Abstract
Functional single-nucleotide polymorphisms (SNPs) of inflammatory cytokines have been previously related to the occurrence of an ischemic stroke (IS). We investigated whether five functional SNPs (i.e., TNF - 308G>A, IL6-174G>C, IL12B 1188A>C, IL4-589C>T, and IL10-1082G>A) might be associated with the age of onset and 6-month outcome of an acute IS. A probe-free real-time PCR methodology was used to genotype 145 consecutively admitted cases with a first-ever IS. Simple Kaplan-Mayer and adjusted Cox regression analyses showed no association between inflammatory genotypes and the age of IS onset. IL6-174G>C, IL12B 1188A>C, IL4-589C>T, and IL10-1082G>A were not found to significantly contribute to the long-term outcome of the disease. However, carriage of the TNF-α 308 GG genotype was significantly associated with reduced odds for an adverse outcome. Larger studies are needed to confirm our results. Copyright © 2011 Stella Marousi et al.
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CITATION STYLE
Marousi, S., Antonacopoulou, A., Kalofonos, H., Papathanasopoulos, P., Karakantza, M., & Ellul, J. (2011). Functional inflammatory genotypes in ischemic stroke: Could we use them to predict age of onset and long-term outcome? Stroke Research and Treatment. https://doi.org/10.4061/2011/792923
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