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首页> 外文期刊>Medicine. >Association between PNPLA3 rs738409 polymorphism and nonalcoholic fatty liver disease (NAFLD) susceptibility and severity: A meta-analysis
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Association between PNPLA3 rs738409 polymorphism and nonalcoholic fatty liver disease (NAFLD) susceptibility and severity: A meta-analysis

机译:pnpla3 rs738409之间的关联多态性和非酒精性脂肪肝病(Nafld)敏感性和严重程度:Meta分析

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Objective: This meta-analysis is to investigate the relationship between the patatin-like phospholipase domain containing 3 (PNPLA3) rs738409 polymorphism and the susceptibility and severity of nonalcoholic fatty liver disease (NAFLD). Methods: Chinese Journal Full-text Database, Wanfang Database, VIP Database, and PubMed Database were subjected to case-control study retrieving, from January 2008 to December 2014. Following key words were used: fatty liver, PNPLA3, and rs738409 gene or variants or polymorphism or alleles. Meta-analysis was performed based on the retrieved articles. Results: In total 65 studies were first retrieved according to the key words, and finally 21 studies with 14,266 subjects were included. Meta-analysis showed that PNPLA3 rs738409 polymorphism exerted strong influence not only on fatty liver but also on the histological injury. PNPLA3 rs738409 [G] allele was a risk factor for NAFLD (GG vs CC, OR = 4.01, 95% CI 2.93–5.49; GC vs CC, OR = 1.88, 95% CI 1.58–2.24). PNPLA3 gene variant was significantly associated with the increased serum alanine aminotransferase (ALT) levels (GG vs CC, standardized mean difference = 0.47, 95% CI 0.14–0.81). In addition, nonalcoholic steatohepatitis (NASH) was more frequently observed in G allele carriers (GG vs CC, OR = 3.24, 95% CI 2.79–3.76; GC vs CC, OR = 2.14, 95% CI 1.43–3.19). Conclusion: PNPLA3 rs738409 polymorphism is not only a factor significantly associated with the susceptibility of NAFLD, but also related to the susceptibility of aggressive diseases.
机译:目的:这种荟萃分析是研究含有3(PNPLA3)RS738409多态性和非酒精性脂肪肝病(NAFLD)的含有3(PNPLA3)RS738409多态性和易感性和严重程度之间的关系。方法:从2008年1月到2014年12月,中文期刊全文数据库,万芳数据库,VIP数据库和PubMed数据库进行案例控制研究检索。使用关键词:脂肪肝,PNPLA3和RS738409基因或变体或多态性或等位基因。基于检索到的文章进行META分析。结果:总共65项根据关键词检出的研究,最后包括14,266个受试者的21项研究。荟萃分析表明,PNPLA3 RS738409多态性不仅对脂肪肝施加强烈的影响,而且对组织学损伤进行了强烈的影响。 PNPLA3 RS738409 [G]等位基因是NAFLD的危险因素(GG VS CC,OR = 4.01,95%CI 2.93-5.49; GC VS CC,OR = 1.88,95%CI 1.58-2.24)。 PNPLA3基因变体与增加的血清丙氨酸氨基转移酶(ALT)水平显着相关(GG VS CC,标准化平均差= 0.47,95%CI 0.10.81)。此外,在G等位基因载体(GG VS CC,OR = 3.24,95%CI 2.79-3.76; GC VS CC,OR = 2.14,95%CI 1.43-3.19)中,更常见的非酒精性脱脂性炎(NASH)更常见。结论:PNPLA3 RS738409多态性不仅是与NAFLD易感性显着相关的因素,也与侵袭性疾病的易感性有关。

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