间质金属蛋白酶基因多态性与中心性肥胖在非酒精性脂肪肝病中交互作用研究

吴鹏波; 舒泳翔; 李明; 罗和生; 张国; 谭诗云

Abstract

吴鹏波,舒泳翔,李明,罗和生,张国,谭诗云.间质金属蛋白酶基因多态性与中心性肥胖在非酒精性脂肪肝病中交互作用研究[J].Chinese journal of Epidemiology,2015,36(12):1415-1418

间质金属蛋白酶基因多态性与中心性肥胖在非酒精性脂肪肝病中交互作用研究

Study on the interaction between matrix metalloproteinases gene polymorphism and central obesity in nonalcoholic fatty liver disease

Received:April 30, 2015

DOI：10.3760/cma.j.issn.0254-6450.2015.12.022

KeyWord: 基质金属蛋白酶非酒精性脂肪肝病多态性中心性肥胖交互作用

English Key Word: Matrix metalloproteinases Nonalcoholic fatty liver disease Polymorphism Central obesity Interaction

FundProject:湖北省自然基金项目(2012CDZ029)

Author Name	Affiliation	E-mail
Wu Pengbo	Department of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan 430060, China
Shu Yongxiang	Department of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan 430060, China
Li Ming	Department of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan 430060, China
Luo Hesheng	Department of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan 430060, China
Zhang Guo	Department of Gastroenterology, the People's Hospital of Guangxi Zhuang Autonomous Region
Tan Shiyun	Department of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan 430060, China	tanshiyun@medmail.com

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Abstract:

目的探讨间质金属蛋白酶-9(MMP-9)-1562C/T(rs3918242)以及MMP-2-1306C/T(rs243865)位点单核苷酸多态性(SNP)与非酒精性脂肪肝(NAFLD)遗传易感性以及与中心性肥胖交互作用。方法对545例NAFLD患者和636例正常对照,采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析rs24386以及rs3918242基因型、非条件logistic分析各基因型与脂肪肝发病易感性关系,利用非条件logistic分析和广义多因子降维(GMDR)法分析rs3918242、rs243865与中心性肥胖的交互作用。结果 MMP-9 rs3918242位点T基因携带者(TT/CT)与非T基因携带者(CC)的NAFLD罹患风险明显增加(OR=1.67,95%CI:1.32～2.12,P=0.001;调整OR=1.65,95%CI:1.31～2.01,P=0.008);而MMP-2 rs243865位点T基因携带者(TT/CT)与非T基因携带者(CC)的NAFLD罹患风险明显降低(OR=0.68,95%CI:0.53～0.86,P=0.001;调整OR=0.66,95%CI:0.49～0.90,P=0.007)。广义多因子降维法分析结果显示,rs3918242与中心性肥胖在NAFLD发病中存在交互作用(P=0.001)。利用非条件logistic校正年龄、性别、腰围、BMI、LDL-C、HDL-C、FPG、胰岛素抵抗指数后,分析显示,携带rs3918242 TT/CT基因型中心性肥胖个体罹患NAFLD的风险高于携带CC基因非吸烟个体(OR=4.50,95%CI:2.78～7.17,P=0.007)。结论 MMP-9基因的rs3918242以及MMP-2基因的rs243865与NAFLD患病罹患风险紧密相关,rs3918242与中心性肥胖在NAFLD发病中具有协同效应。

English Abstract:

Objective To study whether matrix metalloproteinases-9(MMP)-1562C/T(rs3918242) and MMP-2-1306C/T (rs243865) were associated with the susceptibility on nonalcoholic fatty liver disease (NAFLD) and the interactions between the two factors and central obesity. Methods Genotypes of 545 patients and 636 subjects with NAFLD under control were examined by polymerase chain reaction-based restriction fragment length polymorphism(PCR-RFLP). Unconditional logistic regression (ULR) was performed to assess the NAFLD risk. The gene-environment interactions on the risk of NAFLD were explored by generalized multifactor dimensionality reduction (GMDR) and ULR methods. Results Results from the case-control analysis indicated that there was an increased risk of developing NAFLD for MMP-9 rs3918242 (TT/CT) genotype carriers, when compared with the non-carriers (CC), with OR=1.67,95%CI: 1.32-2.12, P=0.001; Adjusted OR=1.65,95%CI:1.31-2.01(P=0.008). However, risk reduction of NAFLD was found when MMP-2 rs243865 (TT/CT) genotype carriers compared with the non-carriers (CC), with OR=0.68, 95%CI:0.53-0.86,P=0.001; with adjusted OR=0.66, 95%CI: 0.49-0.90(P=0.007). Data from the GMDR showed that gene-environment interaction among rs3918242 and central obesity on the risk of NAFLD might be significant (P=0.001). By using the ULR method, subjects as central obesity-positive but with genotype CT/TT, appeared having 4.50 (95%CI:2.78-7.17,P=0.007) times risk of NAFLD, when compared to the central obesity-negative subjects with genotype CC after adjusting for the covariates. Conclusion MMP-9 rs3918242, MMP-2 rs243865 were associated with risk of NAFLD while both rs3918242 and central obesity showing synergistic effects on the risk of the NAFLD.

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