TY - JOUR
T1 - Hepatic Steatosis Is Associated with Increased Disease Severity and Liver Injury in Coronavirus Disease-19
AU - Chen, Vincent L.
AU - Hawa, Fadi
AU - Berinstein, Jeffrey A.
AU - Reddy, Chanakyaram A.
AU - Kassab, Ihab
AU - Platt, Kevin D.
AU - Hsu, Chia Yang
AU - Steiner, Calen A.
AU - Louissaint, Jeremy
AU - Gunaratnam, Naresh T.
AU - Sharma, Pratima
N1 - Funding Information:
VLC was supported by an AASLD Clinical, Translational and Outcomes Research Award. JL was supported by an NIH Training Grant in Epidemiology and Health Services (T32DK062708).
Publisher Copyright:
© 2020, Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2021/9
Y1 - 2021/9
N2 - Background: Coronavirus disease-2019 (COVID-19) is a global pandemic. Obesity has been associated with increased disease severity in COVID-19, and obesity is strongly associated with hepatic steatosis (HS). However, how HS alters the natural history of COVID-19 is not well characterized, especially in Western populations. Aims: To characterize the impact of HS on disease severity and liver injury in COVID-19. Methods: We examined the association between HS and disease severity in a single-center cohort study of hospitalized COVID-19 patients at Michigan Medicine. HS was defined by either hepatic steatosis index > 36 (for Asians) or > 39 (for non-Asians) or liver imaging demonstrating steatosis > 30 days before onset of COVID-19. The primary predictor was HS. The primary outcomes were severity of cardiopulmonary disease, transaminitis, jaundice, and portal hypertensive complications. Results: In a cohort of 342 patients, metabolic disease was highly prevalent including nearly 90% overweight. HS was associated with increased transaminitis and need for intubation, dialysis, and vasopressors. There was no association between HS and jaundice or portal hypertensive complications. In a sensitivity analysis including only patients with liver imaging > 30 days before onset of COVID-19, imaging evidence of hepatic steatosis remained associated with disease severity and risk of transaminitis. Conclusions: HS was associated with increased disease severity and transaminitis in COVID-19. HS may be relevant in predicting risk of complications related to COVID-19.
AB - Background: Coronavirus disease-2019 (COVID-19) is a global pandemic. Obesity has been associated with increased disease severity in COVID-19, and obesity is strongly associated with hepatic steatosis (HS). However, how HS alters the natural history of COVID-19 is not well characterized, especially in Western populations. Aims: To characterize the impact of HS on disease severity and liver injury in COVID-19. Methods: We examined the association between HS and disease severity in a single-center cohort study of hospitalized COVID-19 patients at Michigan Medicine. HS was defined by either hepatic steatosis index > 36 (for Asians) or > 39 (for non-Asians) or liver imaging demonstrating steatosis > 30 days before onset of COVID-19. The primary predictor was HS. The primary outcomes were severity of cardiopulmonary disease, transaminitis, jaundice, and portal hypertensive complications. Results: In a cohort of 342 patients, metabolic disease was highly prevalent including nearly 90% overweight. HS was associated with increased transaminitis and need for intubation, dialysis, and vasopressors. There was no association between HS and jaundice or portal hypertensive complications. In a sensitivity analysis including only patients with liver imaging > 30 days before onset of COVID-19, imaging evidence of hepatic steatosis remained associated with disease severity and risk of transaminitis. Conclusions: HS was associated with increased disease severity and transaminitis in COVID-19. HS may be relevant in predicting risk of complications related to COVID-19.
KW - Acute liver injury
KW - NAFLD
KW - Outcomes
KW - SARS-CoV-2
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U2 - 10.1007/s10620-020-06618-3
DO - 10.1007/s10620-020-06618-3
M3 - Article
C2 - 32980956
AN - SCOPUS:85091510725
SN - 0163-2116
VL - 66
SP - 3192
EP - 3198
JO - Digestive Diseases and Sciences
JF - Digestive Diseases and Sciences
IS - 9
ER -