Serveur d'exploration sur les variants du Covid

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The Interferon-induced transmembrane protein 3 gene (IFITM3) rs12252 C variant is associated with COVID-19.

Identifieur interne : 000005 ( Main/Exploration ); précédent : 000004; suivant : 000006

The Interferon-induced transmembrane protein 3 gene (IFITM3) rs12252 C variant is associated with COVID-19.

Auteurs : Juan G Mez [Espagne] ; Guillermo M. Albaiceta [Espagne] ; Elías Cuesta-Llavona [Espagne] ; Marta García-Clemente [Espagne] ; Carlos L Pez-Larrea [Espagne] ; Laura Amado-Rodríguez [Espagne] ; Inés L Pez-Alonso [Espagne] ; Santiago Mel N [Espagne] ; Marta E. Alvarez-Argüelles [Espagne] ; Helena Gil-Pe A [Espagne] ; José R. Vidal-Casti Eira [Espagne] ; Viviana Corte-Iglesias [Espagne] ; María L. Saiz [Espagne] ; Victoria Alvarez [Espagne] ; Eliecer Coto [Espagne]

Source :

RBID : pubmed:33113474

Descripteurs français

English descriptors

Abstract

BACKGROUND AND AIMS

The interferon-induced transmembrane proteins play an important antiviral role by preventing viruses from traversing the cellular lipid bilayer. IFITM3 gene variants have been associated with the clinical response to influenza and other viruses. Our aim was to determine whether the IFITM3 rs12252 polymorphism was associated with the risk of developing severe symptoms of COVID-19 in our population.

METHODS

A total of 288 COVID-19 patients who required hospitalization (81 in the intensive care unit) and 440 age matched controls were genotyped with a Taqman assay. Linear regression models were used to compare allele and genotype frequencies between the groups, correcting for age and sex.

RESULTS

Carriers of the minor allele frequency (rs12252 C) were significantly more frequent in the patients compared to controls after correcting by age and sex (p = 0.01, OR = 2.02, 95%CI = 1.19-3.42). This genotype was non-significantly more common among patients who required ICU.

CONCLUSIONS

The IFITM3 rs12252 C allele was a risk factor for COVID-19 hospitalization in our Caucasian population. The extent of the association was lower than the reported among Chinese, a population with a much higher frequency of the risk allele.


DOI: 10.1016/j.cyto.2020.155354
PubMed: 33113474


Affiliations:


