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ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R
Issue 10
Oct.  2018
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Association between MBOAT7 rs641738 polymorphism and nonalcoholic fatty liver disease

DOI: 10.3969/j.issn.1001-5256.2018.10.021
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  • Published Date: 2018-10-20
  • Objective To investigate the association between MOBAT7 rs641738 polymorphism and the development of NAFLD in the Chinese Han population in Qingdao, China, and to provide a theoretical basis for the prevention and treatment of NAFLD and its complication.Methods A total of 113 NAFLD patients who were treated in Qingdao Municipal Hospital and 74 healthy controls were enrolled in this study. Blood samples were collected, DNA was extracted, and PCR and time-of-flight mass spectrometry were used to determine the genotype of MBOAT7 rs641738. The chi-square test was used to determine whether the distribution of genotypes met the Hardy-Weinberg equilibrium, in order to assess the group representativeness of samples. Clinical data and biochemical results including liver function were collected.The chi-square test was used for comparison of sex and genotype and allele frequencies between the two groups. The independent samples t-test and Wilcoxon rank sum test were used for comparison of continuous data between the two groups. The relative risk of NAFLD associated with gene polymorphisms was expressed as odds ratio ( OR) and 95% confidence interval ( CI) , and the non-conditional logistic regression model was used to calculate OR and 95% CI. Results There was no significant difference in the distribution of CC, CT, and TT genotypes of MBOAT7 rs641738 between the NAFLD group and the control group ( χ2= 0. 157, P = 0. 692) , and there was also no significant difference in the distribution of C and T alleles between the two groups ( χ2= 0. 365, P = 0. 546) . The non-conditional logistic regression analysis showed that the carriers with CC + CT genotypes of MBOAT7 rs641738 had a similar risk of NAFLD as those with CC genotype ( OR = 0. 923, 95% CI: 0. 685-1. 245, P = 0. 692) ; there was also no significant difference after adjustment for sex, age, and body mass index ( corrected OR = 0. 893, 95% CI: 0. 652-1. 223, P = 0. 481) . In the NAFLD group, the carriers with CC + CT genotypes had significantly lower levels of total cholesterol and low-density lipoprotein than those with CC genotype ( t =-2. 348 and-2. 113, P = 0. 021 and0. 037) , and there were no significant differences in the other indices ( all P > 0. 05) . Conclusion There is no significant association between MBOAT7 rs641738 polymorphism and the risk of NAFLD in the Chinese Han population in Qingdao.

     

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  • [1]COHEN JC, HORTON JD, HOBBS HH.Human fatty liver disease:Old questions and new insights[J].Science, 2011, 332 (6037) :1519-1523.
    [2]LI SP, WANG QC.Progress of the epidemiology of non-alcoholic fatty liver disease[J].Chin J Gastroenterol Hepatol, 2017, 26 (10) :1085-1087. (in Chinese) 李生鹏, 王全楚.非酒精性脂肪性肝病的流行病学进展[J].胃肠病学和肝病学杂志, 2017, 26 (10) :1085-1087.
    [3]SEVERSON TJ, BESUR S, BONKOVSKY HL.Genetic factors that affect nonalcoholic fatty liver disease:A systematic clinical review[J].World J Gastroenterol, 2016, 22 (29) :6742-6756.
    [4]DONGIOVANNI P, VALENTI L.Genetics of nonalcoholic fatty liver disease[J].Metabolism, 2016, 65 (8) :1026-1037.
    [5]HU ZJ, ZHANG J.Current status of research on nonalcoholic fatty liver disease in China[J].J Clin Hepatol, 2016, 32 (3) :552-555. (in Chinese) 胡中杰, 张晶.我国非酒精性脂肪性肝病的研究现状[J].临床肝胆病杂志, 2016, 32 (3) :552-555.
    [6]GIJON MA, RIEKHOF WR, ZARINI S, et al.Lysophospholipid acyltransferases and arachidonate recycling in human neutrophils[J].J Biol Chem, 2008, 283 (44) :30235-30245.
    [7]LEE HC, INOUE T, IMAE R, et al.Caenorhabditis elegans mboa-7, a member of the MBOAT family, is required for selective incorporation of polyunsaturated fatty acids into phosphatidylinositol[J].Mol Biol Cell, 2008, 19 (3) :1174-1184.
    [8]DAUWERSE JG, de VRIES BB, WOUTERS CH, et al.At (4;6) (q12;p23) translocation disrupts a membrane-associated O-acetyl transferase gene (MBOAT1) in a patient with a novel brachydactyly-syndactyly syndrome[J].Eur J Hum Genet, 2007, 15 (7) :743-751.
    [9]PEREZ-CHACON G, ASTUDILLO AM, BALGOMA D, et al.Control of free arachidonic acid levels by phospholipases A2 and lysophospholipid acyltransferases[J].Biochim Biophys Acta, 2009, 1791 (12) :1103-1113.
    [10]LANDS WE.Metabolism of glycerolipides;a comparison of lecithin and triglyceride synthesis[J].J Biol Chem, 1958, 231 (2) :883-888.
    [11]ZARINI S, HANKIN JA, MURPHY RC, et al.Lysophospholipid acyltransferases and eicosanoid biosynthesis in zebrafish myeloid cells[J].Prostaglandins Other Lipid Mediat, 2014, 113-115:52-61.
    [12]KRAWCZYK M, RAU M, SCHATTENBERG JM, et al.Combined effects of the PNPLA3 rs738409, TM6SF2 rs58542926, and MBOAT7 rs641738 variants on NAFLD severity:A multicenter biopsy-based study[J].J Lipid Res, 2017, 58 (1) :247-255.
    [13]MANCINA RM, DONGIOVANNI P, PETTA S, et al.The MBOAT7-TMC4 variant rs641738 increases risk of nonalcoholic fatty liver disease in individuals of european descent[J].Gastroenterology, 2016, 150 (5) :1219-1230.
    [14]THABET K, ASIMAKOPOULOS A, SHOJAEI M, et al.MBOAT7rs641738 increases risk of liver inflammation and transition to fibrosis in chronic hepatitis C[J].Nat Commun, 2016, 7:12757.
    [15]LIN YC, CHANG PF, CHANG MH, et al.Genetic determinants of hepatic steatosis and serum cytokeratin-18 fragment levels in Taiwanese children[J].Liver Int, 2018, 38 (7) :1300-1307.
    [16]Group of Fatty Liver and Alcoholic Liver Diseases, Society of Hepatology, Chinese Medical Association.Guidelines for management of non-alcoholic fatty liver disease[J].J Clin Hepatol, 2010, 26 (2) :120-124. (in Chinese) 中华医学会肝脏病学分会脂肪肝和酒精性肝病学组.非酒精性脂肪性肝病诊疗指南[J].临床肝胆病杂志, 2010, 26 (2) :120-124.
    [17]BUCH S, STICKEL F, TREPO E, et al.A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7as risk loci for alcohol-related cirrhosis[J].Nat Genet, 2015, 47 (12) :1443-1448.
    [18]LUUKKONEN PK, ZHOU Y, HYOTYLAINEN T, et al.The MBOAT7 variant rs641738 alters hepatic phosphatidylinositols and increases severity of non-alcoholic fatty liver disease in humans[J].J Hepatol, 2016, 65 (6) :1263-1265.
    [19]DONATI B, DONGIOVANNI P, ROMEO S, et al.MBOAT7rs641738 variant and hepatocellular carcinoma in non-cirrhotic individuals[J].Sci Rep, 2017, 7 (1) :4492.
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