首页> 外文期刊>American journal of therapeutics >Association of Coagulation Factors VIII/XI/XIII Polymorphisms With Coagulation Factor Activities and Deep Vein Thrombosis After Artificial Joints Replacement
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Association of Coagulation Factors VIII/XI/XIII Polymorphisms With Coagulation Factor Activities and Deep Vein Thrombosis After Artificial Joints Replacement

机译:凝血因子viii / xi / xiii多态性与人工关节置换后的凝血因子活性和深静脉血栓形成

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The study aims at investigating the effects of coagulation factors VIII/XI/XIII polymorphisms in coagulation factor activities and deep vein thrombosis (DVT). A total of 130 patients with history of artificial joint replacement surgery were recruited, including 65 patients with DVT (cases) and 65 patients without DVT (controls). Cases and controls had comparable age, sex, and body mass index. Activities of VIII/XI and XIII were, respectively, detected by 1 phase anticoagulation method and microtitrimetry. Polymorphisms of VIII rs1800291 (3591C>G), XI rs2289252 (25264C>T), and XIII rs5985 (103G>T) were detected by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Activities of VIII/XI were significantly increased in cases than in controls (P < 0.001 for VIII, P = 0.024 for XI). Activity of XI was significantly increased by 11.11% in CT + TT mutant type (25264C>T) compared with wild-type CC (95% confidence interval (CI), 2.28-19.95). In univariate analysis, incidence of DVT for CT mutant was 2.41-fold compared with wild-type CC (95% CI, 1.16-5.03). T allele had 1.83-fold increased risk of DVT than C allele (95% CI, 1.06-3.14). In multivariate analysis, incidence of DVT for CT + TT mutant type was 2.39-fold compared with wild type (95% CI, 1.07-5.35). Distributions of VIII gene 3951C>G and genotypes were not significant between groups (both P > 0.05). The mutation rate of VIII gene 103G>T was low in study population (0.77%) and was not significant between groups. XI 25264C>T genotype is significantly associated with XI activity. T mutation of this locus significantly increases XI activity and is a risk factor for DVT.
机译:该研究旨在研究凝血因子VIII / XI / XIII多态性在凝血因子活性和深静脉血栓形成(DVT)的影响。招募了130例人工置置手术历史历史,包括65例DVT(病例)和65名没有DVT(对照)的患者。病例和对照具有可比年龄,性别和体重指数。通过1相抗凝法和微量滴定法检测VIII / XI和XIII的活性。通过聚合酶链反应限制片段长度多态性(PCR-RFLP)检测VIII RS1800291(3591C> G),XI RS2289252(25264C> T)和XIII RS5985(103g> T)的多态性。在病例中,VIII / XI的活动显着增加,而不是对照(P <0.001用于viII,Xi的P = 0.024)。与野生型CC(95%置信区间(CI),2.28-19.95)相比,CT + TT突变体型(25264C> T)中,XI的活性显着增加11.11%。在单变量分析中,与野生型CC(95%CI,1.16-5.03)相比,CT突变体的DVT的发生率为2.41倍。等位基因对DVT的风险增加1.83倍,而不是C等位基因(95%CI,1.06-3.14)。在多变量分析中,与野生型(95%CI,1.07-5.35)相比,CT + TT突变体型DVT的发病率为2.39倍。 VIII基因3951C> G和基因型之间的分布在基团之间不显着(P> 0.05)。 VIII基因103g> T的突变率在研究人群中较低(0.77%)并且在基团之间并不显着。 XI 25264C> T基因型与XI活动显着相关。该基因座的T突变显着提高了XI活动,是DVT的危险因素。

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