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Published Online
on October 4, 2007

Stroke. 2007
Published online before print October 4, 2007, doi: 10.1161/STROKEAHA.107.492231
A more recent version of this article appeared on November 1, 2007
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Submitted on April 25, 2007
Accepted on April 27, 2007

Interleukin-6 -174G/C Polymorphism and Ischemic Stroke. A Systematic Review

Amy R. Tso BA; José G. Merino MD, MPhil; and Steven Warach MD, PhD*

From the National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Md, USA.

* To whom correspondence should be addressed. E-mail: warachs{at}ninds.nih.gov.

Background and Purpose—Interleukin-6 (IL-6) is associated with atherosclerotic disease and is also a key mediator in the inflammatory response to cerebral ischemia. Although the IL-6 -174G/C promoter polymorphism has been associated with carotid artery atherosclerosis and coronary heart disease, its relation to ischemic stroke is unclear. This review summarizes the current literature and discusses methodological considerations for future studies.

Methods—Electronic searches were conducted in the PubMed MEDLINE, Scopus, and ISI Web of Science databases. Two investigators independently reviewed all abstracts to identify studies examining the association between the IL-6 -174G/C polymorphism and ischemic cerebrovascular events.

Results—Twelve relevant publications were identified. Three reported on a subset of patients from a later publication, leaving 9 independent studies. Two studies found an association between ischemic stroke and the G allele or GG genotype, whereas 4 found an association with the C allele or CC genotype. One study found the CC genotype to be significantly less frequent in retinal artery occlusion patients. Two studies found no association between the -174G/C polymorphism and stroke.

Conclusions—Studies investigating stroke and the -174G/C polymorphism report conflicting results, which may reflect the complex physiology of IL-6 and true differences between stroke subtypes and populations. However, interpretation of published results is hindered by methodological limitations, and greater rigor and consistency in future studies will help unravel the relationship between the -174G/C polymorphism and stroke.


Key words: acute stroke • genetics • inflammation




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[Abstract] [Full Text] [PDF]