Original Investigation

Low VEGF expression in conceptus material and maternal serum AFP and ß-hCG levels as indicators of defective angiogenesis in first-trimester miscarriages

10.5152/jtgga.2012.06

  • Gülşen Kutluer
  • Nedim Mahmut Çiçek
  • Özlem Moraloğlu
  • Pervin Ertargın
  • Esma Sarıkaya
  • İshak Artar
  • Özlem Erdem

Received Date: 20.10.2011 Accepted Date: 18.12.2011 J Turk Ger Gynecol Assoc 2012;13(2):111-117 PMID: 24592019

Objective:

The aims of this study were to assess the relationship between early miscarriages and vascular endothelial growth factor (VEGF) expression and to determine the serum levels of first-trimester maternal alpha-fetoprotein (AFP) and human chorionic gonadotropin (β-hCG) as markers of angiogenesis and predictors of abortion and intrauterine fetal loss.

Material and Methods:

The present study was a prospective, singlecenter, randomized controlled clinical trial. Ninety-five women who were 6-10 weeks pregnant between May and June 2010 were included in the study. The subjects were divided into three groups, i.e., incomplete abortion (IA) (n=31), intrauterine death (IU-D) (n=32) and control (elective pregnancy termination) (n=32). Feto-placental materials were compared based on immune staining for VEGF in the pathology laboratory, and maternal serum samples were tested in the hormone laboratory.

Results:

Serum β-hCG levels in the patient groups were significantly lower than the controls (p=0.001). The serum AFP level was lower than the controls in the IA group while it was higher than the controls in the IU-D (p=0.016). Immunohistochemistry showed that the cytotrophoblast, syncytiotrophoblast and endometrial gland epithelium were weakly stained for VEGF in the patient groups (IA and IU-D) in comparison to the control group (p=0.06, p=0.028, p=0.006).

Conclusion:

Early pregnancy losses are related to insufficient angiogenesis, and maternal serum AFP and β-hCG can be used as markers of angiogenesis in the first trimester.

Keywords: Abortion, implantation, angiogenesis, VEGF, ß, -hCG, AFP