Endoglin gene insertion polymorphism not associated with aneurysmal subarachnoid hemorrhage

J Neurosurg. 2005 May;102(5):879-81. doi: 10.3171/jns.2005.102.5.0879.

Abstract

Object: Data concerning an association between the ENG gene intronic insertion polymorphism and intracrahial aneurysms (IAs) remain inconsistent. In this study the authors investigated whether this polymorphism is associated with a subarachnoid hemorrhage (SAH) caused by a ruptured IA in a Polish population.

Methods: One hundred nineteen patients with aneurysmal SAH and 119 sex-matched healthy volunteers were studied. The insertion ENG gene polymorphism in intron 7 was identified using polymerase chain reaction-single-strand chain polymorphism method. The distribution of the insertion allele did not differ between the SAH (13%) and control (16%) cases (p = 0.36). The homozygous insertion/insertion genotype frequencies in these cases were 3.4 and 0.8%, respectively (p = 0.18).

Conclusions: The authors failed to find an association between the intronic insertion polymorphism of the ENG gene and aneurysmal SAH in a Polish population.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD
  • Endoglin
  • Female
  • Humans
  • Introns / genetics
  • Male
  • Middle Aged
  • Poland
  • Polymorphism, Genetic*
  • Receptors, Cell Surface
  • Subarachnoid Hemorrhage / genetics*
  • Vascular Cell Adhesion Molecule-1 / genetics*
  • White People / genetics

Substances

  • Antigens, CD
  • ENG protein, human
  • Endoglin
  • Receptors, Cell Surface
  • Vascular Cell Adhesion Molecule-1