SARS-CoV-2 Variants of Concern and Clinical Severity in the Mexican Pediatric Population

Author:

Maldonado-Cabrera Anahí12ORCID,Colin-Vilchis Jesus Alejandro3,Haque Ubydul45ORCID,Velazquez Carlos1,Alvarez Villaseñor Andrea Socorro6,Magdaleno-Márquez Luis Eduardo7ORCID,Calleros-Muñoz Carlos Iván8,Figueroa-Enríquez Karen Fernanda8,Angulo-Molina Aracely19,Gallego-Hernández Ana Lucía1

Affiliation:

1. Department of Chemical Biological Sciences, University of Sonora, Hermosillo 83000, Mexico

2. Department of Epidemiology, Family Medicine Unit No. 37, Mexican Social Security Institute (IMSS), Hermosillo 83260, Mexico

3. Department of Medicine, Autonomous University of the Mexico State, Toluca 50000, Mexico

4. Rutgers Global Health Institute, New Brunswick, NJ 08901, USA

5. Department of Biostatistics and Epidemiology, School of Public Health, Rutgers University, Piscataway, NJ 08854, USA

6. Coordination of Medical Health Research, Mexican Social Security Institute (IMSS), La Paz 23920, Mexico

7. University Center for Biological and Agricultural Sciences, University of Guadalajara, Zapopan 44100, Mexico

8. Department of Agriculture, University of Sonora, Hermosillo 83323, Mexico

9. School of Life Sciences, University of Applied Sciences and Arts Northwestern Switzerland, 4132 Muttenz, Switzerland

Abstract

The emergence of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) variants of concern (VOCs) presents global heterogeneity, and their relative effect on pediatric severity is still limited. In this study, we associate VOCs with pediatric clinical severity outcomes in Mexico. Bioinformatics methods were used to characterize VOCs and single amino acid (aa) mutations in 75,348 SARS-CoV-2 genetic sequences from February 2020 to October 2022. High-predominance VOCs groups were calculated and subsequently associated with 372,989 COVID-19 clinical pediatric outcomes. We identified 21 high-frequency mutations related to Omicron lineages with an increased prevalence in pediatric sequences compared to adults. Alpha and the other lineages had a significant increase in case fatality rate (CFR), intensive critical unit (ICU) admission, and automated mechanical ventilation (AMV). Furthermore, a logistic model with age-adjusted variables estimated an increased risk of hospitalization, ICU/AMV, and death in Gamma and Alpha, in contrast to the other lineages. We found that, regardless of the VOCs lineage, infant patients presented the worst severity prognoses. Our findings improve the understanding of the impact of VOCs on pediatric patients across time, regions, and clinical outcomes. Enhanced understanding of the pediatric severity for VOCs would enable the development and improvement of public health strategies worldwide.

Funder

Department of Chemical-Biological Science

Interdisciplinary Faculty of Biological

Health Sciences of the University of Sonora

Publisher

MDPI AG

Subject

Infectious Diseases

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