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Genetic Factors Influencing Warfarin Dose in Black-African Patients: A Systematic Review and Meta-Analysis.
Asiimwe, Innocent G; Zhang, Eunice J; Osanlou, Rostam; Krause, Amanda; Dillon, Chrisly; Suarez-Kurtz, Guilherme; Zhang, Honghong; Perini, Jamila A; Renta, Jessicca Y; Duconge, Jorge; Cavallari, Larisa H; Marcatto, Leiliane R; Beasly, Mark T; Perera, Minoli A; Limdi, Nita A; Santos, Paulo C J L; Kimmel, Stephen E; Lubitz, Steven A; Scott, Stuart A; Kawai, Vivian K; Jorgensen, Andrea L; Pirmohamed, Munir.
Afiliação
  • Asiimwe IG; Department of Molecular and Clinical Pharmacology, The Wolfson Centre for Personalized Medicine, MRC Centre for Drug Safety Science, University of Liverpool, Liverpool, UK.
  • Zhang EJ; Department of Molecular and Clinical Pharmacology, The Wolfson Centre for Personalized Medicine, MRC Centre for Drug Safety Science, University of Liverpool, Liverpool, UK.
  • Osanlou R; Department of Molecular and Clinical Pharmacology, The Wolfson Centre for Personalized Medicine, MRC Centre for Drug Safety Science, University of Liverpool, Liverpool, UK.
  • Krause A; Division of Human Genetics, Faculty of Health Sciences, National Health Laboratory Service, School of Pathology, The University of the Witwatersrand, Johannesburg, South Africa.
  • Dillon C; Department of Neurology & Epidemiology, Hugh Kaul Precision Medicine Institute, The University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Suarez-Kurtz G; Coordenação de Pesquisa, Instituto Nacional de Câncer, Rio de Janeiro, Brazil.
  • Zhang H; Department of Pharmacology, Center for Pharmacogenomics, Northwestern University, Chicago, Illinois, USA.
  • Perini JA; Research Laboratory of Pharmaceutical Sciences, West Zone State University-UEZO, Rio de Janeiro, Brazil.
  • Renta JY; University of Puerto Rico School of Pharmacy, Medical Sciences Campus, San Juan, Puerto Rico.
  • Duconge J; University of Puerto Rico School of Pharmacy, Medical Sciences Campus, San Juan, Puerto Rico.
  • Cavallari LH; Department of Pharmacotherapy and Translational Research, Center for Pharmacogenomics, University of Florida College of Pharmacy, Gainesville, Florida, USA.
  • Marcatto LR; Laboratory of Genetics and Molecular Cardiology, Faculdade de Medicina FMUSP, Heart Institute (InCor), Universidade de São Paulo, São Paulo, Brazil.
  • Beasly MT; Department of Neurology & Epidemiology, Hugh Kaul Precision Medicine Institute, The University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Perera MA; Department of Pharmacology, Center for Pharmacogenomics, Northwestern University, Chicago, Illinois, USA.
  • Limdi NA; Department of Neurology & Epidemiology, Hugh Kaul Precision Medicine Institute, The University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Santos PCJL; Department of Pharmacology, Escola Paulista de Medicina, EPM-Unifesp, Universidade Federal de São Paulo, São Paulo, Brazil.
  • Kimmel SE; Department of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Lubitz SA; Cardiac Arrhythmia Service and Cardiovascular Research Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Scott SA; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Kawai VK; Sema4, a Mount Sinai venture, Stamford, Connecticut, USA.
  • Jorgensen AL; Division of Clinical Pharmacology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Pirmohamed M; Department of Biostatistics, Institute of Translational Medicine, University of Liverpool, Liverpool, UK.
Clin Pharmacol Ther ; 107(6): 1420-1433, 2020 06.
Article em En | MEDLINE | ID: mdl-31869433
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Varfarina / Citocromo P-450 CYP2C9 / Anticoagulantes Tipo de estudo: Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Revista: Clin Pharmacol Ther Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Varfarina / Citocromo P-450 CYP2C9 / Anticoagulantes Tipo de estudo: Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Revista: Clin Pharmacol Ther Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Reino Unido