Association of D-dimer, platelet-activating factor, and soluble vascular endothelial growth factor receptor 1 levels with disease severity and prognosis in gestational hypertension
- PMID: 40821034
- PMCID: PMC12351624
- DOI: 10.62347/WGEX7482
Association of D-dimer, platelet-activating factor, and soluble vascular endothelial growth factor receptor 1 levels with disease severity and prognosis in gestational hypertension
Abstract
Objective: To investigate the associations of D-dimer (D-D), platelet-activating factor (PAF), and soluble vascular endothelial growth factor receptor 1 (sVEGFR-1) levels with disease severity and prognosis in hypertensive disorders complicating pregnancy (HDCP).
Methods: A total of 138 HDCP patients were categorized as the gestational hypertension (GH, n = 62), preeclampsia (PE, n = 45), and severe preeclampsia (SPE, n = 31) groups. Fifty healthy pregnant women served as controls. Plasma D-D and serum PAF and sVEGFR-1 levels were measured and compared. ROC curves assessed their diagnostic and prognostic value. Based on neonatal Apgar score <7 or grade III amniotic fluid contamination, patients were divided into good (n = 73) and poor (n = 65) prognosis groups.
Results: D-D, PAF, and sVEGFR-1 levels increased with disease severity (all P<0.05). The AUCs for diagnosing HDCP severity were 0.893 (D-D), 0.889 (PAF), 0.825 (sVEGFR-1), and 0.944 (combined). Multivariate logistic regression identified D-D, PAF, sVEGFR-1, and 24h RPO as independent prognostic factors (all P<0.05). Combined AUC for prognosis prediction was 0.883.
Conclusion: Elevated D-D, PAF, and sVEGFR-1 levels are closely associated with HDCP severity and prognosis, offering high diagnostic and predictive value.
Keywords: D-dimer; Hypertensive disorders of pregnancy; disease condition; human soluble vascular endothelial growth factor receptor 1; platelet-activating factor; prognosis.
AJTR Copyright © 2025.
Conflict of interest statement
None.
Figures




Similar articles
-
Serum VEGF-A and sVEGFR-1 levels as predictors of disease severity in COVID-19 patients.Diagn Microbiol Infect Dis. 2025 Nov;113(3):117007. doi: 10.1016/j.diagmicrobio.2025.117007. Epub 2025 Jul 14. Diagn Microbiol Infect Dis. 2025. PMID: 40684546
-
Assessment of the relationship between hematologic parameters, (CPD), in screening for COVID-19 severity in women.Future Sci OA. 2025 Dec;11(1):2540749. doi: 10.1080/20565623.2025.2540749. Epub 2025 Aug 2. Future Sci OA. 2025. PMID: 40752013 Free PMC article.
-
[Interaction of α-amylase and inflammatory response in patients with ventilator-associated pneumonia and their prognostic value].Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2025 Jun;37(6):535-541. doi: 10.3760/cma.j.cn121430-20240409-00321. Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2025. PMID: 40820528 Chinese.
-
Accuracy of placental growth factor alone or in combination with soluble fms-like tyrosine kinase-1 or maternal factors in detecting preeclampsia in asymptomatic women in the second and third trimesters: a systematic review and meta-analysis.Am J Obstet Gynecol. 2023 Sep;229(3):222-247. doi: 10.1016/j.ajog.2023.03.032. Epub 2023 Mar 28. Am J Obstet Gynecol. 2023. PMID: 36990308
-
Accuracy of routine laboratory tests to predict mortality and deterioration to severe or critical COVID-19 in people with SARS-CoV-2.Cochrane Database Syst Rev. 2024 Aug 6;8(8):CD015050. doi: 10.1002/14651858.CD015050.pub2. Cochrane Database Syst Rev. 2024. PMID: 39105481 Free PMC article.
References
-
- Zanini MJ, Domínguez C, Fernández-Oliva T, Sánchez O, Toda MT, Foraster M, Dadvand P, Llurba E. Urban-related environmental exposures during pregnancy and placental development and preeclampsia: a review. Curr Hypertens Rep. 2020;22:81. - PubMed
-
- Ives CW, Sinkey R, Rajapreyar I, Tita ATN, Oparil S. Preeclampsia-pathophysiology and clinical presentations: JACC state-of-the-art review. J Am Coll Cardiol. 2020;76:1690–1702. - PubMed
-
- Yang C, Baker PN, Granger JP, Davidge ST, Tong C. Long-term impacts of preeclampsia on the cardiovascular system of mother and offspring. Hypertension. 2023;80:1821–1833. - PubMed
LinkOut - more resources
Full Text Sources