» Articles » PMID: 32309767

Correlation of Anti-Müllerian Hormone Levels with Metabolic Syndrome Events in Polycystic Ovary Syndrome: A Cross-sectional Study

Overview
Date 2020 Apr 21
PMID 32309767
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Various endocrine disorders have been reported in women of reproductive age, 10% of which is affected by polycystic ovary syndrome (PCOS).

Objective: This study aimed to evaluate the correlation of anti-Müllerian hormone (AMH) levels with the metabolic syndrome in patients with PCOS.

Materials And Methods: This cross-sectional study employed a consecutive sampling method using medical records from January 2013 to December 2017 at Dr. Cipto Mangunkusumo General Hospital polyclinic and Yasmin in vitro fertilization Clinic (Kencana), Jakarta, Indonesia. The primary outcome of the study was the AMH levels as independent variable correlated with metabolic syndrome. The secondary outcome was also the AMH levels correlated with each PCOS phenotype. The tertiary outcome was each PCOS phenotype as independent variable correlated with metabolic syndrome.

Results: Women with phenotype 1 of PCOS had a median AMH level of 13.92 (range: 3.88-34.06) ng/ml. 21% patients had metabolic syndrome, with a median AMH level 7.65 (3.77-20.20) ng/ml, higher than the women without metabolic syndrome (p = 0.38). The most frequent phenotype in women with PCOS was phenotype 4, oligo- or anovulation and polycystic ovary morphology (OA/PCOM) in 41.3%. The most frequent phenotype in women with metabolic syndrome was phenotype 1, OA + PCOM + hyperandrogenism in 56.5%.

Conclusion: All PCOS phenotypes exhibited significant correlations with the AMH level. Phenotype 1 (OA + PCOM + hyperandrogenism) was associated with the highest AMH level and was significantly associated with metabolic syndrome.

Citing Articles

Anti-Mullerian Hormone and Fertility Treatment Decisions in Polycystic Ovary Syndrome: A Literature Review.

Shah D, Jirge P J Hum Reprod Sci. 2024; 17(1):16-24.

PMID: 38665612 PMC: 11041323. DOI: 10.4103/jhrs.jhrs_153_23.


Age-group-specific reference intervals for anti-Müllerian hormone and its diagnostic performance for polycystic ovary syndrome in a Korean population.

Song J, Park Y, Cho H, Lee S, Kim S, Lim J J Clin Lab Anal. 2021; 35(7):e23861.

PMID: 34097316 PMC: 8274997. DOI: 10.1002/jcla.23861.

References
1.
Li L, Chen X, He Z, Zhao X, Huang L, Yang D . Clinical and metabolic features of polycystic ovary syndrome among Chinese adolescents. J Pediatr Adolesc Gynecol. 2012; 25(6):390-5. DOI: 10.1016/j.jpag.2012.07.006. View

2.
. Revised 2003 consensus on diagnostic criteria and long-term health risks related to polycystic ovary syndrome. Fertil Steril. 2004; 81(1):19-25. DOI: 10.1016/j.fertnstert.2003.10.004. View

3.
Zahiri Z, Sharami S, Milani F, Mohammadi F, Kazemnejad E, Ebrahimi H . Metabolic Syndrome in Patients with Polycystic Ovary Syndrome in Iran. Int J Fertil Steril. 2016; 9(4):490-6. PMC: 4793169. DOI: 10.22074/ijfs.2015.4607. View

4.
Shroff R, Syrop C, Davis W, Van Voorhis B, Dokras A . Risk of metabolic complications in the new PCOS phenotypes based on the Rotterdam criteria. Fertil Steril. 2007; 88(5):1389-95. DOI: 10.1016/j.fertnstert.2007.01.032. View

5.
Dumont A, Robin G, Catteau-Jonard S, Dewailly D . Role of Anti-Müllerian Hormone in pathophysiology, diagnosis and treatment of Polycystic Ovary Syndrome: a review. Reprod Biol Endocrinol. 2015; 13:137. PMC: 4687350. DOI: 10.1186/s12958-015-0134-9. View