DOI 10.1016/j.placenta.2026.07.009
Levels of soluble Syndecan-1 and VEGF-A in maternal and cord blood in the presence of placental lesions of maternal vascular underperfusion and its association with fetal aortic intima media thickness.
Аннотация
INTRODUCTION
Placenta is an essential organ for a healthy pregnancy, thus maternal vascular hypoperfusion has been associated with adverse outcomes. Syndecan-1 and VEGF-A are involved in the placentation process. However, whether these proteins could serve as early markers of placental damage or fetal vascular damage is still unknown.
METHODS
A clinical study was carried out in 66 healthy pregnant women in the second trimester of pregnancy, with follow-up until delivery. The maternal age, height, and weight were collected. Ultrasound examination was performed to obtain fetal growth measures and fetal abdominal aorta characteristics. At birth, a histopathological study of the placenta was performed, and the newborn's weight and height were recorded. Maternal serum Syndecan-1 and VEGF-A levels were measured by ELISA in the second trimester and in cord blood serum at delivery. Analysis was performed with Student's t-test, and correlation tests.
RESULTS
Placental histopathological analysis revealed a prevalence of 76% multiple infarcts, 64% increased syncytial knots, 27% distal villous hypoplasia, and 12% acute atherosis. Maternal Syndecan-1 levels were significantly lower in the presence of placental multiple infarcts (p < 0.001), acute atherosis (p = 0.018), distal villous hypoplasia (p < 0.001), and increased syncytial knots (p < 0.001). Maternal VEGF-A levels were not different in the presence of placental lesions. Maternal and umbilical cord blood Syndecan-1 levels correlated with fetal abdominal aorta Intima-media thickness (r = -0.57, p < 0.001, and r = 0.74, p < 0.001, respectively). Umbilical cord blood VEGF-A also correlated with fetal abdominal aorta Intima-media thickness (r = 0.43, p < 0.001).
CONCLUSION
Maternal and cord blood Syndecan-1 could be an early marker of placental damage and fetal aortic intima media thickness.
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