Evidence map›Paper›PMID 31869433›Full record

SynthesisClinical pharmacology and therapeutics2020

Genetic Factors Influencing Warfarin Dose in Black-African Patients: A Systematic Review and Meta-Analysis.

Innocent G Asiimwe, Eunice J Zhang, Rostam Osanlou, Amanda Krause, Chrisly Dillon, Guilherme Suarez-Kurtz, Honghong Zhang, Jamila A Perini, Jessicca Y Renta, Jorge Duconge and 12 more

Open access · greenAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Clinical pharmacology and therapeutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 4 pooled it
8.2field-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

28 citing papers in PubMed, 4 syntheses or guidelines pooled it, 63 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Warfarin dosing algorithms: A systematic review.British journal of clinical pharmacology · 2021
    Pooled it
  4. Influence ofCardiovascular therapeutics · 2021
    Pooled it
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Observational
  12. Review
  13. Article
  14. Warfarin Dosing in Patients With CYP2C9*5 Variant Alleles.Clinical pharmacology and therapeutics · 2022
    Article
  15. Article
  16. Article
  17. Ethnic Diversity and Warfarin Pharmacogenomics.Frontiers in pharmacology · 2022
    Review
  18. Article
  19. 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

22 authors at 14 institutions in 5 countries.

Innocent G AsiimweDepartment of Molecular and Clinical Pharmacology, The Wolfson Centre for Personalized Medicine, MRC Centre for Drug Safety Science, University of Liverpool, Liverpool, UK.ORCID 0000-0002-1196-1822
Eunice J ZhangDepartment of Molecular and Clinical Pharmacology, The Wolfson Centre for Personalized Medicine, MRC Centre for Drug Safety Science, University of Liverpool, Liverpool, UK.
Rostam OsanlouDepartment of Molecular and Clinical Pharmacology, The Wolfson Centre for Personalized Medicine, MRC Centre for Drug Safety Science, University of Liverpool, Liverpool, UK.
Amanda KrauseDivision of Human Genetics, Faculty of Health Sciences, National Health Laboratory Service, School of Pathology, The University of the Witwatersrand, Johannesburg, South Africa.
Chrisly DillonDepartment of Neurology & Epidemiology, Hugh Kaul Precision Medicine Institute, The University of Alabama at Birmingham, Birmingham, Alabama, USA.
Guilherme Suarez-KurtzCoordenação de Pesquisa, Instituto Nacional de Câncer, Rio de Janeiro, Brazil.ORCID 0000-0002-1115-8319
Honghong ZhangDepartment of Pharmacology, Center for Pharmacogenomics, Northwestern University, Chicago, Illinois, USA.
Jamila A PeriniResearch Laboratory of Pharmaceutical Sciences, West Zone State University-UEZO, Rio de Janeiro, Brazil.
Jessicca Y RentaUniversity of Puerto Rico School of Pharmacy, Medical Sciences Campus, San Juan, Puerto Rico.
Jorge DucongeUniversity of Puerto Rico School of Pharmacy, Medical Sciences Campus, San Juan, Puerto Rico.
Larisa H CavallariDepartment of Pharmacotherapy and Translational Research, Center for Pharmacogenomics, University of Florida College of Pharmacy, Gainesville, Florida, USA.
Leiliane R MarcattoLaboratory of Genetics and Molecular Cardiology, Faculdade de Medicina FMUSP, Heart Institute (InCor), Universidade de São Paulo, São Paulo, Brazil.ORCID 0000-0002-1141-0246
Mark T BeaslyDepartment of Neurology & Epidemiology, Hugh Kaul Precision Medicine Institute, The University of Alabama at Birmingham, Birmingham, Alabama, USA.
Minoli A PereraDepartment of Pharmacology, Center for Pharmacogenomics, Northwestern University, Chicago, Illinois, USA.ORCID 0000-0002-1146-2791
Nita A LimdiDepartment of Neurology & Epidemiology, Hugh Kaul Precision Medicine Institute, The University of Alabama at Birmingham, Birmingham, Alabama, USA.
Paulo C J L SantosDepartment of Pharmacology, Escola Paulista de Medicina, EPM-Unifesp, Universidade Federal de São Paulo, São Paulo, Brazil.
Stephen E KimmelDepartment of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Steven A LubitzCardiac Arrhythmia Service and Cardiovascular Research Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
Stuart A ScottDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Vivian K KawaiDivision of Clinical Pharmacology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Andrea L JorgensenDepartment of Biostatistics, Institute of Translational Medicine, University of Liverpool, Liverpool, UK.
Munir PirmohamedDepartment of Molecular and Clinical Pharmacology, The Wolfson Centre for Personalized Medicine, MRC Centre for Drug Safety Science, University of Liverpool, Liverpool, UK.
University of Liverpool · GBUniversity of Alabama at Birmingham · USNorthwestern University · USUniversity of Puerto Rico, Medical Sciences Campus · PRAmerican Association of Colleges of Pharmacy · USInstituto Nacional de Câncer - INCA · BRMassachusetts General Hospital · USNational Health Laboratory Service · ZASema4 (United States) · USUniversidade de São Paulo · BRUniversidade Estadual da Zona Oeste · BRUniversidade Federal de São Paulo · BRUniversity of Pennsylvania · USVanderbilt University Medical Center · US

