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The Impact of Liver Chemistries on Respiratory Failure Among Hemodialysis Patients with COVID-19 During the Omicron Wave

Overview
Journal Intern Med
Specialty General Medicine
Date 2023 Jul 5
PMID 37407459
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Abstract

Objective Although the coronavirus disease 2019 (COVID-19) Omicron variant causes less severe symptoms than previous variants, early indicators for respiratory failure are needed in hemodialysis patients, who have a higher mortality rate than the general population. Liver chemistries are known to reflect the severity of COVID-19 in the general population. This study explored the early indicators for worsened respiratory failure based on patient characteristics, including liver chemistries. Methods This retrospective study included 117 patients admitted for COVID-19 during the Omicron wave. Respiratory failure was defined as oxygen requirement during treatment. Information on the symptoms and clinical characteristics, including liver chemistries [aspartate aminotransferase (AST) and alanine aminotransferase (ALT)], at admission was collected. Results Thirty-five patients (29.9%) required oxygen supply during treatment. In the multivariate logistic regression analyses, AST [odds ratio (OR) 1.06, 95% confidence interval (CI) 1.00-1.13, p=0.029], ALT (OR 1.09, 95% CI 1.02-1.18, p=0.009), and moderate COVID-19 illness (Model including AST, OR 6.95, 95% CI 2.23-23.17, p<0.001; Model including ALT, OR 7.19, 95% CI 2.21-25.22, p=0.001) were independent predictors for respiratory failure. Based on the cutoff values determined by the receiver operating characteristic curve, higher AST (≥23 IU/L) and ALT levels (≥14 IU/L) were also independently associated with respiratory failure (higher AST: 64.3% vs. 18.8%, OR 3.44, 95% CI 1.08-11.10, p=0.035; higher ALT: 48.8% vs. 19.7%, OR 4.23, 95% CI 1.34-14.52, p=0.013, respectively). Conclusion The measurement of AST and ALT levels at baseline may help predict oxygen requirement in hemodialysis patients with COVID-19.

References
1.
Hsu C, Weiner D, Aweh G, Miskulin D, Manley H, Stewart C . COVID-19 Among US Dialysis Patients: Risk Factors and Outcomes From a National Dialysis Provider. Am J Kidney Dis. 2021; 77(5):748-756.e1. PMC: 7816961. DOI: 10.1053/j.ajkd.2021.01.003. View

2.
Meng B, Abdullahi A, Ferreira I, Goonawardane N, Saito A, Kimura I . Altered TMPRSS2 usage by SARS-CoV-2 Omicron impacts infectivity and fusogenicity. Nature. 2022; 603(7902):706-714. PMC: 8942856. DOI: 10.1038/s41586-022-04474-x. View

3.
Maslo C, Friedland R, Toubkin M, Laubscher A, Akaloo T, Kama B . Characteristics and Outcomes of Hospitalized Patients in South Africa During the COVID-19 Omicron Wave Compared With Previous Waves. JAMA. 2021; 327(6):583-584. PMC: 8719272. DOI: 10.1001/jama.2021.24868. View

4.
Ono K, Ono T, Matsumata T . The pathogenesis of decreased aspartate aminotransferase and alanine aminotransferase activity in the plasma of hemodialysis patients: the role of vitamin B6 deficiency. Clin Nephrol. 1995; 43(6):405-8. View

5.
Nardo A, Schneeweiss-Gleixner M, Bakail M, Dixon E, Lax S, Trauner M . Pathophysiological mechanisms of liver injury in COVID-19. Liver Int. 2020; 41(1):20-32. PMC: 7753756. DOI: 10.1111/liv.14730. View