Frontiers in Endocrinology (Apr 2024)

Genetic and inflammatory factors underlying gestational diabetes mellitus: a review

  • Gyan Watson Ray,
  • Gyan Watson Ray,
  • Gyan Watson Ray,
  • Qiaoli Zeng,
  • Qiaoli Zeng,
  • Qiaoli Zeng,
  • Phidelia Kusi,
  • Hengli Zhang,
  • Hengli Zhang,
  • Hengli Zhang,
  • Taotao Shao,
  • Taotao Shao,
  • Taili Yang,
  • Yue Wei,
  • Mianqin Li,
  • Xiaoqun Che,
  • Xiaoqun Che,
  • Runmin Guo,
  • Runmin Guo,
  • Runmin Guo

DOI
https://doi.org/10.3389/fendo.2024.1399694
Journal volume & issue
Vol. 15

Abstract

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Gestational diabetes mellitus (GDM) poses a significant global health concern, impacting both maternal and fetal well-being. Early detection and treatment are imperative to mitigate adverse outcomes during pregnancy. This review delves into the pivotal role of insulin function and the influence of genetic variants, including SLC30A8, CDKAL1, TCF7L2, IRS1, and GCK, in GDM development. These genetic variations affect beta-cell function and insulin activity in crucial tissues, such as muscle, disrupting glucose regulation during pregnancy. We propose a hypothesis that this variation may disrupt zinc transport, consequently impairing insulin production and secretion, thereby contributing to GDM onset. Furthermore, we discussed the involvement of inflammatory pathways, such as TNF-alpha and IL-6, in predisposing individuals to GDM. Genetic modulation of these pathways may exacerbate glucose metabolism dysregulation observed in GDM patients. We also discussed how GDM affects cardiovascular disease (CVD) through a direct correlation between pregnancy and cardiometabolic function, increasing atherosclerosis, decreased vascular function, dyslipidemia, and hypertension in women with GDM history. However, further research is imperative to unravel the intricate interplay between inflammatory pathways, genetics, and GDM. This understanding is pivotal for devising targeted gene therapies and pharmacological interventions to rectify genetic variations in SLC30A8, CDKAL1, TCF7L2, IRS1, GCK, and other pertinent genes. Ultimately, this review offers insights into the pathophysiological mechanisms of GDM, providing a foundation for developing strategies to mitigate its impact.

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