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<name sortKey="Saiz, Maria L" sort="Saiz, Maria L" uniqKey="Saiz M" first="María L" last="Saiz">María L. Saiz</name>
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<name sortKey="Alvarez, Victoria" sort="Alvarez, Victoria" uniqKey="Alvarez V" first="Victoria" last="Alvarez">Victoria Alvarez</name>
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<title xml:lang="en">The Interferon-induced transmembrane protein 3 gene (IFITM3) rs12252 C variant is associated with COVID-19.</title>
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<author>
<name sortKey="Vidal Casti Eira, Jose R" sort="Vidal Casti Eira, Jose R" uniqKey="Vidal Casti Eira J" first="José R" last="Vidal-Casti Eira">José R. Vidal-Casti Eira</name>
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<author>
<name sortKey="Corte Iglesias, Viviana" sort="Corte Iglesias, Viviana" uniqKey="Corte Iglesias V" first="Viviana" last="Corte-Iglesias">Viviana Corte-Iglesias</name>
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<name sortKey="Saiz, Maria L" sort="Saiz, Maria L" uniqKey="Saiz M" first="María L" last="Saiz">María L. Saiz</name>
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<name sortKey="Alvarez, Victoria" sort="Alvarez, Victoria" uniqKey="Alvarez V" first="Victoria" last="Alvarez">Victoria Alvarez</name>
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<name sortKey="Coto, Eliecer" sort="Coto, Eliecer" uniqKey="Coto E" first="Eliecer" last="Coto">Eliecer Coto</name>
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<nlm:affiliation>Genética Molecular, Hospital Universitario Central Asturias, Oviedo, Spain; Instituto de Investigación Sanitaria del Principado deAsturias, ISPA, Oviedo, Spain; Universidad de Oviedo, Oviedo, Spain; Red de Investigación Renal (REDINREN), Madrid, Spain. Electronic address: eliecer.coto@sespa.es.</nlm:affiliation>
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<series>
<title level="j">Cytokine</title>
<idno type="eISSN">1096-0023</idno>
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<date when="2021" type="published">2021</date>
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<term>Aged (MeSH)</term>
<term>Asian Continental Ancestry Group (genetics)</term>
<term>COVID-19 (blood)</term>
<term>COVID-19 (epidemiology)</term>
<term>COVID-19 (genetics)</term>
<term>European Continental Ancestry Group (genetics)</term>
<term>Female (MeSH)</term>
<term>Gene Frequency (MeSH)</term>
<term>Genetic Predisposition to Disease (MeSH)</term>
<term>Genotype (MeSH)</term>
<term>Humans (MeSH)</term>
<term>Linear Models (MeSH)</term>
<term>Male (MeSH)</term>
<term>Membrane Proteins (blood)</term>
<term>Membrane Proteins (genetics)</term>
<term>Middle Aged (MeSH)</term>
<term>Polymorphism, Genetic (MeSH)</term>
<term>RNA-Binding Proteins (blood)</term>
<term>RNA-Binding Proteins (genetics)</term>
<term>Risk Factors (MeSH)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Adulte d'âge moyen (MeSH)</term>
<term>Facteurs de risque (MeSH)</term>
<term>Femelle (MeSH)</term>
<term>Fréquence d'allèle (MeSH)</term>
<term>Génotype (MeSH)</term>
<term>Humains (MeSH)</term>
<term>Modèles linéaires (MeSH)</term>
<term>Mâle (MeSH)</term>
<term>Polymorphisme génétique (MeSH)</term>
<term>Population d'origine asiatique (génétique)</term>
<term>Population d'origine européenne (génétique)</term>
<term>Protéines de liaison à l'ARN (génétique)</term>
<term>Protéines de liaison à l'ARN (sang)</term>
<term>Protéines membranaires (génétique)</term>
<term>Protéines membranaires (sang)</term>
<term>Prédisposition génétique à une maladie (MeSH)</term>
<term>Sujet âgé (MeSH)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="blood" xml:lang="en">
<term>Membrane Proteins</term>
<term>RNA-Binding Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="blood" xml:lang="en">
<term>COVID-19</term>
</keywords>
<keywords scheme="MESH" qualifier="epidemiology" xml:lang="en">
<term>COVID-19</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Asian Continental Ancestry Group</term>
<term>COVID-19</term>
<term>European Continental Ancestry Group</term>
<term>Membrane Proteins</term>
<term>RNA-Binding Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>Population d'origine asiatique</term>
<term>Population d'origine européenne</term>
<term>Protéines de liaison à l'ARN</term>
<term>Protéines membranaires</term>
</keywords>
<keywords scheme="MESH" qualifier="sang" xml:lang="fr">
<term>Protéines de liaison à l'ARN</term>
<term>Protéines membranaires</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Aged</term>
<term>Female</term>
<term>Gene Frequency</term>
<term>Genetic Predisposition to Disease</term>
<term>Genotype</term>
<term>Humans</term>
<term>Linear Models</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Polymorphism, Genetic</term>
<term>Risk Factors</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Adulte d'âge moyen</term>
<term>Facteurs de risque</term>
<term>Femelle</term>
<term>Fréquence d'allèle</term>
<term>Génotype</term>
<term>Humains</term>
<term>Modèles linéaires</term>
<term>Mâle</term>
<term>Polymorphisme génétique</term>
<term>Prédisposition génétique à une maladie</term>
<term>Sujet âgé</term>
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<front>
<div type="abstract" xml:lang="en">
<p>
<b>BACKGROUND AND AIMS</b>
</p>