Funding

Upstream Regulation and Downstream effectors of c-MYC in Ovarian CancerU54MD007600 · NIMHD · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI Emma Fernandez-Repollet · 2017 to 2026
$35.8M
Predictors of hemorrhage among patients on direct acting oral anticoagulantsR01HL092173 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LIMDI, NITA A · 2008 to 2023
$10.4M
Genomics of Cardiac ArrhythmiasR01HL139731 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI ELLINOR, PATRICK THOMAS · 2018 to 2022
$3.3M
Health disparity in pharmacogenomics: African American SNPs and drug metabolismR01MD009217 · NIMHD · UNIVERSITY OF CHICAGO · PI PERERA, MINOLI A · 2014 to 2018
$2.0M
Patient Oriented Research in Personalized Antithrombotic TherapyK24HL133373 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LIMDI, NITA A · 2016 to 2025
$1.2M
A Genomic Approach to Warfarin Dose Prescription in Admixed Caribbean Hispanics.SC1HL123911 · NHLBI · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI DUCONGE, JORGE · 2014 to 2017
$982k
Pharmacogenetic Determinants of Variability in Response to GlucocorticoidsK23GM117395 · NIGMS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI KAWAI, VIVIAN K · 2015 to 2018
$736k
Comprehensive studies of novel SNPs affecting warfarin dose in African AmericansR21HL106097 · NHLBI · UNIVERSITY OF CHICAGO · PI PERERA, MINOLI A · 2011 to 2012
$437k
NHLBI NIH HHS K24 HL133373NHLBI NIH HHS R01 HL092173NHLBI NIH HHS R01 HL139731NHLBI NIH HHS R21 HL106097NHLBI NIH HHS SC1 HL123911NIGMS NIH HHS K23 GM117395NIMHD NIH HHS R01 MD009217NIMHD NIH HHS U54 MD007600
6 · The paper itself

Abstract

Warfarin is the most commonly used oral anticoagulant in sub-Saharan Africa. Dosing is challenging due to a narrow therapeutic index and high interindividual variability in dose requirements. To evaluate the genetic factors affecting warfarin dosing in black-Africans, we performed a meta-analysis of 48 studies (2,336 patients). Significant predictors for CYP2C9 and stable dose included rs1799853 (CYP2C9*2), rs1057910 (CYP2C9*3), rs28371686 (CYP2C9*5), rs9332131 (CYP2C9*6), and rs28371685 (CYP2C9*11) reducing dose by 6.8, 12.5, 13.4, 8.1, and 5.3 mg/week, respectively. VKORC1 variants rs9923231 (-1639G>A), rs9934438 (1173C>T), rs2359612 (2255C>T), rs8050894 (1542G>C), and rs2884737 (497T>G) decreased dose by 18.1, 21.6, 17.3, 11.7, and 19.6 mg/week, respectively, whereas rs7294 (3730G>A) increased dose by 6.9 mg/week. Finally, rs12777823 (CYP2C gene cluster) was associated with a dose reduction of 12.7 mg/week. Few studies were conducted in Africa, and patient numbers were small, highlighting the need for further work in black-Africans to evaluate genetic factors determining warfarin response.

Indexed as

AnticoagulantsBlack PeopleCytochrome P-450 CYP2C9Dose-Response Relationship, DrugHumansPolymorphism, Single NucleotideVitamin K Epoxide ReductasesWarfarinAnticoagulantsCYP2C9 protein, humanCytochrome P-450 CYP2C9Vitamin K Epoxide ReductasesVKORC1 protein, humanWarfarin

Identifiers

PMID31869433
PMCPMC7217737
OpenAlexW2995598335

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Registered trials

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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 OpenQuestion graph.