ANTI-MULLERIAN HORMONE AND OVARIAN RESERVE DISPARITY AMONG WOMEN OF THREE DIFFERENT ETHNIC GROUPS IN THE NIGER DELTA REGION, NIGERIA

Authors

  • Ezeiruaku, Ferdinand Chukwuma Department of Medical Laboratory Science, Niger Delta University, Nigeria. Author
  • Ogon, Agnes Oyovwevotu Department of Chemical Pathology, Medical Laboratory Services, Federal Medical Centre, Nigeria. Author
  • Onitsha, Enebrayi Nelson Department of Medical Laboratory Science, Niger Delta University, Nigeria. Author

Keywords:

Anti-Mullerian Hormone (AMH), Ethnicity, Ovarian Reserve, Infertility

Abstract

Background: Increasing research indicates that reproductive function and potential may vary among racial and ethnic groups. Timing of puberty, infertility, and reproductive aging have all been shown to vary. Anti-mullerian hormone (AMH) levels are one of the novel diagnostic biomarkers for ovarian reserve. Ethnic variations in anti-Mullerian hormone (AMH) levels may influence fertility outcomes. Aims: This cross-sectional study evaluated the difference in ovarian reserve marker (anti-mullerian hormone) in women from three ethnic groups (Ikwerre, Kalabari and Ijaws) in Niger Delta Region, Nigeria. Materials/Method: For the purpose of the study, a total of 1,773 women in good health were used, including 580 from Ikwerre tribe, 593 from Kalabari tribe, and 600 from Ijaws tribes. Four age groups of the women were created; 20-30, 31-40, 41-50 and 51-60 years old. After completing the questionnaire with questions about age, tribe, last menstrual date, and whether or not they were taking medication for infertility problems, the women were chosen at random. Blood serums were collected from the women and Enzyme Linked Immunoassay method was used to analyze serum level of Anti-Mullerian Hormone. Results: The result obtained revealed that Anti-Mullerian Hormone levels were significantly higher amongst Kalabari women, and significantly lower amongst the Ikwerre women compared to the other tribes. The result also showed that that ovarian reserve significantly decreases with age. However, the negative correlation of Anti-Mullerian Hormone with age was stronger among women of the Ijaw tribes, suggesting that the Ijaw women have a longer reproductive age compared to the other tribes. Conclusions: This study has established that different tribes exhibit significant Anti-Mullerian Hormone levels at different age group, with the Kalabari Women having the highest AMH levels, and Ikwerre women having the lowest Anti-Mullerian Hormone levels in all age groups. Ethnicity may play significant role in ovarian reserve, and therefore, it should be considered during patient counselling and personalized management.

References

C. Iglesias, M. Banker, N. Mahajan, L. Herrero, M. Meseguer, and J.A. Garcia-Velasco, (2014). Ethnicity as a determinant of ovarian reserve: differences in ovarian aging between Spanish and Indian women. Fertility and sterility. 102(1):244-9.

Tal R, Seifer DB. (2013). Potential mechanisms for racial and ethnic differences in antimüllerian hormone and ovarian reserve. International journal of endocrinology. (1):818912.

Marsh EE, Shaw ND, Klingman KM, Tiamfook-Morgan TO, Yialamas MA, Sluss PM, Hall JE. (2011). Estrogen levels are higher across the menstrual cycle in African-American women compared with Caucasian women. The Journal of Clinical Endocrinology & Metabolism. 1;96(10):3199-206.

Zhu X, Wong F, Bensoussan A, Lo SK, Zhou C, Yu J. (2010). Are there any cross‐ethnic differences in menstrual profiles? A pilot comparative study on Australian and Chinese women with primary dysmenorrhea. Journal of Obstetrics and Gynaecology Research. 36(5):1093-101.

Begum K, Muttukrishna S, Sievert LL, Sharmeen T, Murphy L, Chowdhury O, Kasim A, Gunu R, Bentley GR. (2016). Ethnicity or environment: effects of migration on ovarian reserve among Bangladeshi women in the United Kingdom. Fertility and sterility. Mar 1;105(3):744-54.

Mangalesh S, Katiyar P, Dudani S. (2020). Ethnic Differences in Anti-mullerian Hormone and Ovarian Reserve Retrospective Analysis of Indian and Ethiopian Women. Tropical Journal of Obstetrics and Gynaecology. 37(2):318-25.

