[1] Krawczyk M, Bonfrate L, Portincasa P. Nonalcoholic fatty liver disease[J]. Best Pract Res Clin Gastroenterol,2010, 24(5):695-708. [2] 胡翠兰, 王军, 彭浩, 等. 二氯乙酸二异丙胺片治疗非酒精性脂肪肝病40例[J]. 医药导报,2009, 28(11):1460-1461. [3] Yang Z, Wang X, Wen J, et al. Prevalence of non-alcoholic fatty liver disease and its relation to hypoadiponectinaemia in the middle-aged and elderly Chinese population[J]. Arch Med Sci,2011, 7(4):665-672. [4] Browning JD, Szczepaniak LS, Dobbins R, et al. Prevalence of hepatic steatosis in an urban population in the United States: impact of ethnicity[J]. Hepatology,2004, 40(6): 1387-1395. [5] Browning JD, Kumar KS, Saboorian MH, et al. Ethnic differences in the prevalence of cryptogenic cirrhosis[J]. Am J Gastroenterol,2004, 99(2): 292-298. [6] Caldwell SH, Harris DM, Patrie JT, et al. Is NASH underdiagnosed among African Americans [J] ?Am J Gastroenterol,2002, 97(6): 1496-1500. [7] Day CP, James DF. Steatohepatitis: a table of two "hit" [J] ?Gastroenterology, 1998, 114(4): 842-845. [8] Namikawa C, Shu-Ping Z, Vyselaar JR, et al. Polymorphisms of microsomal triglyceride transfer protein gene and manganese superoxide dismutase gene in non-alcoholic steatohepatitis[J]. J Hepatol,2004, 40(5): 781-786 . [9] Oliveira CP, Stefano JT, Cavaleiro AM, et al. Association of polymorphisms of glutamate-cystein ligase and microsomal triglyceride transfer protein genes in non-alcoholic fatty liver disease[J]. J Gastroenterol Hepatol,2010, 25(2): 357-361. [10] Hashemi M, Hoseini H, Yaghmaei P, et al. Association of Polymorphisms in Glutamate-Cysteine Ligase Catalytic Subunit and Microsomal Triglyceride Transfer Protein Genes with Nonalcoholic Fatty Liver Disease[J]. DNA Cell biol,2011, 30(8): 569-575. [11] Song J, da Costa KA, Fischer LM, et al. Polymorphism of the PEMT gene and susceptibility to nonalcoholic fatty liver disease (NAFLD)[J]. FASEB J,2005, 19(10): 1266-1271. [12] Dong H, Wang J, Li C, et al. The phosphatidylethanolamine N-methyltransferase gene V175M single nucleotide polymorphism confers the susceptibility to NASH in Japanese population[J]. J Hepatol, 2007, 46(5): 915-920 . [13] Zhang B, Xie W, Krasowski MD. PXR: a xenobiotic receptor of diverse function implicated in pharmacogenetics[J]. Pharmacogenomics,2008, 9(11): 1695-1709 . [14] Sookoian S, Castano GO, Burgueno AL, et al. The nuclear receptor PXR gene variants are associated with liver injury in nonalcoholic fatty liver disease[J]. Pharmacogenet Genomics,2010, 20(1):1-8 . [15] Everett L, Galli A, Crabb D. The role of hepatic peroxisome proliferator-activated receptors(PPARs) in health and disease[J]. Liver, 2000, 20(3):191-199. [16] Ferré P. The biology of peroxisome proliferator-activated receptors: relationship with lipid metabolism and insulin sensitivity[J]. Diabetes,2004, 53(Suppl):S43-50. [17] Chen S, Li Y, Li S, et al. A Val227Ala substitution in the peroxisome proliferator activated receptor alpha(PPAR alpha) gene associated with non-alcoholic fatty liver disease and decreased waist circumference and waist-to-hip ratio[J]. Gastroenterol Hepatol,2008, 23(9):1415-418. [18] Petersen KF, Dufour S, Hariri A, et al. Apolipoprotein C3 gene variants in nonalcoholic fatty liver disease[J]. N Engl J Med,2010, 362(12): 1082-1089 . [19] Kozlitina J, Boerwinkle E, Cohen JC, et al. Dissociation between APOC3 variants, hepatic triglyceride content and insulin