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Record W2163331125 · doi:10.1016/s1474-4422(12)70234-x

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

2012· review· en· W2163331125 on OpenAlexafffund
Matthew Traylor, Martin Farrall, Cathie Sudlow, Jemma C. Hopewell, Yu‐Ching Cheng, Myriam Fornage, M. Arfan Ikram, Rainer Malik, Steve Bevan, Unnur Þorsteinsdóttir, Mike A. Nalls, W. T. Longstreth, Kerri L. Wiggins, Sunaina Yadav, Eugenio Parati, Anita L. DeStefano, Bradford B. Worrall, Steven J. Kittner, Muhammad Saleem Khan, Alex P. Reiner, Anna Helgadóttir, Sefanja Achterberg, Israel Fernández‐Cadenas, Shérine Abboud, Reinhold Schmidt, James Walters, Wei‐Min Chen, E. Bernd Ringelstein, Martin O’Donnell, Weang-Kee Ho, Joanna Pera, Robin Lemmens, Bo Norrving, Peter Higgins, Marianne Benn, Michèle M. Sale, Gregor Kuhlenbäumer, Alex S. F. Doney, Astrid M. Vicente, Hossein Delavaran, Ale Algra, Gail Davies, Sofia A. Oliveira, Ian J. Deary, Helena Schmidt, Massimo Pandolfo, Joan Montaner, Cara L. Carty, Paul I. W. de Bakker, Konstantinos Kostulas, José M. Ferro, Natalie R. van Zuydam, Einar Már Valdimarsson, Børge G. Nordestgaard, Vincent Thijs, Agnieszka Słowik, Danish Saleheen, Guillaume Paré, Klaus Berger, Guðmar Þorleifsson, Albert Hofman, Thomas H. Mosley, Braxton D. Mitchell, Karen L. Furie, Robert Clarke, Christopher Levi, Sudha Seshadri, Andreas Gschwendtner, Giorgio B. Boncoraglio, Pankaj Sharma, Sólveig Grétarsdóttir, Bruce M. Psaty, Peter M. Rothwell, Jonathan Rosand, James F. Meschia, Kāri Stefánsson, Martin Dichgans, Hugh S. Markus

Bibliographic record

VenueThe Lancet Neurology · 2012
Typereview
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicGenetic Associations and Epidemiology
Canadian institutionsMcMaster University
FundersNational Center for Research ResourcesNational Institute of Neurological Disorders and StrokeNational Institute of Diabetes and Digestive and Kidney DiseasesNational Human Genome Research InstituteNational Center for Advancing Translational SciencesMedical Research CouncilFonds Wetenschappelijk OnderzoekSTROKE-RiksförbundetCanadian Institutes of Health ResearchDirectorate for Biological SciencesNational Institutes of HealthNational Institute on AgingNational Institute for Health and Care ResearchCentre for Cognitive Ageing and Cognitive EpidemiologyOffice of Research on Women's HealthNational Heart, Lung, and Blood InstituteDeutsche Migräne- und Kopfschmerzgesellschaft e.V.Vlaamse regeringWellcome TrustBiotechnology and Biological Sciences Research CouncilAustrian Science FundLunds UniversitetEconomic and Social Research CouncilSkånes universitetssjukhusUniversity of EdinburghBundesministerium für Bildung und ForschungHeart and Stroke Foundation of CanadaNational Heart Foundation of AustraliaEngineering and Physical Sciences Research CouncilAstraZenecaVetenskapsrådetCanadian Stroke Network
KeywordsGenome-wide association studyMeta-analysisIschaemic strokeStroke (engine)Genetic associationMedicineComputational biologyBiologyGeneticsInternal medicineGenotypeGeneSingle-nucleotide polymorphismIschemiaEngineering

Abstract

fetched live from OpenAlex

BACKGROUND: Various genome-wide association studies (GWAS) have been done in ischaemic stroke, identifying a few loci associated with the disease, but sample sizes have been 3500 cases or less. We established the METASTROKE collaboration with the aim of validating associations from previous GWAS and identifying novel genetic associations through meta-analysis of GWAS datasets for ischaemic stroke and its subtypes. METHODS: We meta-analysed data from 15 ischaemic stroke cohorts with a total of 12 389 individuals with ischaemic stroke and 62 004 controls, all of European ancestry. For the associations reaching genome-wide significance in METASTROKE, we did a further analysis, conditioning on the lead single nucleotide polymorphism in every associated region. Replication of novel suggestive signals was done in 13 347 cases and 29 083 controls. FINDINGS: We verified previous associations for cardioembolic stroke near PITX2 (p=2·8×10(-16)) and ZFHX3 (p=2·28×10(-8)), and for large-vessel stroke at a 9p21 locus (p=3·32×10(-5)) and HDAC9 (p=2·03×10(-12)). Additionally, we verified that all associations were subtype specific. Conditional analysis in the three regions for which the associations reached genome-wide significance (PITX2, ZFHX3, and HDAC9) indicated that all the signal in each region could be attributed to one risk haplotype. We also identified 12 potentially novel loci at p<5×10(-6). However, we were unable to replicate any of these novel associations in the replication cohort. INTERPRETATION: Our results show that, although genetic variants can be detected in patients with ischaemic stroke when compared with controls, all associations we were able to confirm are specific to a stroke subtype. This finding has two implications. First, to maximise success of genetic studies in ischaemic stroke, detailed stroke subtyping is required. Second, different genetic pathophysiological mechanisms seem to be associated with different stroke subtypes. FUNDING: Wellcome Trust, UK Medical Research Council (MRC), Australian National and Medical Health Research Council, National Institutes of Health (NIH) including National Heart, Lung and Blood Institute (NHLBI), the National Institute on Aging (NIA), the National Human Genome Research Institute (NHGRI), and the National Institute of Neurological Disorders and Stroke (NINDS).

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.014
metaresearch head score (Gemma)0.025
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Meta-analysis · Consensus signal: Meta-analysis
GenreCandidate signal: Empirical · Consensus signal: none
Teacher disagreement score0.014
Threshold uncertainty score0.076

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0140.025
Meta-epidemiology (narrow)0.0020.001
Meta-epidemiology (broad)0.0100.027
Bibliometrics0.0050.006
Science and technology studies0.0010.000
Scholarly communication0.0020.001
Open science0.0020.002
Research integrity0.0020.001
Insufficient payload (model declined to judge)0.0020.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.118
GPT teacher head0.353
Teacher spread0.236 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designMeta-analysis
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations487
Published2012
Admission routes2
Has abstractyes

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