Grynnerup AG, Lindhard A, Sørensen S. (2014). Recent progress in the utility of anti-Müllerian hormone in female infertility. Current Opinion in Obstetrics and Gynecology. 1;26(3):162-7.

Practice Committee of the American Society for Reproductive Medicine. (2015). Testing and interpreting measures of ovarian reserve: a committee opinion. Fertility and sterility 103(3):e9-17

Lunsford AJ, Whelan K, McCormick K, McLaren JF. (2014). Anti-müllerian hormone as a measure of reproductive function in female childhood cancer survivors. Fertility and Sterility. 101(1):227-31.

Ibrahim MA, Siddiq-Fgeer SA, Elhassan TH, Mohamed-Salih FE, Babiker AE, Ahmaed AY. (2017). The influence of Sickle Cell Anaemia on LH, FSH, AMH, Estradiol, Vitamin D and Ferritin levels of Sudanese females. Am. J. Innov. Res. Appl. Sci., 4(1):15-21

Rzeszowska M, Leszcz A, Putowski L, Hałabiś M, Tkaczuk-Włach J, Kotarski J, Polak G. (2016). Anti-Müllerian hormone: structure, properties and appliance. Ginekologia polska. 87(9).

Fong SL, Schipper I, Valkenburg O, de Jong FH, Visser JA, Laven JS. (2015). The role of anti-Müllerian hormone in the classification of anovulatory infertility. European Journal of Obstetrics & Gynecology and Reproductive Biology. 186:75-9.

Dewailly D, Andersen CY, Balen A, Broekmans F, Dilaver N, Fanchin R, Griesinger G, Kelsey TW, La Marca A, Lambalk C, Mason H. (2014). The physiology and clinical utility of anti-Müllerian hormone in women. Human reproduction update. 20(3):370-85.

Silva JB, Panaino TR, Tamm MA, Lira P, Arêas PC, Mancebo AC, Souza MM, Antunes RA, Souza MD. (2016). Prediction of metaphase II oocytes according to different serum Anti-Müllerian hormone (AMH) levels in antagonist ICSI cycles. JBRA Assisted Reproduction. 20(4):222-6

La Marca A, Minasi MG, Sighinolfi G, Greco P, Argento C, Grisendi V, Fiorentino F, Greco E. (2017). Female age, serum antimüllerian hormone level, and number of oocytes affect the rate and number of euploid blastocysts in in vitro fertilization/intracytoplasmic sperm injection cycles. Fertility and sterility. 108(5):777-83.

Tarasconi B, Tadros T, Ayoubi JM, Belloc S, de Ziegler D, Fanchin R. (2017). Serum antimüllerian hormone levels are independently related to miscarriage rates after in vitro fertilization–embryo transfer. Fertility and sterility. 108(3):518-24.

Arnanz A. Anti-Müllerian Hormone as a Quantitative and Qualitative Marker of Euploid Blastocysts’. InVienna: ESHRE Congress 2019.

Melado L, Arnanz A, Bayram A, Elkhatib I, De Munck N, Navarro AT, Coughlan C, Lawrenz B, Fatemi HM. (2020). Anti-Müllerian hormone is an independent marker for oocyte survival after vitrification. Reproductive BioMedicine Online. 41(1):119-27.

Dąbkowska-Huć A, Lemm M, Sikora J, Witek A, Skałba P. (2013). Anti-Müllerian hormone dynamics during ovulation induction treatment with recombinant follicle-stimulating hormone in women with polycystic ovary syndrome. Endokrynologia Polska. 64(3):203-7

Gnoth C, Schuring AN, Friol K, Tigges J, Mallmann P, Godehardt E. (2008). Relevance of anti-Mullerian hormone measurement in a routine IVF program. Human Reproduction. 23(6):1359-65.

Dunlop CE, Anderson RA. (2015). Uses of anti-Müllerian hormone (AMH) measurement before and after cancer treatment in women. Maturitas. 80(3):245-50.

Ezeiruaku FC, Ezeani CL. (2018). Anti-Mullerian Hormone: Establishing the Ovarian Reserve Range with Age in Rivers State Women, Niger Delta Region of Nigeria. Open Journal of Endocrine and Metabolic Diseases. 8(9):167-75.

Liu H, Hong, L. (2017). Anti-Mullerian Hormone as Examination for Ovulatory Dysfunction of Female. Biomedical Research; 28: 55-64.

