Changes in circulating forms of anti-Muüllerian hormone and androgens in women with and without PCOS: a systematic longitudinal study throughout pregnancy.


Journal

Human reproduction (Oxford, England)
ISSN: 1460-2350
Titre abrégé: Hum Reprod
Pays: England
ID NLM: 8701199

Informations de publication

Date de publication:
02 05 2023
Historique:
received: 12 12 2022
revised: 23 02 2023
medline: 3 5 2023
pubmed: 16 3 2023
entrez: 15 3 2023
Statut: ppublish

Résumé

What are the changes in serum concentration of total and cleaved anti-Muüllerian hormone (AMH) molecular forms and of androgens before and throughout pregnancy in women with and without polycystic ovary syndrome (PCOS) in a longitudinal follow-up investigation? Serum levels of total and cleaved AMH are higher from preconception to the third trimester of pregnancy in women with PCOS as compared to controls, whereas testosterone and androstenedione levels are higher in women with PCOS than in control women before pregnancy and during the second and third trimester of pregnancy. Cross-sectional or partial longitudinal studies have shown higher AMH and androgen levels in pregnant women with PCOS as compared with non-PCOS women. To date, no complete longitudinal dynamic monitoring of the circulating forms of AMH and androgens from pre-conception to the third trimester of pregnancy have compared women with and without PCOS. This systematic prospective quarterly longitudinal monocentric study was a comparative follow-up of 30 women with PCOS and 29 controls before and during pregnancy from April 2019 to July 2022. Women aged 18-43 years with a pre-conception measurement of AMH were included during the first trimester of a singleton pregnancy. The PCOS group was defined according to the Rotterdam diagnostic criteria. The control group patients included in the study had normal ovarian reserves. Circulating total and cleaved AMH, and serum estradiol, LH, and androgen levels were measured during the first, second, and third trimester of pregnancy in all study participants. Before pregnancy, patients with PCOS had higher levels of AMH than controls. The total and cleaved AMH forms were significantly higher in women with PCOS than controls from pre-conception to the third trimester of pregnancy (all P < 0.001). Androgens (total testosterone and androstenedione) were higher in women with PCOS than controls from mid-pregnancy onwards. Our control population was a population of infertile women with no ovarian problems but most of them had undergone ART treatments to achieve pregnancy. These results strengthen the hypothesis that gestational hyperandrogenism as well as exposure to elevated AMH levels in utero could be driving forces predisposing female progeny to develop PCOS. Funding was provided by INSERM, France (grant number U1172) and the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation program, ERC-2016-CoG to P.G. grant agreement n° 725149/REPRODAMH. The authors have nothing to declare. NCT03483792.

Identifiants

pubmed: 36921289
pii: 7078527
doi: 10.1093/humrep/dead050
pmc: PMC10152173
doi:

Substances chimiques

Androgens 0
Androstenedione 409J2J96VR
Anti-Mullerian Hormone 80497-65-0
Testosterone 3XMK78S47O

Banques de données

ClinicalTrials.gov
['NCT03483792']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

938-950

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of European Society of Human Reproduction and Embryology.

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Auteurs

M Peigné (M)

Laboratory of Development and Plasticity of the Neuroendocrine Brain, University of Lille, Inserm, CHU Lille, Lille Neuroscience and Cognition, UMR-S 1172, Lille, France.
Department of Reproductive Medicine and Fertility Preservation, AP-HP-Université Sorbonne Paris-Nord, Jean Verdier Hospital, Bondy, France.
Department of Medical Gynecology, CHU Lille, Jeanne de Flandre Hospital, Lille, France.

V Simon (V)

Laboratory of Development and Plasticity of the Neuroendocrine Brain, University of Lille, Inserm, CHU Lille, Lille Neuroscience and Cognition, UMR-S 1172, Lille, France.
Department of Medical Gynecology, CHU Lille, Jeanne de Flandre Hospital, Lille, France.

P Pigny (P)

Department of Biochemistry and Hormonology, CHU Lille, Centre de Biologie Pathologie, Lille, France.

N E H Mimouni (NEH)

Laboratory of Development and Plasticity of the Neuroendocrine Brain, University of Lille, Inserm, CHU Lille, Lille Neuroscience and Cognition, UMR-S 1172, Lille, France.

C Martin (C)

Department of Biostatistics, CHU Lille, Lille, France.

D Dewailly (D)

Laboratory of Development and Plasticity of the Neuroendocrine Brain, University of Lille, Inserm, CHU Lille, Lille Neuroscience and Cognition, UMR-S 1172, Lille, France.
Department of Medical Gynecology, CHU Lille, Jeanne de Flandre Hospital, Lille, France.

S Catteau-Jonard (S)

Laboratory of Development and Plasticity of the Neuroendocrine Brain, University of Lille, Inserm, CHU Lille, Lille Neuroscience and Cognition, UMR-S 1172, Lille, France.
Department of Medical Gynecology, CHU Lille, Jeanne de Flandre Hospital, Lille, France.

P Giacobini (P)

Laboratory of Development and Plasticity of the Neuroendocrine Brain, University of Lille, Inserm, CHU Lille, Lille Neuroscience and Cognition, UMR-S 1172, Lille, France.

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