Poster Session 3
Category: Medical/Surgical/Diseases/Complications
Poster Session 3
Zezhen Xiang, MS (he/him/his)
Washington University School of Medicine
Saint Louis, Missouri, United States
Jeannie C. Kelly, MD, MS (she/her/hers)
Associate Professor
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
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
Associate Professor
Washington University School of Medicine
St. Louis, 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
Peinan Zhao, PhD
Washington University School of Medicine
Washington University School of Medicine, Missouri, United States
Yong Wang, PhD (he/him/his)
Washington University School of Medicine
Washington University School of Medicine, Missouri, United States
21 participants (6 POE; 4 controls; 11 SPTB) with similar demographics were included; The control patients were all term births with no POE. SPTB occurred at a mean gestation of 34 weeks. Immune cell ratios in placental vessels increased over pregnancy in both SPTB (R2 = 0.714, p < 0.0001) and POE (R2 = 0.690, p=0.0055), but not controls (R2 = 0.018, p = 0.6809); SPTB demonstrated a steeper increase than both POE (F = 3.69, p =0.0389) and controls (F = 10.02, p = 0.0005) (Fig. B). No longitudinal changes in tissue T2* were observed within groups, but SPTB showed persistently lower oxygenation compared to controls (F=14.96, p < 0.0001), but not POE (F=0.89, p=0.4196) (Fig. C).
Conclusion:
Both POE and SPTB demonstrated increasing immune cells within placental vessels and persistently lower oxygenation within placental tissue, suggesting shared pathways for placental dysregulation. However, SPTB showed a steeper immune response, potentially distinguishing a threshold for risk of preterm birth.