Seifer DB, Golub ET, Lambert-Messerlian G, Benning L, Anastos K, Watts DH, Cohen MH, Karim R, Young MA, Minkoff H, Greenblatt RM. (2009). Variations in serum müllerian inhibiting substance between white, black, and Hispanic women. Fertility and sterility. 1;92(5):1674-8.

Kaur M, Arora M. (2013). Diminished ovarian reserve, causes, assessment and management. Int J Infertil Fetal Med. 4(2):45-55.

Amballi AA, Dada OA, Adeleye AO, Jide S. (2007). Evaluation of the determination of reference ranges for reproductive hormones (prolactin, FSH, LH, and testosterone) using enzyme immunoassay method. Sci Res Essays. 2(4):135-8.

Iliodromiti S, Kelsey TW, Wu O, Anderson RA, Nelson SM. (2014). The predictive accuracy of anti-Müllerian hormone for live birth after assisted conception: a systematic review and meta-analysis of the literature. Human reproduction update. 20(4):560-70.

Jayaprakasan K, Pandian D, Hopkisson J, Campbell BK, Maalouf WE. (2014). Effect of ethnicity on live birth rates after in vitro fertilisation or intracytoplasmic sperm injection treatment. BJOG: An International Journal of Obstetrics & Gynaecology. 121(3):300-7

Bleil ME, Gregorich SE, Adler NE, Sternfeld B, Rosen MP, Cedars MI. (2014). Race/ethnic disparities in reproductive age: an examination of ovarian reserve estimates across four race/ethnic groups of healthy, regularly cycling women. Fertility and sterility. 101(1):199-207.

Jindal S, Greenseid K, Berger D, Santoro N, Pal L. (2012). Impaired gremlin 1 (GREM1) expression in cumulus cells in young women with diminished ovarian reserve (DOR). Journal of assisted reproduction and genetics. 29:159-62.

Freeman EW, Gracia CR, Sammel MD, Lin H, Lim LC, Strauss III JF. (2007). Association of anti-mullerian hormone levels with obesity in late reproductive-age women. Fertility and sterility. 87(1):101-6.

Dennis NA, Houghton LA, Jones GT, Van Rij AM, Morgan K, McLennan IS. (2012). The level of serum anti-Müllerian hormone correlates with vitamin D status in men and women but not in boys. The Journal of Clinical Endocrinology & Metabolism. 97(7):2450-5.

Sowers MF, Eyvazzadeh AD, McConnell D, Yosef M, Jannausch ML, Zhang D, Harlow S, Randolph JF. (2008). Anti-mullerian hormone and inhibin B in the definition of ovarian aging and the menopause transition. The Journal of Clinical Endocrinology & Metabolism. 93(9):3478-83.

Schuh-Huera SM, Johnson MP, Rosen B, Stemfeld MI, Cedas R.D. (2012). Genetic various and environmental factors associated with hormonal matters of ovarian reserve in gausian and American women, “Human Reproduction, 594 -602.

Faddy MJ, Gosden RG, Gougeon A, Richardson SJ, Nelson JF. (1992). Accelerated disappearance of ovarian follicles in mid-life: implications for forecasting menopause. Human reproduction. 7(10):1342-6.

van Disseldorp J, Faddy MJ, Themmen AP, De Jong FH, Peeters PH, Van der Schouw YT, Broekmans FJ. Relationship of serum antimullerian hormone concentration to age at menopause. The Journal of Clinical Endocrinology & Metabolism. 2008 Jun 1;93(6):2129-34.

Gleicher N, Barad DH. (2011). Dehydroepiandrosterone (DHEA) supplementation in diminished ovarian reserve (DOR). Reproductive Biology and Endocrinology, 9:1-2.

van Rooij IA, Broekmans FJ, Scheffer GJ, Looman CW, Habbema JD, de Jong FH, Fauser BJ, Themmen AP, te Velde ER. (2005). Serum antimüllerian hormone levels best reflect the reproductive decline with age in normal women with proven fertility: a longitudinal study. Fertility and sterility. 83(4):979-87.

Downloads

Published

2024-08-08

How to Cite

ANTI-MULLERIAN HORMONE AND OVARIAN RESERVE DISPARITY AMONG WOMEN OF THREE DIFFERENT ETHNIC GROUPS IN THE NIGER DELTA REGION, NIGERIA. (2024). INTERNATIONAL JOURNAL OF ENDOCRINOLOGY (IJEN), 2(2), 1-12. https://iaeme-library.com/index.php/IJEN/article/view/IJEN_02_02_001