Role of ACE2 and TMPRSS2 polymorphisms in clinical severity and outcomes of COVID-19 in Egypt

African Journal of Laboratory Medicine

 
 
Field Value
 
Title Role of ACE2 and TMPRSS2 polymorphisms in clinical severity and outcomes of COVID-19 in Egypt
 
Creator Samy, Walaa Gaber, Osama A. Amer, Rania M. El-Deeb, Nahawand A. Abdelmoaty, Ahmed A. Sharaf, Ahmed L. El-Gebaly, Ahmed M. Mosbah, Rasha Alsadik, Maha E. Fawzy, Amal Ahmed, Alshymaa A.
 
Subject Molecular; genetics; virus; susceptability ACE2 gene; TMPRSS2 gene; single nucleotide polymorphisms; COVID-19; severity; outcome
Description Background: The clinical presentations of coronavirus disease 2019 (COVID-19) exhibit significant variation, ranging from asymptomatic cases to mortality resulting from severe pneumonia. Host genetics can partially explain this variation.Objective: This study evaluated possible associations between severity and outcome of COVID-19 and single nucleotide polymorphism (SNP) rs2285666 in the ACE2 gene and SNP rs2070788 in the TMPRSS2 gene.Methods: The study included a sample of 100 consecutive adult patients admitted to the COVID-19 Isolation and Intensive Care Units of the Zagazig University Hospitals, Zagazig, Egypt from July 2021 to November 2021. For rs2285666, polymerase chain reaction-restriction fragment length polymorphism was carried out. For rs2070788, real-time polymerase chain reaction was performed.Results: For rs2285666, the GA genotype was the most frequent among female patients (39% [16/41]) and the A genotype was more prevalent among male patients (54.2% [32/59]). For rs2070788, the AA genotype was the most frequent among all patients (46% [46/100]). No rs2285666 or rs2070788 genotypes or allele frequencies had significant associations with either severity or outcomes of patients.Conclusion: This study found no significant associations of COVID-19 severity or outcomes of patients with genotypes or allele frequencies of the rs2285666 SNP in the ACE2 gene or the rs2070788 SNP of the TMPRSS2 gene. The search for other genetic associations with COVID-19 infection is still required.What this study adds: The study reveals that host genetics explain the variation observed in the disease. Specific genetic variants can confer either increased susceptibility or resistance to the disease.
 
Publisher AOSIS
 
Contributor non
Date 2024-08-27
 
Type info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion — molecular genetics
Format text/html application/epub+zip text/xml application/pdf application/pdf
Identifier 10.4102/ajlm.v13i1.2375
 
Source African Journal of Laboratory Medicine; Vol 13, No 1 (2024); 8 pages 2225-2010 2225-2002
 
Language eng
 
Relation
The following web links (URLs) may trigger a file download or direct you to an alternative webpage to gain access to a publication file format of the published article:

https://ajlmonline.org/index.php/ajlm/article/view/2375/2949 https://ajlmonline.org/index.php/ajlm/article/view/2375/2950 https://ajlmonline.org/index.php/ajlm/article/view/2375/2951 https://ajlmonline.org/index.php/ajlm/article/view/2375/2957 https://ajlmonline.org/index.php/ajlm/article/view/2375/2952
 
Coverage Zagzig; El-Sharkia; Egypt COVID19 panadimic adults; both genders; same ethnicity
Rights Copyright (c) 2024 Walaa Samy, Osama A. Gaber, Rania M. Amer, Nahawand A. El-Deeb, Ahmed A. Abdelmoaty, Ahmed L. Sharaf, Ahmed M. El-Gebaly, Rasha Mosbah, Maha E. Alsadik, Amal Fawzy, Alshymaa A. Ahmed https://creativecommons.org/licenses/by/4.0
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