Open AccessGenetic variants associated with metabolic dysfunction‐associated fatty liver disease in western China
Author(s) -
Liao Shenling,
An Kang,
Liu Zhi,
He He,
An Zhenmei,
Su Qiaoli,
Li Shuangqing
Publication year - 2022
Publication title -
journal of clinical laboratory analysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.536
H-Index - 50
eISSN - 1098-2825
pISSN - 0887-8013
DOI - 10.1002/jcla.24626
Subject(s) - single nucleotide polymorphism , snp , biology , fatty liver , odds ratio , medicine , multifactor dimensionality reduction , genetics , endocrinology , genotype , disease , gene
Abstract Introduction We aimed to confirm the association between some single nucleotide polymorphisms (SNPs) and metabolic dysfunction‐associated fatty liver disease (MAFLD) in western China. Methods A total of 286 cases and 250 healthy controls were enrolled in our study. All samples were genotyped for patatin‐like phospholipase domain containing 3 ( PNPLA3 ) rs738409, transmembrane 6 superfamily member 2 ( TM6SF2 ) rs58542926, membrane‐bound O‐acyltransferase domain containing 7 ( MBOAT7 ) rs641738, glucokinase regulator ( GCKR ) rs1260326 and rs780094, and GATA zinc finger domain containing 2A ( GATAD2A ) rs4808199. Using logistic regression analysis, we evaluated the association between MAFLD and each SNP under different models. Multiple linear regression was used to find the association between SNPs and laboratory characteristics. Multifactor dimensionality reduction was applied to test SNP–SNP interactions. Results The recessive model and additive model of PNPLA3 rs738409 variant were related to MAFLD (odds ratio [OR] = 1.791 and 1.377, respectively, p = 0.038 and 0.027, respectively). However, after Benjamini‐Hochberg adjustment for multiple tests, all associations were no longer statistically significant. PNPLA3 rs738409 correlated with AST levels. GCKR rs780094 and rs1260326 negatively correlated with serum glucose but positively correlated with triglycerides in MAFLD. Based on MDR analysis, the best single‐locus and multilocus models for MAFLD risk were rs738409 and six‐locus models, respectively. Conclusions In the Han population in western China, no association was found between these SNPs and the risk of MAFLD. PNPLA3 rs738409 was associated with aspartate aminotransferase levels in MAFLD patients. GCKR variants were associated with increased triglyceride levels and reduced serum fasting glucose in patients with MAFLD.