resistance[J]. Hepatology, 2011, 53(2): 467-474. [20] Maddux BA, Goldfine ID. Membrane glycoprotein PC-1 inhibition of insulin receptor function occurs via direct interaction with the receptor -subunit[ J]. Diabetes,2000, 49(1): 13-19. [21] Carulli L, Canedi I, Rondinella S, et al. Genetic polymorphisms in non-alcoholic fatty liver disease: interleukin-6-174G/C polymorphism is associated with non-alcoholic steatohepatitis[J]. Dig Liver Dis,2009, 41(11): 823-828 . [22] Dongiovanni P, Valenti L, Rametta R, et al. Genetic variants regulating insulin receptor signalling are associated with the severity of liver damage in patients with non-alcoholic fatty liver disease[J]. Gut,2010, 59(2): 267-273. [23] Johannes W Rey, Andrea Noetel, Aline Hardt, et al. Pro12Ala polymorphism of the peroxisome proliferator-activated receptor γ2 in patients with fatty liver diseases[J]. World J Gastroenterol, 2010, 16(46): 5830-5837. [24] AC Gupta, AK Chaudhory, Sukriti, et al. Peroxisome proliferators-activated receptor γ2 Pro12Ala variant is associated with body mass index in non-alcoholic fatty liver disease patients[J]. Hepatol Int, 2010, 5(1): 575-580. [25] Dongiovanni P, Rametta R, Fracanzani AL, et al. Lack of association between peroxisome proliferator-activated receptors alpha and gamma-polymorphisms and progressive liver damage in patients with non-alcoholic fatty liver disease: a case control study[J]. BMC Gastroenterol,2010, 10:102-108. [26] Yang Z, Wen J, Li Q, et al. PPARG gene Pro12Ala variant contributes to the development of non-alcoholic fatty liver in middle-aged and older Chinese population[J]. Molecular and Cellular Endocrinology, 2012, 348(1):255-259. [27] Musso G, Gambino R, De Michieli F, et al. Adiponectin gene polymorphisms modulate acute adiponectin response to dietary fat: Possible pathogenetic role in NASH[J]. Hepatology, 2008, 47(4): 1167-1177. [28] Nobili V, Daly AK, Al-Serri A, et al. The mitochondrial superoxide dismutase 2 (SOD2) targeting sequence polymorphism is associated with fibrotic NAFLD: consistent evidence from case-control and intra-familial allelic association studies[J]. Hepatology, 2007, 46(4): 760A-760A. [29] Dongiovanni P, Rametta R, Fracanzani AL, et al. The SOD2 C47T polymorphism influences NAFLD fibrosis severity: Evidence from case-control and intra-familial allele association studies[J]. Journal of Hepatology,2012, 56(2):448-454. [30] Chen Y, Yang Y, Miller ML, et al. Hepatocyte-specific GCLC deletion leads to rapid onset of steatosis with mitochondrial injury and liver failure[J]. Hepatology, 2007, 45(5): 1118-1128 . [31] Oliveira CP, Stefano JT, Cavaleiro AM, et al. Association of polymorphisms of glutamate-cystein ligase and microsomal triglyceride transfer protein genes in non-alcoholic fatty liver disease[J]. J Gastroenterol Hepatol,2010, 25(2): 357-361 . [32] Lin YC, Chang PF, Hu FC, et al. Variants in the UGT1A1 gene and the risk of pediatric nonalcoholic fatty liver disease[J]. Pediatrics,2009, 124(6): e1221-e1227. [33] Kowdley KV. The role of iron in nonalcoholic fatty liver disease: the story continues[J]. Gastroenterology, 2010, 138(3): 817-819 . [34] George DK, Goldwurm S, MacDonald GA, et al. Increased hepatic iron concentration in nonalcoholic steatohepatitis is associated with increased fibrosis[J]. Gastroenterology,1998,114(2): 311-318 . [35] Nelson JE, Bhattacharya