sofie
  • Department of Reproduction, Obstetrics and Herd Health, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.
Gerits, Ilse
  • Department of Reproduction, Obstetrics and Herd Health, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.
Van de Velde, Margot
  • Department of Reproduction, Obstetrics and Herd Health, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.
Angel-Velez, Daniel
  • Department of Reproduction, Obstetrics and Herd Health, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.
  • Research Group in Animal Sciences-INCA-CES, Universidad CES, 050021 Medellin, Colombia.
De Coster, Tine
  • Department of Reproduction, Obstetrics and Herd Health, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.
Van Soom, Ann
  • Department of Reproduction, Obstetrics and Herd Health, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.
Smits, Katrien
  • Department of Reproduction, Obstetrics and Herd Health, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.

Grant Funding

  • 1222317 / Fonds Wetenschappelijk Onderzoek

Conflict of Interest Statement

The authors declare no conflict of interest.

References

This article includes 60 references
  1. Lazzari G, Colleoni S, Crotti G, Turini P, Fiorini G, Barandalla M, Landriscina L, Dolci G, Benedetti M, Duchi R. Laboratory production of equine embryos.. J. Equine Vet. Sci. 2020;89:103097.
    doi: 10.1016/j.jevs.2020.103097pubmed: 32563445google scholar: lookup
  2. Hinrichs K. Assisted reproductive techniques in mares.. Reprod. Domest. Anim. 2018;53:4–13.
    doi: 10.1111/rda.13259pubmed: 30238661google scholar: lookup
  3. Stout T.A.E. Clinical application of in vitro embryo production in the horse.. J. Equine Vet. Sci. 2020;89:103011.
    doi: 10.1016/j.jevs.2020.103011pubmed: 32563449google scholar: lookup
  4. Lazzari G, Crotti G, Turini P, Duchi R, Mari G, Zavaglia G, Barbacini S, Galli C. Equine embryos at the compacted morula and blastocyst stage can obtained by intracytoplasmic sperm injection (ICSI) of in vitro matured oocytes with frozen-thawed spermatozoa from semen of different fertilities.. Theriogenology 2002;58:709–712.
  5. Claes A.N.J, Galli C, Colleoni S, Necchi D, Lazzari G, Deelen C, Beitma M, Stout T. Factors influencing oocyte recovery and in-vitro production of equine embryos in a commercial OPU/ISCI program.. J. Equine Vet. Sci. 2016;41:51–84.
  6. Cuervo-Arango J, Claes A.N, Stout T.A.E. Mare and stallion effects on blastocyst production in a commercial equine ovum pick-up-intracytoplasmic sperm injection program.. Reprod. Fertil. Dev. 2019;31:1894–1903.
    doi: 10.1071/RD19201pubmed: 31634435google scholar: lookup
  7. Galli C, Colleoni S, Duchi R, Lazzari G. Male factors affecting the success of equine in vitro embryo production by ovum pickup-intracytoplasmic sperm injection in a clinical setting.. J. Equine Vet. Sci. 2016;43:S6–S10.
  8. Josso N, Cate R.L, Picard J.Y, Vigier B, Di Clemente N, Wilson C, Imbeaud S, Pepinsky R.B, Guerrier D, Boussin L. Anti-müllerian hormone: The Jost factor.. Recent Prog. Horm. Res. 1993;48:1–59.
  9. Durlinger A.L, Visser J.A, Themmen A.P. Regulation of ovarian function: The role of anti-Müllerian hormone.. Reproduction 2002;124:601–609.
    doi: 10.1530/rep.0.1240601pubmed: 12416998google scholar: lookup
  10. Josso N, Picard J.Y. Anti-Müllerian hormone.. Physiol. Rev. 1986;66:1938–1990.
    doi: 10.1152/physrev.1986.66.4.1038pubmed: 3532142google scholar: lookup
  11. Durlinger A.L, Kramer P, Karels B, de Jong F.H, Uilenbroek J.T, Grootegoed J.A, Themmen A.P. Control of primordial follicle recruitment by anti-Müllerian hormone in the mouse ovary.. Endocrinology 1999;140:5789–5796.
