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Genetic variation on chromosome 9p21 shows association with large vessel disease in a Swedish sample aged ≤70 years

Journal article
Authors Sandra Olsson
Katarina Jood
Christian Blomstrand
Christina Jern
Published in European Journal of Neurology
Volume 18
Issue 2
Pages 365-67
ISSN 1351-5101
Publication year 2011
Published at Institute of Neuroscience and Physiology, Department of Clinical Neuroscience and Rehabilitation
Pages 365-67
Language en
Links dx.doi.org/10.1111/j.1468-1331.2010...
https://gup.ub.gu.se/file/86209
Keywords functional outcome; genetics; ischaemic stroke; single nucleotide polymorphism; TOAST
Subject categories Medical and Health Sciences

Abstract

Background:  The aim of this study was to investigate whether we could replicate a recent finding of an association between genetic variants on chromosome 9p21 and the ischaemic stroke (IS) subtype large-vessel disease (LVD). Methods:  The Sahlgrenska Academy Study on Ischemic Stroke comprises 844 patients with IS, who suffered IS before reaching the age of 70, and 668 healthy controls. IS subtype was defined according to the TOAST criteria, and 111 patients were categorized as LVD. Seven single-nucleotide polymorphisms (SNPs) on 9p21 were analyzed. Functional outcome was assessed 3 months after IS using the modified Rankin scale. Results:  The SNP rs7857345 showed a significant association with the subtype LVD independent of traditional vascular risk factors. In addition, an association between rs7857345 and functional outcome after LVD was observed. Conclusion:  In this relatively young sample of patients with IS, genetic variation on 9p21 is associated with LVD.

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