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Impact of CYP2C19 gene polymorphisms on warfarin dose requirement: a systematic review and meta-analysis

    Dongxu Wang

    Arrhythmia Center, National Center for Cardiovascular Diseases & Fuwai Hospital, CAMS & PUMC, Beijing, 100037, China

    ,
    Ling Yong

    Department of Pharmacy Administration & Clinical Pharmacy, School of Pharmaceutical Sciences, Peking University, Beijing, 100191, China

    ,
    Qing Zhang

    Department of Cardiovascular, Beijing Hospital, National Centre of Gerontology, Beijing, 100730, China

    &
    Hao Chen

    *Author for correspondence:

    E-mail Address: dr.chenhaomd_bjh@vip.163.com

    Department of Cardiovascular, Beijing Hospital, National Centre of Gerontology, Beijing, 100730, China

    Published Online:https://doi.org/10.2217/pgs-2022-0106

    Background: Various genetic factors influence warfarin maintenance dose. Methods: A literature search was performed on PubMed, Embase and the Cochrane Library, and a meta-analysis to analyze the impact of CYP2C19 polymorphisms on warfarin maintenance dose was conducted. Results: From nine studies encompassing 1393 patients, three CYP2C19 SNPs were identified: rs4244285, rs4986893 and rs3814637. Warfarin maintenance dose was significantly reduced by 10% in individuals with the rs4986893 A allele compared with the GG carriers and was 34%, 16% and 18% lower in patients with rs3814637 TT and CT genotypes and T allele, respectively, than that in CC carriers. No significant dose difference was observed among the rs4244285 genotypes. Conclusion:CYP2C19 rs4986893 and rs3814637 are associated with significantly reduced warfarin dose requirements.

    Papers of special note have been highlighted as: • of interest

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