Literature DB >> 25653287

Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease.

Kristiina Rannikmäe1, Gail Davies1, Pippa A Thomson1, Steve Bevan1, William J Devan1, Guido J Falcone1, Matthew Traylor1, Christopher D Anderson1, Thomas W K Battey1, Farid Radmanesh1, Ranjan Deka1, Jessica G Woo1, Lisa J Martin1, Jordi Jimenez-Conde1, Magdy Selim1, Devin L Brown1, Scott L Silliman1, Chelsea S Kidwell1, Joan Montaner1, Carl D Langefeld1, Agnieszka Slowik1, Björn M Hansen1, Arne G Lindgren1, James F Meschia1, Myriam Fornage1, Joshua C Bis1, Stéphanie Debette1, Mohammad A Ikram1, Will T Longstreth1, Reinhold Schmidt1, Cathy R Zhang1, Qiong Yang1, Pankaj Sharma1, Steven J Kittner1, Braxton D Mitchell1, Elizabeth G Holliday1, Christopher R Levi1, John Attia1, Peter M Rothwell1, Deborah L Poole1, Giorgio B Boncoraglio1, Bruce M Psaty1, Rainer Malik1, Natalia Rost1, Bradford B Worrall1, Martin Dichgans1, Tom Van Agtmael1, Daniel Woo1, Hugh S Markus1, Sudha Seshadri1, Jonathan Rosand1, Cathie L M Sudlow2.   

Abstract

OBJECTIVES: We hypothesized that common variants in the collagen genes COL4A1/COL4A2 are associated with sporadic forms of cerebral small vessel disease.
METHODS: We conducted meta-analyses of existing genotype data among individuals of European ancestry to determine associations of 1,070 common single nucleotide polymorphisms (SNPs) in the COL4A1/COL4A2 genomic region with the following: intracerebral hemorrhage and its subtypes (deep, lobar) (1,545 cases, 1,485 controls); ischemic stroke and its subtypes (cardioembolic, large vessel disease, lacunar) (12,389 cases, 62,004 controls); and white matter hyperintensities (2,733 individuals with ischemic stroke and 9,361 from population-based cohorts with brain MRI data). We calculated a statistical significance threshold that accounted for multiple testing and linkage disequilibrium between SNPs (p < 0.000084).
RESULTS: Three intronic SNPs in COL4A2 were significantly associated with deep intracerebral hemorrhage (lead SNP odds ratio [OR] 1.29, 95% confidence interval [CI] 1.14-1.46, p = 0.00003; r(2) > 0.9 between SNPs). Although SNPs associated with deep intracerebral hemorrhage did not reach our significance threshold for association with lacunar ischemic stroke (lead SNP OR 1.10, 95% CI 1.03-1.18, p = 0.0073), and with white matter hyperintensity volume in symptomatic ischemic stroke patients (lead SNP OR 1.07, 95% CI 1.01-1.13, p = 0.016), the direction of association was the same. There was no convincing evidence of association with white matter hyperintensities in population-based studies or with non-small vessel disease cerebrovascular phenotypes.
CONCLUSIONS: Our results indicate an association between common variation in the COL4A2 gene and symptomatic small vessel disease, particularly deep intracerebral hemorrhage. These findings merit replication studies, including in ethnic groups of non-European ancestry.
© 2015 American Academy of Neurology.

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Year:  2015        PMID: 25653287      PMCID: PMC4351667          DOI: 10.1212/WNL.0000000000001309

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  36 in total

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Journal:  Am J Hum Genet       Date:  2011-12-29       Impact factor: 11.025

2.  COL4A1 mutations in patients with sporadic late-onset intracerebral hemorrhage.

Authors:  Yi-Chinn Weng; Akshata Sonni; Cassandre Labelle-Dumais; Michelle de Leau; W Berkeley Kauffman; Marion Jeanne; Alessandro Biffi; Steven M Greenberg; Jonathan Rosand; Douglas B Gould
Journal:  Ann Neurol       Date:  2012-04       Impact factor: 10.422

3.  Burden of blood pressure-related alleles is associated with larger hematoma volume and worse outcome in intracerebral hemorrhage.

