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Multicenter Study
. 2020 Jul;115(7):1075-1083.
doi: 10.14309/ajg.0000000000000717.

Liver Enzyme Elevation in Coronavirus Disease 2019: A Multicenter, Retrospective, Cross-Sectional Study

Affiliations
Multicenter Study

Liver Enzyme Elevation in Coronavirus Disease 2019: A Multicenter, Retrospective, Cross-Sectional Study

Shao-Rui Hao et al. Am J Gastroenterol. 2020 Jul.

Abstract

Introduction: Elevated liver enzyme levels are observed in patients with coronavirus disease 2019 (COVID-19); however, these features have not been characterized.

Methods: Hospitalized patients with COVID-19 in Zhejiang Province, China, from January 17 to February 12, 2020, were enrolled. Liver enzyme level elevation was defined as alanine aminotransferase level >35 U/L for men and 25 U/L for women at admission. Patients with normal alanine aminotransferase levels were included in the control group. Reverse transcription polymerase chain reaction was used to confirm severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, and patients symptomatic with SARS-CoV-2 infection were defined as patients with COVID-19. Epidemiological, demographic, clinical, laboratory, treatment, and outcome data were collected and compared.

Results: Of 788 patients with COVID-19, 222 (28.2%) patients had elevated liver enzyme levels (median [interquartile range {IQR}] age, 47.0 [35.0-55.0] years; 40.5% women). Being male, overweight, and smoking increased the risk of liver enzyme level elevation. The liver enzyme level elevation group had lesser pharyngalgia and more diarrhea than the control group. The median time from illness onset to admission was 3 days for liver enzyme level elevation groups (IQR, 2-6), whereas the median hospitalization time for 86 (38.7%) discharged patients was 13 days (IQR, 11-16). No differences in disease severity and clinical outcomes were noted between the groups.

Discussion: We found that 28.2% of patients with COVID-19 presented with elevated liver enzyme levels on admission, which could partially be related to SARS-CoV-2 infection. Male patients had a higher risk of liver enzyme level elevation. With early medical intervention, liver enzyme level elevation did not worsen the outcomes of patients with COVID-19.

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Conflict of interest statement

Guarantor of the article: Shao-Rui Hao, MD, Shan-Yan Zhang, MD, Jiang-Shan Lian, MD, Xi Jin, MD, and Cheng-Yin Ye, PhD, contributed equally to this article. Yi-Da Yang, MD, accepts full responsibility for the conduct of the study and had full access to the data and control of the decision to publish.

Specific author contributions: Y.-D.Y., T.-B.L., J.-F.S., and L.-J.L. designed the study. S.-R.H. and S.-Y.Z. managed the full deidentified data set. S.-R.H. and C.-Y.Y. performed the statistical analyses. S.-R.H. and J.-S.L. authored the initial draft of the manuscript. X.J. and Y.-D.Y. critically revised the manuscript. All authors were involved in the review and interpretation of data and approved the final copy.

Financial support: This work was supported by National Natural Science Foundation of China (81700549) and National Major Science and Technology Research Projects for the Control and Prevention of Major Infectious Diseases in China (2017ZX10202202).

Potential competing interests: All the authors have no conflict of interest to declare.

Figures

Figure 1.
Figure 1.
Kaplan-Meier analysis showed no differences in hospitalization time between the liver enzyme elevation group and the control group.
Figure 2.
Figure 2.
The Sankey diagram showing the status flow of all 788 patients with COVID-19 by the final follow-up. Columns on the left stand for disease severity and corresponding number of patients with COVID-19 on admission, “L” stands for the liver enzyme elevation group, “N” stands for control group. Columns on the right stand for patient status and relative number by the final follow-up on February 12, 2020. COVID-19 = coronavirus disease 2019.

Comment in

  • Elevated Liver Chemistries in COVID-19-Is It Not a Concern?
    Kumar K, Kulkarni A. Kumar K, et al. Am J Gastroenterol. 2021 Feb 1;116(2):424. doi: 10.14309/ajg.0000000000000914. Am J Gastroenterol. 2021. PMID: 32947321 Free PMC article. No abstract available.
  • Reply to Kumar and Kulkarni.
    Hao S, Yang Y. Hao S, et al. Am J Gastroenterol. 2021 Feb 1;116(2):424-425. doi: 10.14309/ajg.0000000000001067. Am J Gastroenterol. 2021. PMID: 33284185 No abstract available.

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