Hypertension
Poster Session 3
Rupsa C. Boelig, MD, MS (she/her/hers)
Assistant Professor
Thomas Jefferson University Hospital
Philadelphia, PA, United States
James Michael, PhD
Thomas Jefferson University
Philadelpia, PA, United States
Antonios Tawk, MD, MSc
Sidney Kimmel Medical College at Thomas Jefferson University Hospital
Philadelphia, PA, United States
Walter Kraft, MD
Sidney Kimmel Medical College at Thomas Jefferson University Hospital
Philadelphia, PA, United States
Steven McKenzie, MD, PhD
Sidney Kimmel Medical College at Thomas Jefferson University Hospital
Philadelphia, PA, United States
This is a prospective study of singletons at high risk for preeclampsia taking aspirin daily. Blood was drawn at baseline prior to aspirin (10-16 weeks’), 2-4 weeks after aspirin initiation (follow-up 1), and at 28-32 weeks’ (follow-up 2). PFA-100 epinephrine closure time (PFA-100 (epi)) is a known marker of aspirin response that increases with platelet inhibition. miRNAs (16, 18a, 181a, 126, 155, 223) were quantified in highly purified platelets and reported as fold-change from baseline. Pearson correlation coefficient was used to correlate PFA-100(epi) and miRNA fold change. Regression analysis was used to correlate fold-change in miRNAs and outcome of preeclampsia and preterm birth.
Results:
Of N=130 participants in parent study, N=57 had sufficient sample for miRNA extraction and reliable, reproducible quantification. At follow up-1, an increase in PFA-100(epi) was associated with a reduced miRNAs 223 (r=-0.33, p=0.017), 18a (r=-0.29, p=0.035), and 181a(r=-0.28, p=0.046). No miRNA at follow up-1 was associated with outcomes. At follow up-2, increased miRNA 223 was associated with preterm birth (B=6.5 (1.5-27.2), p=0.01) but not preeclampsia (B=2.0 (0.7-6.3, p=0.22).
Conclusion:
MicroRNAs are markers of both aspirin response in pregnancy and adverse pregnancy outcome. Platelet derived miRNA 223 has been associated with platelet activity and activation of inflammatory pathways, and is a promising marker for both tracking aspirin response and prediction of adverse pregnancy outcome.