Authors:  Guido J Falcone; Alessandro Biffi; William J Devan; H Bart Brouwers; Christopher D Anderson; Valerie Valant; Alison M Ayres; Kristin Schwab; Natalia S Rost; Joshua N Goldstein; Anand Viswanathan; Steven M Greenberg; Magdy Selim; James F Meschia; Devin L Brown; Bradford B Worrall; Scott L Silliman; David L Tirschwell; Jonathan Rosand
Journal:  Stroke       Date:  2013-01-15       Impact factor: 7.914

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6.  Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease.

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Journal:  Nucleic Acids Res       Date:  2013-12-06       Impact factor: 16.971

8.  Chemical chaperone treatment reduces intracellular accumulation of mutant collagen IV and ameliorates the cellular phenotype of a COL4A2 mutation that causes haemorrhagic stroke.

Authors:  Lydia S Murray; Yinhui Lu; Aislynn Taggart; Nicole Van Regemorter; Catheline Vilain; Marc Abramowicz; Karl E Kadler; Tom Van Agtmael
Journal:  Hum Mol Genet       Date:  2013-09-02       Impact factor: 6.150

9.  17q25 Locus is associated with white matter hyperintensity volume in ischemic stroke, but not with lacunar stroke status.

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Journal:  Stroke       Date:  2013-05-14       Impact factor: 7.914

10.  Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.

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Journal:  Lancet Neurol       Date:  2012-10-05       Impact factor: 59.935

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  54 in total

1.  Comparative genomic analysis of collagen gene diversity.

Authors:  Farhan Haq; Nabeel Ahmed; Muhammad Qasim
Journal:  3 Biotech       Date:  2019-02-14       Impact factor: 2.406

Review 2.  Monogenic causes of stroke: now and the future.

Authors:  Rhea Y Y Tan; Hugh S Markus
Journal:  J Neurol       Date:  2015-06-03       Impact factor: 4.849

Review 3.  Neuroimaging in Dementia.

Authors:  Adam M Staffaroni; Fanny M Elahi; Dana McDermott; Kacey Marton; Elissaios Karageorgiou; Simone Sacco; Matteo Paoletti; Eduardo Caverzasi; Christopher P Hess; Howard J Rosen; Michael D Geschwind
Journal:  Semin Neurol       Date:  2017-12-05       Impact factor: 3.420

Review 4.  Advancing stroke genomic research in the age of Trans-Omics big data science: Emerging priorities and opportunities.

Authors:  Mayowa Owolabi; Emmanuel Peprah; Huichun Xu; Rufus Akinyemi; Hemant K Tiwari; Marguerite R Irvin; Kolawole Wasiu Wahab; Donna K Arnett; Bruce Ovbiagele
Journal:  J Neurol Sci       Date:  2017-09-18       Impact factor: 3.181

Review 5.  Genetic factors in cerebral small vessel disease and their impact on stroke and dementia.

Authors:  Christof Haffner; Rainer Malik; Martin Dichgans
Journal:  J Cereb Blood Flow Metab       Date:  2016-01       Impact factor: 6.200

Review 6.  Emerging insights from the genetics of cerebral small-vessel disease.

Authors:  Loes C A Rutten-Jacobs; Natalia S Rost
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7.  17p12 Influences Hematoma Volume and Outcome in Spontaneous Intracerebral Hemorrhage.

Authors:  Sandro Marini; William J Devan; Farid Radmanesh; Laura Miyares; Timothy Poterba; Björn M Hansen; Bo Norrving; Jordi Jimenez-Conde; Eva Giralt-Steinhauer; Roberto Elosua; Elisa Cuadrado-Godia; Carolina Soriano; Jaume Roquer; Christina E Kourkoulis; Alison M Ayres; Kristin Schwab; David L Tirschwell; Magdy Selim; Devin L Brown; Scott L Silliman; Bradford B Worrall; James F Meschia; Chelsea S Kidwell; Joan Montaner; Israel Fernandez-Cadenas; Pilar Delgado; Steven M Greenberg; Arne Lindgren; Charles Matouk; Kevin N Sheth; Daniel Woo; Christopher D Anderson; Jonathan Rosand; Guido J Falcone
Journal:  Stroke       Date:  2018-06-18       Impact factor: 7.914

Review 8.  Genetics of Spontaneous Intracerebral Hemorrhage.

Authors:  Guido J Falcone; Daniel Woo
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9.  Endothelial depletion of murine SRF/MRTF provokes intracerebral hemorrhagic stroke.

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10.  Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke.

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Journal:  Stroke       Date:  2020-03-16       Impact factor: 7.914

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