<p>The interferon-induced transmembrane proteins play an important antiviral role by preventing viruses from traversing the cellular lipid bilayer. IFITM3 gene variants have been associated with the clinical response to influenza and other viruses. Our aim was to determine whether the IFITM3 rs12252 polymorphism was associated with the risk of developing severe symptoms of COVID-19 in our population.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>METHODS</b>
</p>
<p>A total of 288 COVID-19 patients who required hospitalization (81 in the intensive care unit) and 440 age matched controls were genotyped with a Taqman assay. Linear regression models were used to compare allele and genotype frequencies between the groups, correcting for age and sex.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>Carriers of the minor allele frequency (rs12252 C) were significantly more frequent in the patients compared to controls after correcting by age and sex (p = 0.01, OR = 2.02, 95%CI = 1.19-3.42). This genotype was non-significantly more common among patients who required ICU.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSIONS</b>
</p>
<p>The IFITM3 rs12252 C allele was a risk factor for COVID-19 hospitalization in our Caucasian population. The extent of the association was lower than the reported among Chinese, a population with a much higher frequency of the risk allele.</p>
</div>
</front>
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<Year>2021</Year>
<Month>01</Month>
<Day>04</Day>
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<Day>04</Day>
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<Volume>137</Volume>
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<Year>2021</Year>
<Month>01</Month>
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<Title>Cytokine</Title>
<ISOAbbreviation>Cytokine</ISOAbbreviation>
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<ArticleTitle>The Interferon-induced transmembrane protein 3 gene (IFITM3) rs12252 C variant is associated with COVID-19.</ArticleTitle>
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<AbstractText Label="BACKGROUND AND AIMS">The interferon-induced transmembrane proteins play an important antiviral role by preventing viruses from traversing the cellular lipid bilayer. IFITM3 gene variants have been associated with the clinical response to influenza and other viruses. Our aim was to determine whether the IFITM3 rs12252 polymorphism was associated with the risk of developing severe symptoms of COVID-19 in our population.</AbstractText>
<AbstractText Label="METHODS">A total of 288 COVID-19 patients who required hospitalization (81 in the intensive care unit) and 440 age matched controls were genotyped with a Taqman assay. Linear regression models were used to compare allele and genotype frequencies between the groups, correcting for age and sex.</AbstractText>
<AbstractText Label="RESULTS">Carriers of the minor allele frequency (rs12252 C) were significantly more frequent in the patients compared to controls after correcting by age and sex (p = 0.01, OR = 2.02, 95%CI = 1.19-3.42). This genotype was non-significantly more common among patients who required ICU.</AbstractText>
<AbstractText Label="CONCLUSIONS">The IFITM3 rs12252 C allele was a risk factor for COVID-19 hospitalization in our Caucasian population. The extent of the association was lower than the reported among Chinese, a population with a much higher frequency of the risk allele.</AbstractText>
<CopyrightInformation>Copyright © 2020 Elsevier Ltd. All rights reserved.</CopyrightInformation>
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<name sortKey="Corte Iglesias, Viviana" sort="Corte Iglesias, Viviana" uniqKey="Corte Iglesias V" first="Viviana" last="Corte-Iglesias">Viviana Corte-Iglesias</name>
<name sortKey="Coto, Eliecer" sort="Coto, Eliecer" uniqKey="Coto E" first="Eliecer" last="Coto">Eliecer Coto</name>
<name sortKey="Cuesta Llavona, Elias" sort="Cuesta Llavona, Elias" uniqKey="Cuesta Llavona E" first="Elías" last="Cuesta-Llavona">Elías Cuesta-Llavona</name>
<name sortKey="Garcia Clemente, Marta" sort="Garcia Clemente, Marta" uniqKey="Garcia Clemente M" first="Marta" last="García-Clemente">Marta García-Clemente</name>
<name sortKey="Gil Pe A, Helena" sort="Gil Pe A, Helena" uniqKey="Gil Pe A H" first="Helena" last="Gil-Pe A">Helena Gil-Pe A</name>
<name sortKey="L Pez Alonso, Ines" sort="L Pez Alonso, Ines" uniqKey="L Pez Alonso I" first="Inés" last="L Pez-Alonso">Inés L Pez-Alonso</name>
<name sortKey="L Pez Larrea, Carlos" sort="L Pez Larrea, Carlos" uniqKey="L Pez Larrea C" first="Carlos" last="L Pez-Larrea">Carlos L Pez-Larrea</name>
<name sortKey="Mel N, Santiago" sort="Mel N, Santiago" uniqKey="Mel N S" first="Santiago" last="Mel N">Santiago Mel N</name>
<name sortKey="Saiz, Maria L" sort="Saiz, Maria L" uniqKey="Saiz M" first="María L" last="Saiz">María L. Saiz</name>
<name sortKey="Vidal Casti Eira, Jose R" sort="Vidal Casti Eira, Jose R" uniqKey="Vidal Casti Eira J" first="José R" last="Vidal-Casti Eira">José R. Vidal-Casti Eira</name>
</country>
</tree>
</affiliations>
</record>

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{{Explor lien
   |wiki=    Sante
   |area=    CovidVariantV1
   |flux=    Main
   |étape=   Exploration
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   |clé=     pubmed:33113474
   |texte=   The Interferon-induced transmembrane protein 3 gene (IFITM3) rs12252 C variant is associated with COVID-19.
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Data generation: Tue Jan 26 18:10:18 2021. Site generation: Tue Jan 26 18:10:59 2021