Association of PNPLA3 rs738409 G/C gene polymorphism with nonalcoholic fatty liver disease in children: a meta-analysis.

4区 医学 Q4 Medicine BMC Medical Genetics Pub Date : 2020-08-18 DOI:10.1186/s12881-020-01098-8
Shan Tang, Jing Zhang, Ting Ting Mei, Hai Qing Guo, Xin Huan Wei, Wen Yan Zhang, Ya Li Liu, Shan Liang, Zuo Peng Fan, Li Xia Ma, Wei Lin, Yi Rong Liu, Li Xia Qiu, Hai Bin Yu
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引用次数: 11

Abstract

Background: Nonalcoholic fatty liver disease (NAFLD) is one of the most common causes of chronic liver disease worldwide. Current studies have shown that PNPLA3 (Patatin-like phospholipase domain containing 3) rs738409 G/C gene polymorphism is associated with adult nonalcoholic fatty liver disease [1, 2].But there is no consensus on the relationship between PNPLA3 rs738409 G/C gene polymorphism and children NAFLD due to differences in population samples. To this end, a meta-analysis of published research is conducted to comprehensively assess the relationship between PNPLA3 gene polymorphism and NAFLD in children.

Methods: We searched MEDLINE, PubMed, EMBASE, and CENTRAL databases from inception to May 2019. Case-control studies assessing the relationship between PNPLA3 rs738409 G/C gene polymorphism with non-alcoholic fatty liver disease in children were selected according to inclusion and exclusion criteria. Random effects model was used to quantify the association between the PNPLA3 rs738409 G/C gene polymorphism and the susceptibility of children's NAFLD. Fixed effects model was used to quantify the relationship between the PNPLA3 rs738409 G/C gene polymorphism and the severity of NAFLD in children. The Stata 12.0 software was employed for data analysis.

Results: A total of nine case-control studies were included in this meta-analysis containing data of 1173 children with NAFLD and 1792 healthy controls. Five studies compared NAFLD children and non-NAFLD healthy populations. Statistical analysis showed that PNPLA3 gene polymorphism was significantly associated with children's NAFLD in the allele contrast, dominant, recessive and over dominant models (G vs C,OR = 3.343, 95% CI = 1.524-7.334; GG + GC vs CC,OR = 3.157, 95% CI = 1.446-6.892;GG vs GC + CC,OR = 5.692, 95% CI = 1.941-16.689; GG + CC vs GC,OR = 2.756, 95% CI = 1.729-4.392). Four case-control studies compared Children with nonalcoholic fatty liver (NAFL) and children with nonalcoholic steatohepatitis (NASH). The results showed that the PNPLA3 gene polymorphism was also significantly associated with the severity of NAFLD in children in recessive gene model (GG vs GC + CC,OR = 14.43, 95% CI = 5.985-34.997); The Egger's test revealed no significant publication bias.

Conclusions: Meta-analysis showed that PNPLA3 gene polymorphism was significantly associated with susceptibility and severity of NAFLD in children.

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PNPLA3 rs738409 G/C基因多态性与儿童非酒精性脂肪肝的关联:一项荟萃分析
背景:非酒精性脂肪性肝病(NAFLD)是世界范围内最常见的慢性肝病之一。目前研究表明PNPLA3 (Patatin-like phospholipase domain containing 3) rs738409 G/C基因多态性与成人非酒精性脂肪肝相关[1,2]。但由于群体样本的差异,PNPLA3 rs738409 G/C基因多态性与儿童NAFLD的关系尚未达成共识。为此,我们对已发表的研究进行荟萃分析,全面评估PNPLA3基因多态性与儿童NAFLD之间的关系。方法:检索MEDLINE、PubMed、EMBASE和CENTRAL数据库,检索时间从成立到2019年5月。根据纳入和排除标准选择评估PNPLA3 rs738409 G/C基因多态性与儿童非酒精性脂肪性肝病关系的病例对照研究。采用随机效应模型量化PNPLA3 rs738409 G/C基因多态性与儿童NAFLD易感性的关系。采用固定效应模型量化PNPLA3 rs738409 G/C基因多态性与儿童NAFLD严重程度的关系。采用Stata 12.0软件进行数据分析。结果:本荟萃分析共纳入9项病例对照研究,包含1173名NAFLD儿童和1792名健康对照者的数据。五项研究比较了NAFLD儿童和非NAFLD健康人群。统计分析显示,PNPLA3基因多态性在等位基因对比、显性、隐性和超显性模型中与儿童NAFLD显著相关(G vs C,OR = 3.343, 95% CI = 1.524 ~ 7.334;GG + GC vs CC或= 3.157,95% CI = 1.446 - -6.892, GG vs GC + CC = 5.692, 95% CI = 1.941 - -16.689;GG + CC vs GC,OR = 2.756, 95% CI = 1.729-4.392)。四项病例对照研究比较了非酒精性脂肪肝(NAFL)儿童和非酒精性脂肪性肝炎(NASH)儿童。在隐性基因模型中,PNPLA3基因多态性也与儿童NAFLD的严重程度显著相关(GG vs GC + CC,OR = 14.43, 95% CI = 5.985 ~ 34.997);艾格检验未发现显著的发表偏倚。结论:荟萃分析显示,PNPLA3基因多态性与儿童NAFLD的易感性和严重程度显著相关。
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BMC Medical Genetics
BMC Medical Genetics 医学-遗传学
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12 months
期刊介绍: BMC Medical Genetics is an open access journal publishing original peer-reviewed research articles in the effects of genetic variation in individuals, families and among populations in relation to human health and disease. Note: BMC Medical Genetics is now closed. This journal has merged with BMC Medical Genomics, a broad-scope, open access community journal for all medical genetics and genomics research.
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