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Front Med (Lausanne) . Allelic Variants Within the ABO Blood Group Phenotype Confer Protection Against Critical COVID-19 Hospital Presentation

tetano

Editor, Senior Moderator
Front Med (Lausanne)


. 2022 Jan 13;8:759648.
doi: 10.3389/fmed.2021.759648. eCollection 2021.
Allelic Variants Within the ABO Blood Group Phenotype Confer Protection Against Critical COVID-19 Hospital Presentation


Herbert F Jelinek[SUP] 1 2 3 [/SUP], Mira Mousa[SUP] 1 4 [/SUP], Nawal Alkaabi[SUP] 5 [/SUP], Eman Alefishat[SUP] 1 6 [/SUP], Gihan Daw Elbait[SUP] 1 [/SUP], Hussein Kannout[SUP] 1 [/SUP], Hiba AlHumaidan[SUP] 7 [/SUP], Francis Amirtharaj Selvaraj[SUP] 7 [/SUP], Hala Imambaccus[SUP] 7 [/SUP], Stefan Weber[SUP] 7 [/SUP], Maimunah Uddin[SUP] 5 [/SUP], Fatema Abdulkarim[SUP] 8 [/SUP], Bassam Mahboub[SUP] 8 [/SUP], Guan Tay[SUP] 1 9 10 [/SUP], Habiba Alsafar[SUP] 1 2 11 [/SUP]



Affiliations

Abstract

Introduction: Coronavirus disease 2019 (COVID-19) disease severity differs widely due to numerous factors including ABO gene-derived susceptibility or resistance. The objective of this study was to investigate the association of the ABO blood group and genetic variations of the ABO gene with COVID-19 severity in a heterogeneous hospital population sample from the United Arab Emirates, with the use of an epidemiological and candidate gene approach from a genome-wide association study (GWAS). Methods: In this cross-sectional study, a total of 646 participants who tested positive for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) were recruited from multiple hospitals and population-based (quarantine camps) recruitment sites from March 2020 to February 2021. The participants were divided into two groups based on the severity of COVID-19: noncritical (n = 453) and critical [intensive care unit (ICU) patients] (n = 193), as per the COVID-19 Reporting and Data System (CO-RADS) classification. The multivariate logistic regression analysis demonstrated the association of ABO blood type as well as circulating anti-A antibodies and anti-B antibodies as well as A and B antigens, in association with critical COVID-19 hospital presentation. A candidate gene analysis approach was conducted from a GWAS where we examined 240 single nucleotide polymorphisms (SNPs) (position in chr9: 136125788-136150617) in the ABO gene, in association with critical COVID-19 hospital presentation. Results: Patients with blood group O [odds ratio (OR): 0.51 (0.33, 0.79); p = 0.003] were less likely to develop critical COVID-19 symptoms. Eight alleles have been identified to be associated with a protective effect of blood group O in ABO 3'untranslated region (UTR): rs199969472 (p = 0.0052), rs34266669 (p = 0.0052), rs76700116 (p = 0.0052), rs7849280 (p = 0.0052), rs34039247 (p = 0.0104), rs10901251 (p = 0.0165), rs9411475 (p = 0.0377), and rs13291798 (p = 0.0377). Conclusion: Our findings suggest that there are novel allelic variants that link genetic variants of the ABO gene and ABO blood groups contributing to the reduced risk of critical COVID-19 disease. This study is the first study to combine genetic and serological evidence of the involvement of the ABO blood groups and the ABO gene allelic associations with COVID-19 severity within the Middle Eastern population.

Keywords: ABO blood group; COVID-19 pandemic; Middle East; SARS-CoV-2; UAE; disease severity; infection–immunology.
 
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