    doi: 10.1210/endo.140.12.7204pubmed: 10579345google scholar: lookup
  12. Durlinger A.L, Gruijters M.J, Kramer P, Karels B, Kumar T.R, Matzuk M.M, Rose U.M, de Jong F.H, Iulenbroek J.T, Grootegoed J.A. Anti-Müllerian hormone attenuates the effects of FSH on follicle development in the mouse ovary.. Endocrinoly 2001;142:4891–4899.
    doi: 10.1210/endo.142.11.8486pubmed: 11606457google scholar: lookup
  13. La Marca A, Sighinolfi G, Radi D, Argento C, Baraldi E, Carducci Artenisio A, Stabile G, Volpe A. Anti-Müllerian (AMH) as a predictive marker in assisted reproductive technology (ART). Hum. Reprod. Update 2010;16:113–130.
    doi: 10.1093/humupd/dmp036pubmed: 19793843google scholar: lookup
  14. Umer S, Zhao S.J, Sammad A, Weldegebriall Sahlu B, Pang Y.W, Zhu H. AMH: Could it be used as a biomarker for fertility and superovulation in domestic animals?. Genes 2019;10:1009.
    doi: 10.3390/genes10121009pmc: PMC6947652pubmed: 31817280google scholar: lookup
  15. Monniaux D, Drouilhet L, Rico C, Estienne A, Jarrier P, Touzé J.L, Sapa J, Phocas F, Dupont J, Dalbiès-Tran R. Regulation of anti-Müllerian hormone production in domestic animals.. Reprod. Fertil. Dev. 2013;25:1–16.
    doi: 10.1071/RD12270pubmed: 23244824google scholar: lookup
  16. Fanchin R, Schonäuer L.M, Righini C, Guibourdenche J, Frydman R, Taieb J. Serum anti-Müllerian hormone is more strongly related to ovarian follicular status than serum inhibin B, estradiol, FSH and LH on day 3.. Hum. Reprod. 2003;18:323–327.
    doi: 10.1093/humrep/deg042pubmed: 12571168google scholar: lookup
  17. Hansen K.R, Hodenett G.M, Knowlton N, Craig L.B. Correlation of ovarian reserve tests with histologically determined primordial follicle number.. Fertil. Steril. 2011;95:170–175.
  18. Kevenaar M.E, Meerasahib M.F, Kramer P, van de Lang-Born B.M.N, de Jong F.H, Groome N.P, Themmen A.P.N. Serum anti-Müllerian hormone level reflects the size of the primordial follicle pool in mice.. Endocrinology 2006;147:3228–3234.
    doi: 10.1210/en.2005-1588pubmed: 16556768google scholar: lookup
  19. Batista E.O.S, Macedo G.G, Sala R.V, Ortolan M.D.D.V, Filho M.F.S, Del Valle T.A, Jesus E.F, Lopes R.N.V.R, Rennó F.P, Baruselli P.S. Plasma antimullerian hormone as a predictor of ovarian antral follicular population in Bos indicus (Nelore) and Bos Taurus (Holstein) heifers.. Reprod. Domest. Anim. 2014;49:448–452.
    doi: 10.1111/rda.12304pubmed: 24689827google scholar: lookup
  20. Nagashima J.B, Hansen B.S, Songsasen N, Travis A.J, Place N.J. Anti-Müllerian hormone in the domestic dog during the anestrus to oestrus transition.. Reprod. Domest. Anim. 2016;51:158–164.
    doi: 10.1111/rda.12660pubmed: 26708613google scholar: lookup
  21. Vernunft A, Schneider F, Tuchscherer F, Becker F, Kanitz W. Anti-Müllerian hormone (AMH) can help to predict follicular growth in mare.. Pferdeheilkunde 2011;27:293–296.
    doi: 10.21836/PEM20110315google scholar: lookup
  22. Claes A.N.J, Ball B.A, Troedsson M.H.T, Curry JR T.E, Squires E.L, Scoggin K.E. Molecular changes in the equine follicles in relation to variations in antral follicle count and anti-Müllerian hormone concentrations.. Equine Vet. J. 2015;48:741–748.
    doi: 10.1111/evj.12514pubmed: 26403213google scholar: lookup
  23. Jayaprakasan K, Deb S, Batcha M, Hopkisson J, Johnson I, Campbell B, Raine-Fenning N. The cohort of antral follicles measuring 2–6 mm reflects the quantitative status of ovarian reserve as assessed by serum levels of anti-Müllerian hormone and response to controlled ovarian stimulation.. Fertil. Steril. 2010;94:1775–1781.
