Cytochrome P450 (CYP2C9*2,*3) & vitamin-K epoxide reductase complex (VKORC1-1639G<A) gene polymorphisms & their effect on acenocoumarol dose in patients with mechanical heart valve replacement

被引:0
|
作者
Kaur, Anupriya [1 ]
Khan, Farah [1 ]
Agrawal, Suraksha S. [1 ]
Kapoor, Aditya [2 ]
Agarwal, Surendra K. [3 ]
Phadke, Shubha R. [1 ]
机构
[1] Sanjay Gandhi Postgrad Inst Med Sci, Dept Med Genet, Lucknow 226014, Uttar Pradesh, India
[2] Sanjay Gandhi Postgrad Inst Med Sci, Dept Cardiol, Lucknow 226014, Uttar Pradesh, India
[3] Sanjay Gandhi Postgrad Inst Med Sci, Dept Cardiovasc & Thorac Surg, Lucknow 226014, Uttar Pradesh, India
关键词
Acenocoumarol; CYP2C9; dose requirements; INR; oral anticoagulants; VKORC1; ALLELIC VARIANTS; WARFARIN; CYP2C9; PHARMACOGENETICS; REQUIREMENTS; FREQUENCIES; VKORC1;
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background & objectives: Studies have demonstrated the effect of CYP2C9 (cytochrome P450) and VKORC1 (vitamin K epoxide reductase complex) gene polymorphisms on the dose of acenocoumarol. The data from India about these gene polymorphisms and their effects on acenocoumarol dose are scarce. The aim of this study was to determine the occurrence of CYP2C9*2,*3 and VKORC 1 -1639G>A gene polymorphisms and to study their effects on the dose of acenocoumarol required to maintain a target International Normalized Ratio (INR) in patients with mechanical heart valve replacement. Methods: Patients from the anticoagulation clinic of a tertiary care hospital in north India were studied. The anticoagulation profile, INR (International Normalized Ratio) values and administered acenocoumarol dose were obtained from the clinical records of patients. Determination of the CYP2C9*2,*3 and VKORC1 -1639G>A genotypes was done by PCR-RFLP (restriction fragment length polymorphism). Results: A total of 111 patients were studied. The genotype frequencies of CYP2C9 *1/*1,*1/*2,*1/*3 were as 0.883, 0.072, 0.036 and that of VKORC1 -1639G>A for GG, AG, and AA genotypes were 0.883, 0.090, and 0.027, respectively. The percentage of patients carrying any of the variant alleles of CYP2C9 and VKORC1 in heterozygous or homozygous form was 34% among those receiving a low dose of <= 20 mg/wk while it was 13.8 per cent in those receiving >20 mg/wk (P=0.014). A tendency of lower dose requirements was seen among carriers of the studied polymorphisms. There was considerable variability in the dose requirements of patients with and without variant alleles. Interpretation & conclusions: The study findings point towards the role of CYP2C9 and VKORC1 gene polymorphisms in determining the inter-individual dose variability of acenocoumarol in the Indian patients with mechanical heart valve replacement.
引用
收藏
页码:203 / 209
页数:7
相关论文
共 47 条
  • [1] Effect of different genetics variants: CYP2C9*2, CYP2C9*3 of cytochrome P-450 CYP2C9 and 1639G&gt;A of the VKORC1 gene; On acenocoumarol requirement in Moroccan patients
    Smires, F. Z.
    Habbal, R.
    Moreau, C.
    Assaidi, A.
    Loriot, M. A.
    Nadifi, S.
    PATHOLOGIE BIOLOGIE, 2013, 61 (03): : 88 - 92
  • [2] Cytochrome P4502C9 (CYP2C9) and vitamin K epoxide reductase (VKORC1) genotypes as determinants of acenocoumarol sensitivity
    Bodin, L
    Verstuyft, C
    Tregouet, DA
    Robert, A
    Dubert, L
    Funck-Brentano, C
    Jaillon, P
    Beaune, P
    Laurent-Puig, P
    Becquemont, L
    Loriot, MA
    BLOOD, 2005, 106 (01) : 135 - 140
  • [3] Effects of cytochrome P450 2C9 (CYP2C9) and vitamin K epoxide reductase (VKORC1) genotypes on fluindione anticoagulation status
    Lacut, K.
    Verstuyft, C.
    Gourhant, L.
    Poulhazan, E.
    Becquemont, L.
    Mottier, D.
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2009, 7 : 689 - 689
  • [4] Warfarin dose requirement and cytochrome P450 2C9 and Vitamin K epoxide reductase complex subunit 1-1639 genetic polymorphisms in Thai patients
    Subsuphan, Burassakorn
    Chinpaisal, Chatchai
    Pongchaidecha, Manat
    Phanthabordeekorn, Wibun
    Watana, Surawut
    ARCHIVES OF PHARMACY PRACTICE, 2016, 7 (01) : 18 - 25
  • [5] Effect of different genetic variants (2C9*2, 2C9*3 of cytochrome P-450 CYP2C9 and-1639G&gt;A of the VKORC1 gene) on acenocoumarol requirement in Moroccan patients
    Smires, F. -Z.
    Assaidi, A.
    Loriot, M. A.
    Moreau, C.
    Habbal, R.
    Nadifi, S.
    EUROPEAN JOURNAL OF CARDIOVASCULAR NURSING, 2011, 10 : S38 - S38
  • [6] Genotypes of the cytochrome p450 isoform, CYP2C9, and the vitamin K epoxide reductase complex subunit 1 conjointly determine stable warfarin dose: a prospective study
    John F. Carlquist
    Benjamin D. Horne
    Joseph B. Muhlestein
    Donald L. Lappé
    Bryant M. Whiting
    Matthew J. Kolek
    Jessica L. Clarke
    Brent C. James
    Jeffrey L. Anderson
    Journal of Thrombosis and Thrombolysis, 2006, 22 : 191 - 197
  • [7] Genotypes of the cytochrome p450 isoform, CYP2C9, and the vitamin K epoxide reductase complex subunit 1 conjointly determine stable warfarin dose:: a prospective study
    Carlquist, John F.
    Horne, Benjamin D.
    Muhlestein, Joseph B.
    Lappe, Donald L.
    Whiting, Bryant M.
    Kolek, Matthew J.
    Clarke, Jessica L.
    James, Brent C.
    Anderson, Jeffrey L.
    JOURNAL OF THROMBOSIS AND THROMBOLYSIS, 2006, 22 (03) : 191 - 197
  • [8] Influence of CYP2C9 and vitamin k oxide reductase complex (VKORC)1 polymorphisms on time to determine the warfarin maintenance dose
    Aomori, T.
    Obayashi, K.
    Fujita, Y.
    Araki, T.
    Nakamura, K.
    Nakamura, T.
    Kurabayashi, M.
    Yamamoto, K.
    PHARMAZIE, 2011, 66 (03): : 222 - 225
  • [9] Influence of VKORC1 and CYP2C9 Polymorphisms on Daily Acenocoumarol Dose Requirement in South Indian Patients With Mechanical Heart Valves
    Kalpana, S. R.
    Bharath, G.
    Manjunath, C. N.
    Christopher, Rita
    CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS, 2017, 23 (07) : 876 - 882
  • [10] Effects of cytochrome P4502C9 (CYP2C9) and vitamin K epoxide reductase (VKORC1) genotypes on fluindione anticoagulation status
    Lacut, K.
    Gourhant, L.
    Letierce, A.
    Mottier, D.
    Becquemont, L.
    Verstuyft, C.
    FUNDAMENTAL & CLINICAL PHARMACOLOGY, 2008, 22 : 56 - 56