Poster Session 3
Jasmine Rios, MPH (she/her/hers)
Medical Student
Pritzker School of Medicine, University of Chicago
Chicago, Illinois, United States
Renee Odom-Konja, MPH
Research Coordinator, Department of Obstetrics and Gynecology
Endeavor Health
Evanston, Illinois, United States
Lauren S. Keenan-Devlin, MPH, PhD
Research Scientist, Research Assistant Professor
Endeavor Health/ University of Chicago Pritzker School of Medicine
Endeavor Health, Illinois, United States
Linda M. Ernst, MD
Endeavor Health
Evanston, Illinois, United States
Alexa A. Freedman, PhD (she/her/hers)
Northwestern University
Chicago, Illinois, United States
Greg E. Miller, PhD
Professor
Northwestern University
Chicago, Illinois, United States
Ann EB Borders, MD, MPH, MSc (she/her/hers)
Ian Bernard Horowitz Chair of Obstetrics, Clinical Professor
Endeavor Health, Evanston Hospital
Evanston, IL, United States
COVID-19 infection during pregnancy has been linked to adverse birth outcomes, potentially due to increased inflammation. This study compared placental inflammation in individuals with COVID-19 infection during pregnancy to placentas of those who delivered prior to the pandemic to understand inflammation associated with COVID-19 infection and timing.
Study Design:
Participants were enrolled in the Stress, Pregnancy, and Health study from 2018-2022. Placentas were collected < 2 hours from delivery and histologically examined. Medical records were manually reviewed for evidence of COVID-19; infection timing, severity, symptoms, vaccination status were abstracted for those infected. The control group included placentas from births before December 1, 2019. Models were adjusted for maternal age, race/ethnicity, and socioeconomic characteristics.
Results:
Among the 605 participants, 57 had confirmed COVID-19 infections and 214 delivered before December 1, 2019. Of the 57 positive cases, 5(8.7%) were asymptomatic, 39(68.4%) mild, 1(1.7%) severe, and 6(10.5%) did not have documented symptoms. Those infected with COVID-19 during pregnancy had increased odds of high-grade placental chronic inflammation (OR=2.23, CI 1.06-4.69), particularly amongst those infected before 20 weeks gestation (OR=3.57, CI 1.25-10.18). Prevalence of chronic basal villitis was higher in those infected with COVID-19 (p< 0.001). There were no significant differences in acute inflammation (p=0.169), fetal vascular pathology (p=0.488), or maternal vascular pathology (p=0.255) between the infected and uninfected cohorts.
Conclusion:
In a cohort of predominantly mild COVID-19 infections during pregnancy, COVID-19 was associated with increased odds of placental chronic inflammation, driven primarily by chronic basal villitis. Inflammatory patterns differed by timing of infection, with increased odds of chronic placental lesions among those infected early in pregnancy. These findings enhance understanding of COVID-19 infection's inflammatory effects in pregnancy, aiding in prevention and treatment of at-risk pregnant patients.