基因分型
基因型
医学
2019年冠状病毒病(COVID-19)
肥胖
白细胞介素17
免疫学
代谢综合征
人口
多态性(计算机科学)
疾病
内科学
基因
细胞因子
遗传学
生物
传染病(医学专业)
环境卫生
作者
Richard Salama-Frisbie,Cinthia Analí Molina-Flores,Arguiñe Ivonne Urraza-Robledo,Maria Elena Gutiérrez-Pérez,Alberto Alejandro Miranda-Pérez,Alhi A Gutiérrez-Salas,Jorge Haro-Santa Cruz,Francisco Carlos López-Márquez
标识
DOI:10.1089/jir.2023.0101
摘要
Coronavirus disease 2019 (COVID-19) is caused by Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV2). COVID-19 can cause a cytokine release syndrome in which cytokines, including interleukin 17 (IL-17), are massively secreted in response to a specific stimulus. This can contribute to mortality and severe forms of COVID-19. The study aimed to determine the association of SARS-CoV2 infection with the IL-17A rs2275913 and IL-17F rs763780 variants, as well as with the associated comorbidities in COVID-19-positive Mexican patients. The study included 178 patients positive to COVID-19 and 177 COVID-19 negative subjects. For genotyping, the samples were amplified with a TaqMan® probe. There was no association between the AA genotype and A allele of IL-17A variant or the IL-17F C allele with the presence of COVID-19. In regard to comorbidities, a statistically significant association was found between IL-17A rs2275913 AA genotype and hypertension, as well as with the presence of obesity (P = 0.003, OR 23, 95% CI: 2.97-178.092 and P = 0.025, OR 28, 95% CI: 1.52-178.029, respectively) in patients with COVID-19. In conclusion, rs2275913 IL-17A polymorphism in COVID-19 patients seems to confer a higher susceptibility to the presence of hypertension and obesity, increasing the risk of premature cardiovascular disease in this population. However, more studies should be conducted for a better understanding of their relation.
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