TY - JOUR
T1 - Sustained Improvements in Markers of Liver Disease Severity After Hepatitis C Treatment
AU - Wong, Robert J.
AU - Jain, Mamta K.
AU - Therapondos, George
AU - Shiffman, Mitchell L.
AU - Kshirsagar, Onkar
AU - Clark, Christopher
AU - Thamer, Mae
N1 - Funding Information:
RJW receives research funding from Gilead Sciences and Abbvie, has served as a consultant and member of the advisory board for Gilead Sciences, and serves on the speaker's bureau for Gilead Sciences, Salix, and Bayer. RJW is also funded by an AASLD Foundational Clinical and Translational Research Award in Liver Diseases.MKJ receives research funding from Gilead Sciences, Merck, Janssen, and GlaxoSmithKline / ViiV Healthcare and has served as an advisor for GlaxoSmithKline.MLS receives grant funding from Abbvie, Bristol Myers-Squibb, Conatus, CymaBay, Exalenz, Galectin, Genfit, Gilead, Intercept, Immuron, Merck, NGMBio, Novartis, and Shire. He is also an advisor/speaker for Abbvie, Bayer, Bristol Myers-Squibb, Daiichi Sankyo, Gilead, Intercept, Merck, and Salix and serves as a consultant for Optum Rx.This study was supported by an investigator-initiated study research grant from Gilead Sciences. Robert Wong is supported by an AASLD Foundation Clinical and Translational Research Award in Liver Diseases.
Funding Information:
RJW receives research funding from Gilead Sciences and Abbvie , has served as a consultant and member of the advisory board for Gilead Sciences, and serves on the speaker's bureau for Gilead Sciences, Salix, and Bayer. RJW is also funded by an AASLD Foundational Clinical and Translational Research Award in Liver Diseases.
Publisher Copyright:
© 2019 Indian National Association for Study of the Liver
PY - 2020/3/1
Y1 - 2020/3/1
N2 - Background & aims: Although serological markers of disease severity improve after hepatitis C virus (HCV) treatment, it is unclear if all patients experience sustained improvement. We aim to evaluate longitudinal changes in aspartate (AST), alanine (ALT) aminotransferase, platelet count (PLT), and fibrosis-4 (FIB-4) after HCV treatment. Methods: All adult chronic HCV patients who received antiviral therapy from January 2011 to February 2017 at four large urban hospital systems were evaluated to assess changes in AST, ALT, PLT, and FIB-4 from pre-treatment to post-treatment annually up to 4 years after HCV therapy. Comparisons used Student's t-test and analysis of variance, and were stratified by sex, race, ethnicity, age, body mass index (BMI), and diabetes mellitus. Results: Among 2691 patients (62.2% men, 76.9% aged 45–65 years, 56.5% white), all markers of disease severity demonstrated sustained improvements from pre-treatment to 4 years post-treatment (AST 53 U/L to 27.5 U/L, ALT 53 U/L to 29 U/L, PLT 168 × 103 to 176 × 103, FIB-4 2.51 to 1.68). However, Hispanics and patients with BMI >30 kg/m2 experienced rebound increases in AST, ALT, and FIB-4 at 4 years post-treatment after experiencing initial improvements in these serological markers in the first-year post-treatment. Sustained improvements in PLT were observed in all groups, including Hispanics and patients with BMI >30 kg/m2. Conclusion: HCV treatment in a large community-based cohort demonstrated sustained improvements in AST, ALT, PLT, and FIB-4. Rebound increases in AST, ALT, and FIB-4 observed in Hispanics and those with BMI >30 kg/m2 may reflect persisting nonalcoholic fatty liver disease.
AB - Background & aims: Although serological markers of disease severity improve after hepatitis C virus (HCV) treatment, it is unclear if all patients experience sustained improvement. We aim to evaluate longitudinal changes in aspartate (AST), alanine (ALT) aminotransferase, platelet count (PLT), and fibrosis-4 (FIB-4) after HCV treatment. Methods: All adult chronic HCV patients who received antiviral therapy from January 2011 to February 2017 at four large urban hospital systems were evaluated to assess changes in AST, ALT, PLT, and FIB-4 from pre-treatment to post-treatment annually up to 4 years after HCV therapy. Comparisons used Student's t-test and analysis of variance, and were stratified by sex, race, ethnicity, age, body mass index (BMI), and diabetes mellitus. Results: Among 2691 patients (62.2% men, 76.9% aged 45–65 years, 56.5% white), all markers of disease severity demonstrated sustained improvements from pre-treatment to 4 years post-treatment (AST 53 U/L to 27.5 U/L, ALT 53 U/L to 29 U/L, PLT 168 × 103 to 176 × 103, FIB-4 2.51 to 1.68). However, Hispanics and patients with BMI >30 kg/m2 experienced rebound increases in AST, ALT, and FIB-4 at 4 years post-treatment after experiencing initial improvements in these serological markers in the first-year post-treatment. Sustained improvements in PLT were observed in all groups, including Hispanics and patients with BMI >30 kg/m2. Conclusion: HCV treatment in a large community-based cohort demonstrated sustained improvements in AST, ALT, PLT, and FIB-4. Rebound increases in AST, ALT, and FIB-4 observed in Hispanics and those with BMI >30 kg/m2 may reflect persisting nonalcoholic fatty liver disease.
KW - HCV
KW - diabetes
KW - fibrosis
KW - hispanic
KW - obesity
UR - http://www.scopus.com/inward/record.url?scp=85073713056&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85073713056&partnerID=8YFLogxK
U2 - 10.1016/j.jceh.2019.09.001
DO - 10.1016/j.jceh.2019.09.001
M3 - Article
C2 - 32189926
AN - SCOPUS:85073713056
SN - 0973-6883
VL - 10
SP - 114
EP - 123
JO - Journal of Clinical and Experimental Hepatology
JF - Journal of Clinical and Experimental Hepatology
IS - 2
ER -