Literature DB >> 18340101

Whole genome analyses suggest ischemic stroke and heart disease share an association with polymorphisms on chromosome 9p21.

Mar Matarin, W Mark Brown, Andrew Singleton, John A Hardy, James F Meschia.   

Abstract

BACKGROUND AND
PURPOSE: Recently independent studies reported an association between coronary heart disease and single-nucleotide polymorphisms (SNPs) located at chromosome 9p21, near CDKN2A and CDKN2B genes. Given that stroke is a common complication after myocardial infarction, we investigated if the same SNPs were associated with ischemic stroke in our population.
METHODS: We recently initiated a whole genome analysis of ischemic stroke and published the first stage of a case control study using >400,000 SNPs from Illumina Infinium Human-1 and HumanHap300 assays. We focused on SNPs recently associated with heart disease by Helgadottir and colleagues and SNPs from the same haplotype block.
RESULTS: In analyses both unadjusted and adjusted for stroke risk factors, significant associations with ischemic stroke were observed for SNPs from the same haplotype block previously associated with myocardial infarction. Significant association was also seen between disease and haplotypes involving these SNPs, both with and without adjustment for stroke risk factors (odd ratios: 1.01 to 2.65).
CONCLUSIONS: These data are important for 3 reasons: first, they suggest a genetic association for stroke; second, they suggest that this association shares pathogenic mechanisms with heart disease and diabetes; and third, they illustrate, that public release of data can facilitate rapid risk locus discovery.

Entities:  

Mesh:

Year:  2008        PMID: 18340101      PMCID: PMC3932672          DOI: 10.1161/STROKEAHA.107.502963

Source DB:  PubMed          Journal:  Stroke        ISSN: 0039-2499            Impact factor:   7.914


  12 in total

1.  A common variant on chromosome 9p21 affects the risk of myocardial infarction.

Authors:  Anna Helgadottir; Gudmar Thorleifsson; Andrei Manolescu; Solveig Gretarsdottir; Thorarinn Blondal; Aslaug Jonasdottir; Adalbjorg Jonasdottir; Asgeir Sigurdsson; Adam Baker; Arnar Palsson; Gisli Masson; Daniel F Gudbjartsson; Kristinn P Magnusson; Karl Andersen; Allan I Levey; Valgerdur M Backman; Sigurborg Matthiasdottir; Thorbjorg Jonsdottir; Stefan Palsson; Helga Einarsdottir; Steinunn Gunnarsdottir; Arnaldur Gylfason; Viola Vaccarino; W Craig Hooper; Muredach P Reilly; Christopher B Granger; Harland Austin; Daniel J Rader; Svati H Shah; Arshed A Quyyumi; Jeffrey R Gulcher; Gudmundur Thorgeirsson; Unnur Thorsteinsdottir; Augustine Kong; Kari Stefansson
Journal:  Science       Date:  2007-05-03       Impact factor: 47.728

2.  Two common gene variants on chromosome 9 and risk of atherothrombosis.

Authors:  Robert Y L Zee; Paul M Ridker
Journal:  Stroke       Date:  2007-08-23       Impact factor: 7.914

Review 3.  The regulation of INK4/ARF in cancer and aging.

Authors:  William Y Kim; Norman E Sharpless
Journal:  Cell       Date:  2006-10-20       Impact factor: 41.582

4.  A community-based study of stroke incidence after myocardial infarction.

Authors:  Brandi J Witt; Robert D Brown; Steven J Jacobsen; Susan A Weston; Barbara P Yawn; Véronique L Roger
Journal:  Ann Intern Med       Date:  2005-12-06       Impact factor: 25.391

5.  A common allele on chromosome 9 associated with coronary heart disease.

Authors:  Ruth McPherson; Alexander Pertsemlidis; Nihan Kavaslar; Alexandre Stewart; Robert Roberts; David R Cox; David A Hinds; Len A Pennacchio; Anne Tybjaerg-Hansen; Aaron R Folsom; Eric Boerwinkle; Helen H Hobbs; Jonathan C Cohen
Journal:  Science       Date:  2007-05-03       Impact factor: 47.728

6.  Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.

Authors:  Richa Saxena; Benjamin F Voight; Valeriya Lyssenko; Noël P Burtt; Paul I W de Bakker; Hong Chen; Jeffrey J Roix; Sekar Kathiresan; Joel N Hirschhorn; Mark J Daly; Thomas E Hughes; Leif Groop; David Altshuler; Peter Almgren; Jose C Florez; Joanne Meyer; Kristin Ardlie; Kristina Bengtsson Boström; Bo Isomaa; Guillaume Lettre; Ulf Lindblad; Helen N Lyon; Olle Melander; Christopher Newton-Cheh; Peter Nilsson; Marju Orho-Melander; Lennart Råstam; Elizabeth K Speliotes; Marja-Riitta Taskinen; Tiinamaija Tuomi; Candace Guiducci; Anna Berglund; Joyce Carlson; Lauren Gianniny; Rachel Hackett; Liselotte Hall; Johan Holmkvist; Esa Laurila; Marketa Sjögren; Maria Sterner; Aarti Surti; Margareta Svensson; Malin Svensson; Ryan Tewhey; Brendan Blumenstiel; Melissa Parkin; Matthew Defelice; Rachel Barry; Wendy Brodeur; Jody Camarata; Nancy Chia; Mary Fava; John Gibbons; Bob Handsaker; Claire Healy; Kieu Nguyen; Casey Gates; Carrie Sougnez; Diane Gage; Marcia Nizzari; Stacey B Gabriel; Gung-Wei Chirn; Qicheng Ma; Hemang Parikh; Delwood Richardson; Darrell Ricke; Shaun Purcell
Journal:  Science       Date:  2007-04-26       Impact factor: 47.728