  24. Rico C, Fabre S, Médigue C, di Clemente N, Clément F, Bontoux M, Touzé J.L, Dupont M, Briant E, Rémy B. Anti-Müllerian hormone is an endocrine marker of ovarian gonadotropin-responsive follicles and can help to predict superovulatory response in cow.. Biol. Reprod. 2009;80:50–59.
    doi: 10.1095/biolreprod.108.072157pubmed: 18784351google scholar: lookup
  25. Monniaux D, Baril G, Laine A.L, Jarrier P, Poulin N, Cognié J, Fabre S. Anti-Müllerian hormone as a predictive endocrine marker for embryo production in the goat.. Reproduction 2011;142:845–854.
    doi: 10.1530/REP-11-0211pubmed: 21930684google scholar: lookup
  26. Claes A.N.J, Ball B.A, Scoggin K.E, Esteller-Vico A, Kalmar J.J, Conley A.J, Squires E.L, Troedsson M.H.T. The interrelationship between anti-Müllerian hormone, ovarian follicular populations and age in mares.. Equine Vet. J. 2015;47:537–541.
    doi: 10.1111/evj.12328pubmed: 25124401google scholar: lookup
  27. Dewailly D, Yding Andersen C, Balen A, Broekmans F, Dilaver N, Fanchin R, Griesinger G, Kelsey T.W, La Marca A, Lambalk C. The physiology and clinical utility of anti-Müllerian hormone in women.. Hum. Reprod. Update 2014;20:370–385.
    doi: 10.1093/humupd/dmt062pubmed: 24430863google scholar: lookup
  28. Ebner T, Sommergruber M, Moser M, Shebl O, Schreier-Lechner E, Tews G. Basal level of anti-Müllerian hormone is associated with oocyte quality in stimulated cycled.. Hum. Reprod. 2006;21:2022–2026.
    doi: 10.1093/humrep/del127pubmed: 16679324google scholar: lookup
  29. Brodin T, Hadziosmanovic N, Berglund L, Olovsson M, Holte J. Comparing four ovarian reserve markers—Associations with ovarian response and live births after assisted reproduction.. Acta Obstet. Gynecol. Scand. 2015;94:1056–1063.
    doi: 10.1111/aogs.12710pubmed: 26184379google scholar: lookup
  30. Hu K.L, Liu F.T, Xu H, Li R, Qiao J. Association of serum anti-Müllerian hormone and other factors with cumulative live birth rate following IVF.. RBMO 2020;40:675–683.
    doi: 10.1016/j.rbmo.2020.01.024pubmed: 32268980google scholar: lookup
  31. Rico C, Drouilhet L, Salvetti P, Dalbiès-Tran R, Jarrier P, Touzé J.L, Pillet E, Ponsart C, Fabre S, Monniaux D. Determination of anti-Müllerian hormone concentrations in blood as a tool to select Holstein donor cows for embryo production: From the laboratory to the farm.. Reprod. Fertil. Dev. 2012;24:932–944.
    doi: 10.1071/RD11290pubmed: 22935154google scholar: lookup
  32. Fushimi Y, Okawa H, Monniaux D, Takagi M. Efficacy of a single blood anti-Müllerian hormone (AMH) concentration measurement for the selection of Japanese Black heifer embryo donors in herd breeding program.. J. Reprod. Dev. 2020;66:593–598.
    doi: 10.1262/jrd.2020-069pmc: PMC7768178pubmed: 32938834google scholar: lookup
  33. Steel A, Athorn R.Z, Grupen C.G. Anti-Müllerian hormone and oestradiol as markers of future reproductive success in juveniles gilts.. Anim. Reprod. Sci. 2018;195:197–206.
