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The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm
Authors:Helgadottir Anna  Thorleifsson Gudmar  Magnusson Kristinn P  Grétarsdottir Solveig  Steinthorsdottir Valgerdur  Manolescu Andrei  Jones Gregory T  Rinkel Gabriel J E  Blankensteijn Jan D  Ronkainen Antti  Jääskeläinen Juha E  Kyo Yoshiki  Lenk Guy M  Sakalihasan Natzi  Kostulas Konstantinos  Gottsäter Anders  Flex Andrea  Stefansson Hreinn  Hansen Torben  Andersen Gitte  Weinsheimer Shantel  Borch-Johnsen Knut  Jorgensen Torben  Shah Svati H  Quyyumi Arshed A  Granger Christopher B  Reilly Muredach P  Austin Harland  Levey Allan I  Vaccarino Viola  Palsdottir Ebba  Walters G Bragi  Jonsdottir Thorbjorg  Snorradottir Steinunn
Institution:deCODE Genetics, Sturlugata 8, IS-101 Reykjavik, Iceland.
Abstract:Recently, two common sequence variants on 9p21, tagged by rs10757278-G and rs10811661-T, were reported to be associated with coronary artery disease (CAD) and type 2 diabetes (T2D), respectively. We proceeded to further investigate the contributions of these variants to arterial diseases and T2D. Here we report that rs10757278-G is associated with, in addition to CAD, abdominal aortic aneurysm (AAA; odds ratio (OR) = 1.31, P = 1.2 x 10(-12)) and intracranial aneurysm (OR = 1.29, P = 2.5 x 10(-6)), but not with T2D. This variant is the first to be described that affects the risk of AAA and intracranial aneurysm in many populations. The association of rs10811661-T to T2D replicates in our samples, but the variant does not associate with any of the five arterial diseases examined. These findings extend our insight into the role of the sequence variant tagged by rs10757278-G and show that it is not confined to atherosclerotic diseases.
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