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首页> 外文期刊>Current pharmaceutical design >Impact of the 719Arg Variant of KIF6 and Major Cardiovascular Events on Patients who Received Statins: A Systematic Review and Meta-Analysis
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Impact of the 719Arg Variant of KIF6 and Major Cardiovascular Events on Patients who Received Statins: A Systematic Review and Meta-Analysis

机译:KIF6 719ARG变体对接受他汀类药物的患者的影响:系统审查和荟萃分析

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Purpose: The purpose of this study was to determine the relationship between Kinesin like protein 6(KIF6) gene Trp719Arg and major cardiovascular events (MACEs) risk in subjects who received statin therapy.Methods: PubMed, EmBase, and the Cochrane Library were searched from inception through September 2017.The selected studies evaluated the association of Trp719Arg with MACEs in individuals who received statins.Relative risk (RR) and 95% confidence interval (CI) were used to evaluate the effect of statin therapy on MACEsin subjects carrying polymorphisms, and the odds ratio (OR) and 95% CI were used to evaluate the relationshipbetween Trp719Arg and MACE risk in individuals who received statins, using the random-effects model.Results: Seven studies were included (N=48,885). Overall, we found that statin therapy significantly reduced therisk for MACEs in subjects carrying ArgArg (RR: 0.79; 95% CI: 0.69-0.90; P=0.001), ArgTrp (RR: 0.71; 95%CI: 0.60 -0.83; P<0.001), ArgArg+ArgTrp (RR: 0.71; 95% CI: 0.63 -0.81; P<0.001), and TrpTrp (RR: 0.79; 95%CI: 0.73-0.85; P<0.001). Furthermore, there was no significant difference between subjects carrying ArgArg andthose carrying TrpTrp (OR: 1.11; 95% CI: 0.92-1.34; P=0.265). However, ArgTrp (OR: 1.29; 95% CI: 1.07-1.55;P=0.007) and ArgArg+ArgTrp (OR: 1.26; 95% CI: 1.05-1.51; P=0.012) were associated with an increased riskfor MACEs when compared with TrpTrp.Conclusions: Statin therapy significantly reduced the risk for MACEs in subjects carrier specific KIF6 geneTrp719Arg polymorphisms. Further, subjects carrying ArgTrp or ArgArg+ArgTrp had a greater incidence ofMACEs as compared with TrpTrp when they received statins.
机译:目的:本研究的目的是确定接受他汀类药物治疗的受试者的蛋白质6(KIF6)基因TRP719ARG和主要心血管事件(拟合)风险的蛋白质6(KIF6)基因患者的关系。方法:被搜查了PUBMED,EMBASE和Cochrane图书馆从2017年9月开始的。所选研究评估了TRP719ARG在接受他汀类药物的个体中与次数的关联。使用风险(RR)和95%置信区间(CI)来评估他汀类药物治疗对携带多态性的甘露素对象的影响。使用随机效应模型,使用差距(或)和95%CI来评估TRP719ARG和接受他汀类药物的个体的坐标风险的关系。结果:包括七项研究(n = 48,885)。总体而言,我们发现,他汀类药物治疗在携带argarg的受试者中显着减少了患者的次数(RR:0.79; 95%CI:0.69-0.90; p = 0.001),Arctrp(Rr:0.71; 95%Ci:0.60 -0.83; P < 0.001),Argarg + Argtrp(RR:0.71; 95%CI:0.63 -0.81; P <0.001)和TRPTRP(RR:0.79; 95%CI:0.73-0.85; P <0.001)。此外,携带携带TRPTRP的Argarg患有argarg患者的受试者没有显着差异(或:1.11; 95%CI:0.92-1.34; P = 0.265)。然而,Arctrp(或:1.29; 95%Ci:1.07-1.55; p = 0.007)和argarg + Argtrp(或:1.26; 95%Ci:1.05-1.51; p = 0.012)与比较时的迈出的巨大风险增加有关使用TRPTRP.CONCLUSIONS:他汀类药物治疗显着降低了受试者载体特异性KIF6 GENETRP719ARG多态性的迈占的风险。此外,携带argtrp或argarg + argtrp的受试者与他们接受他汀类药物时,与Trptrp相比具有更大的距离。

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