Polymorphism impact on AGTR1 gene in Covid-19 patients in Babylon Province
NeuroQuantology
; 20(8):6196-6202, 2022.
Artigo
em Inglês
| EMBASE | ID: covidwho-2010515
ABSTRACT
Infection by the Covid-19 produces in people an illness of profoundly factor and erratic seriousness. The presence of continuous hereditary single nucleotide polymorphisms (SNPs) in the population could prompt a more prominent weakness to infections or an overstated provocative reaction. We concentrated on the relationship between SNP from AGTR1 gene and the seriousness of the infection created by the SARS-Cov-2 infection. Methods:
30 (18 of male and 12 of Female) Covid-19 patients with age range from 55-60 years were assembled in light of the seriousness of side effects.Results:
one SNP rs5186 in AGTR1 gene were related with the seriousness of illness. Our results were showed that the rs5186 (C) allele in AGTR1 gene is associated with increased risk for Covid 19 based on OR value homozygous allele CC has 2.5(0.7-8.5), allele C with allele frequency 20 more than control group, and with OR=2.5(1.5-5.9) with significant P values (P=0.03).
adult; allele; article; clinical article; controlled study; coronavirus disease 2019; female; gene frequency; genetic association; genetic polymorphism; genetic susceptibility; homozygosity; human; male; middle aged; side effect; single nucleotide polymorphism; angiotensin 1A receptor; endogenous compound
Texto completo:
Disponível
Coleções:
Bases de dados de organismos internacionais
Base de dados:
EMBASE
Tipo de estudo:
Estudo experimental
Idioma:
Inglês
Revista:
NeuroQuantology
Ano de publicação:
2022
Tipo de documento:
Artigo
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