Oral Concurrent Session 1 - Medical and Surgical Complications of Pregnancy
Oral Concurrent Sessions
Jeannie C. Kelly, MD, MS (she/her/hers)
Associate Professor
Washington University School of Medicine
Washington University School of Medicine, Missouri, United States
Zezhen Xiang, MS (he/him/his)
Washington University School of Medicine
Saint Louis, Missouri, United States
Sam A. S. Williams, BS
Clinical Research Coordinator
Washington University School of Medicine
Washington University School of Medicine, Missouri, United States
Melissa Mills, BS
Research Coordinator
Washington University School of Medicine
Saint Louis, Missouri, United States
Emily Diveley, BSN, BS
Washington University School of Medicine
Washington University School of Medicine, Missouri, United States
Nandini Raghuraman, MD, MSCI (she/her/hers)
Associate Professor
Washington University School of Medicine
Washington University School of Medicine, Missouri, United States
Peinan Zhao, PhD
Washington University School of Medicine
Washington University School of Medicine, Missouri, United States
Nardhy Gomez-Lopez, PhD (she/her/hers)
Professor
Washington University School of Medicine
Washington University School of Medicine, Missouri, United States
Antonina I. Frolova, MD, PhD (she/her/hers)
Assistant Professor of Ob&Gyn
Washington University School of Medicine
St. Louis, Missouri, United States
Yong Wang, PhD (he/him/his)
Washington University School of Medicine
Washington University School of Medicine, Missouri, United States
20 participants (10 POE; 10 controls) with similar demographics were included (Table). Longitudinal analysis showed a progressive increase in immune cell infiltration from the first to the third trimester in POE cases, which was not observed in controls (Fig. B). Consistently, immune cell ratios in the third trimester were higher in POE cases than in controls (Fig. C). Although overall mean T2* values did not differ between groups (54.4±16.9 vs. 71.3±9.6 ms; p = 0.095), longitudinal analysis revealed persistently lower T2* values in POE placental tissue (F = 11.04, p = 0.0005; Fig. D), with no differences in placental vessels or intervillous space.
Conclusion:
POE reshapes the placental environment, with increased immune cell infiltration in the third trimester and reduced placental tissue oxygenation throughout gestation. This study provides the first noninvasive evidence of POE-induced placental immune pathology, suggesting a mechanism for adverse outcomes and a target for future interventions.