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Current and Past Infections of HBV Do Not Increase Mortality in Patients With COVID-19
Terry Cheuk-Fung Yip1,2,3, Vincent Wai-Sun Wong1,2,3, Grace Chung-Yan Lui1,2,4
1Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong SAR, China.
Insights
Hepatitis B virus (HBV) infection did not increase the risk of liver injury or death in COVID-19 patients. This study found no significant association between current or past HBV infection and adverse outcomes in this population.
Area of Science:
- Hepatology
- Infectious Diseases
- Public Health
Background:
- Hepatitis B virus (HBV) infection is a global health concern.
- The interaction between HBV and COVID-19 outcomes requires further investigation.
- Understanding these interactions is crucial for managing patients with co-existing conditions.
Purpose of the Study:
- To compare the risk of acute liver injury and mortality in COVID-19 patients with current, past, or no HBV infection.
- To identify factors associated with acute liver injury in COVID-19 patients.
- To inform clinical management strategies for COVID-19 patients with HBV.
Main Methods:
- A territory-wide retrospective cohort study was conducted in Hong Kong.
- COVID-19 patients diagnosed between January 2020 and January 2021 were identified and analyzed.
- Exclusion criteria included hepatitis C infection or missing HBsAg results. Acute liver injury and mortality were primary outcomes.
Main Results:
- Of 5,639 patients, 6.3% had current HBV and 6.4% had past HBV infection.
- Acute liver injury occurred in 1.2% (no HBV), 2.3% (current HBV), and 3.1% (past HBV) of patients.
- Acute liver injury was associated with mortality (aHR, 2.45), but HBV infection status was not.
Conclusions:
- Current or past HBV infections were not associated with increased acute liver injury or mortality in COVID-19 patients.
- Hepatitis B virus coinfection does not appear to significantly worsen COVID-19 outcomes regarding liver injury and mortality.
- Further research may explore the long-term effects and specific management nuances.
Background And Aims:
We compared risk of acute liver injury and mortality in patients with COVID-19 and current, past, and no HBV infection.
Approach And Results:
This was a territory-wide retrospective cohort study in Hong Kong. Patients with COVID-19 between January 23, 2020, and January 1, 2021, were identified. Patients with hepatitis C or no HBsAg results were excluded. The primary outcome was mortality. Acute liver injury was defined as alanine aminotransferase or aspartate aminotransferase ≥2 × upper limit of normal (ULN; i.e., 80 U/L), with total bilirubin ≥2 × ULN (i.e., 2.2 mg/dL) and/or international normalized ratio ≥1.7. Of 5,639 patients included, 353 (6.3%) and 359 (6.4%) had current and past HBV infection, respectively. Compared to patients without known HBV exposure, current HBV-infected patients were older and more likely to have cirrhosis. Past HBV-infected patients were the oldest, and more had diabetes and cardiovascular disease. At a median follow-up of 14 (9-20) days, 138 (2.4%) patients died; acute liver injury occurred in 58 (1.2%), 8 (2.3%), and 11 (3.1%) patients with no, current, and past HBV infection, respectively. Acute liver injury (adjusted HR [aHR], 2.45; 95% CI, 1.52-3.96; P < 0.001), but not current (aHR, 1.29; 95% CI, 0.61-2.70; P = 0.507) or past (aHR, 0.90; 95% CI, 0.56-1.46; P = 0.681) HBV infection, was associated with mortality. Use of corticosteroid, antifungal, ribavirin, or lopinavir-ritonavir (adjusted OR [aOR], 2.55-5.63), but not current (aOR, 1.93; 95% CI, 0.88-4.24; P = 0.102) or past (aOR, 1.25; 95% CI, 0.62-2.55; P = 0.533) HBV infection, was associated with acute liver injury.
Conclusion:
Current or past HBV infections were not associated with more liver injury and mortality in COVID-19.
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