  34. Am-in N, Suwimonteerabutr J, Kirkwood R.N. Serum anti-Müllerian hormone and estradiol concentrations in gilts and their age at puberty.. Animals 2020;10:2189.
    doi: 10.3390/ani10112189pmc: PMC7700628pubmed: 33238427google scholar: lookup
  35. Almeida J, Ball B.A, Conley A.J, Place N.J, Liu I.K.M, Scholtz E.L, Mathewson L, Stanley S.D, Moeller B.C. Biological and clinical significance of Anti-Müllerian hormone determination in blood serum of the mare.. Theriogenology 2011;76:1393–1403.
  36. Claes A.N.J, Ball B.A. Biological functions and clinical applications of anti-Müllerian hormone in stallions and mares.. Vet. Clin. Equine 2016;32:451–464.
    doi: 10.1016/j.cveq.2016.07.004pubmed: 27726984google scholar: lookup
  37. Claes A.N.J, Ball B.A, Corbin C.J, Conley A.J. Anti-Müllerian hormone as a diagnostic marker for equine cryptorchidism in three cases with equivocal testosterone concentrations.. J. Equine Vet. Sci. 2014;34:442–445.
  38. Ball B.A, Conley A.J, MacLaughlin D.T, Grundy S.A, Sabeur K, Liu I.K.M. Expression of anti-Müllerian hormone (AMH) in equine granulosa-cell tumor and in normal equine ovaries.. Theriogenology 2008;70:968–977.
  39. Scarlet D, Wulf M, Kuhl J, Köhne M, Ille N, Conley A.J, Aurich C. Anti-Müllerian hormone profiling in prepubertal horses and its relationship with gonadal function.. Theriogenology 2018;117:72–77.
  40. Joonè C.J, Schulman M.L, Fosgate G.T, Claes A.N.J, Gupta S.K, Botha A.E, Human A, Bertschinger H.J. Serum anti-Müllerian hormone dynamics in mares following immunocontraception with anti-zona pellucida or -GnRH vaccines.. Theriogenology 2018;106:214–220.
  41. Ball B.A, El-Sheikh Ali H, Scoggin K.E, Riddle W.T, Schnobrich M, Bradecamp E, Agnew M, Squires E.L, Troedsson M.H.T. Relation between anti-Müllerian hormone and fertility in the mare.. Theriogenology 2019;125:335–341.
  42. Uliani R.C, Conley A.J, Corbin C.J, Friso A.M, Maciel L.F.S, Alvarenga M.A. Anti-Müllerian hormone and ovarian aging in mares.. J. Endocrinol. 2019;240:147–156.
    doi: 10.1530/JOE-18-0391pubmed: 30400031google scholar: lookup
  43. Ortiz-Escribano N, Bogado Pascottini O, Woelders H, Vandenberghe L, De Schauwer C, Govaere J, Van den Abbeel E, Vullers T, Ververs C, Roels K. An improved vitrification protocol for equine immature oocytes resulting in a first live foal.. Equine Vet. J. 2018;50:391–397.
    doi: 10.1111/evj.12747pubmed: 28833413google scholar: lookup
  44. Choi Y.H, Love L.B, Varner D.D, Hinrichs K. Holding immature equine oocytes in the absence of meiotic inhibitors: Effect on germinal vesicle chromatin and blastocyst development after intracytoplasmic sperm injection.. Theriogenology 2006;66:955–963.
  45. Cuervo-Arango J, Claes A.N, Stout T.A. A retrospective comparison of the efficiency of different assisted reproductive techniques in the horse, emphasizing the impact of maternal age.. Theriogenology 2019;132:36–44.
