# Anti-Müllerian hormone, sex steroids, and metabolic profile in cord blood of pregnancies with type 2 diabetes and gestational diabetes

**Authors:** Claudio Villarroel, Patricia López, Soledad Henriquez, Paulina Kohen, Ethel Codner

PMC · DOI: 10.3389/fendo.2025.1589541 · Frontiers in Endocrinology · 2025-07-28

## TL;DR

This study shows that type 2 diabetes in mothers affects the intrauterine environment, altering hormone and metabolic levels in the cord blood of female infants.

## Contribution

The study is the first to examine ovarian markers and metabolic profiles in cord blood of preterm infants from pregnancies with type 2 diabetes and gestational diabetes.

## Key findings

- AMH levels in cord blood were significantly higher in pregnancies with type 2 diabetes compared to gestational diabetes and controls.
- Type 2 diabetes was associated with lower adiponectin and higher insulin and IGF-1 levels in cord blood.
- No significant correlations were found between maternal and cord blood levels of AMH, insulin, IGF-1, and androgens.

## Abstract

The prevalence of type 2 diabetes (T2D) and gestational diabetes (GD)among women of reproductive age has increased in recent decades, making it the most common pregnancy complication. Many studies have examined pregnancy complications in women with diabetes; however, the impact of diabetes on the intrauterine environment, specifically ovarian markers and metabolic profiles in very preterm infants at birth, has not been studied. This study aimed to investigate AMH, sex steroid levels, and the metabolic profile in venous cord blood (VCB) in gestations affected by type 2 diabetes (T2D) and gestational diabetes (GD).

Hormonal profile was evaluated in VCB of pregnancies with T2D (n=24), GD (n=26), and pregnancies without diabetes (C, n=25). Only pregnancies carrying a female offspring were included. AMH, sex steroids, and metabolic function biomarkers, including glucose, insulin, IGF-1, and adiponectin (APN) were measured. Clinical and anthropometric data were assessed in the mothers and offspring.

AMH VCB levels were significantly higher in T2D than in GD and C pregnancies (P<0.01 and P<0.005, respectively). Dehydroepiandrosterone sulfate (DHEAS) and sex hormone-binding globulin (SHBG) VCB levels were lower in T2D pregnancies than in GD and C (P < 0.01, P < 0.0001, respectively). APN levels were lower in T2D pregnancies than in C (P < 0.05). Additionally, higher insulin and IGF-1 VCB levels and HOMA-IR index were observed in T2D than in C and GD (P < 0.001, P<0.05, and P<0.05, respectively). No significant correlations were observed between maternal and AMH, insulin, IGF-1, and androgen VCB levels.

T2D disrupts the intrauterine environment, leading to increased insulin, IGF-1, HOMA-IR, and AMH concentrations and decreased adiponectin levels in VCB. These findings describe the impact that maternal T2D may have on the health and development of their offspring.

## Linked entities

- **Proteins:** AMH (anti-Mullerian hormone), SULT2A1 (sulfotransferase family 2A member 1), SHBG (sex hormone binding globulin), PIN (insulin precursor), IGF1 (insulin like growth factor 1)
- **Diseases:** type 2 diabetes (MONDO:0005148), gestational diabetes (MONDO:0005406)

## Full-text entities

- **Genes:** AMH (anti-Mullerian hormone) [NCBI Gene 268] {aka MIF, MIS}, ADIPOQ (adiponectin, C1Q and collagen domain containing) [NCBI Gene 9370] {aka ACDC, ACRP30, ADIPQTL1, ADPN, APM-1, APM1}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, SHBG (sex hormone binding globulin) [NCBI Gene 6462] {aka ABP, SBP, TEBG}
- **Diseases:** GD (MESH:D016640), diabetes (MESH:D003920), T2D (MESH:D003924)
- **Chemicals:** steroid (MESH:D013256), DHEAS (MESH:D019314), glucose (MESH:D005947)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12336012/full.md

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Source: https://tomesphere.com/paper/PMC12336012