No association of the -105 promoter polymorphism of the selenoprotein S encoding gene SEPS1 with cerebrovascular disease

Eur J Neurol. 2007 Oct;14(10):1173-5. doi: 10.1111/j.1468-1331.2007.01898.x.

Abstract

A common pro-inflammatory promoter variant of the selenoprotein S encoding gene (SEPS1) was studied in young stroke patients from Italy and Germany and in healthy control subjects. The -105A-allele was found in 56 of 205 (27.3%) patients with ischemic stroke IS because of a spontaneous cervical artery dissection (CAD), and in 69 of 295 (23.4%) patients <50 years with IS of non-CAD origin. The SEPS -105A promoter variant was detected in 87 of 393 healthy control subjects (22.1%) and in 11 of 55 CAD patients without IS (20%). The non-significant differences of SEPS1 allele frequencies between disease groups and healthy controls suggest that the SEPS1 -105A allele is not a major-risk factor for stroke.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Alleles
  • Cerebrovascular Disorders / etiology
  • Cerebrovascular Disorders / genetics*
  • Female
  • Humans
  • Male
  • Membrane Proteins / genetics*
  • Middle Aged
  • Polymorphism, Genetic*
  • Promoter Regions, Genetic / genetics*
  • Risk Factors
  • Selenoproteins / genetics*

Substances

  • Membrane Proteins
  • SELENOS protein, human
  • Selenoproteins