7.  A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release.

Authors:  Mar Matarín; W Mark Brown; Sonja Scholz; Javier Simón-Sánchez; Hon-Chung Fung; Dena Hernandez; J Raphael Gibbs; Fabienne Wavrant De Vrieze; Cynthia Crews; Angela Britton; Carl D Langefeld; Thomas G Brott; Robert D Brown; Bradford B Worrall; Michael Frankel; Scott Silliman; L Douglas Case; Andrew Singleton; John A Hardy; Stephen S Rich; James F Meschia
Journal:  Lancet Neurol       Date:  2007-05       Impact factor: 44.182

8.  Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.

Authors:  Eleftheria Zeggini; Michael N Weedon; Cecilia M Lindgren; Timothy M Frayling; Katherine S Elliott; Hana Lango; Nicholas J Timpson; John R B Perry; Nigel W Rayner; Rachel M Freathy; Jeffrey C Barrett; Beverley Shields; Andrew P Morris; Sian Ellard; Christopher J Groves; Lorna W Harries; Jonathan L Marchini; Katharine R Owen; Beatrice Knight; Lon R Cardon; Mark Walker; Graham A Hitman; Andrew D Morris; Alex S F Doney; Mark I McCarthy; Andrew T Hattersley
Journal:  Science       Date:  2007-04-26       Impact factor: 47.728

9.  Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.

Authors: 
Journal:  Nature       Date:  2007-06-07       Impact factor: 49.962

10.  The Ischemic Stroke Genetics Study (ISGS) Protocol.

Authors:  James F Meschia; Thomas G Brott; Robert D Brown; Richard J P Crook; Michael Frankel; John Hardy; José G Merino; Stephen S Rich; Scott Silliman; Bradford Burke Worrall
Journal:  BMC Neurol       Date:  2003-07-08       Impact factor: 2.474

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  67 in total

1.  Stroke Genetics Update: 2011.

Authors:  John W Cole; James F Meschia
Journal:  Curr Cardiovasc Risk Rep       Date:  2011-12-01

2.  Heterozygote genotypes at rs2222823 and rs2811712 SNP loci are associated with cerebral small vessel disease in Han Chinese population.

Authors:  Wei Li; Bo Hu; Gui-Lin Li; Xing-Quan Zhao; Bao-Zhong Xin; Jin-Xi Lin; Yuan Shen; Xian-Hong Liang; Gai-Fen Liu; Han-Qing Gao; Xiao-Ling Liao; Zhi-Gang Liang; Yong-Jun Wang
Journal:  CNS Neurosci Ther       Date:  2012-05-24       Impact factor: 5.243

3.  A Polymorphism Within the 3'UTR of NLRP3 is Associated with Susceptibility for Ischemic Stroke in Chinese Population.

Authors:  Zhansheng Zhu; Jing Yan; Chunsong Geng; Dagang Wang; Chaoyang Li; Shuai Feng; Huiping Wang
Journal:  Cell Mol Neurobiol       Date:  2015-12-21       Impact factor: 5.046

4.  A common variant in chromosome 9p21 associated with coronary artery disease in Asian Indians.

Authors:  Arindam Maitra; Debabrata Dash; Shibu John; Prathima R Sannappa; Anupam P Das; Jayashree Shanker; Veena S Rao; H Sridhara; Vijay V Kakkar
Journal:  J Genet       Date:  2009-04       Impact factor: 1.166

Review 5.  Stroke Risk Factors, Genetics, and Prevention.

Authors:  Amelia K Boehme; Charles Esenwa; Mitchell S V Elkind
Journal:  Circ Res       Date:  2017-02-03       Impact factor: 17.367

6.  A quantitative model for age-dependent expression of the p16INK4a tumor suppressor.

Authors:  Denis Tsygankov; Yan Liu; Hanna K Sanoff; Norman E Sharpless; Timothy C Elston
Journal:  Proc Natl Acad Sci U S A       Date:  2009-09-14       Impact factor: 11.205

7.  Fluid phase biopsy for detection and characterization of circulating endothelial cells in myocardial infarction.

Authors:  Kelly Bethel; Madelyn S Luttgen; Samir Damani; Anand Kolatkar; Rachelle Lamy; Mohsen Sabouri-Ghomi; Sarah Topol; Eric J Topol; Peter Kuhn
Journal:  Phys Biol       Date:  2014-01-09       Impact factor: 2.583

8.  Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression.

Authors:  Michael S Cunnington; Mauro Santibanez Koref; Bongani M Mayosi; John Burn; Bernard Keavney
Journal:  PLoS Genet       Date:  2010-04-08       Impact factor: 5.917

9.  Mitochondrial DNA haplogroups and risk of transient ischaemic attack and ischaemic stroke: a genetic association study.

Authors:  Patrick F Chinnery; Hannah R Elliott; Anila Syed; Peter M Rothwell
Journal:  Lancet Neurol       Date:  2010-03-31       Impact factor: 44.182

10.  Expression of linear and novel circular forms of an INK4/ARF-associated non-coding RNA correlates with atherosclerosis risk.

Authors:  Christin E Burd; William R Jeck; Yan Liu; Hanna K Sanoff; Zefeng Wang; Norman E Sharpless
Journal:  PLoS Genet       Date:  2010-12-02       Impact factor: 5.917

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