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Integrated analysis of clinical and genetic factors on the interindividual variation of warfarin anticoagulation efficacy in clinical practice.
Sun, Bao; Ma, Siqing; Xiao, Feiyan; Luo, Jianquan; Liu, Mouze; Liu, Wenhui; Luo, Zhiying.
Afiliação
  • Sun B; Department of Pharmacy, The Second Xiangya Hospital, Central South University, No.139, People's Middle Street, Furong District, Changsha City, 40013, Hunan Porv., China.
  • Ma S; Institute of Clinical Pharmacy, Central South University, Changsha, China.
  • Xiao F; Department of Pharmacy, Hunan Institute for Tuberculosis Control, Changsha, China.
  • Luo J; Department of Pharmacy, Hunan Chest Hospital, Changsha, China.
  • Liu M; Center for Clinical Trial and Research, The Second Xiangya Hospital, Central South University, Changsha, China.
  • Liu W; Department of Pharmacy, The Second Xiangya Hospital, Central South University, No.139, People's Middle Street, Furong District, Changsha City, 40013, Hunan Porv., China.
  • Luo Z; Institute of Clinical Pharmacy, Central South University, Changsha, China.
BMC Cardiovasc Disord ; 23(1): 279, 2023 05 31.
Article em En | MEDLINE | ID: mdl-37254053
ABSTRACT

AIM:

The anticoagulation effect of warfarin is usually evaluated by percentage of time in therapeutic range (PTTR), which is negatively correlated with the risk of warfarin adverse reactions. This study aimed to explore the effects of genetic and nongenetic factors on anticoagulation efficacy of warfarin during different therapeutic range.

METHODS:

We conducted an observational retrospective study aiming at evaluating the impact of clinical and genetic factors on PTTR from initial to more than six months treatment. This analysis included patients with heart valve replace (HVR) surgery who underwent long-term or life-long time treatment with standard-dose warfarin for anticoagulation control in Second Xiangya Hospital. All patients were followed for at least 6 months. We genotyped single nucleotide polymorphisms in VKORC1 and CYP2C9 associated with altered warfarin dose requirements and tested their associations with PTTR.

RESULTS:

A total of 629 patients with intact clinical data and available genotype data were enrolled in this study, and only 38.63% patients achieved good anticoagulation control (PTTR > 0.6). Clinical factors, including male gender, older age, overweight, AVR surgery and stroke history, were associated with higher PTTR. Patients with VKORC1 -1639AA genotype had significantly higher PTTR level compared with GA/GG genotype carriers only in the first month of treatment. Patients with CYP2C9*3 allele had higher PTTR compared with CYP2C9*1*1 carriers. Moreover, compared with VKORC1 -1639 AG/GG carriers, INR > 4 was more likely to be present in patients with AA genotype. The frequency of CYP2C9*1*3 in patients with INR > 4 was significantly higher than these without INR > 4.

CONCLUSION:

We confirmed the relevant factors of warfarin anticoagulation control, including genetic factors (VKORC1 -1639G > A and CYP2C9*3 polymorphisms) and clinical factors (male gender, older age, overweight, AVR surgery and stroke history), which could be helpful to individualize warfarin dosage and improve warfarin anticoagulation control during different treatment period.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hidrocarboneto de Aril Hidroxilases / Acidente Vascular Cerebral Tipo de estudo: Diagnostic_studies / Observational_studies / Risk_factors_studies Limite: Humans / Male Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hidrocarboneto de Aril Hidroxilases / Acidente Vascular Cerebral Tipo de estudo: Diagnostic_studies / Observational_studies / Risk_factors_studies Limite: Humans / Male Idioma: En Ano de publicação: 2023 Tipo de documento: Article