Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/12629
Title: Impact of COX-2 rs5275 and rs20417 and GPIIIa rs5918 polymorphisms on 90-day ischemic stroke functional outcome: A novel finding
Authors: Jane Maguire
Ammarin Thakkinstian
Christopher Levi
Lisa Lincz
Linda Bisset
Jonathan Sturm
Rodney Scott
Scott Whyte
John Attia
University of Newcastle Faculty of Medicine and Health Sciences
Hunter Medical Research Institute, Australia
University of Newcastle, Australia
Mahidol University
Hunter Haematology Research Group
John Hunter Hospital
Gosford Hospital
Keywords: Medicine
Issue Date: 1-Mar-2011
Citation: Journal of Stroke and Cerebrovascular Diseases. Vol.20, No.2 (2011), 134-144
Abstract: We hypothesized that polymorphisms in 5 genes related to thrombolytic and inflammation pathways will independently influence occurrence, severity, and 3-month functional outcome in patients with ischemic stroke. This was a case-control design with ischemic stroke patients recruited from 4 public hospitals (n = 640) and community controls (n = 627). Baseline clinical data were collected, and follow-up telephone interviews were conducted with 520 patients at 90 days postevent to determine stroke outcome using the Barthel Index (BI), Modified Rankin Scale (mRS) and Glasgow Outcome Scale (GOS). Blood samples were collected and genotyped for polymorphisms in platelet glycoprotein Ibα (GPIbα) rs224309 and rs6065, glycoprotein IIIa (GPIIIa) rs5918, tissue plasminogen activator (tPA) rs63020761, plasminogen activating inhibitor (PAI-1) rs72578597, and cyclooxygenase-2 (COX-2) rs5275 and rs20417. COX-2 polymorphism rs5275 demonstrated a significant association with poststroke mRS, with a dominant genetic model demonstrating the best fit (CC + TC) (adjusted odds ratio [aOR] = 1.61; P = .026). The COX-2 rs20417 C allele showed an association with GOS (aOR = 1.95; P = .012), and again a dominant genetic model demonstrated the best fit (CC + GC). GPIIIa rs5918 (A1A2) was associated with poststroke BI, with a dominant model demonstrating the best fit (A1A2 + A2A2) (aOR = 0.56; P = .014). There was a significant association between stroke severity and tPA rs63020761 TT allele (aOR = 1.96; 95% CI = 1.03-3.72; P = .040). This is the first study to demonstrate associations between stroke functional outcome and 2 COX-2 variants (rs20417 and rs5275) and a GPIIIa variant (rs5918). © 2011 by National Stroke Association.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79951866750&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/12629
ISSN: 10523057
Appears in Collections:Scopus 2011-2015

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