中华医学遗传学杂志
中華醫學遺傳學雜誌
중화의학유전학잡지
Chinese Journal of Medical Genetics
2015年
5期
629-634
,共6页
侯江龙%董鑫%王玉庆%王刚%董力%李岭
侯江龍%董鑫%王玉慶%王剛%董力%李嶺
후강룡%동흠%왕옥경%왕강%동력%리령
华法林%抗凝%基因多态性%个性化用药
華法林%抗凝%基因多態性%箇性化用藥
화법림%항응%기인다태성%개성화용약
Warfarin%Anti-coagulation%Gene polymorphism%Personalized medicine
目的 评价非遗传因素和基因多态性对中国人群患者华法林用药稳定剂量的影响,为华法林个体化用药提供临床指导.方法 选取正在服用华法林进行抗凝、连续2次国际标准化比值(international normalized ratio,INR)达标的门诊及住院患者200人,记录其基本信息和临床用药情况,用Sanger直接测序法进行4种基因共8种多态性的检测,用统计学分析评价遗传与非遗传因素对华法林用药剂量的影响并建立数学模型.结果 在非遗传因素中,年龄和身高对华法林用药剂量有显著的影响,用药剂量随年龄增长有降低的趋势,而随身高的增长有升高的趋势.20岁年龄组与60岁年龄组华法林用药剂量差异达到1.81 mg/天,身高140 cm组与180 cm组的用药剂量差异达1.06 mg/天.在遗传因素中,VKORC1-1639G/A位点、CYP2C9 430C/T位点、CYP2C9 1075A/C位点、CYP4F2 V433M位点对华法林用药剂量有显著影响,野生型和突变型患者华法林用药剂量的差异从0.35 mg/天到0.84 mg/天不等.结论 遗传和非遗传因素均为影响华法林个体化用药的重要因素,临床上应尽可能全面地考虑这些因素.建立合理的华法林稳定剂量的预测算法对华法林用药的安全性和有效性具有重要的意义.
目的 評價非遺傳因素和基因多態性對中國人群患者華法林用藥穩定劑量的影響,為華法林箇體化用藥提供臨床指導.方法 選取正在服用華法林進行抗凝、連續2次國際標準化比值(international normalized ratio,INR)達標的門診及住院患者200人,記錄其基本信息和臨床用藥情況,用Sanger直接測序法進行4種基因共8種多態性的檢測,用統計學分析評價遺傳與非遺傳因素對華法林用藥劑量的影響併建立數學模型.結果 在非遺傳因素中,年齡和身高對華法林用藥劑量有顯著的影響,用藥劑量隨年齡增長有降低的趨勢,而隨身高的增長有升高的趨勢.20歲年齡組與60歲年齡組華法林用藥劑量差異達到1.81 mg/天,身高140 cm組與180 cm組的用藥劑量差異達1.06 mg/天.在遺傳因素中,VKORC1-1639G/A位點、CYP2C9 430C/T位點、CYP2C9 1075A/C位點、CYP4F2 V433M位點對華法林用藥劑量有顯著影響,野生型和突變型患者華法林用藥劑量的差異從0.35 mg/天到0.84 mg/天不等.結論 遺傳和非遺傳因素均為影響華法林箇體化用藥的重要因素,臨床上應儘可能全麵地攷慮這些因素.建立閤理的華法林穩定劑量的預測算法對華法林用藥的安全性和有效性具有重要的意義.
목적 평개비유전인소화기인다태성대중국인군환자화법림용약은정제량적영향,위화법림개체화용약제공림상지도.방법 선취정재복용화법림진행항응、련속2차국제표준화비치(international normalized ratio,INR)체표적문진급주원환자200인,기록기기본신식화림상용약정황,용Sanger직접측서법진행4충기인공8충다태성적검측,용통계학분석평개유전여비유전인소대화법림용약제량적영향병건립수학모형.결과 재비유전인소중,년령화신고대화법림용약제량유현저적영향,용약제량수년령증장유강저적추세,이수신고적증장유승고적추세.20세년령조여60세년령조화법림용약제량차이체도1.81 mg/천,신고140 cm조여180 cm조적용약제량차이체1.06 mg/천.재유전인소중,VKORC1-1639G/A위점、CYP2C9 430C/T위점、CYP2C9 1075A/C위점、CYP4F2 V433M위점대화법림용약제량유현저영향,야생형화돌변형환자화법림용약제량적차이종0.35 mg/천도0.84 mg/천불등.결론 유전화비유전인소균위영향화법림개체화용약적중요인소,림상상응진가능전면지고필저사인소.건립합리적화법림은정제량적예측산법대화법림용약적안전성화유효성구유중요적의의.
Objective To assess the influence of genetic polymorphisms and non-genetic factors on warfarin maintenance dose variations in order to provide guidance for personalized use of warfarin.Methods Two hundred patients from outpatient and inpatient with stable international normalized ratio(INR) were recruited.Clinical data and blood samples were collected.Genotypes of 4 genes involved in warfarin metabolic pathways were determined with Sanger sequencing.Based on statistical analysis of warfarin maintenance dosage, a mathematical model was established.Results Among non-genetic factors, the age and height have significant influence in warfarin dosage.The dosage is negatively correlated with age but positively correlated with height.The difference in dosage for between the 20-year-old group and 60-year-old group has reached 1.81 mg/day, and that for between the 140 cm in height and 180 cm in height groups has reached 1.06 mg/day.VKORC1-1639G/A, CYP2C9 430C/T, CYP2C9 1075A/C and CYP4F2 V433M polymorphisms have significant influence on stable warfarin dosage.The dosage for patients with wild type and mutant genotypes has varied from 0.35 mg/day to 0.84 mg/day.Conclusion Non-genetic factors and genetic polymorphisms play important roles in personalized variations of warfarin maintenance dose.The establishment of mathematical models considering multiple factors is helpful in evaluating the safety and effectiveness of warfarin dosage.