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. 2023 Feb 1;227(3):344-352.
doi: 10.1093/infdis/jiac411.

Alpha to Omicron: Disease Severity and Clinical Outcomes of Major SARS-CoV-2 Variants

Affiliations

Alpha to Omicron: Disease Severity and Clinical Outcomes of Major SARS-CoV-2 Variants

Frank P Esper et al. J Infect Dis. .

Abstract

Background: Four severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants predominated in the United States since 2021. Understanding disease severity related to different SARS-CoV-2 variants remains limited.

Method: Viral genome analysis was performed on SARS-CoV-2 clinical isolates circulating March 2021 through March 2022 in Cleveland, Ohio. Major variants were correlated with disease severity and patient outcomes.

Results: In total 2779 patients identified with either Alpha (n 1153), Gamma (n 122), Delta (n 808), or Omicron variants (n 696) were selected for analysis. No difference in frequency of hospitalization, intensive care unit (ICU) admission, and death were found among Alpha, Gamma, and Delta variants. However, patients with Omicron infection were significantly less likely to be admitted to the hospital, require oxygen, or admission to the ICU (2 12.8, P .001; 2 21.6, P .002; 2 9.6, P .01, respectively). In patients whose vaccination status was known, a substantial number had breakthrough infections with Delta or Omicron variants (218/808 [26.9] and 513/696 [73.7], respectively). In breakthrough infections, hospitalization rate was similar regardless of variant by multivariate analysis. No difference in disease severity was identified between Omicron subvariants BA.1 and BA.2.

Conclusions: Disease severity associated with Alpha, Gamma, and Delta variants is comparable while Omicron infections are significantly less severe. Breakthrough disease is significantly more common in patients with Omicron infection.

Keywords: COVID-19; Delta; Omicron; SARS-CoV-2; clinical severity; variant.

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Conflict of interest statement

Potential conflicts of interest. D. D. R. performs collaborative research that is sponsored by industry collaborators BD, bioMerieux, Cepheid, Cleveland Diagnostics, Hologic, Luminex, Q-Linea, Qiagen, Roche, Specific Diagnostics, Thermo Fisher, and Vela; and is or has been on advisory boards for Luminex, Talis Biomedical, and Thermo Fisher. F. E. serves as consultant to Proctor and Gamble. All other authors report no potential conflicts.

Figures

Figure 1.
Figure 1.
Weekly prevalence of major severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) over the study period (11 March 2021 through 22 March 2022). Isolates of screened clinical samples were determined and categorized into variant groups. Isolates that did not categorize into the 3 major variant groups (eg, epsilon, lambda, etc.) were designated as other. Weekly prevalence for each variant is displayed and raw totals are quantified.
Figure 2.
Figure 2.
Comparison of laboratory abnormalities among different SARS-CoV-2 variants. Box and whiskers plot displaying first through 99th percentile results among patients infected with 1 of the 4 major SARS-CoV-2 variants. Horizontal lines represent mean value. P values for ANOVA performed at a significance level of .05 is displayed. Abbreviations: CRP, C-reactive protein; PLT, platlets; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2; WBC, white blood cells; ALC, absolute lymphocyte count.

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