AMH as part of the diagnostic PCOS workup in large epidemiological studies

Author:

Piltonen Terhi T1ORCID,Komsi Elina1,Morin-Papunen Laure C1,Korhonen Elisa1,Franks Stephen2,Järvelin Marjo-Riitta3456,Arffman Riikka K1ORCID,Ollila Meri-Maija1ORCID

Affiliation:

1. Department of Obstetrics and Gynaecology, Medical Research Center Oulu, Research Unit of Clinical Medicine, University of Oulu and Oulu University Hospital , FI-90029, Oulu , Finland

2. Institute of Reproductive and Developmental Biology, Imperial College London, W12 0NN , London , United Kingdom

3. Faculty of Medicine, Center for Life Course Health Research, University of Oulu , FI-90014, Oulu , Finland

4. Unit of Primary Care, Oulu University Hospital , FI-90220, Oulu , Finland

5. Department of Epidemiology and Biostatistics, School of Public Health, MRC Centre for Environment and Health, Imperial College London , W2 1PG, London , United Kingdom

6. Department of Life Sciences, College of Health and Life Sciences, Brunel University London , UB8 3PH, London , United Kingdom

Abstract

Abstract Objectives Previous studies have shown good correlation between polycystic ovarian morphology (PCOM) and serum anti-Müllerian hormone (AMH) levels. We evaluated the utility of AMH as a surrogate for PCOM as a part of the polycystic ovary syndrome (PCOS) diagnosis by describing how the use of different AMH cut-off values would change the prevalence of PCOS. Methods A general population-based birth cohort study. Anti-Müllerian hormone concentrations were measured from serum samples taken at age 31 years (n = 2917) using the electrochemiluminescence immunoassay (Elecsys). Anti-Müllerian hormone data were combined with data on oligo/amenorrhoea and hyperandrogenism to identify women with PCOS. Results The addition of AMH as a surrogate marker for PCOM increased the number of women fulfilling at least two PCOS features in accordance with the Rotterdam criteria. The prevalence of PCOS was 5.9% when using the AMH cut-off based on the 97.5% quartile (10.35 ng/mL) and 13.6% when using the recently proposed cut-off of 3.2 ng/mL. When using the latter cut-off value, the distribution of PCOS phenotypes A, B, C, and D was 23.9%, 4.7%, 36.6%, and 34.8%, respectively. Compared with the controls, all PCOS groups with different AMH concentration cut-offs showed significantly elevated testosterone (T), free androgen index (FAI), luteinizing hormone (LH), LH/follicle-stimulating hormone (FSH) ratio, body mass index (BMI), waist circumference, and homoeostatic model assessment of insulin resistance (HOMA-IR) values, as well as significantly decreased sex hormone-binding globulin (SHBG) values. Conclusions Anti-Müllerian hormone could be useful surrogate for PCOM in large data sets, where transvaginal ultrasound is not feasible, to aid the capturing of women with typical PCOS characteristics. Anti-Müllerian hormone measurement from archived samples enables retrospective PCOS diagnosis when combined with oligo/amenorrhoea or hyperandrogenism.

Funder

Academy of Finland

Sigrid Juselius Foundation

Medical Research Center Oulu

Novo Nordisk Foundation

Roche Diagnostics International Ltd

University of Oulu

Oulu University Hospital

Ministry of Health and Social Affairs

National Institute for Health and Welfare

Regional Institute of Occupational Health, Oulu, Finland

European Regional Development Fund

DynaHEALTH

LifeCycle

LongITools

EDCMET

Medical Research Council, UK

MRC

Publisher

Oxford University Press (OUP)

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism

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