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IFNL4 genetic variant can predispose to COVID-19.
Saponi-Cortes, Jose Maria R; Rivas, Maria Dolores; Calle-Alonso, Fernando; Sanchez, Juan F; Costo, Alberto; Martin, Carlos; Zamorano, Jose.
  • Saponi-Cortes JMR; Servicio de Medicina Interna, Complejo Hospitalario Universitario de Caceres, Caceres, Spain.
  • Rivas MD; Unidad de Investigacion, Complejo Hospitalario Universitario de Caceres, Avenida Pablo Naranjo s/n, 10003, Caceres, Spain.
  • Calle-Alonso F; Departamento de Didactica de Matematicas, Universidad de Extremadura, Caceres, Spain.
  • Sanchez JF; Servicio de Medicina Interna, Complejo Hospitalario Universitario de Caceres, Caceres, Spain.
  • Costo A; Servicio de Medicina Interna, Complejo Hospitalario Universitario de Caceres, Caceres, Spain.
  • Martin C; Servicio de Medicina Interna, Complejo Hospitalario Universitario de Caceres, Caceres, Spain.
  • Zamorano J; Unidad de Investigacion, Complejo Hospitalario Universitario de Caceres, Avenida Pablo Naranjo s/n, 10003, Caceres, Spain. jose.zamorano@salud-juntaex.es.
Sci Rep ; 11(1): 21185, 2021 10 27.
Article in English | MEDLINE | ID: covidwho-1493214
Preprint
This scientific journal article is probably based on a previously available preprint. It has been identified through a machine matching algorithm, human confirmation is still pending.
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ABSTRACT
Interferon lambda 4 (IFNλ4) has shown antiviral activity against RNA viruses, including some coronaviruses. Besides, genetic variants of IFNL4 can be predictive of the clearance of RNA viruses. However, little is known about the effect of these genetic variants on SARS-CoV-2 infection. In this study, we investigated whether there was a relationship of the rs12979860 polymorphism of IFNL4 with COVID-19. We found that the T allele of rs12979860 was overexpressed in COVID-19 patients with regard to the general population without this disease (36.16% vs. 26.40%, p = 6.4 × 10-4; OR 0.633 C vs T; 95% CI 0.487, 0.824), suggesting that this allele could be a risk factor for COVID-19. Accordingly, the CC genotype was significantly lower in COVID-19 patients compared to controls (37.85% vs. 55.51%, p = 8 × 10-5; OR 0.488; 95% CI 0.342, 0.698). These results were not affected by sex, age, and disease severity in patients with COVID-19. Our findings suggest that, like other infectious diseases caused by RNA viruses, genetic variants of IFNL4 can predispose to COVID-19. Confirmation of our results may contribute to better understanding the mechanisms of this disease.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Interleukins / Polymorphism, Single Nucleotide / SARS-CoV-2 / COVID-19 Type of study: Observational study / Prognostic study Topics: Variants Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: English Journal: Sci Rep Year: 2021 Document Type: Article Affiliation country: S41598-021-00747-z

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Interleukins / Polymorphism, Single Nucleotide / SARS-CoV-2 / COVID-19 Type of study: Observational study / Prognostic study Topics: Variants Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: English Journal: Sci Rep Year: 2021 Document Type: Article Affiliation country: S41598-021-00747-z