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Influence of APOE locus on poor prognosis of COVID-19

The COVID-19 pandemic has infected over 25 million of people worldwide, 5% of whom evolved to death and, among of the active cases, more than 60 thousand are classified as critical or severe. Recent studies revealed that ApoE, a protein encoded by APOE gene, may increase the risk of severe COVID-19...

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Autores principales: Rodrigues, Juliana Carla Gomes, Pinto, Pablo, Leitão, Luciana Pereira Colares, Vinagre, Lui Wallacy Morikawa Souza, Monte, Natasha, Fernandes, Marianne Rodrigues, Khayat, André Salim, de Assumpção, Paulo Pimentel, Santos, Ney Pereira Carneiro dos, Santos, Sidney Emanuel Batista dos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8220252/
https://www.ncbi.nlm.nih.gov/pubmed/34179542
http://dx.doi.org/10.1016/j.heliyon.2021.e07379
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author Rodrigues, Juliana Carla Gomes
Pinto, Pablo
Leitão, Luciana Pereira Colares
Vinagre, Lui Wallacy Morikawa Souza
Monte, Natasha
Fernandes, Marianne Rodrigues
Khayat, André Salim
de Assumpção, Paulo Pimentel
Santos, Ney Pereira Carneiro dos
Santos, Sidney Emanuel Batista dos
author_facet Rodrigues, Juliana Carla Gomes
Pinto, Pablo
Leitão, Luciana Pereira Colares
Vinagre, Lui Wallacy Morikawa Souza
Monte, Natasha
Fernandes, Marianne Rodrigues
Khayat, André Salim
de Assumpção, Paulo Pimentel
Santos, Ney Pereira Carneiro dos
Santos, Sidney Emanuel Batista dos
author_sort Rodrigues, Juliana Carla Gomes
collection PubMed
description The COVID-19 pandemic has infected over 25 million of people worldwide, 5% of whom evolved to death and, among of the active cases, more than 60 thousand are classified as critical or severe. Recent studies revealed that ApoE, a protein encoded by APOE gene, may increase the risk of severe COVID-19 cases. ApoE has been involved with prevention of tissue damage and promotion of adaptative immune response in the lungs. This study investigated frequencies distribution of alleles that alter the ApoE expression in lung tissues to trace a profile of these variants and associate them to COVID-19 clinical outcomes. Data about APOE expression levels was obtained from the Genotype-Tissue Expression Project and the allele frequencies of APOE variants was acquired from the populations included in the phase 3 release of the 1000 Genomes Project. A total of 128 variants showed a significant impact on the APOE expression in lung tissues (p < 0.0001). Linkage Disequilibrium analysis revealed that 98 variants were closely grouped into seven distinct haplotype blocks, of which six were composed of variants that significantly decrease APOE gene expression in the lungs. Most of the haplotypes with higher impact on APOE expression showed greater frequencies in Europeans and lower in Africans, which implies that European populations might be more susceptible to SARS-CoV-2 infection. The present study indicates a potential genetic contribution of APOE expression-modifying variants in modulating the prognosis of COVID-19.
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spelling pubmed-82202522021-06-23 Influence of APOE locus on poor prognosis of COVID-19 Rodrigues, Juliana Carla Gomes Pinto, Pablo Leitão, Luciana Pereira Colares Vinagre, Lui Wallacy Morikawa Souza Monte, Natasha Fernandes, Marianne Rodrigues Khayat, André Salim de Assumpção, Paulo Pimentel Santos, Ney Pereira Carneiro dos Santos, Sidney Emanuel Batista dos Heliyon Research Article The COVID-19 pandemic has infected over 25 million of people worldwide, 5% of whom evolved to death and, among of the active cases, more than 60 thousand are classified as critical or severe. Recent studies revealed that ApoE, a protein encoded by APOE gene, may increase the risk of severe COVID-19 cases. ApoE has been involved with prevention of tissue damage and promotion of adaptative immune response in the lungs. This study investigated frequencies distribution of alleles that alter the ApoE expression in lung tissues to trace a profile of these variants and associate them to COVID-19 clinical outcomes. Data about APOE expression levels was obtained from the Genotype-Tissue Expression Project and the allele frequencies of APOE variants was acquired from the populations included in the phase 3 release of the 1000 Genomes Project. A total of 128 variants showed a significant impact on the APOE expression in lung tissues (p < 0.0001). Linkage Disequilibrium analysis revealed that 98 variants were closely grouped into seven distinct haplotype blocks, of which six were composed of variants that significantly decrease APOE gene expression in the lungs. Most of the haplotypes with higher impact on APOE expression showed greater frequencies in Europeans and lower in Africans, which implies that European populations might be more susceptible to SARS-CoV-2 infection. The present study indicates a potential genetic contribution of APOE expression-modifying variants in modulating the prognosis of COVID-19. Elsevier 2021-06-23 /pmc/articles/PMC8220252/ /pubmed/34179542 http://dx.doi.org/10.1016/j.heliyon.2021.e07379 Text en © 2021 The Authors. Published by Elsevier Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Rodrigues, Juliana Carla Gomes
Pinto, Pablo
Leitão, Luciana Pereira Colares
Vinagre, Lui Wallacy Morikawa Souza
Monte, Natasha
Fernandes, Marianne Rodrigues
Khayat, André Salim
de Assumpção, Paulo Pimentel
Santos, Ney Pereira Carneiro dos
Santos, Sidney Emanuel Batista dos
Influence of APOE locus on poor prognosis of COVID-19
title Influence of APOE locus on poor prognosis of COVID-19
title_full Influence of APOE locus on poor prognosis of COVID-19
title_fullStr Influence of APOE locus on poor prognosis of COVID-19
title_full_unstemmed Influence of APOE locus on poor prognosis of COVID-19
title_short Influence of APOE locus on poor prognosis of COVID-19
title_sort influence of apoe locus on poor prognosis of covid-19
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8220252/
https://www.ncbi.nlm.nih.gov/pubmed/34179542
http://dx.doi.org/10.1016/j.heliyon.2021.e07379
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