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Are 25 SNPs from the CARDIoGRAM study associated with ischaemic stroke?

Artikel i vetenskaplig tidskrift
Författare H. Lovkvist
M. Sjogren
P. Hoglund
G. Engstrom
Christina Jern
Sandra Olsson
J. G. Smith
B. Hedblad
G. Andsberg
H. Delavaran
Katarina Jood
U. Kristoffersson
B. Norrving
O. Melander
A. Lindgren
Publicerad i European Journal of Neurology
Volym 20
Nummer/häfte 9
Sidor 1284-1291
ISSN 1351-5101
Publiceringsår 2013
Publicerad vid Institutionen för neurovetenskap och fysiologi, sektionen för klinisk neurovetenskap och rehabilitering
Sidor 1284-1291
Språk en
Länkar dx.doi.org/10.1111/ene.12183
Ämnesord CARDIoGRAM, coronary artery disease, genetic risk score, genome-wide association study, ischaemic, coronary-artery-disease, genome-wide association, single-nucleotide, polymorphisms, myocardial-infarction, genetic-variants, chromosome 9p21, heart-disease, blood-pressure, confers risk, susceptibility, rsimonian r, 1986, controlled clinical trials
Ämneskategorier Klinisk medicin

Sammanfattning

Background and purpose: The Coronary Artery Disease Genome-Wide Replication and Meta-Analysis Study (CARDIoGRAM) reported 25 single-nucleotide polymorphisms (SNPs) on 15 chromosomes to be associated with coronary artery disease (CAD) risk. Because common vascular risk factors are shared between CAD and ischaemic stroke (IS), these SNPs may also be related to IS overall or one or more of its pathogenetic subtypes. Methods: We performed a candidate gene study comprising 3986 patients with IS and 2459 control subjects. The 25 CAD-associated SNPs reported by CARDIoGRAM were examined by allelic association analysis including logistic regression. Weighted and unweighted genetic risk scores (GRSs) were also compiled and likewise analysed against IS. We furthermore considered the IS main subtypes large-vessel disease (LVD), small-vessel disease and cardioembolic stroke [according to Trial of Org 10172 in Acute Stroke Treatment (TOAST)] separately. Results: SNP rs4977574 on chromosome 9p21.3 was associated with overall IS [odds ratio (OR) = 1.12; 95% confidence interval (CI): 1.04-1.20; P = 0.002] as well as LVD (OR = 1.36; 95% CI: 1.13-1.64; P = 0.001). No other SNP was significantly associated with IS or any of its main subtypes. Analogously, the GRSs did not show any noticeable effect. Conclusions: Besides the previously reported association with SNPs on chromosome 9p21, this study did not detect any significant association between IS and CAD-susceptible genetic variants. Also, GRSs compiled from these variants did not predict IS or any pathogenetic IS subtype, despite a total sample size of 6445 participants.

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