ABSTRACT
Background: The use of biomarkers for diagnosis of Preeclampsia [PE], a life-threatening pregnancy disorder, could reduce serious complications of this disease. In this study, we investigated dysregulation of endoglin [Eng] expression and diagnostic accuracy of soluble endoglin [sEng] in PE patients
Methods: For this case-control study, 26 mild and 15 severe preeclamptic women along with 20 normotensive controls were recruited. The expression level of Eng [the co-receptor of TGF-[31] was evaluated using qRT-PCR
Also, the serum concentration of soluble Eng and expression of membranous Eng were determined by ELISA and immunohistochemistry
Results: A significant up-regulation in Eng mRNA and sEng levels was observed in PE patients versus normal controls. Immunohistochemistry [IHC] showed up-regulation of membranous Eng staining in syncytiotrophoblast and cytotrophoblast cells of PE patients
The serum levels of sEng were significantly increased in all patients [mild, sever, early- and late-onset] as compared to healthy pregnant women [P<0.001]. Receiver-operating characteristic [ROC] curve analysis revealed that sEng had the highest accuracy in distinguishing PE from normal pregnancies with cut-off value of 20.4, sensitivity of 92.1%, specificity of 90%, and area under the curve [AUC] of 0.94 [95% Cl: 0.88-1.00]
Conclusions: Our data showed that the up-regulation of Eng mRNA along with its membranous and soluble form in PE patients leads to defect in angiogenesis pathway. Also, the results of this study revealed sEng potential as a marker for diagnosis of PE and its severity