Gaikwad Tejasvita, Ghosh Kanjaksha, Shetty Shrimati
National Institute of Immunohaematology (ICMR), Department of Thrombosis and Haemostasis, 13th Floor, KEM Hospital, Parel, Mumbai, India.
National Institute of Immunohaematology (ICMR), Department of Thrombosis and Haemostasis, 13th Floor, KEM Hospital, Parel, Mumbai, India.
Thromb Res. 2014 Sep;134(3):537-44. doi: 10.1016/j.thromres.2014.05.028. Epub 2014 May 27.
Warfarin is the most widely used anticoagulant all over the world for prevention and treatment of different thrombotic conditions. Polymorphisms in two genes i.e. CYP2C9 (Cytochrome P450 2C9) and VKORC1 (Vitamin K epoxide reductase complex subunit 1) play a major role in warfarin dose variation and its related adverse effects. Different ethnic groups have shown significant differences in dose requirement.
A systematic electronic search was carried out in PUBMED and ScienceDirect using different key words like, 'warfarin', 'CYP2C9', 'VKORC1', 'pharmacokinetics', 'metabolites' and 'genetic'. Till date, data from 15 Asian countries for CYP2C9 genotypes and 14 Asian countries for VKORC1 genotypes could be retrieved.
Approximately 90% of the subjects from East Asian countries were found to be carriers for VKORC1 1639 'A' or 1173 'T' allele (associated with low dose warfarin), while the prevalence of these alleles in the rest of the Asian countries (except Iran) i.e. South, South East, West and Central Asia ranged between 14 and 80%. Interestingly, an increase in carrier rate for CYP2C9 2 or 3 alleles was observed as we move from East to West Asia and an opposite trend was observed with VKORC1 1639 'A' or 1173 'T' alleles. Countries like Iran, Oman, India and Russia showed a drastic variation in the distribution pattern of these genotypes from that of the neighboring countries.
The analysis further highlights the importance of genotype based warfarin dosing in each country. Since many Asian countries are still underrepresented in pharmacogenomic research, addition of data from these underrepresented countries will be beneficial for safe warfarin dosing in these patients.
华法林是全球用于预防和治疗不同血栓形成疾病的最广泛使用的抗凝剂。细胞色素P450 2C9(CYP2C9)和维生素K环氧化物还原酶复合物亚基1(VKORC1)这两个基因的多态性在华法林剂量变化及其相关不良反应中起主要作用。不同种族群体在剂量需求上表现出显著差异。
在PUBMED和ScienceDirect中使用“华法林”“CYP2C9”“VKORC1”“药代动力学”“代谢物”和“基因”等不同关键词进行系统的电子检索。截至目前,可检索到来自15个亚洲国家的CYP2C9基因型数据和14个亚洲国家的VKORC1基因型数据。
发现东亚国家约90%的受试者是VKORC1 1639 'A'或1173 'T'等位基因(与低剂量华法林相关)的携带者,而这些等位基因在其他亚洲国家(伊朗除外)即南亚、东南亚、西亚和中亚的流行率在14%至80%之间。有趣的是,随着从东亚到西亚移动,观察到CYP2C9 2或3等位基因的携带者率增加,而VKORC1 1639 'A'或1173 'T'等位基因则呈现相反趋势。伊朗、阿曼、印度和俄罗斯等国家这些基因型的分布模式与邻国相比有巨大差异。
该分析进一步强调了各国基于基因型的华法林给药的重要性。由于许多亚洲国家在药物基因组学研究中的代表性仍然不足,增加这些代表性不足国家的数据将有利于这些患者的华法林安全给药。