Evidence map›Paper›PMID 31220337›Full record

SynthesisClinical pharmacology and therapeutics2019

Genomewide Association Study of Statin-Induced Myopathy in Patients Recruited Using the UK Clinical Practice Research Datalink.

Daniel F Carr, Ben Francis, Andrea L Jorgensen, Eunice Zhang, Hector Chinoy, Susan R Heckbert, Joshua C Bis, Jennifer A Brody, James S Floyd, Bruce M Psaty and 6 more

Open access · hybridAbstract readMeta-AnalysisValidation Study
In one paragraph

Synthesis in Clinical pharmacology and therapeutics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
7.7field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 61 citations in OpenAlex.

  1. Trial
  2. Polygenic risk scores in pharmacogenomics: methodological challenges, current applications, and perspectives for clinical implementation.Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V · 2026
    Article
  3. Article
  4. Article
  5. Retrospective Evaluation of the Impact ofJournal of personalized medicine · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. International journal of molecular sciences · 2024
    Article
  12. Article
  13. Review
  14. PharmVar GeneFocus: SLCO1B1.Clinical pharmacology and therapeutics · 2023
    Review
  15. Cardiovascular precision medicine - A pharmacogenomic perspective.Cambridge prisms. Precision medicine · 2023
    Review
  16. Genetic VariantPharmaceutics · 2022
    Article
  17. Article
  18. Ethnic Diversity and Warfarin Pharmacogenomics.Frontiers in pharmacology · 2022
    Review
  19. Personalizing treatments for patients based on cardiovascular phenotyping.Expert review of precision medicine and drug development · 2022
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 8 institutions in 5 countries.

Daniel F CarrWolfson Centre for Personalised Medicine, Department of Molecular and Clinical Pharmacology, Institute of Translational Medicine, University of Liverpool, Liverpool, UK.
Ben FrancisDepartment of Biostatistics, Institute of Translational Medicine, University of Liverpool, Liverpool, UK.
Andrea L JorgensenDepartment of Biostatistics, Institute of Translational Medicine, University of Liverpool, Liverpool, UK.
Eunice ZhangWolfson Centre for Personalised Medicine, Department of Molecular and Clinical Pharmacology, Institute of Translational Medicine, University of Liverpool, Liverpool, UK.
Hector ChinoyRheumatology Department, Salford Royal NHS Foundation Trust, Manchester Academic Health Science Centre, Salford, UK.
Susan R HeckbertCardiovascular Health Research Unit, Department of Epidemiology, University of Washington, Seattle, Washington, USA.
Joshua C BisCardiovascular Health Research Unit, Department of Medicine, University of Washington, Seattle, Washington, USA.
Jennifer A BrodyCardiovascular Health Research Unit, Department of Medicine, University of Washington, Seattle, Washington, USA.
James S FloydCardiovascular Health Research Unit, Department of Medicine, University of Washington, Seattle, Washington, USA.
Bruce M PsatyCardiovascular Health Research Unit, Department of Medicine, University of Washington, Seattle, Washington, USA.
Mariam MolokhiaSchool of Population Health and Environmental Sciences, King's College London, London, UK.
Maryse Lapeyre-MestreMedical and Clinical Pharmacology, CHU Toulouse, Toulouse, France.
Anita ConfortiUniversity Hospital, Verona, Italy.
Ana AlfirevicWolfson Centre for Personalised Medicine, Department of Molecular and Clinical Pharmacology, Institute of Translational Medicine, University of Liverpool, Liverpool, UK.
Tjeerd van StaaHealth e-Research Centre, School of Health Sciences, Faculty of Biology, Medicine, and Health, University of Manchester, Manchester, UK.
Munir PirmohamedWolfson Centre for Personalised Medicine, Department of Molecular and Clinical Pharmacology, Institute of Translational Medicine, University of Liverpool, Liverpool, UK.
University of Liverpool · GBUniversity of Washington · USCentre Hospitalier Universitaire de Toulouse · FRKaiser Permanente Washington Health Research Institute · USKing's College London · GBManchester Academic Health Science Centre · GBSalford Royal NHS Foundation Trust · GBUniversity of Verona · IT

Funding

CHS research resources for the cardiovascular health of older adultsU01HL130114 · NHLBI · UNIVERSITY OF WASHINGTON · PI BURKE, GREGORY L, KRONMAL, RICHARD A · 2016 to 2019
$6.6M
Department of HealthMedical Research Council MC_QA137929Medical Research Council MR/L006758/1Medical Research Council MR/N003322/1NHLBI NIH HHS U01 HL130114Wellcome Trust
6 · The paper itself

Abstract

Statins can be associated with myopathy. We have undertaken a genomewide association study (GWAS) to discover and validate genetic risk factors for statin-induced myopathy in a "real-world" setting. One hundred thirty-five patients with statin myopathy recruited via the UK Clinical Practice Research Datalink were genotyped using the Illumina OmniExpress Exome version 1.0 Bead Chip and compared with the Wellcome Trust Case-Control Consortium (n = 2,501). Nominally statistically significant single nucleotide polymorphism (SNP) signals in the GWAS (P < 5 × 10

Indexed as

Adverse Drug Reaction Reporting SystemsPharmacogenomic VariantsPolymorphism, Single NucleotideCase-Control StudiesDatabases, FactualGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansHydroxymethylglutaryl-CoA Reductase InhibitorsLiver-Specific Organic Anion Transporter 1Muscular DiseasesReproducibility of ResultsRisk FactorsSeverity of Illness IndexUnited KingdomHydroxymethylglutaryl-CoA Reductase InhibitorsLiver-Specific Organic Anion Transporter 1SLCO1B1 protein, human

Identifiers

PMID31220337
PMCPMC6896237
OpenAlexW2950340165

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.