Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Meta-Analysis
. 2021 Apr;73(4):1521-1530.
doi: 10.1002/hep.31472.

Elevated Liver Biochemistries in Hospitalized Chinese Patients With Severe COVID-19: Systematic Review and Meta-analysis

Affiliations
Meta-Analysis

Elevated Liver Biochemistries in Hospitalized Chinese Patients With Severe COVID-19: Systematic Review and Meta-analysis

Alexander J Kovalic et al. Hepatology. 2021 Apr.

Abstract

Background and aims: Several recent studies have reported an abnormal liver chemistry profile among patients with coronavirus disease 2019 (COVID-19), although its clinical significance remains unknown.

Approach and results: This systematic review and meta-analysis identified six studies of 586 patients delineating liver chemistries among patients with severe/critical illness versus mild cases of COVID-19 infection. Patients with severe/critical illness with COVID-19 infection have increased prevalence of coronary artery disease, cerebrovascular disease, and chronic obstructive pulmonary disease as compared with mild cases. A significant association between severe/critical COVID-19 infections with elevations in aspartate aminotransferase (pooled mean difference [MD], 11.70 U/L; 95% confidence interval [CI], 2.97, 20.43; P = 0.009), elevated total bilirubin (pooled MD, 0.14 mg/dL; 95% CI, 0.06, 0.22; P = 0.0005), and decreased albumin (pooled MD, -0.68 g/L; 95% CI, -0.81, -0.55; P < 0.00001) was noted. There was also a trend toward elevated alanine aminotransferase levels among these severe cases (pooled MD, 8.84 U/L; 95% CI, -2.28, 19.97; P = 0.12); however, this did not reach statistical significance. More severe/critically ill cases were associated with leukocytosis, neutrophilia, lymphopenia, elevated creatinine kinase, elevated lactate dehydrogenase (LDH), and elevated prothrombin time (PT).

Conclusions: Comorbidities, including coronary artery disease, cerebrovascular disease and chronic obstructive pulmonary disease, are more prevalent in hospitalized Chinese patients with severe/critical illness from COVID-19, and these patients are more likely to manifest with abnormal liver chemistries. Further prospective studies are crucial to understand the pathophysiologic mechanisms underlying the hepatic manifestations of the novel COVID-19 infection and its clinical significance.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
Study flow diagram.
Fig. 2
Fig. 2
Forest plot comparison of demographic data with respect to gender, hypertension, diabetes mellitus, coronary artery disease, and cerebrovascular disease [Figure 2A] as well as smoking, chronic obstructive pulmonary disease, chronic liver disease, chronic kidney disease, malignancy, and ACEi/ARB treatment [Figure 2B] among patients with severe/critical illness versus mild COVID‐19 infection.
Fig. 3
Fig. 3
Forest plot comparison of liver chemistries among patients with severe/critical illness versus mild COVID‐19 infection. Abbreviation; IV, inverse variance.
Fig. 4
Fig. 4
Forest plot comparison of mortality reported among patients with severe/critical illness versus mild COVID‐19 infection.

Comment in

References

    1. Sohrabi C, Alsafi Z, O'Neill N, Khan M, Kerwan A, Al‐Jabir A, et al. World Health Organization declares global emergency: a review of the 2019 novel coronavirus (COVID‐19). Int J Surg 2020;76:71‐76. - PMC - PubMed
    1. Zhang C, Shi L, Wang FS. Liver injury in COVID‐19: management and challenges. Lancet Gastroenterol Hepatol 2020;5:428‐430. - PMC - PubMed
    1. Moher D, Liberati A, Tetzlaff J, Altman DG, PRISMA Group . Preferred reporting items for systematic reviews and meta‐analyses: the PRISMA statement. Ann Intern Med 2009;151:264‐269, w64. - PubMed
    1. Stroup DF, Berlin JA, Morton SC, Olkin I, Williamson GD, Rennie D, et al. Meta‐analysis of observational studies in epidemiology: a proposal for reporting. Meta‐analysis of Observational Studies in Epidemiology (MOOSE) group. JAMA 2000;283:2008‐2012. - PubMed
    1. Wells G, Shea B, O’Connell D, Peterson J, Welch V, Losos M, et al. The Newcastle‐Ottawa Scale [NOS] for assessing the quality of nonrandomised studies in meta‐analyses. 2013. http://www.ohri.ca/programs/clinical_epidemiology/oxford.asp. Accessed March 30, 2020.

MeSH terms