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Ischemic stroke is associated with the ABO locus: The EuroCLOT study
Frances M. K. Williams, Angela M. Carter, Pirro G. Hysi and 56 more
Annals of Neurology · 2013 · Meta-analysis
Abstract
Objective : End‐stage coagulation and the structure/function of fibrin are implicated in the pathogenesis of ischemic stroke. We explored whether genetic variants associated with end‐stage coagulation in healthy REFVIDunteers account for the genetic predisposition to ischemic stroke and examined their influence on stroke subtype. Methods : Common genetic variants identified through genome‐wide association studies of coagulation factors and fibrin structure/function in healthy twins (n = 2,100, Stage 1) were examined in ischemic stroke (n = 4,200 cases) using 2 independent samples of European ancestry (Stage 2). A third clinical collection having stroke subtyping (total 8,900 cases, 55,000 controls) was used for replication (Stage 3). Results : Stage 1 identified 524 single nucleotide polymorphisms (SNPs) from 23 linkage disequilibrium blocks having significant association ( p < 5 × 10 –8 ) with 1 or more coagulation/fibrin phenotypes. The most striking associations included SNP rs5985 with factor XIII activity ( p = 2.6 × 10 –186 ), rs10665 with FVII ( p = 2.4 × 10 –47 ), and rs505922 in the ABO gene with both von Willebrand factor ( p = 4.7 × 10 –57 ) and factor VIII ( p = 1.2 × 10 –36 ). In Stage 2, the 23 independent SNPs were examined in stroke cases/noncases using MOnica Risk, Genetics, Archiving and Monograph (MORGAM) and Wellcome Trust Case Control Consortium 2 collections. SNP rs505922 was nominally associated with ischemic stroke (odds ratio = 0.94, 95% confidence interval = 0.88–0.99, p = 0.023). Independent replication in Meta‐Stroke confirmed the rs505922 association with stroke, beta (standard error, SE) = 0.066 (0.02), p = 0.001, a finding specific to large‐vessel and cardioembolic stroke ( p = 0.001 and p = < 0.001, respectively) but not seen with small‐vessel stroke ( p = 0.811). Interpretation : ABO gene variants are associated with large‐vessel and cardioembolic stroke but not small‐vessel disease. This work sheds light on the different pathogenic mechanisms underpinning stroke subtype. Ann Neurol 2013
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References 41
- 1.
Lopez AD, Mathers CD, Ezzati M, et al. Global and regional burden of disease and risk factors, 2001: systematic analysis of population health data. Lancet. 2006;367:1747-1757.
Not in our library10.1016/s0140-6736(06)68770-9
- 2.
Souto JC, Almasy L, Borrell M, et al. Genetic susceptibility to thrombosis and its relationship to physiological risk factors: the GAIT study. Genetic Analysis of Idiopathic Thrombophilia. Am J Hum Genet. 2000;67:1452-1459.
Not in our library10.1086/316903
- 3.
Carter AM, Cymbalista CM, Spector TD, Grant PJ. Heritability of clot formation, morphology, and lysis. The EuroCLOT study. Arterioscler Thromb Vasc Biol. 2007;27:2783-2789.
Not in our library10.1161/atvbaha.107.153221
- 4.
Williams FM, Carter AM, Kato B, et al. Identification of quantitative trait loci for fibrin clot phenotypes: the EuroCLOT study. Arterioscler Thromb Vasc Biol. 2009;29:600-605.
Not in our library10.1161/atvbaha.108.178103
- 5.
Samani NJ, Erdmann J, Hall AS, et al. Genomewide association analysis of coronary artery disease. N Engl J Med. 2007;357:443-453.
Not in our library10.1056/nejmoa072366
- 6.
Manolio TA. Collaborative genome-wide association studies of diverse diseases: programs of the NHGRI's office of population genomics. Pharmacogenomics. 2009;10:235-241.
Not in our library10.2217/14622416.10.2.235
- 7.
Spector TD, Williams FM. The UK Adult Twin Registry (TwinsUK). Twin Res Hum Genet. 2006;9:899-906.
Not in our library10.1375/183242706779462462
- 8.
Andrew T, Hart DJ, Snieder H, et al. Are twins and singletons comparable? A study of disease-related and lifestyle characteristics in adult women. Twin Res. 2001;4:464-477.
Not in our library10.1375/1369052012803
- 9.
Carter AM, Catto AJ, Mansfield MW, et al. Predictive variables for mortality after acute ischemic stroke. Stroke. 2007;38:1873-1880.
Not in our library10.1161/strokeaha.106.474569
- 10.
de Lange M, Snieder H, Ariens RA, et al. The genetics of haemostasis: a twin study. Lancet. 2001;357:101-105.
Not in our library10.1016/s0140-6736(00)03541-8
- 11.
Freeman MS, Mansfield MW, Barrett JH, Grant PJ. Genetic contribution to circulating levels of hemostatic factors in healthy families with effects of known genetic polymorphisms on heritability. Arterioscler Thromb Vasc Biol. 2002;22:506-510.
Not in our library10.1161/hq0302.104906
- 12.
Freeman MS, Mansfield MW, Barrett JH, Grant PJ. Heritability of features of the insulin resistance syndrome in a community-based study of healthy families. Diabet Med. 2002;19:994-999.
Not in our library10.1046/j.1464-5491.2002.00843.x
- 13.
Evans A, Salomaa V, Kulathinal S, et al. MORGAM (an international pooling of cardiovascular cohorts). Int J Epidemiol. 2005;34:21-27.
Not in our library10.1093/ije/dyh327
- 14.
Kulathinal S, Karvanen J, Saarela O, Kuulasmaa K. Case-cohort design in practice—experiences from the MORGAM Project. Epidemiol Perspect Innov. 2007;4:15.
