The role of OLR1 polymorphisms in determining the risk and prognosis of ischemic stroke in a Chinese population

NeuroRehabilitation. 2013;32(2):391-6. doi: 10.3233/NRE-130860.

Abstract

Aim: To explore the role of rs11053646 polymorphism of oxidized low-density lipoprotein receptor 1 (OLR-1) gene in the susceptibility and prognosis of ischemic stoke (IS).

Methods: A total of 304 IS patients and 377 age and sex-matched healthy controls were recruited. Patients were followed up for 6 months for recovery evaluation of stroke. Genotyping analyses of the rs11053646 G > C polymorphisms of OLR1 gene were performed.

Results: The genotype frequencies and alleles frequencies at rs11053646 were significantly differed between stroke subjects and control subjects (both P < 0.001). The presence of CC genotype was significantly higher in IS subjects than in controls (38% vs. 25%, P = 0.001). Similarly, the C allele carriage in IS was significantly higher than controls (59% vs. 49%, P < 0.001). Regression analysis showed the CC homozygote had a significantly increased risk for stroke (adjusted OR = 2.080; P = 0.001). The genotype of rs11053646 were not associated with the IS subtype and severity at admission, but determine the clinical outcome at 6 months after discharge from hospital.

Conclusion: The rs11053646 polymorphism of OLR1 gene be used as a molecular marker for the susceptibility and prognosis of IS in Chinese population.

MeSH terms

  • Aged
  • Asian People / genetics
  • Brain Ischemia / complications
  • Case-Control Studies
  • Female
  • Gene Frequency
  • Genetic Predisposition to Disease / genetics*
  • Genotype
  • Humans
  • Male
  • Middle Aged
  • Nociceptin Receptor
  • Polymorphism, Single Nucleotide / genetics*
  • Receptors, Opioid / genetics*
  • Recovery of Function
  • Severity of Illness Index
  • Stroke* / diagnosis
  • Stroke* / etiology
  • Stroke* / genetics

Substances

  • Receptors, Opioid
  • Nociceptin Receptor
  • OPRL1 protein, human