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PNPLA3和RNF7基因变异与东欧人群发生肝纤维化和肝硬化的风险相关。

PNPLA3 and RNF7 Gene Variants are Associated with the Risk of Developing Liver Fibrosis and Cirrhosis in an Eastern European Population.

作者信息

Kupcinskas Juozas, Valantiene Irena, Varkalaitė Greta, Steponaitiene Ruta, Skieceviciene Jurgita, Sumskiene Jolanta, Petrenkiene Vitalija, Kondrackiene Jurate, Kiudelis Gediminas, Lammert Frank, Kupcinskas Limas

机构信息

Institute for Digestive Research, Lithuanian University of Health Sciences, Kaunas; Department of Gastroenterology, Lithuanian University of Health Sciences, Kaunas, Lithuania.

Institute for Digestive Research, Lithuanian University of Health Sciences, Kaunas, Lithuania.

出版信息

J Gastrointestin Liver Dis. 2017 Mar;26(1):37-43. doi: 10.15403/jgld.2014.1121.261.pnp.

Abstract

BACKGROUND AND AIMS

Genome-wide association studies have revealed an association between the risk of developing liver fibrosis or cirrhosis and the single nucleotide polymorphisms (SNPs) of the PNPLA3, RNF7, MERTK and PCSK7 genes. We aimed to validate these results in an Eastern European population.

METHODS

We evaluated the associations between the PNPLA3 (rs738409), RNF7 (rs16851720), MERTK (rs4374383) and PCSK7 (rs236918) variants and liver fibrosis and cirrhosis in a series of consecutive patients recruited at the Department of Gastroenterology, Lithuanian University of Health Sciences Hospital, during the period 2012-2015. The study included 317 individuals with liver cirrhosis, 154 individuals with liver fibrosis, and 498 controls. The studied SNPs were determined using RT-PCR TaqMan assays.

RESULTS

MERTK and PCSK7 SNPs were not associated with liver fibrosis or cirrhosis. The PNPLA3 SNP rs738409 was associated with a higher risk of developing liver fibrosis (aOR: 1.65, P=0.001) and cirrhosis (aOR: 1.92, P=5.5710-7). PNPLA3 genotypes were also associated with higher risk of developing liver fibrosis and cirrhosis in dominant (aOR: 1.98, P=2.2010-5; aOR: 1.67, P=0.008, respectively) and recessive (aOR: 3.94, P=5.16*10-5; aOR: 3.02, P=0.003, respectively) models. RNF7 rs16851720 was associated with liver cirrhosis comparing CC vs. AA + CA genotypes (aOR: 0.26, P=0.020).

CONCLUSION

Our study showed that PNPLA3 rs738409 and RNF7 rs16851720 confer an increased risk of developing liver fibrosis and cirrhosis in this Eastern European population, while the MERTK and PCSK7 SNPs are not associated with these conditions.

摘要

背景与目的

全基因组关联研究揭示了肝脏纤维化或肝硬化发生风险与PNPLA3、RNF7、MERTK和PCSK7基因的单核苷酸多态性(SNP)之间存在关联。我们旨在在东欧人群中验证这些结果。

方法

我们评估了2012年至2015年期间在立陶宛健康科学大学医院胃肠病科招募的一系列连续患者中,PNPLA3(rs738409)、RNF7(rs16851720)、MERTK(rs4374383)和PCSK7(rs236918)变异与肝纤维化和肝硬化之间的关联。该研究纳入了317例肝硬化患者、154例肝纤维化患者和498例对照。使用RT-PCR TaqMan分析法确定所研究的SNP。

结果

MERTK和PCSK7的SNP与肝纤维化或肝硬化无关。PNPLA3 SNP rs738409与发生肝纤维化(调整后比值比:1.65,P = 0.001)和肝硬化(调整后比值比:1.92,P = 5.57×10⁻⁷)的较高风险相关。PNPLA3基因型在显性(调整后比值比:1.98,P = 2.20×10⁻⁵;调整后比值比:1.67,P = 0.008)和隐性(调整后比值比:3.94,P = 5.16×10⁻⁵;调整后比值比:3.02,P = 0.003)模型中也与发生肝纤维化和肝硬化的较高风险相关。与CC基因型相比,RNF7 rs16851720的AA + CA基因型与肝硬化相关(调整后比值比:0.26,P = 0.020)。

结论

我们的研究表明,在这个东欧人群中,PNPLA3 rs738409和RNF7 rs16851720会增加发生肝纤维化和肝硬化的风险,而MERTK和PCSK7的SNP与这些情况无关。

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