TY - JOUR
T1 - Chronic hepatitis-C infection in COVID-19 patients is associated with in-hospital mortality
AU - Ronderos, Diana
AU - Omar, Alaa Mabrouk Salem
AU - Abbas, Hafsa
AU - Makker, Jasbir
AU - Baiomi, Ahmed
AU - Sun, Haozhe
AU - Mantri, Nikhitha
AU - Choi, Yongsun
AU - Fortuzi, Ked
AU - Shin, Dongmin
AU - Patel, Harish
AU - Chilimuri, Sridhar
N1 - Publisher Copyright:
© 2021 The Author(s). Published by Baishideng Publishing Group Inc. All Rights Reserved.
PY - 2021
Y1 - 2021
N2 - BACKGROUND There is little evidence about the association of pre-existing hepatitis C infection (HCV) with outcomes in patients with coronavirus disease 2019 (COVID-19). AIM To assess the prevalence of history of HCV among patients with COVID-19 and to study the relationship of in-hospital mortality in relation with other predictors of poor outcomes in the presence or absence of COVID-19 induced acute liver injury. METHODS In a retrospective single-center study design, 1193 patients with COVID-19 infection were studied. Patients were then classified into those with and without a history of HCV, 50 (4.1%) and 1157 (95.9%) respectively. RESULTS Multivariate cox-regression models showed that age, HCV, D-Dimer, and ferritin were the only predictors of in-hospital mortality. Acute liver injury and fibrosis score (Fib-4 score) were not different between both groups. Multivariate coxregression model for liver profile revealed that aspartate aminotransferase/ alanine aminotransferase ratio, Fib-4 score, and HCV were predictors of inhospital mortality. After propensity score matching HCV was the only predictor of mortality in the multivariate cox-regression model. A model including HCV was found to add predictive value to clinical and laboratory parameters. CONCLUSION In patients with COVID-19, history of HCV infection leads to an accentuated severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virulence, irrespective of baseline comorbidities, admission laboratory variables, or COVID-19-induced liver injury, which may be related to extrahepatic effects of HCV leading to enhanced ACE-2/TMPRSS mechanisms of SARS-CoV-2 viral entry, baseline cytokine-mediated pro-inflammation, and endothelial dysfunction.
AB - BACKGROUND There is little evidence about the association of pre-existing hepatitis C infection (HCV) with outcomes in patients with coronavirus disease 2019 (COVID-19). AIM To assess the prevalence of history of HCV among patients with COVID-19 and to study the relationship of in-hospital mortality in relation with other predictors of poor outcomes in the presence or absence of COVID-19 induced acute liver injury. METHODS In a retrospective single-center study design, 1193 patients with COVID-19 infection were studied. Patients were then classified into those with and without a history of HCV, 50 (4.1%) and 1157 (95.9%) respectively. RESULTS Multivariate cox-regression models showed that age, HCV, D-Dimer, and ferritin were the only predictors of in-hospital mortality. Acute liver injury and fibrosis score (Fib-4 score) were not different between both groups. Multivariate coxregression model for liver profile revealed that aspartate aminotransferase/ alanine aminotransferase ratio, Fib-4 score, and HCV were predictors of inhospital mortality. After propensity score matching HCV was the only predictor of mortality in the multivariate cox-regression model. A model including HCV was found to add predictive value to clinical and laboratory parameters. CONCLUSION In patients with COVID-19, history of HCV infection leads to an accentuated severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virulence, irrespective of baseline comorbidities, admission laboratory variables, or COVID-19-induced liver injury, which may be related to extrahepatic effects of HCV leading to enhanced ACE-2/TMPRSS mechanisms of SARS-CoV-2 viral entry, baseline cytokine-mediated pro-inflammation, and endothelial dysfunction.
KW - Acute liver injury
KW - COVID-19
KW - Hepatitis C
KW - Mortality
KW - Seropositive
UR - http://www.scopus.com/inward/record.url?scp=85118938632&partnerID=8YFLogxK
U2 - 10.12998/wjcc.v9.i29.8749
DO - 10.12998/wjcc.v9.i29.8749
M3 - Article
AN - SCOPUS:85118938632
SN - 2307-8960
VL - 9
SP - 8749
EP - 8762
JO - World Journal of Clinical Cases
JF - World Journal of Clinical Cases
IS - 29
ER -