Abstract

Gestational diabetes mellitus is a transient form of glucose intolerance occurring during pregnancy. Pregnancies affected by gestational diabetes mellitus are at risk for the development of preeclampsia, a severe life threatening condition, associated with significant feto-maternal morbidity and mortality. It is a risk factor for long-term health in women and their offspring. Pregnancy has been shown to be associated with a subliminal degree of neutrophil activation and tightly regulated generation of neutrophil extracellular traps (NETs). This response is excessive in cases with preeclampsia, leading to the presence of large numbers of NETs in affected placentae. We have recently observed that circulatory neutrophils in cases with gestational diabetes mellitus similarly exhibit an excessive pro-NETotic phenotype, and pronounced placental presence, as detected by expression of neutrophil elastase. Furthermore, exogenous neutrophil elastase liberated by degranulating neutrophils was demonstrated to alter trophoblast physiology and glucose metabolism by interfering with key signal transduction components. In this review we examine whether additional evidence exists suggesting that altered neutrophil activity in gestational diabetes mellitus may contribute to the development of preeclampsia.

Highlights

  • Gestational diabetes mellitus (GDM) is defined as glucose intolerance manifesting during pregnancy in women with no prior history of diabetes [1,2,3,4]

  • Pregnancies complicated by GDM, or other diabetic conditions, are associated with poor outcome and are frequently affected by further complications such as PE, a severe life-threatening condition [6, 31]

  • In this review we have attempted to discern whether overt neutrophil activity and NETosis in pregnancies affected by GDM, could contribute to the subsequent development of PE

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Summary

Introduction

Gestational diabetes mellitus (GDM) is defined as glucose intolerance manifesting during pregnancy in women with no prior history of diabetes [1,2,3,4].

Results
Conclusion

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