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Association of sFlt-1 and C-reactive protein with outcomes in severe preeclampsia: A cohort study
Leandro Nóbrega1, Leila Katz, Luis Lippo
1Department of Maternal and Child Health, Instituto de Medicina Integral Prof.Fernando Figueira (IMIP), Recife, Pernambuco, Brazil,Department of Obstetrics,Universidade Federal de Campina Grande (UFCG), Campina Grande, Paraíba,Brazil,Faculdade Pernambucana de Saúde (FPS), Recife, Pernambuco, Brazil.
Insights
Soluble FMS-like tyrosine kinase-1 (sFlt-1) is elevated in preeclampsia with severe features and predicts adverse maternal and fetal outcomes, unlike hs-CRP. These biomarkers, though predictive, do not correlate, suggesting varied pathogenic pathways in preeclampsia.
Area of Science:
- Obstetrics and Gynecology
- Maternal-Fetal Medicine
- Biomarker Research
Background:
- Preeclampsia (PE) with severe features presents significant maternal and perinatal risks.
- Understanding the role of biomarkers like soluble FMS-like tyrosine kinase-1 (sFlt-1) and high-sensitivity C-reactive protein (hs-CRP) is crucial for predicting PE outcomes.
Purpose of the Study:
- To investigate the association between serum sFlt-1 and hs-CRP levels and maternal/perinatal outcomes in patients with preeclampsia with severe features.
- To evaluate the predictive capabilities of sFlt-1 and hs-CRP for adverse outcomes in severe preeclampsia.
Main Methods:
- A cohort study involving 100 third-trimester pregnant women (60 with PE, 40 controls).
- Serum sFlt-1 and hs-CRP levels were measured alongside clinical and epidemiological data.
- Hierarchical multiple regression and ROC curves were used to assess predictive abilities for adverse outcomes.
Main Results:
- Patients with PE had significantly higher sFlt-1 levels, but hs-CRP levels were not significantly different compared to controls.
- Both sFlt-1 and hs-CRP showed reasonable predictive ability for composite adverse maternal outcomes, but were not correlated with each other.
- sFlt-1, but not hs-CRP, was strongly associated with lower birth weight and Apgar score < 7 at 5 minutes.
Conclusions:
- Elevated sFlt-1 levels are characteristic of preeclampsia with severe features.
- While both biomarkers can predict adverse maternal outcomes, they exhibit distinct associations with perinatal morbidity, suggesting different underlying pathophysiological mechanisms in PE.
- Maternal age, prior hypertension, sFlt-1, and hs-CRP are independently associated with adverse maternal outcomes in severe preeclampsia.
Abstract:
To determine the association between soluble FMS-like tyrosine kinase-1 (sFlt-1) and high-sensitivity C-reactive protein (hs-CRP) with maternal and perinatal outcomes in patients with preeclampsia (PE) with severe features.A cohort study was conducted on 100 patients, 60 with PE with severe features, and 40 healthy women in the third trimester of pregnancy. Admission serum levels of sFlt-1 and hs-CRP and clinical and epidemiological parameters were evaluated to quantify the predictive ability of adverse maternal and perinatal outcomes using hierarchical multiple regression and receiver operating characteristic curves.Compared to controls, patients with PE and severe features had significantly higher levels of sFlt-1 but not hs-CRP. sFlt-1 and hs-CRP proved to be reasonable parameters for the prediction of composite adverse maternal outcomes. However, we found no correlation between these 2 biomarkers. PE integrated estimate of risk scores were correlated only with sFlt-1 levels. Regarding fetal outcomes, unlike hs-CRP, sFlt-1 was strongly associated with birth weight and Apgar score < 7 at 5 minutes. Following multivariate analysis, maternal age, previous hypertension, sFlt-1, and hs-CRP levels remained independently associated with composite adverse maternal outcomes.sFlt-1 levels were elevated in patients with PE and severe features. Both sFlt-1 and hs-CRP may predict composite adverse maternal outcomes but do not correlate with each other and differ in perinatal morbidity patterns. These data support the hypothesis that the varied outcomes in PE may result from different pathogenic pathways.
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