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γ-谷氨酰羧化酶基因多态性对华法林剂量需求的影响:一项系统评价和荟萃分析。

Impact of gamma-glutamyl carboxylase gene polymorphisms on warfarin dose requirement: a systematic review and meta-analysis.

作者信息

Sun Yifan, Wu Zhitong, Li Shan, Qin Xue, Li Taijie, Xie Li, Deng Yan, Chen Junqing

机构信息

Department of Clinical Laboratory, Liuzhou Hospital of Traditional Chinese Medicine, 32 Jiefang North Road, Liuzhou 545001, Guangxi, People's Republic of China.

Department of Clinical Laboratory, Guigang City People's Hospital, 1 Zhongshan Middle Road, Guigang 537100, Guangxi, People's Republic of China.

出版信息

Thromb Res. 2015 Apr;135(4):739-47. doi: 10.1016/j.thromres.2015.01.029. Epub 2015 Feb 7.

Abstract

BACKGROUND

The Gamma-glutamyl carboxylase (GGCX) gene, as with Vitamin K Epoxide Reductase Complex Subunit 1 (VKORC1), CytochromeP450 Complex Subunit 14 F2 (CYP4F2) and CytochromeP450 Complex Subunit2C9 (CYP2C9), is a candidate predictor for appropriate maintenance warfarin dose. However, the association between GGCX gene polymorphisms and warfarin dose requirement is still controversial. To quantify the influence of GGCX polymorphisms on warfarin dose requirements, we performed a systematic review and meta-analysis.

METHODS

According to PRISRM statement (Preferred reporting items for systematic reviews and meta-analyses), a comprehensive literature search was undertaken through August 2014 looking for eligible studies in Embase, Pubmed,Web of Science and the Cochrane Library. The impact of GGCX polymorphisms on mean daily warfarin dose (MDWD) was counted by means of Z test. RevMan 5.2.7 software (developed by the Cochrane Collaboration) was applied to analyze the relationship between GGCX gene polymorphisms and warfarin dose requirements.

RESULTS

Nineteen articles including 21 studies with a total of 6957 patients were included in the meta-analysis. Among three investigated single nucleotide polymorphisms (SNPs), rs11676382 showed higher CC genotype frequencies in Asian than those in Caucasian (97.7% vs. 86.9%); patients who were "G carriers" (that is, carried the GGCX rs11676382 CG or GG genotypes) required 27% lower warfarin dose than CC genotype [95%Confidence Interval (CI)=17%-37%, P=0.000, I(2)%=82.0 and PQ=0.000], moreover, stratified analysis by ethnicity showed similar results in Caucasian (23% lower, 95%CI=12%-33%), but not in Asian. With respect to genetic variation of rs699664 and rs121714145 SNPs, no significant impact on warfarin dose requirements were demonstrated.

CONCLUSIONS

This meta-analysis suggested that GGCX rs11676382 polymorphism may be one of factors affecting the dose of warfarin requirement, and the effects are different in different ethnicities. Further studies about this topic in different ethnicities with larger samples are expected to be conducted to validate our results.

摘要

背景

γ-谷氨酰羧化酶(GGCX)基因与维生素K环氧化物还原酶复合物亚基1(VKORC1)、细胞色素P450复合物亚基14 F2(CYP4F2)和细胞色素P450复合物亚基2C9(CYP2C9)一样,是合适的华法林维持剂量的候选预测指标。然而,GGCX基因多态性与华法林剂量需求之间的关联仍存在争议。为了量化GGCX多态性对华法林剂量需求的影响,我们进行了一项系统评价和荟萃分析。

方法

根据PRISRM声明(系统评价和荟萃分析的首选报告项目),截至2014年8月进行了全面的文献检索,在Embase、PubMed、科学网和考克兰图书馆中查找符合条件的研究。通过Z检验计算GGCX多态性对平均每日华法林剂量(MDWD)的影响。应用RevMan 5.2.7软件(由考克兰协作组织开发)分析GGCX基因多态性与华法林剂量需求之间的关系。

结果

荟萃分析纳入了19篇文章,包括21项研究,共6957例患者。在研究的三个单核苷酸多态性(SNP)中,rs11676382在亚洲人中的CC基因型频率高于白种人(97.7%对86.9%);“G携带者”(即携带GGCX rs11676382 CG或GG基因型)的患者所需华法林剂量比CC基因型低27%[95%置信区间(CI)=17%-37%,P=0.000,I²%=82.0,PQ=0.000],此外,按种族进行的分层分析在白种人中显示出相似的结果(低23%,95%CI=12%-33%),但在亚洲人中并非如此。关于rs699664和rs121714145 SNP的基因变异,未显示对华法林剂量需求有显著影响。

结论

这项荟萃分析表明,GGCX rs11676382多态性可能是影响华法林剂量需求的因素之一,且在不同种族中的影响不同。预计将在不同种族中进行更大样本量的关于该主题的进一步研究以验证我们的结果。

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