TY - JOUR
T1 - Factors associated with high alanine aminotransferase (ALT) and cirrhosis in people living with HIV on combination antiretroviral treatment (cART) in the Asia-Pacific
AU - TREAT Asia HIV Observational Database (TAHOD) of IeDEA Asia-Pacific
AU - Rupasinghe, Dhanushi
AU - Choi, Jun Yong
AU - Yunihastuti, Evy
AU - Kiertiburanakul, Sasisopin
AU - Ross, Jeremy
AU - Ly, Penh Sun
AU - Chaiwarith, Romanee
AU - Do, Cuong Duy
AU - Chan, Yu Jiun
AU - Kumarasamy, Nagalingeswaran
AU - Avihingsanon, Anchalee
AU - Kamarulzaman, Adeeba
AU - Khusuwan, Suwimon
AU - Zhang, Fujie
AU - Lee, Man Po
AU - Van Nguyen, Kinh
AU - Merati, Tuti Parwati
AU - Sangle, Sashikala
AU - Oon Tek, Ng
AU - Tanuma, Junko
AU - Ditangco, Rossana
AU - Sim, Benedict Lim Heng
AU - Pujari, Sanjay
AU - Jiamsakul, Awachana
N1 - Funding Information:
The study team would like to acknowledge all TAHOD study members, steering committee, and patients for their support. This study was supported by the TREAT Asia HIV Observational Database, which is funded by International Epidemiology Databases to Evaluate AIDS (IeDEA; U01AI069907). The Kirby Institute is funded by the Australian Government Department of Health and is affiliated with the Faculty of Medicine, University of New South Wales Sydney. Dr. Oon Tek Ng was supported by the Singapore Ministry of Health's National Medical Research Council (NMRC) Clinician Scientist Award (MOH‐000276).
Publisher Copyright:
© 2022 Wiley Periodicals LLC.
PY - 2022/11
Y1 - 2022/11
N2 - Liver disease is a growing burden among people living with HIV (PLHIV) in resource-limited settings. As an indicator of liver disease, risk factors of high alanine aminotransferase (ALT) and cirrhosis were assessed among PLHIV in the TREAT Asia HIV Observational Database (TAHOD). Patients on combination antiretroviral therapy (cART) with a pre-cART ALT measurement and at least one follow-up ALT measurement were included. Factors associated with high ALT (ALT levels > 5 times its upper limit of normal) were analyzed using repeated measure logistic regression over a 10-year follow-up period. Liver cirrhosis was defined as having an AST to Platelet Ratio Index score > 1.5, fibrosis-4 score > 3.25, or a clinical diagnosis of cirrhosis. Cox regression analysis stratified by site was used to analyze factors associated with cirrhosis among those in follow-up after 2015. Of 5182 patients, 101 patients (1.9%) had high ALT levels with hepatitis C virus (HCV) antibody positive (odds ratio [OR]: 4.98, 95% confidence interval [CI]: 2.82–8.77, p < 0.001) and ever high alcohol consumption (OR: 2.33, 95% CI: 1.00–5.46, p = 0.050) as likely factors. Among 6318 PLHIV in the liver cirrhosis analysis, 151 (2%) developed cirrhosis (incidence rate = 0.82 per 100 person-years). Those HCV-antibody positive (hazard ratio [HR]: 5.54, 95% CI: 3.75–8.18, p < 0.001) and had high alcohol consumption (HR: 2.06, 95% CI: 1.23–3.45, p = 0.006) were associated with liver cirrhosis. HCV-antibody positive and high alcohol consumption are factors associated with high ALT. With raised ALT levels as a known factor associated with liver cirrhosis, greater efforts are required in managing ALT levels and reducing the risk of developing liver cirrhosis among those positive for HCV-antibody and those who consume alcohol.
AB - Liver disease is a growing burden among people living with HIV (PLHIV) in resource-limited settings. As an indicator of liver disease, risk factors of high alanine aminotransferase (ALT) and cirrhosis were assessed among PLHIV in the TREAT Asia HIV Observational Database (TAHOD). Patients on combination antiretroviral therapy (cART) with a pre-cART ALT measurement and at least one follow-up ALT measurement were included. Factors associated with high ALT (ALT levels > 5 times its upper limit of normal) were analyzed using repeated measure logistic regression over a 10-year follow-up period. Liver cirrhosis was defined as having an AST to Platelet Ratio Index score > 1.5, fibrosis-4 score > 3.25, or a clinical diagnosis of cirrhosis. Cox regression analysis stratified by site was used to analyze factors associated with cirrhosis among those in follow-up after 2015. Of 5182 patients, 101 patients (1.9%) had high ALT levels with hepatitis C virus (HCV) antibody positive (odds ratio [OR]: 4.98, 95% confidence interval [CI]: 2.82–8.77, p < 0.001) and ever high alcohol consumption (OR: 2.33, 95% CI: 1.00–5.46, p = 0.050) as likely factors. Among 6318 PLHIV in the liver cirrhosis analysis, 151 (2%) developed cirrhosis (incidence rate = 0.82 per 100 person-years). Those HCV-antibody positive (hazard ratio [HR]: 5.54, 95% CI: 3.75–8.18, p < 0.001) and had high alcohol consumption (HR: 2.06, 95% CI: 1.23–3.45, p = 0.006) were associated with liver cirrhosis. HCV-antibody positive and high alcohol consumption are factors associated with high ALT. With raised ALT levels as a known factor associated with liver cirrhosis, greater efforts are required in managing ALT levels and reducing the risk of developing liver cirrhosis among those positive for HCV-antibody and those who consume alcohol.
KW - ALT elevations
KW - Asia-Pacific
KW - cirrhosis
KW - HIV
UR - http://www.scopus.com/inward/record.url?scp=85136124877&partnerID=8YFLogxK
U2 - 10.1002/jmv.28019
DO - 10.1002/jmv.28019
M3 - Article
C2 - 35869413
AN - SCOPUS:85136124877
SN - 0146-6615
VL - 94
SP - 5451
EP - 5464
JO - Journal of Medical Virology
JF - Journal of Medical Virology
IS - 11
ER -