  46. Traversari J, Aepli H, Knutti B, Lüttgenau J, Bruckmaier R, Bollwein H. Relationships between antral follicle count, blood serum concentration of anti-Müllerian hormone and fertility in mares.. Schweiz. Arch. Tierheilkd. 2019;161:627–638.
    doi: 10.17236/sat00225pubmed: 31586925google scholar: lookup
  47. Pacheco A, Cruz M, Iglesias C, García-Velasco J.A. Very low anti-müllerian hormone concentrations are not an independent predictor of embryo quality and pregnancy rate.. Reprod. Biomed. Online. 2018;37:113–119.
    doi: 10.1016/j.rbmo.2018.03.015pubmed: 29703435google scholar: lookup
  48. Melado Vidales L, Fernández-Nistal A, Martínez Fernández V, Verdú Merino V, Bruna Catalán I, Bajo Arenas J.M. Anti-Müllerian hormone levels to predict oocyte maturity and embryo quality during controlled ovarian hyperstimulation.. Minerva Ginecol. 2017;69:225–235.
  49. Scheffer J.B, de Carvalho R.F, Aguiar A.P.S, Machado I.J.M, France J.B, Lozano D.M, Fanchin R. Which ovarian reserve marker relates to embryo quality on day 3 and blastocyst; age, AFC, AMH?. JBRA Assist. Reprod. 2021;25:109–114.
    doi: 10.5935/1518-0557.20200060pmc: PMC7863095pubmed: 32960526google scholar: lookup
  50. Wu W, Wang X, Li Y, Zhang Y. Analysis of the women with the AMH concentrations below the limit of reference range but with the ideal number of retrieved oocytes.. Arch. Gynecol. Obstet. 2020;301:1089–1094.
    doi: 10.1007/s00404-020-05491-9pubmed: 32179967google scholar: lookup
  51. Vernunft A, Schwerhoff M, Viergutz T, Dierderich M, Kuwer A. Anti-Müllerian hormone levels in plasma of Holstein-Friesian heifers as a predictive parameter for ovum pick-up and embryo production outcomes.. J. Reprod. Dev. 2015;61:74–79.
    doi: 10.1262/jrd.2014-091pmc: PMC4354234pubmed: 25482112google scholar: lookup
  52. Sadruddin S, Barnett B, Ku L, Havemann D, Mucowski S, Herrington R, Burggren W. Maternal serum concentration of anti-Müllerian hormone is a better predictor than basal follicle stimulating hormone of successful blastocysts development during IVF treatment.. PLoS ONE 2020;15:e0239779.
  53. Casadei L, Manicuti C, Puca F, Madrigale A, Emidi E, Piccione E. Can anti-Müllerian hormone be predictive of sponteneus onset of pregnancy in women with unexplained infertility?. J. Obstet. Gynaecol. 2013;33:857–861.
    doi: 10.3109/01443615.2013.831050pubmed: 24219729google scholar: lookup
  54. Lahoz B, Alabart J.L, Cocero M.J, Monniaux D, Echegoyen E, Sánchez P, Folch J. Anti-Müllerian hormone concentration in sheep and its dependence of age an independence of BMP15 genotype: An endocrine predictor to select the best donors for embryo technologies.. Theriogenology 2014;81:347–357.
  55. Squires E.L, McCue P.M. Superovulation in mares.. Anim. Reprod. Sci. 2007;99:1–8.
  56. Raz T, Hunter B, Carley S, Card C. Reproductive performance of donor mares subsequent to eFSH treatment in early vernal transition: Comparison between the first, second, and mid-season estrous cycles of the breedinf season.. Anim. Reprod. Sci. 2009;116:107–118.
  57. Meyers-Brown G.A, McCue P.M, Troedsson M.H.T, Klein C, Zent W, Ferris R.A, Lindholm A.R.G, Scofield D.B, Claes A.N, Morganti M. Induction of ovulation in seasonally anestrous mares under ambient lights using recombinant equine FSH (reFSH). Theriogenology 2013;80:456–462.
  58. Raz T, Card C. Efficiency of superovulation and in vivo embryo production in eFSH-treated donor mares after estrus synchronization with progesterone and estradiol-17β.. Theriogenology 2009;72:169–178.
