Hypertension
Poster Session 1
Caroline Smith, BA (she/her/hers)
University of Pittsburgh School of Medicine
Pittsburgh, PA, United States
Carrie Bennett, MD
University of Pittsburgh Medical Center
Pittsburgh, PA, United States
Lara S. Lemon, PhD, PharmD
Assistant Research Professor
University of Pittsburgh
Pittsburgh, PA, United States
Agnes Koczo, MD
UPMC Magee-Womens Hospital
Pittsburgh, PA, United States
Taylor Snisky, BS
MWRI
Pittsburgh, PA, United States
Christina J. Megli, MD,PhD
Research Assistant Professor
Magee- Womens Hospital UPMC
Pittsburgh, PA, United States
Alisse Hauspurg, MD
Assistant Professor
UPMC Magee-Womens Hospital
Pittsburgh, PA, United States
Activin A is a pleotropic protein and marker of endothelial dysfunction and cardiac fibrosis in pregnant and non-pregnant individuals. We sought to assess the relationship between maternal serum activin A concentration at delivery, severity of hypertensive disorder of pregnancy (HDP) and postpartum blood pressure (BP) following a HDP.
Study Design:
We conducted a cohort study of individuals with a HDP who delivered between 3/2019 and 3/2022 co-enrolled in our institution’s biospecimen repository and our remote (BP) monitoring program. Eligible individuals had a physician adjudicated HDP diagnosis, no pre-pregnancy hypertension, a serum specimen collected at the time of delivery and reported at least five home BPs in the first six weeks postpartum. Serum activin A was measured by R&D Systems ELISA. Aspirin use during pregnancy was ascertained from the medical record. We used nonparametric Spearman correlations to compare activin concentrations and continuous variables and Wilcoxon rank sum and non-parametric test for trend to compare concentrations across categorical variables.
Results:
We included 76 individuals who contributed 2121 home BPs to this analysis. Maternal serum activin concentration increased in a stepwise fashion with severity of HDP (non-parametric test for trend p< 0.01) but did not differ significantly by aspirin use in pregnancy. Activin concentration was also significantly correlated with peak systolic (r:0.33, p< 0.01) and diastolic (r: 0.24, p=0.03) postpartum BP, but was not correlated with pre-delivery peak systolic (r: 0.11, p=0.35) or diastolic BP (r: 0.06, p=0.58). Individuals requiring initiation of anti-hypertensive medications had higher activin concentrations compared to those never requiring medications (p=0.001).
Conclusion:
In our study, higher serum activin concentrations at the time of delivery were related to increasing severity of HDP, higher peak postpartum BP and need for anti-hypertensive medication. Our results suggest the potential of activin A as a promising biomarker for improving postpartum risk stratification among individuals with HDP.