Loss of E‐Cadherin Staining Continuity in the Trophoblastic Basal Membrane Correlates with Increased Resistance in Uterine Arteries and Proteinuria in Patients with Pregnancy‐Induced Hypertension

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Abstract

Pregnancy‐induced hypertension (PIH), especially when complicated with pre‐eclampsia (PE), could be a life‐threatening complication of pregnancy. Pre‐eclampsia is one of the leading causes of perinatal morbidity and mortality in women. Pre‐eclampsia is mainly characterized by hypertension and kidney damage with proteinuria. Abnormal placentation and altered structure of the placental barrier are believed to participate in the pathogenesis of pregnancy‐induced hypertension, leading to PE. In the current study, we aimed to analyze the immunohistochemical expression pattern of E‐cadherin and p120, two markers of epithelial–mesenchymal transition, in placental samples derived from a group of 55 patients with pregnancy‐induced hypertension, including pre‐eclampsia and 37 healthy pregnant controls. The results were correlated with the presence of an obtained early uterine artery flow notching during diastole on Doppler ultrasound. We observed a higher frequency of discontinuous E‐cadherin staining in the basement membrane of syncytiotrophoblast in patients with PIH/PE compared to controls (p < 0.001, Fisher’s exact test). Moreover, the loss of continuity of E‐cadherin expression correlated with the presence of a bilateral early diastolic notch on Doppler ultrasound (p < 0.001, Fisher’s exact test) and the presence of proteinuria (p = 0.013, Fisher’s exact test). These findings suggest that E‐cadherin contributes to the integrity of the placental barrier, and its loss could be an immunohistochemical marker of PE.

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Pęksa, M., Kamieniecki, A., Gabrych, A., Lew‐tusk, A., Preis, K., & Świątkowska‐freund, M. (2022). Loss of E‐Cadherin Staining Continuity in the Trophoblastic Basal Membrane Correlates with Increased Resistance in Uterine Arteries and Proteinuria in Patients with Pregnancy‐Induced Hypertension. Journal of Clinical Medicine, 11(3). https://doi.org/10.3390/jcm11030668

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