Most importantly, previous studies have not examined the relationship between each of the three distinct patterns of hepatic iron deposition and histological severity among patients with NASH. The goal of the current study was to analyze the relationships between the pattern of hepatic iron deposition and liver histology in liver biopsy specimens from an unselected cohort of NAFLD patients prospectively enrolled in the National Institutes for Health–funded selleck products Nonalcoholic Steatohepatitis Clinical Research Network (NASH CRN) from eight participating centers in the United States. ALT, alanine aminotransferase; AST, aspartate aminotransferase; BMI, body mass index;

CI, confidence interval; HC, hepatocellular; HCC, hepatocellular carcinoma; HDL, high-density lipoprotein; HFE, hemochromatosis gene; HJV, hemojuvelin; HOMA-IR, homeostasis model assessment of insulin resistance; IL, interleukin; LDL, low-density lipoprotein; NAFLD, nonalcoholic fatty liver disease; NAS, nonalcoholic fatty liver disease activity score; NASH, nonalcoholic steatohepatitis; NASH CRN, Nonalcoholic Steatohepatitis Clinical Research Network; OR, odds ratio; RES, reticuloendothelial system; ROS, reactive oxygen species;

TFR, transferrin receptor; TIBC, total iron-binding capacity; TS, transferrin saturation. Participants were Wnt inhibitor review enrolled in the NASH CRN studies from October 2005 to February 2008 according to inclusion criteria described elsewhere.18, 19 Briefly, NASH CRN study participants at least 18 years of age constituted the MCE patient population for this study. Patients with known hemochromatosis (defined as a hepatic iron index ≥ 1.9 or the removal of >4 g of iron by phlebotomy), C282Y homozygosity for the HFE gene, or unexplained hepatic iron overload (≥3+ stainable iron on liver biopsy) were excluded from all NASH CRN studies. Demographic information such as age, gender, ethnicity, and race was obtained. A medical history was obtained for all subjects; it included a menstrual history for

women, the presence of comorbid conditions, and medication usage. The total dietary consumption of iron, vitamin C, tea, and coffee was determined with the Block 98 food frequency questionnaire; alcohol consumption was determined with the Alcohol Use Disorders Identification Test–Consumption questionnaire during the NASH CRN studies closest to the time of biopsy. A physical examination, which included body weight and height measures, was performed for all subjects. The histological evaluation was based on 849 liver biopsy samples with hepatic iron staining results, which were read centrally by the pathology committee of NASH CRN. In addition, clinical and laboratory data obtained within 6 months of liver biopsy were compared between iron stain–positive subjects and iron stain–negative subjects if they were available (n = 573).