Association of Apolipoprotein E Polymorphisms in Patients with Non-Alcoholic Steatohepatitis

• Published in: Digestive diseases and sciences 2008-12, Vol.53 (12), p.3218-3224
• Main Authors: Sazci, Ali, Akpinar, Gurler, Aygun, Cem, Ergul, Emel, Senturk, Omer, Hulagu, Sadettin
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Aged; Apolipoprotein E3 - genetics; Apolipoproteins E - genetics; Biochemistry; Biological and medical sciences; Case-Control Studies; Cohort Studies; Fatty Liver - ethnology; Fatty Liver - genetics; Feeding. Feeding behavior; Female; Fundamental and applied biological sciences. Psychology; Gastroenterology; Gastroenterology. Liver. Pancreas. Abdomen; Gene Frequency - genetics; Genetic Predisposition to Disease - genetics; Genotype; Hepatitis - ethnology; Hepatitis - genetics; Hepatology; Humans; Liver. Biliary tract. Portal circulation. Exocrine pancreas; Male; Medical sciences; Medicine; Medicine & Public Health; Metabolic diseases; Middle Aged; Obesity; Oncology; Original Paper; Other diseases. Semiology; Polymorphism, Genetic - genetics; Transplant Surgery; Turkey; Vertebrates: anatomy and physiology, studies on body, several organs or systems; Young Adult
• ISSN: 0163-2116; 1573-2568
• DOI: 10.1007/s10620-008-0271-5

Non-alcoholic fatty liver disease (NAFLD) is the most common cause of abnormal hepatic steatosis in the absence of alcohol abuse worldwide. Non-alcoholic steatohepatitis (NASH) is the most progressive form of NAFLD. The aim of this study was to investigate the role of apolipoprotein E (APOE) polymorphisms in the development of NASH. We analysed 57 NASH patients and 245 healthy controls using a polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method in a case-control study. The diagnosis of the patients was based on liver biopsy. The serum levels of glucose, lipids, vitamin B12, folic acid, homocysteine, insulin, total biluribin, total protein, albumin, ferritin, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) were determined in all of the subjects. Body mass index (BMI), waist circumference (WC), AST, ALT, fasting blood sugar (FBS), total cholesterol, triglyceride (TG), low-density lipoprotein (LDL) cholesterol, very low-density lipoprotein (VLDL) cholesterol, insulin and ferritin levels were significantly higher in the 57 patients with NASH compared with the 245 healthy controls. The APOE ε3 allele was overrepresented in the whole group of NASH patients (ε3=97.37% in NASH versus 82.45% in controls). The APOE polymorphism was statistically significantly associated with NASH (χ²=15.741; p=0.008). The APOE3/3 genotype (odds ratio [OR]=7.941; p=0.000) was strongly associated with increased risk for NASH in all NASH patients. Consequently, the APOE3/3 genotype may play a role in the aetiopathogenesis of NASH.