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首页> 外文期刊>Systematic Reviews >Effect of CYP2C9, VKORC1, and CYP4F2 polymorphisms on warfarin maintenance dose in children aged less than 18?years: a protocol for systematic review and meta-analysis
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Effect of CYP2C9, VKORC1, and CYP4F2 polymorphisms on warfarin maintenance dose in children aged less than 18?years: a protocol for systematic review and meta-analysis

机译:CYP2C9,VKORC1和CYP4F2多态性对18岁以下儿童华法林维持剂量的影响:系统评价和荟萃分析的方案

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Background Despite its shortcomings, warfarin is still the most commonly prescribed anticoagulant to prevent thromboembolism in children. In adults, numerous studies confirmed the robust relationship between warfarin maintenance doses and single nucleotide polymorphisms of cytochrome P450 2C9 (CYP2C9), vitamin K epoxide reductase (VKORC1), and cytochrome P450 4F2 (CYP4F2). However, their effect in children still remains to be determined. The primary objective of the present systematic review and meta-analysis is to assess the effect of genotypes of CYP2C9, VKORC1, and CYP4F2 on warfarin maintenance dose in children. Methods/design A comprehensive literature review search using the OVID platform will be conducted by a specialized librarian, without language restrictions (i.e., MEDLINE/EMBASE/Cochrane Central Register of Controlled Trials), and all s will be reviewed by two authors. Data ion from each eligible study will be extracted individually by two authors (MT and TK), and disagreements will be resolved through discussion with a third person (SI). Critical appraisal of the included analysis of the primary objective will follow the Newcastle–Ottawa Scale, in addition to the Strengthening the Reporting of Genetic Association study (STREGA) statement, and data reporting will follow the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement. For the meta-analysis, the presence vs. absence of each genetic polymorphism will be pursued, respectively, using a random effect model with effect size expressed as a mean difference plus 95?% confidence interval. Discussion Our study will provide a comprehensive systematic review and meta-analysis on the potential effects of CYP2C9, VKORC1, or CYP4F2 on the warfarin maintenance dose in children, exploring the feasibility of the development of pharmacogenetic-guided warfarin dosing algorithm for children on oral vitamin K antagonists. Systematic review registration The review has been registered with PROSPERO (registration number CRD42015016172 ).
机译:背景技术尽管华法林有其缺点,但华法林仍然是预防儿童血栓栓塞的最常用处方抗凝剂。在成人中,大量研究证实了华法林维持剂量与细胞色素P450 2C9(CYP2C9),维生素K环氧还原酶(VKORC1)和细胞色素P450 4F2(CYP4F2)的单核苷酸多态性之间存在牢固的关系。但是,它们对儿童的影响尚待确定。本系统综述和荟萃分析的主要目的是评估CYP2C9,VKORC1和CYP4F2基因型对儿童华法林维持剂量的影响。方法/设计由一名专业的图书管理员在没有语言限制的情况下(即MEDLINE / EMBASE / Cochrane对照试验中央注册),使用OVID平台进行全面的文献综述搜索,所有这些都将由两位作者复审。每个合格研究的数据将由两位作者(MT和TK)分别提取,分歧将通过与第三者(SI)讨论解决。对主要目标包括的分析的关键评价将按照纽卡斯尔-渥太华量表进行,除加强遗传协会报告研究(STREGA)声明外,数据报告将遵循系统评价和荟萃分析的首选报告项目。 (PRISMA)声明。对于荟萃分析,将使用随机效应模型分别追踪每种遗传多态性的存在与否,其效应大小表示为平均差异加95%置信区间。讨论我们的研究将对CYP2C9,VKORC1或CYP4F2对儿童华法林维持剂量的潜在影响进行全面的系统回顾和荟萃分析,探讨开发药物遗传学指导的华法林口服维生素儿童剂量算法的可行性K拮抗剂。系统评价注册该评价已在PROSPERO中注册(注册号CRD42015016172)。

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