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Background The genes underlying the risk of stroke in the general population remain undetermined.
Methods We carried out an analysis of genomewide association data generated from four large cohorts composing the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium, including 19,602 white persons (mean [±SD] age, 63±8 years) in whom 1544 incident strokes (1164 ischemic strokes) developed over an average follow-up of 11 years. We tested the markers most strongly associated with stroke in a replication cohort of 2430 black persons with 215 incident strokes (191 ischemic strokes), another cohort of 574 black persons with 85 incident strokes (68 ischemic strokes), and 652 Dutch persons with ischemic stroke and 3613 unaffected persons.
Results Two intergenic single-nucleotide polymorphisms on chromosome 12p13 and within 11 kb of the gene NINJ2 were associated with stroke (P<5x10–8). NINJ2 encodes an adhesion molecule expressed in glia and shows increased expression after nerve injury. Direct genotyping showed that rs12425791 was associated with an increased risk of total (i.e., all types) and ischemic stroke, with hazard ratios of 1.30 (95% confidence interval [CI], 1.19 to 1.42) and 1.33 (95% CI, 1.21 to 1.47), respectively, yielding population attributable risks of 11% and 12% in the discovery cohorts. Corresponding hazard ratios were 1.35 (95% CI, 1.01 to 1.79; P=0.04) and 1.42 (95% CI, 1.06 to 1.91; P=0.02) in the large cohort of black persons and 1.17 (95% CI, 1.01 to 1.37; P=0.03) and 1.19 (95% CI, 1.01 to 1.41; P=0.04) in the Dutch sample; the results of an underpowered analysis of the smaller black cohort were nonsignificant.
Conclusions A genetic locus on chromosome 12p13 is associated with an increased risk of stroke.
Source Information
The authors' affiliations are listed in the Appendix.
Drs. Ikram, Seshadri, Bis, Fornage, DeStefano, Mosley, van Duijn, Breteler, Longstreth, and Wolf contributed equally to this article.
This article (10.1056/NEJMoa0900094) was published at NEJM.org on April 15, 2009.
Address reprint requests to Dr. Seshadri at the Department of Neurology, Boston University School of Medicine, 72 E. Concord St., Boston, MA 02118, or at suseshad{at}bu.edu.
Related Letters:
Genomewide Association Studies of Stroke
Kim J., Chae Y. K., Ikram M. A., Seshadri S., Bis J. C., the Cohorts in Heart and Aging Research Consortium
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N Engl J Med 2009;
361:722, Aug 13, 2009.
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