  59. Dal G.E, Kasikci G. Serum anti-Müllerian hormone levels during estrus and diestrus in mares.. Med. Weter. 2020;76:282–284.
    doi: 10.21521/mw.6392google scholar: lookup
  60. Claes A.N.J, Cuervo-Arango J, Derks S, Stout T.A.E. The usefulness of anti-Müllerian hormone in predicting oocyte recovery and in vitro production of equine embryos.. J. Equine Vet. Sci. 2020;89:103049.

Citations

This article has been cited 9 times.
  1. Scarlet D, Schuler G, Malama E, Bollwein H, Bocci C, Colleoni S, Lazzari G, Galli C, Kowalewski MP. Endocrine profile and OPU-ICSI outcomes in mares: a comparative study. Reprod Fertil 2025 Jul 1;6(3).
    doi: 10.1530/RAF-25-0027pubmed: 40539920google scholar: lookup
  2. Van den Branden E, Salamone M, Broothaers K, Peere S, Polfliet E, Dewulf M, Van Steenkiste G, van Loon G, Smits K, Govaere J. Physiological and behavioral parameters of pain and stress in mares during and after transvaginal ultrasound-guided follicular aspiration. Front Vet Sci 2025;12:1574351.
    doi: 10.3389/fvets.2025.1574351pubmed: 40271484google scholar: lookup
  3. Khan IU, Khairullah AR, Khan AY, Rehman AU, Mustofa I. Strategic approaches to improve equine breeding and stud farm outcomes. Vet World 2025 Feb;18(2):311-328.
  4. Cuervo-Arango J, Sala-Ayala L, Márquez-Moya A, Martínez-Boví R. The Influence of Aspiration Pressure, Follicle Flushing Method and Needle Rotation During Single-Operator OPU Technique on Oocyte Recovery and Embryo Production in the Mare. Animals (Basel) 2025 Mar 14;15(6).
    doi: 10.3390/ani15060832pubmed: 40150362google scholar: lookup
  5. Heidary Z, Masoumi M, Dashtkoohi M, Sharifinejad N, Dehghan Tarzjani M, Ghaemi M, Hossein Rashidi B. The Association of AMH Level with the Number and Quality of Oocytes in Women Undergoing IVF/ICSI: A Single-Center Study. J Reprod Infertil 2024 Jan-Mar;25(1):38-45.
    doi: 10.18502/jri.v25i1.15197pubmed: 39157280google scholar: lookup
  6. Koca D, Aktar A, Turgut AO, Sagirkaya H, Alcay S. Elecsys(®) AMH assay: Determination of Anti-Müllerian hormone levels and evaluation of the relationship between superovulation response in Holstein dairy cows. Vet Med Sci 2024 Jul;10(4):e1509.
    doi: 10.1002/vms3.1509pubmed: 38889090google scholar: lookup
  7. De Coster T, Zhao Y, Tšuiko O, Demyda-Peyrás S, Van Soom A, Vermeesch JR, Smits K. Genome-wide equine preimplantation genetic testing enabled by simultaneous haplotyping and copy number detection. Sci Rep 2024 Jan 23;14(1):2003.
    doi: 10.1038/s41598-023-48103-7pubmed: 38263320google scholar: lookup
  8. Hildebrandt TB, Holtze S, Colleoni S, Hermes R, Stejskal J, Lekolool I, Ndeereh D, Omondi P, Kariuki L, Mijele D, Mutisya S, Ngulu S, Diecke S, Hayashi K, Lazzari G, de Mori B, Biasetti P, Quaggio A, Galli C, Goeritz F. In vitro fertilization program in white rhinoceros. Reproduction 2023 Dec 1;166(6):383-399.
    doi: 10.1530/REP-23-0087pubmed: 37877686google scholar: lookup
  9. Angel-Velez D, De Coster T, Azari-Dolatabad N, Fernandez-Montoro A, Benedetti C, Bogado Pascottini O, Woelders H, Van Soom A, Smits K. New Alternative Mixtures of Cryoprotectants for Equine Immature Oocyte Vitrification. Animals (Basel) 2021 Oct 28;11(11).
    doi: 10.3390/ani11113077pubmed: 34827809google scholar: lookup