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Impact of interferon-induced transmembrane protein 3 gene rs12252 polymorphism on COVID-19 mortality

BACKGROUND AND AIMS: Interferon-induced transmembrane protein 3 (IFITM3) plays a critical role in the adaptive and innate immune response by preventing membrane hemifusion between the host and viral cell cytoplasm. This study aimed to evaluate whether IFITM3 rs12252 polymorphism is related to an inc...

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Autores principales: Ahmadi, Iraj, Afifipour, Alireza, Sakhaee, Fatemeh, Zamani, Mohammad Saber, Mirzaei Gheinari, Fahimeh, Anvari, Enayat, Fateh, Abolfazl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9250290/
https://www.ncbi.nlm.nih.gov/pubmed/35792282
http://dx.doi.org/10.1016/j.cyto.2022.155957
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author Ahmadi, Iraj
Afifipour, Alireza
Sakhaee, Fatemeh
Zamani, Mohammad Saber
Mirzaei Gheinari, Fahimeh
Anvari, Enayat
Fateh, Abolfazl
author_facet Ahmadi, Iraj
Afifipour, Alireza
Sakhaee, Fatemeh
Zamani, Mohammad Saber
Mirzaei Gheinari, Fahimeh
Anvari, Enayat
Fateh, Abolfazl
author_sort Ahmadi, Iraj
collection PubMed
description BACKGROUND AND AIMS: Interferon-induced transmembrane protein 3 (IFITM3) plays a critical role in the adaptive and innate immune response by preventing membrane hemifusion between the host and viral cell cytoplasm. This study aimed to evaluate whether IFITM3 rs12252 polymorphism is related to an increased mortality rate of coronavirus disease 2019 (COVID-19). METHODS: The IFITM3 rs12252 polymorphism was genotyped using the amplification refractory mutation system-polymerase chain reaction (ARMS-PCR) in 548 dead and 630 improved patients positive for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). RESULTS: In the present study, the minor allele frequency of IFITM3 rs12252 (C) was significantly more frequent in dead patients than in improved cases. The results of the multivariate logistic regression analysis indicated that the lower lipid profiles, PCR Ct value, 25-hydroxyvitamin D, and uric acid and higher levels of erythrocyte sedimentation rate (ESR), liver enzymes, and creatinine, and IFITM3 rs12252 CC genotypes were related to the COVID-19 infection mortality. CONCLUSIONS: In summary, our findings suggested a possible link between the mortality of COVID-19 infection, the CC genotypes of IFITM3 rs12252, and clinical parameters. Further investigations are required worldwide to prove the link relationship of COVID-19 mortality with host genetic factors.
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spelling pubmed-92502902022-07-05 Impact of interferon-induced transmembrane protein 3 gene rs12252 polymorphism on COVID-19 mortality Ahmadi, Iraj Afifipour, Alireza Sakhaee, Fatemeh Zamani, Mohammad Saber Mirzaei Gheinari, Fahimeh Anvari, Enayat Fateh, Abolfazl Cytokine Article BACKGROUND AND AIMS: Interferon-induced transmembrane protein 3 (IFITM3) plays a critical role in the adaptive and innate immune response by preventing membrane hemifusion between the host and viral cell cytoplasm. This study aimed to evaluate whether IFITM3 rs12252 polymorphism is related to an increased mortality rate of coronavirus disease 2019 (COVID-19). METHODS: The IFITM3 rs12252 polymorphism was genotyped using the amplification refractory mutation system-polymerase chain reaction (ARMS-PCR) in 548 dead and 630 improved patients positive for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). RESULTS: In the present study, the minor allele frequency of IFITM3 rs12252 (C) was significantly more frequent in dead patients than in improved cases. The results of the multivariate logistic regression analysis indicated that the lower lipid profiles, PCR Ct value, 25-hydroxyvitamin D, and uric acid and higher levels of erythrocyte sedimentation rate (ESR), liver enzymes, and creatinine, and IFITM3 rs12252 CC genotypes were related to the COVID-19 infection mortality. CONCLUSIONS: In summary, our findings suggested a possible link between the mortality of COVID-19 infection, the CC genotypes of IFITM3 rs12252, and clinical parameters. Further investigations are required worldwide to prove the link relationship of COVID-19 mortality with host genetic factors. Elsevier Ltd. 2022-09 2022-07-02 /pmc/articles/PMC9250290/ /pubmed/35792282 http://dx.doi.org/10.1016/j.cyto.2022.155957 Text en © 2022 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Ahmadi, Iraj
Afifipour, Alireza
Sakhaee, Fatemeh
Zamani, Mohammad Saber
Mirzaei Gheinari, Fahimeh
Anvari, Enayat
Fateh, Abolfazl
Impact of interferon-induced transmembrane protein 3 gene rs12252 polymorphism on COVID-19 mortality
title Impact of interferon-induced transmembrane protein 3 gene rs12252 polymorphism on COVID-19 mortality
title_full Impact of interferon-induced transmembrane protein 3 gene rs12252 polymorphism on COVID-19 mortality
title_fullStr Impact of interferon-induced transmembrane protein 3 gene rs12252 polymorphism on COVID-19 mortality
title_full_unstemmed Impact of interferon-induced transmembrane protein 3 gene rs12252 polymorphism on COVID-19 mortality
title_short Impact of interferon-induced transmembrane protein 3 gene rs12252 polymorphism on COVID-19 mortality
title_sort impact of interferon-induced transmembrane protein 3 gene rs12252 polymorphism on covid-19 mortality
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9250290/
https://www.ncbi.nlm.nih.gov/pubmed/35792282
http://dx.doi.org/10.1016/j.cyto.2022.155957
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