Abstract 4514

Introduction

Ischemic cerebrovascular disease (ICD) is a multifactorial entity whose anatomopathological substrate is the pro-inflammatory state links to atherosclerosis. The inflammatory cells migrate to vascular endothelium unleashing atheroma plaque formation and pro-inflammatory cytoquine release.

Objective

The purpose of this case-control study is to analyze the ICD risk associated to polymorphisms MCP-1 -2518 G/A, IL6 -174 G/C, IL 1B -511 C/T, IL1B +3954 C/T, IL1A -889 C/T.

Methods and patients

A total of 282 ICD diagnosed patients (134 female and 148 male; mean age 68,2±14,9 years) and 287 controls without thrombotic history (143 Female and 144 male; mean age 65,8±14 years) were analysed. AH, DM, dyslipidemia and smoking habit data were collected for each group. Polymorphisms were analysed by PCR-RFLP. Seric IL6 was measured by ELISA. Statistic Analysis was made with Stata v.10 software.

Results

Stroke subtype distribution was: atherothrombotic (32,8%), inhabitual and indeterminate (28,9%), cardioembolic (24,5%), and lacunar (13,7%). Risk factors were more frequent in patients with AH and DM showed a higher prevalence: (OR: 1.684 IC 95%:1.161- 2.443, p:0.006) and (OR: 2.393, IC95%:1.447- 3.956, p:0.01) respectively. Logistic regression was used to determinate polymorphisms distribution. Results are shown in table 1. Analysis of IL-1 polymorphisms showed a synergic relation in IL1A -889 C/T (p:0.05; OR: 0.625; IC95%:0.388-1.008). The G allele IL6 –174 G/C carriers group presented higher seric IL6 levels than C allele carriers, 5.85 pg/ml (2.9- 34.5) vs 4.94pg/ml (2.5- 11.4) respectively. IL-6 genotype frequency G/G + G/C vs C/C was analyzed. Atherothrombotic stroke IL-6 genotype frequency was G/G + G/C (24.3%) vs C/C (12.0%) (p: 0.082).

Conclusion

There is no association between MCP-1 -2518 G/A, IL6 -174 G/C, IL 1B -511 C/T, IL1B +3954 C/T, IL1A -889 C/T polymorphisms and ischemic stroke. We found a synergic effect between IL1 mutations. The G allele IL6 –174 G/C carriers group presented higher seric IL6 levels than C allele carriers. The analysis performed by ICD subtypes showed an association between IL6 G allele and atherothrombotic subtype.

* SETH and MMA GRANT

Table 1
pORIC 95%
MCP-1 -2518 G/A G/G + G/A vs A/A 0,383 0.844 0.578-1.234 
IL6 -174 G/C G/G + G/C vs C/C 0.696 0.877 0.453-1.696 
IL 1B -511 C/T C/C + C/T vs T/T 0.343 0.820 0.545-1.235 
IL1B +3954 C/T C/T + T/T vs C/C 0.676 0.915 0.602-1.389 
IL1A -889 C/T C/T + T/T vs C/C 0.273 0.799 0.536-1.193 
pORIC 95%
MCP-1 -2518 G/A G/G + G/A vs A/A 0,383 0.844 0.578-1.234 
IL6 -174 G/C G/G + G/C vs C/C 0.696 0.877 0.453-1.696 
IL 1B -511 C/T C/C + C/T vs T/T 0.343 0.820 0.545-1.235 
IL1B +3954 C/T C/T + T/T vs C/C 0.676 0.915 0.602-1.389 
IL1A -889 C/T C/T + T/T vs C/C 0.273 0.799 0.536-1.193 
Disclosures:

No relevant conflicts of interest to declare.

Author notes

*

Asterisk with author names denotes non-ASH members.

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