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Record W7081584268

Genetic analysis for a shared biological basis between migraine and coronary artery disease

2022· other· en· W7081584268 on OpenAlex

Why this work is in the frame

A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.

fundA Canadian funder is recorded on the work.
no affNo Canadian affiliation: this work is invisible to an affiliation-only frame.
No Canadian affiliation. An affiliation-only frame, the usual design, would never have seen this work. It is one of the works that make the case for inverting the frame.

Bibliographic record

Venuenot available
Typeother
Languageen
FieldComputer Science
TopicGeochemistry and Geologic Mapping
Canadian institutionsnot available
FundersU.S. National Library of MedicineNational Institute of Neurological Disorders and StrokeNational Institute of Allergy and Infectious DiseasesNational Cancer InstituteNational Heart, Lung, and Blood InstituteUniversitätsmedizin der Johannes Gutenberg-Universität MainzUniversitätsklinikum Hamburg-EppendorfCanadian Institutes of Health ResearchAllerganDaiichi Sankyo EuropeSt. Jude MedicalNational Institutes of HealthJanssen Prevention CenterAvera Institute for Human GeneticsCentre for Medical Systems BiologyPaavo Nurmen SäätiöTampereen TuberkuloosisäätiöUniversité de BordeauxSydäntutkimussäätiöTurun YliopistoNorges ForskningsrådTampereen YliopistoJuho Vainion SäätiöTechnische Universität MünchenDeutsche ForschungsgemeinschaftNederlandse Organisatie voor Wetenschappelijk OnderzoekBritish Heart FoundationHáskóli ÍslandsBundesministerium für Bildung und ForschungVrije Universiteit AmsterdamOulun YliopistoSuomen KulttuurirahastoZonMwEberhard Karls Universität TübingenUniversiteit LeidenUnited States-Israel Binational Science FoundationSchool of Medicine, Stanford UniversityInstitut National de la Santé et de la Recherche MédicaleFondation LeducqInstitute of GeneticsAgence Nationale de la RechercheUniversität HeidelbergKarl-Franzens-Universität GrazUniversity of BristolAstraZenecaEuropean CommissionKelaUniversity of LeedsTerveyden ja hyvinvoinnin laitosAcademy of FinlandKing's College LondonRegeneron PharmaceuticalsNational Institute of Mental HealthHelse Sør-Øst RHFTelomere DiagnosticsWellcome TrustInternationale Stichting Alzheimer OnderzoekSanofiNorges Teknisk-Naturvitenskapelige UniversitetDeutsches Zentrum für Herz-KreislaufforschungUniversity of OttawaFP7 HealthImperial College LondonSamfundet FolkhälsanUniversität zu LübeckPfizerSuomen Lääketieteen SäätiöBoston Scientific CorporationMedicinska Understödsföreningen Liv och HälsaTurun Yliopistollinen KeskussairaalaHelsingin ja Uudenmaan SairaanhoitopiiriFoundation for Cardiovascular ResearchMedizinische Universität GrazEmil Aaltosen SäätiöUniversity of PennsylvaniaMedical Research CouncilInstitute for Translational Medicine and TherapeuticsBiocenter, University of OuluFolkhälsanin TutkimussäätiöNational Institute for Health and Care ResearchTeva Pharmaceutical IndustriesAmgen
KeywordsMigraineMigraine with auraCoronary artery diseaseGenetic associationAuraDiseaseAllelePathogenesis
DOInot available

Abstract

fetched live from OpenAlex

<div> Objective: To apply genetic analysis of genome-wide association data to study the extent and nature of a shared biological basis between migraine and coronary artery disease (CAD). </div><div> Methods: Four separate methods for cross-phenotype genetic analysis were applied on data from 2 large-scale genome-wide association studies of migraine (19,981 cases, 56,667 controls) and CAD (21,076 cases, 63,014 controls). The first 2 methods quantified the extent of overlapping risk variants and assessed the load of CAD risk loci in migraineurs. Genomic regions of shared risk were then identified by analysis of covariance patterns between the 2 phenotypes and by querying known genome-wide significant loci. </div><div> Results: We found a significant overlap of genetic risk loci for migraine and CAD. When stratified by migraine subtype, this was limited to migraine without aura, and the overlap was protective in that patients with migraine had a lower load of CAD risk alleles than controls. Genes indicated by 16 shared risk loci point to mechanisms with potential roles in migraine pathogenesis and CAD, including endothelial dysfunction (<em>PHACTR1</em>) and insulin homeostasis (<em>GIP</em>). </div><div> Conclusions: The results suggest that shared biological processes contribute to risk of migraine and CAD, but surprisingly this commonality is restricted to migraine without aura and the impact is in opposite directions. Understanding the mechanisms underlying these processes and their opposite relationship to migraine and CAD may improve our understanding of both disorders. </div>

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.

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesInsufficient payload (model declined to judge)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Not applicable · Consensus signal: none
GenreCandidate signal: Other · Consensus signal: none
Teacher disagreement score0.582
Threshold uncertainty score0.991

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0010.001
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0100.000

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 head0.029
GPT teacher head0.233
Teacher spread0.204 · 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

Quick stats

Citations0
Published2022
Admission routes1
Has abstractyes

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