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The Roles of Genetic Factors in Kawasaki Disease: A Systematic Review and Meta-analysis of Genetic Association Studies

机译:遗传因素在川崎病中的作用:遗传关联研究的系统综述与荟萃分析

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摘要

This systematic review and meta-analysis aimed to better elucidate the roles of genetic factors in Kawasaki disease (KD), and determine the potential genetic biomarkers of KD. The systematic literature search of PubMed, Medline, Embase, Web of Science and CNKI identified 164 eligible studies. The qualitative synthesis revealed that 62 genes may be correlated with the susceptibility to KD, and 47 genes may be associated with the incidence of coronary artery lesions (CALs) in KD. A total of 53 polymorphisms in 34 genes were investigated in further quantitative synthesis. Of these, 23 gene polymorphisms were found to be significantly correlated with KD susceptibility, and 10 gene polymorphisms were found to be significantly associated with the incidence of CALs in KD. In conclusion, our findings indicate that gene polymorphisms of ACE, BLK, CASP3, CD40, FCGR2A, FG beta, HLA-E, IL1A, IL6, ITPKC, LTA, MPO, PD1, SMAD3, CCL17 and TNF may affect KD susceptibility. Besides, genetic variations in BTNL2, CASP3, FCGR2A, FGF23, FG beta, GRIN3A, HLA-E, IL10, ITPKC and TGFBR2 may serve as biomarkers of CALs in KD.
机译:这种系统审查和荟萃分析旨在更好地阐明川崎病(KD)的遗传因素的作用,并确定KD的潜在遗传生物标志物。系统的文献搜索PubMed,Medline,Embase,Science和CNKI鉴定了164名符合条件的研究。定性合成揭示了62个基因可以与Kd的敏感性相关,47个基因可能与Kd中冠状动脉病变(Cals)的发生率相关。在进一步的定量合成中研究了34个基因中的总共53种多态性。其中,发现23种基因多态性与KD易感性显着相关,发现10个基因多态性与KD中CAL的发生率显着相关。总之,我们的研究结果表明ACE,BLK,CASP3,CD40,FCGR2A,FGβ,HLA-E,IL1A,IL6,ITPKC,LTA,MPO,PD1,SMAD3,CCL17和TNF的基因多态性可能影响KD易感性。此外,BTN12,CASP3,FCGR2A,FGF23,FGβ,GRIN3A,HLA-E,IL10,ITPKC和TGFBR2中的遗传变异可以用作KD中CAL的生物标志物。

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