Background: The genetic basis of complex diseases like ischemic stroke probably consists of several predisposing risk factors, such as genes involved in inflammation and thrombotic pathways. On this basis the aim of our study was to evaluate the role of SNPs (single nucleotide polymorphisms) of some pro-inflammatory/anti-inflammatory and coagulation/fibrinolytic genes in patients with acute ischemic stroke.Methods: The study population consisted of 144 consecutive Caucasian adult patients who were hospitalized in the Internal Medicine Department at the University of Palermo between November 2006 and January 2008, and who met inclusion criteria. The cases were patients admitted with a diagnosis of acute ischemic stroke, and age-matched (±3 years) control subjects: patients admitted to our Internal Medicine Department for any cause other than acute cardiovascular and cerebrovascular events and for routine checkup examinations.Molecular analysis of alleles at the -308 nucleotide (-308G/A) of TNF-a gene, -1082/-819 haplotypes of IL-10 gene, IL-1RN exon 2 VNR polymorphism, alleles at the 174 nucleotide ( 174G/C)of IL-6 gene, PAI-1675 5G/4G polymorphism, alleles at the 7351 nucleotide (7351C/T) of tPA gene was undertaken in both patient groups.Results: We analyzed 96 subjects with acute ischemic stroke and 48 control subjects. We observed a significantlyhigher frequency of IL-10 1082 AA genotype in stroke patients with a significant risk trend. Wealso reported a higher frequency in stroke subjects with a significant risk trend of the TPA 7351-CT genotypeand of IL-1RN-VNTR 86 bp 2/2 genotype. Moreover, we observed a significant relationship withTOAST subtype only with regard to CC TPA genotype and 1/1 IL-1 VNTR 86 bp and lacunar strokes.Conclusions: Ischemic stroke is a common multifactor disease, which is affected by a number of geneticmutations and environmental factors. Our findings showing a relationship between pro-inflammatory/anti-inflammatory and thrombotic/fibrinolytic genes SNPs and ischemic stroke may contribute to delineatea possible stroke risk profile in subjects with cerebrovascular risk factors.
|Number of pages||8|
|Publication status||Published - 2012|
- Immunology and Allergy
- Molecular Biology