Kucukbas, Gokce NazKara, OzgurYuce, DenizUygur, Dilek2025-05-102025-05-1020221476-70581476-495410.1080/14767058.2020.17495912-s2.0-85083838591https://doi.org/10.1080/14767058.2020.1749591https://hdl.handle.net/20.500.14720/6014Yuce, Deniz/0000-0003-0725-5447; Kara, Ozgur/0000-0002-4204-0014; Kucukbas, Gokce Naz/0000-0002-2755-3700; Sahin, Dilek/0000-0001-8567-9048Objectives: Intrauterine growth restriction (IUGR) is diagnosed when the estimated fetal weight remains below the 10th percentile of gestational age based on pathological restriction of growth and/or accompanying Doppler abnormalities. Endothelial dysfunction is a common pathogenetic pathway underlying IUGR etiology. Endocan (ESM-1) is a novel marker of endothelial dysfunction and inflammation found in the maternal circulation. This study was designed to compare plasma endocan levels between pregnancies complicated with IUGR and a control group. Study design: Forty-four pregnancies complicated with IUGR and 47 healthy pregnancies were included. Maternal plasma endocan levels were detected by ELISA. Parametric data was studied by Student's t-test. Mann-Whitney U-test was used in analyzing non-parametric data. Categorical variables underwent chi-square test. ROC analysis was performed to define the cutoff value of endocan in detecting IUGR. Spearman correlation test was performed. Results: Maternal plasma endocan level varied significantly between IUGR and healthy pregnancies and was 1.8 fold higher in the IUGR group (793.0 (IQR:544.4-1896.0) ng/L vs. 441.8 (IQR: 408.3-512.4) ng/L, p < .001). There was a weak negative correlation between endocan level and 5th and 10th minute APGAR Scores (r = -0.256; p = .015 and r = -0.215; p = .042, respectively), a weak positive correlation with umbilical artery pulsatility index, and a moderate negative correlation with cerebroplacental ratio (r = 0.394; p < .001 and r = -0.459; p < .001, respectively). Conclusions: There was a significant difference between endocan levels of IUGR and healthy pregnancies. Further studies might be designed to investigate the performance of endocan in predicting neonatal outcomes for pregnancies complicated with IUGR.eninfo:eu-repo/semantics/closedAccessIntrauterine Growth RestrictionFetal Growth RestrictionEndocanEsm-1Endothelial DysfunctionInflammationMaternal Plasma Endocan Levels in Intrauterine Growth RestrictionArticle357Q4Q21295130032290736WOS:000526652300001