Cell death resulting from apoptosis was calculated by the following equation: % Apoptosis = [(M30 CK18/M65 CK18)*100]; likewise, by definition, the remaining amount of cell death is considered to be the result of necrosis and was calculated according to the formula, 100 − [(M30 CK18/M65 CK18)*100]. TUNEL was performed using the ApopTag Plus Peroxidase In Situ Apoptosis Detection Kit (Chemicon, Billerica, MA), following

the manufacturer’s KU-60019 in vivo instructions; diaminobenzidine (DAB; Invitrogen, Carlsbad, CA), prepared just before use, and 5 μL of NiCl2 (8% in distilled water) per milliliter of DAB was substituted for the peroxidase substrate to enhance visualization of dye. Specimens were counterstained using 2% methyl green for 4 minutes at room temperature, followed Selumetinib in vivo by three washes each of distilled

water, absolute ethanol, and xylene. Quantification of apoptosis was determined by counting apoptotic cells in five random fields per patient at 400× magnification. Because the number of cells in each field varies widely between patients with ranging levels of steatosis, it was important to obtain a measure of cellularity for each patient. To estimate the total number of cells per field, two representative fields per patient were selected and overlaid with a 10 × 10 grid in ImageJ (National Institutes of Health, Bethesda, MD). Ten squares within the grid were analyzed for the number of cells and this number was multiplied by 10 to approximate the total number of cells per

field. Percent apoptosis was expressed as the average number of apoptotic cells/average total number of cells for each group. Scoring was performed in a blinded fashion through two independent assessments, 上海皓元 and the mean of these two scores was used for final analysis. Demographic, clinical, and laboratory characteristics were recorded as number and percentage for categorical data and means and standard error or median and interquartile range for continuous data. Categorical data were analyzed using Fisher’s exact test. Continuous variables, including laboratory measures, were not normally distributed and were analyzed using nonparametric statistics, including Mann-Whitney’s rank-sum test and Spearman’s rank-correlation test or linear regression modeling adjusting for sex as a potential confounding variable. Differences in mean histological scores, such as HC and RES iron grade, steatosis grade, fibrosis stage, lobular inflammation grade, and NAS between groups, were analyzed using ordinal logistic regression. Multivariate stepwise linear regression (cutoff: P < 0.20) analysis was used to investigate the independent association of HC iron and percent CK18 levels resulting from necrosis after adjustment for sex, age, body mass index (BMI), alanine aminotransferase (ALT), and presence of diabetes.