N WONG,1 S ROBERTS,1 P LEWIS,1 E PAUL,2 M KITSON,1 D ISER,1 W KEMP1 1Alfred Hospital, Department of Gastroenterology, Commercial Rd, Melbourne, Australia, 2Monash University, Department of Epidemiology and Preventive Medicine, Melbourne, Australia

Background: Detecting GPCR Compound Library fibrosis progression is important in the management of chronic hepatitis C (CHC). However factors influencing the evolution of liver fibrosis in CHC using transient elastography (TE) are unclear. BMI, alcohol use and HIV co-infection are cofactors in progression of CHC although the impact on liver stiffness (LSM) progression in CHC has not been demonstrated. Aim: To determine the impact of BMI, alcohol use and HIV co-infection on fibrosis progression using TE. Methods: Patients with CHC and at least two TE assessments 12 months or more apart were identified from a prospectively maintained database. Baseline demographic, anthropometric and TE data were extracted. Data were cross-matched with information prospectively collected via patient reported questionnaire at the time of TE examination. Change in LSM (ΔLSM) was

adjusted for follow up time, and CHC treatment response. Results: From March 2010 to December 2013, 508 patients (62% Male, age 50.8 ± 10 yrs) with CHC and at least two TE examinations were identified. TE was performed on average 21 ± 9 months (range 12–41 months) apart. Overall there was no difference in LSM between the first (LSM1; median 7.1 ± 8.5 kPa) and second (LSM2; median 7.0 ± 9.2 kPa) assessments (mean ± SD ΔLSM = 0.25 ± 0.25). Neither BMI or alcohol LBH589 clinical trial use were associated with change in LSM. HIV co-infection (n = 62) was associated with a significant increase in LSM (ΔLSM = +1.84 kPa, p = 0.018). 47% of patients who underwent CHC treatment between LSM1 and LSM2 achieved an SVR (18/37). SVR was associated with a non-significant reduction in LSM (ΔLSM = −3.9 vs −1.0 kPa, p = 0.2) Conclusion: This

data supports the reproducibility of LSM but neither BMI nor alcohol intake were associated with change in LSM over a 21 month follow up. HIV co-infection was associated with significant LSM increase in this study with relatively short follow up. This supports the increased rates fibrosis progression in the HIV cohort. LT GAN,1 B SHADBOLT,2 V WONG,3 MCE公司 L ADAMS,4 T DWYER,1 H CHAN,3 N TEOH,1 S CHITTURI,1 G FARRELL1 1Liver Research Group, and 2Biostatistician, ANU Medical School and The Canberra Hospital, ACT, 3Department of Medicine and Therapeutics, Chinese University of Hong Kong, Shatton, Hong Kong, 4Gastroenterology and Hepatology Unit, Charles Gairdner Hospital, Perth, WA Introduction: Non-alcoholic fatty liver disease (NAFLD) affects 27% of the Hong Kong population1 with similar or higher prevalence in Australia. While ∼75% of patients do not have significant liver disease, identifying those with non-alcoholic steatohepatitis (NASH) and/or significant liver fibrosis is challenging.