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(Stroke. 2005;36:2278.)
© 2005 American Heart Association, Inc.
Research Reports |
From the Cardiovascular Research Institute (L.P., C.H., P.Y.K.), Departments of Anesthesia and Perioperative Care and Center for Cerebrovascular Research (M.N.T., A.A., W.L.Y.), Departments of Epidemiology and Biostatistics (C.E.M.), Neurological Surgery (M.T.L., W.L.Y.), Neurology (W.L.Y.), and Medicine (E.B., S.C., R.C., J.Z.), University of California, San Francisco; and the Department of Genetics, Duke University Medical Center, Durham, NC (D.A.M.).
Correspondence to William L. Young, MD, UCSF, 1001 Potrero Ave, Room 3C-38, San Francisco, CA 94110. E-mail ccr{at}anesthesia.ucsf.edu
Background and Purpose Mutations in endoglin (ENG) and activin-like kinase (ALK1) cause hereditary hemorrhagic telangiectasias, disorders characterized by pulmonary and brain arteriovenous malformations (BAVMs). We investigated whether polymorphisms in these genes are also associated with sporadic BAVM.
Methods A total of 177 sporadic BAVM patients and 129 controls (all subjects white) were genotyped for 2 variants in ALK1 and 7 variants in ENG.
Results The ALK1 IVS3-35A>G polymorphism was associated with BAVM: (AnyA [AA+AG] genotype: odds ratio, 2.47; 95% CI, 1.38 to 4.44; P=0.002). Two ENG polymorphisms, ENG 1742A>G and ENG 207G>A, showed a trend toward association with BAVM that did not reach statistical significance.
Conclusions A common polymorphism in ALK1 is associated with sporadic BAVM, suggesting that genetic variation in genes mutated in familial BAVM syndromes may play a role in sporadic BAVMs.
Key Words: case-control studies genetics vascular malformations
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