tetano
Editor, Senior Moderator
Viral Immunol
. 2023 Nov 29.
doi: 10.1089/vim.2023.0091. Online ahead of print. Relationship Between Human FC γ RIIA rs1801274 G Allele and Risk of Death Among Different SARS-CoV-2 Variants
Nazanin Moghaddam[SUP] 1 [/SUP], Mohammad Taghi Goodarzi[SUP] 1 [/SUP], Sina Moghaddam[SUP] 2 [/SUP], Fatemeh Sakhaee[SUP] 2 [/SUP], Iraj Ahmadi[SUP] 3 [/SUP], Enayat Anvari[SUP] 4 [/SUP], Abolfazl Fateh[SUP] 2 5 [/SUP]
Affiliations
Coronavirus disease 2019 (COVID-19), the illness caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), emerged in late 2019 and spread very quickly across the world. Different responses to infections have been related to fragment crystallizable gamma-receptor II alpha (FcγRIIA) polymorphisms. The purpose of this investigation was to determine if FCγRIIA rs1801274 polymorphism was related to COVID-19 mortality among different variants of SARS-CoV-2. The FCγRIIA rs1801274 polymorphism was genotyped using the polymerase chain reaction-restriction fragment length polymorphism technique in 1,734 recovered and 1,450 deceased patients. Deceased patients had significantly higher minor allele frequency of the FCγRIIA rs1801274 G allele than in the recovered cases. The COVID-19 mortality was associated with FCγRIIA rs1801274 GG and AG genotypes in the Delta variant and with FCγRIIA rs1801274 GG genotypes in the Alpha and Omicron BA.5 variants. The reverse transcription-quantitative polymerase chain reaction Ct values revealed statistically significant differences between individuals with a G allele and those with an A allele. In conclusion, among the several SARS-CoV-2 variants, there may be a correlation between the mortality rate of COVID-19 and the G allele of FCγRIIA rs1801274. To confirm our findings, thorough research is still required.
Keywords: COVID-19; FcγRIIA; RT-qPCR Ct values; SARS-CoV-2 variants.
. 2023 Nov 29.
doi: 10.1089/vim.2023.0091. Online ahead of print. Relationship Between Human FC γ RIIA rs1801274 G Allele and Risk of Death Among Different SARS-CoV-2 Variants
Nazanin Moghaddam[SUP] 1 [/SUP], Mohammad Taghi Goodarzi[SUP] 1 [/SUP], Sina Moghaddam[SUP] 2 [/SUP], Fatemeh Sakhaee[SUP] 2 [/SUP], Iraj Ahmadi[SUP] 3 [/SUP], Enayat Anvari[SUP] 4 [/SUP], Abolfazl Fateh[SUP] 2 5 [/SUP]
Affiliations
- PMID: 38029355
- DOI: 10.1089/vim.2023.0091
Coronavirus disease 2019 (COVID-19), the illness caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), emerged in late 2019 and spread very quickly across the world. Different responses to infections have been related to fragment crystallizable gamma-receptor II alpha (FcγRIIA) polymorphisms. The purpose of this investigation was to determine if FCγRIIA rs1801274 polymorphism was related to COVID-19 mortality among different variants of SARS-CoV-2. The FCγRIIA rs1801274 polymorphism was genotyped using the polymerase chain reaction-restriction fragment length polymorphism technique in 1,734 recovered and 1,450 deceased patients. Deceased patients had significantly higher minor allele frequency of the FCγRIIA rs1801274 G allele than in the recovered cases. The COVID-19 mortality was associated with FCγRIIA rs1801274 GG and AG genotypes in the Delta variant and with FCγRIIA rs1801274 GG genotypes in the Alpha and Omicron BA.5 variants. The reverse transcription-quantitative polymerase chain reaction Ct values revealed statistically significant differences between individuals with a G allele and those with an A allele. In conclusion, among the several SARS-CoV-2 variants, there may be a correlation between the mortality rate of COVID-19 and the G allele of FCγRIIA rs1801274. To confirm our findings, thorough research is still required.
Keywords: COVID-19; FcγRIIA; RT-qPCR Ct values; SARS-CoV-2 variants.