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. 2020 Nov 28;553:131–134. doi: 10.1016/j.virol.2020.11.012

Table 1.

The COVID-19 progression, the intensity of anti-NP response, and liver injury after acute SARS-CoV-2 infection in patients with or without chronic hepatitis B.

All patients (n = 67) COVID-19 patients with HBsAg positive (n = 7) COVID-19 patients without HBV (n = 60) p-value
HBsAg positive 7 (10.4) 7 (100.0) 0
HBeAg positive 0 0 0
Comorbidity besides Hepatitis B 21/67 (31.3) 2/7 (28.6) 19/60 (31.7) >0.999
 Pulmonary disease † 3 (4.5) 1 (14.3) 2 (3.3)
 Diabetes and/or Hypertension 15 (22.3) 1 (14.3) 14 (23.3)
 Hyperlipemia and/or CHD 3 (4.5) 0 3 (5.0)
Liver injury at admission # 5/67 (7.5) 0 5/60 (8.3) >0.999
Liver injury admission & during hospitalization 19/67 (28.4) 3/7 (42.9) 16/60 (26.7) 0.395
Liver injury type # 0.432
 Hepatocellular 3/67 (4.5) 1/7 (14.3) 2/60 (3.3)
 Ductular 11/67 (16.4) 2/7 (28.6) 9/60 (15.0)
 Mix 5/67 (7.5) 0 5/60 (8.3)
COVID-19 progression after admission 14/67 (20.9) 2/7 (28.6) 12/60 (20.0) 0.63
COVID-19 stable after admission 53/67 (79.1) 5/7 (71.4) 48/60 (80.0) 0.63
Shedding time of SARS-CoV-2, days* 25.0 ± 9.4 27.1 ± 9.0 24.7 ± 9.5 0.52
anti-NP-IgM development 28/58 (48.3) 4/7 (57.1) 24/51 (47.1) 0.701
 weak-response 10/58 (17.2) 1/7 (14.3) 9/51 (17.6) >0.999
 strong-response 18/58 (31.0) 3/7 (42.9) 15/51 (29.4) 0.665
Days of anti-NP-IgM first detectable § 12.3 ± 4.4 12.5 ± 3.7 12.2 ± 4.6 0.909
anti-NP-IgG development 45/54 (83.3) 6/7 (85.7) 39/47 (83.0) >0.999
 weak-response 33/54 (61.1) 4/7 (57.1) 29/47 (61.7) >0.999
 strong-response 12/54 (22.2) 2/7 (28.6) 10/47 (21.3) 0.645
Days of anti-NP-IgG first detectable § 14.3 ± 4.9 15.8 ± 6.2 14.0 ± 4.7 0.405
Duration of Hospitalization, days 21.0 ± 9.1 25.0 ± 10.7 20.6 ± 8.9 0.228
COVID-19 course, days 27.6 ± 9.2 32.0 ± 10.4 27.0 ± 9.0 0.178
Discharge 67/67 (100.0) 7/7 (100.0) 60/60 (100.0) >0.999

† Includes one patient with bronchiectasis and chronic bronchitis, one patient with pulmonary tuberculosis, and one patient with asthma. CHD, coronary heart disease. # In this study, we defined ALT and/or AST more than 3 times of the upper limit units (ULN), GGT, and/or TBIL more than 2 × ULN as liver injury. ALT and/or AST over 3 × ULN were classified as hepatocellular type, GGT and/or TBIL over 2 × ULN as ductular type, while combined with ALT and/or AST over 3 × ULN and GGT and/or TBIL over 2 × ULN as mix type. * Virus shedding in any type of sample, including nasopharyngeal swab, sputum, and stool. § Days from symptom onset. Data are mean ± standard deviation or n/N (%), where N is the total number of patients with available data.