Not in our library10.1186/1742-5573-4-15
- 15.
Adams HP, Bendixen BH, Kappelle LJ, et al. Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment. Stroke. 1993;24:35-41.
Not in our library10.1161/01.str.24.1.35
- 16.
Bellenguez C, Bevan S, Gschwendtner A, et al. Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke. Nat Genet. 2012;44:328-333.
Not in our library10.1038/ng.1081
- 17.
Hysi PG, Young TL, Mackey DA, et al. A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25. Nat Genet. 2010;42:902-905.
Not in our library10.1038/ng.664
- 18.
Marchini J, Howie B, Myers S, et al. A new multipoint method for genome-wide association studies by imputation of genotypes. Nat Genet. 2007;39:906-913.
Not in our library10.1038/ng2088
- 19.
Silander K, Alanne M, Kristiansson K, et al. Gender differences in genetic risk profiles for cardiovascular disease. PLoS One. 2008;3:e3615.
Not in our library10.1371/journal.pone.0003615
- 20.
Purcell S, Neale B, Todd-Brown K, et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet. 2007;81:559-575.
Not in our library10.1086/519795
- 21.
Willer CJ, Li Y, Abecasis GR. METAL: fast and efficient meta-analysis of genomewide association scans. Bioinformatics. 2010;26:2190-2191.
Not in our library10.1093/bioinformatics/btq340
- 22.
Abecasis GR, Cherny SS, Cookson WO, Cardon LR. Merlin—rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet. 2002;30:97-101.
Not in our library10.1038/ng786
- 23.
Smith NL, Chen MH, Dehghan A, et al. Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: the CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium. Circulation. 2010;121:1382-1392.
Not in our library10.1161/circulationaha.109.869156
- 24.
Ionescu DA, Marcu I, Bicescu E. Cerebral thrombosis, cerebral haemorrhage, and ABO blood-groups. Lancet. 1976;1:278-280.
Not in our library10.1016/s0140-6736(76)91405-7
- 25.
Wu O, Bayoumi N, Vickers MA, Clark P. ABO(H) blood groups and vascular disease: a systematic review and meta-analysis. J Thromb Haemost. 2008;6:62-69.
Not in our library10.1111/j.1538-7836.2007.02818.x
- 26.
Reilly MP, Li M, He J, et al. Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies. Lancet. 2011;377:383-392.
Not in our library10.1016/s0140-6736(10)61996-4
- 27.
Schunkert H, Konig IR, Kathiresan S, et al. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat Genet. 2011;43:333-338.
Not in our library10.1038/ng.784
- 28.
Wiggins KL, Smith NL, Glazer NL, et al. ABO genotype and risk of thrombotic events and hemorrhagic stroke. J Thromb Haemost. 2009;7:263-269.
Not in our library10.1111/j.1538-7836.2008.03243.x
- 29.
Wolpin BM, Kabrhel C, Varraso R, et al. Prospective study of ABO blood type and the risk of pulmonary embolism in two large cohort studies. Thromb Haemost. 2010;104:962-971.
Not in our library10.1160/th10-05-0312
- 30.
Tregouet DA, Heath S, Saut N, et al. Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach. Blood. 2009;113:5298-5303.
Not in our library10.1182/blood-2008-11-190389
- 31.
Suhre K, Shin SY, Petersen AK, et al. Human metabolic individuality in biomedical and pharmaceutical research. Nature. 2011;477:54-60.
Not in our library10.1038/nature10354
- 32.
King A, Markus HS. Doppler embolic signals in cerebrovascular disease and prediction of stroke risk: a systematic review and meta-analysis. Stroke. 2009;40:3711-3717.
Not in our library10.1161/strokeaha.109.563056
- 33.
Markus HS, McCollum C, Imray C, et al. The von Willebrand inhibitor ARC1779 reduces cerebral embolization after carotid endarterectomy: a randomized trial. Stroke. 2011;42:2149-2153.
Not in our library10.1161/strokeaha.111.616649
- 34.
Pantoni L. Cerebral small vessel disease: from pathogenesis and clinical characteristics to therapeutic challenges. Lancet Neurol. 2010;9:689-701.
Not in our library10.1016/s1474-4422(10)70104-6
- 35.
Gretarsdottir S, Thorleifsson G, Manolescu A, et al. Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke. Ann Neurol. 2008;64:402-409.
Not in our library10.1002/ana.21480
- 36.
Gudbjartsson DF, Holm H, Gretarsdottir S, et al. A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. Nat Genet. 2009;41:876-878.
Not in our library10.1038/ng.417
- 37.
Gschwendtner A, Bevan S, Cole JW, et al. Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke. Ann Neurol. 2009;65:531-539.
Not in our library10.1002/ana.21590
- 38.
Kubo M, Hata J, Ninomiya T, et al. A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction. Nat Genet. 2007;39:212-217.
Not in our library10.1038/ng1945
- 39.
Bernardi F, Arcieri P, Bertina RM, et al. Contribution of factor VII genotype to activated FVII levels. Differences in genotype frequencies between northern and southern European populations. Arterioscler Thromb Vasc Biol. 1997;17:2548-2553.
Not in our library10.1161/01.atv.17.11.2548
- 40.
Calafell F, Almasy L, Sabater-Lleal M, et al. Sequence variation and genetic eREFVIDution at the human F12 locus: mapping quantitative trait nucleotides that influence FXII plasma levels. Hum Mol Genet. 2010;19:517-525.
Not in our library10.1093/hmg/ddp517
- 41.
Nothnagel M, Ellinghaus D, Schreiber S, et al. A comprehensive evaluation of SNP genotype imputation. Hum Genet. 2009;125:163-171.
Not in our library10.1007/s00439-008-0606-5
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