Platelet protease-activated receptor 4 genotype and response to aspirin in pregnancy.
Publication/Presentation Date
8-1-2025
Abstract
The platelet protease-activated receptor 4 (PAR4) threonine 120 (Thr120) allele is an activating allele associated with reduced aspirin response in vitro. Aspirin is recommended in high-risk pregnancies to prevent preeclampsia and preterm birth. We evaluated the impact of PAR4 genotype on aspirin response in pregnancy, as measured by platelet function assay 100 (PFA-100) epinephrine closure time, and perinatal outcomes. We conducted a prospective cohort study of high-risk pregnant patients who took 81-mg aspirin daily. PFA-100 was assessed at baseline, 2 to 4 weeks after aspirin initiation (follow-up 1), and 28 to 32 weeks' gestation (follow-up 2). Primary outcome was difference in PFA-100 by genotype. Exposure was defined as PAR4-Thr120 homozygous vs not. Of the 122 participants were included, 24 (19.6%) were PAR4-Thr120 homozygous, and 106 completed follow-up 1 with >75% adherence. Participants homozygous for PAR4-Thr120 had a significantly higher rate of prior preterm birth (50.0% vs 16.1%;
Volume
2
Issue
3
First Page
100085
Last Page
100085
ISSN
2950-3272
Published In/Presented At
Boelig, R. C., Michael, J. V., Tawk, A., Zhan, T., Chan, J. S. Y., Kraft, W. K., & McKenzie, S. E. (2025). Platelet protease-activated receptor 4 genotype and response to aspirin in pregnancy. Blood vessels, thrombosis & hemostasis, 2(3), 100085. https://doi.org/10.1016/j.bvth.2025.100085
Disciplines
Business Administration, Management, and Operations | Health and Medical Administration | Management Sciences and Quantitative Methods
PubMedID
40918740
Department(s)
Administration and Leadership
Document Type
Article