R, Lindor KD, et al. HFE C282Y mutations are associated with advanced hepatic fibrosis in Caucasians with nonalcoholic steatohepatitis[J]. Hepatology,2007, 46(3): 723-729 . [36] Valenti L, Fracanzani AL, Bugianesi E, et al. HFE genotype, parenchymal iron accumulation, and liver fibrosis in patients with nonalcoholic fatty liver disease[J]. Gastroenterology, 2010, 138(3): 905-912 . [37] Valenti L, Fracanzani AL, Dongiovanni P, et al. Tumor necrosis factor α promoter polymorphisms and insulin resistance in nonalcoholic fatty liver disease[J]. Gastroenterology,2002, 122(2): 274-280. [38] Tokushige K, Takakura M, Tsuchiya-Matsushita N, et al. Influence of TNF gene polymorphisms in Japanese patients with NASH and simple steatosis[J]. J Hepatol,2007, 46(6): 1104-1110 . [39] Wong VW, Wong GL, Tsang SW, et al.Genetic polymorphisms of adiponectin and tumor necrosis factor alpha and nonalcoholic fatty liver disease in Chinese people[J]. J Gastroenterol Hepatol, 2008, 23(6): 914-921. [40] Dixon JB, Bhathal PS, Jonsson JR, et al. Pro-fibrotic polymorphisms predictive of advanced liver fibrosis in the severely obese[J]. J Hepatol,2003, 39(6): 967-971 . [41] Yoneda M, Hotta K, Nozaki Y, et al. Association between angiotensin II type 1 receptor polymorphisms and the occurrence of nonalcoholic fatty liver disease[J]. Liver Int, 2009, 29(7): 1078-1085 . [42] Georgescu EF. Angiotensin receptor blockers in the treatment of NASH/NAFLD: could they be a first-class option [J] ? Adv Ther,2008, 25(11): 1141-1174 . [43] Starkel P, Sempoux C, Leclercq I, et al. Oxidative stress, KLF6 and transforming growth factor-b up-regulation differentiate non-alcoholic steatohepatitis progressing to fibrosis from uncomplicated steatosis in rats[J]. J Hepatol,2003, 39(4): 538-546 . [44] Miele L, Beale G, Patman G, et al. The Kruppel-like factor 6 genotype is associated with fibrosis in nonalcoholic fatty liver disease[J]. Gastroenterology,2008, 135(1): 282-291 e281 . [45] Espino A, Villagrán A, Vollrath V, et al. Plasminogen activator inhibitor type 1 serum levels and 4G/5G gene polymorphism in morbidly obese Hispanic patients with non-alcoholic fatty liver disease[J]. Ann hepatolo,2011, 10(4): 493-501. [46] Sookoian S, Castaño G, Gemma C, et al. Common genetic variations in CLOCK transcription factor are associated with nonalcoholic fatty liver disease[J]. World J Gastroenterolo,2007, 13(31): 4242-4248. [47] Jarvelainen HA, Orpana A, Perola M, et al. Promotor polymorphism of the CD14 endotoxin receptor gene as a risk factor for alcoholic liver disease[J]. Hepatology,2001, 33(5): 1148-1153. [48] Day CP, Leathart J, McTernan P, et al. Genetic evidence for a role of gut flora in the pathogenesis of NASH in humans[J]. Hepatology,2006, 44(Suppl 1): 261A- 261A. [49] Romeo S, Sentinelli F, Cambuli VM, et al. The 148M allele of the PNPLA3 gene is associated with indices ofliver damage early in life[J]. J Hepatol,2010, 53(2): 335-338. [50] Lynne E,Wagenknecht, Nicholette D,et al. Association of PNPLA3 with non-alcoholic fatty liver disease in a minority cohort: the Insulin Resistance Atherosclerosis Family Study[J]. Liver International,2011, 31(3): 412-416. [51] Krawczyk M, Grünhage F, Zimmer V, et al. Variant adiponutrin (PNPLA3) represents a commonfibrosis risk gene: Non-invasive elastography-based study in chronic liver disease[J]. J Hepatol,2011, 55(2): 299-306. |