Labor Could Increase Systemic Inflammation and Cause or Deteriorate Cytokine Storm in COVID-19

Amir Hossein Norooznezhad1, Alireza A Shamshirsaz, Sedigheh Hantoushzadeh

  • 1Medical Biology Research Center, Health Technology Institute, Kermanshah University of Medical Sciences, Kermanshah, Iran.

Insights

Pregnant women with COVID-19 face increased risks. Labor and delivery can exacerbate inflammation through cytokine storm pathways, increasing maternal morbidity and mortality.

Area of Science:

  • Obstetrics and Gynecology
  • Infectious Diseases
  • Immunology

Background:

  • Pregnant women with COVID-19 exhibit higher morbidity and mortality rates.
  • COVID-19 is associated with a cytokine storm, an overrelease of pro-inflammatory cytokines like IL-1β, IL-6, and TNF-α.
  • Labor, particularly preterm labor and cesarean sections, involves inflammatory processes and cytokine release.

Purpose of the Study:

  • To explore the inflammatory pathways linking COVID-19 in pregnant women to adverse outcomes during and after labor.
  • To elucidate the role of cytokine storm, tissue injury, and postpartum hemorrhage in escalating inflammation.

Main Methods:

  • Review of existing literature on COVID-19, pregnancy, labor inflammation, and cytokine storm.
  • Analysis of proposed pathways involving cytokine storm, NFκB activation, and hypoxia-inducible factor 1α.

Main Results:

  • COVID-19 patients experience cytokine storms, increasing morbidity and mortality.
  • Labor involves inflammatory cytokines (IL-1β, IL-6, TNF-α) crucial in cytokine storm.
  • Tissue injury (e.g., C-section) and postpartum hemorrhage with hypoxemia activate inflammatory pathways (NFκB, HIF-1α).

Conclusions:

  • Clinicians must monitor and manage the escalating inflammatory status in pregnant COVID-19 patients during and post-labor.
  • Understanding these pathways is critical for mitigating risks associated with COVID-19 in pregnancy.
  • Interventions targeting inflammatory pathways may improve outcomes for pregnant women with COVID-19.

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