Serveur d'exploration sur la COVID chez les séniors

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Angiotensin-converting enzymes (ACE, ACE2) gene variants and COVID-19 outcome.

Identifieur interne : 000939 ( Main/Exploration ); précédent : 000938; suivant : 000940

Angiotensin-converting enzymes (ACE, ACE2) gene variants and COVID-19 outcome.

Auteurs : Juan G Mez [Espagne] ; Guillermo M. Albaiceta [Espagne] ; Marta García-Clemente [Espagne] ; Carlos L Pez-Larrea [Espagne] ; Laura Amado-Rodríguez [Espagne] ; Inés Lopez-Alonso [Espagne] ; Tamara Hermida [Espagne] ; Ana I. Enriquez [Espagne] ; Pablo Herrero [Espagne] ; Santiago Mel N [Espagne] ; Marta E. Alvarez-Argüelles [Espagne] ; José A. Boga [Espagne] ; Susana Rojo-Alba [Espagne] ; Elías Cuesta-Llavona [Espagne] ; Victoria Alvarez [Espagne] ; Rebeca Lorca [Espagne] ; Eliecer Coto [Espagne]

Source :

RBID : pubmed:32882331

Descripteurs français

English descriptors

Abstract

The Angiotensin system is implicated in the pathogenesis of COVID-19. First, ACE2 is the cellular receptor for SARS-CoV-2, and expression of the ACE2 gene could regulate the individuaĺs susceptibility to infection. In addition, the balance between ACE1 and ACE2 activity has been implicated in the pathogenesis of respiratory diseases and could play a role in the severity of COVID-19. Functional ACE1/ACE2 gene polymorphisms have been associated with the risk of cardiovascular and pulmonary diseases, and could thus also contribute to the outcome of COVID-19. We studied 204 COVID-19 patients (137 non-severe and 67 severe-ICU cases) and 536 age-matched controls. The ACE1 insertion/deletion and ACE2 rs2285666 polymorphism were determined. Variables frequencies were compared between the groups by logistic regression. We also sequenced the ACE2 coding nucleotides in a group of patients. Severe COVID-19 was associated with hypertension male gender (p < 0.001), hypertension (p = 0.006), hypercholesterolaemia (p = 0.046), and the ACE1-DD genotype (p = 0.049). In the multiple logistic regression hypertension (p = 0.02, OR = 2.26, 95%CI = 1.12-4.63) and male gender (p = 0.002; OR = 3.15, 95%CI = 1.56-6.66) remained as independent significant predictors of severity. The ACE2 polymorphism was not associated with the disease outcome. The ACE2 sequencing showed no coding sequence variants that could explain an increased risk of developing COVID-19. In conclusion, an adverse outcome of COVID-19 was associated with male gender, hypertension, hypercholesterolemia and the ACE1 genotype. Our work suggested that the ACE1-I/D might influence COVID-19 severity, but the effect was dependent on the hypertensive status. This result requires further validation in other large cohorts.

DOI: 10.1016/j.gene.2020.145102
PubMed: 32882331
PubMed Central: PMC7456966


Affiliations:


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Le document en format XML

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<name sortKey="Rojo Alba, Susana" sort="Rojo Alba, Susana" uniqKey="Rojo Alba S" first="Susana" last="Rojo-Alba">Susana Rojo-Alba</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="Enriquez, Ana I" sort="Enriquez, Ana I" uniqKey="Enriquez A" first="Ana I" last="Enriquez">Ana I. Enriquez</name>
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<name sortKey="Rojo Alba, Susana" sort="Rojo Alba, Susana" uniqKey="Rojo Alba S" first="Susana" last="Rojo-Alba">Susana Rojo-Alba</name>
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<name sortKey="Cuesta Llavona, Elias" sort="Cuesta Llavona, Elias" uniqKey="Cuesta Llavona E" first="Elías" last="Cuesta-Llavona">Elías Cuesta-Llavona</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="Lorca, Rebeca" sort="Lorca, Rebeca" uniqKey="Lorca R" first="Rebeca" last="Lorca">Rebeca Lorca</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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<term>Adult (MeSH)</term>
<term>Aged (MeSH)</term>
<term>Aged, 80 and over (MeSH)</term>
<term>Betacoronavirus (MeSH)</term>
<term>Case-Control Studies (MeSH)</term>
<term>Coronavirus Infections (genetics)</term>
<term>Female (MeSH)</term>
<term>Genotyping Techniques (MeSH)</term>
<term>Humans (MeSH)</term>
<term>Hypercholesterolemia (complications)</term>
<term>Hypertension (complications)</term>
<term>INDEL Mutation (MeSH)</term>
<term>Male (MeSH)</term>
<term>Middle Aged (MeSH)</term>
<term>Pandemics (MeSH)</term>
<term>Peptidyl-Dipeptidase A (genetics)</term>
<term>Pneumonia, Viral (genetics)</term>
<term>Polymorphism, Single Nucleotide (MeSH)</term>
<term>Risk Factors (MeSH)</term>
<term>Spain (MeSH)</term>
<term>Young Adult (MeSH)</term>
</keywords>
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<term>Adulte (MeSH)</term>
<term>Adulte d'âge moyen (MeSH)</term>
<term>Betacoronavirus (MeSH)</term>
<term>Espagne (MeSH)</term>
<term>Facteurs de risque (MeSH)</term>
<term>Femelle (MeSH)</term>
<term>Humains (MeSH)</term>
<term>Hypercholestérolémie (complications)</term>
<term>Hypertension artérielle (complications)</term>
<term>Infections à coronavirus (génétique)</term>
<term>Jeune adulte (MeSH)</term>
<term>Mutation de type INDEL (MeSH)</term>
<term>Mâle (MeSH)</term>
<term>Pandémies (MeSH)</term>
<term>Peptidyl-Dipeptidase A (génétique)</term>
<term>Pneumopathie virale (génétique)</term>
<term>Polymorphisme de nucléotide simple (MeSH)</term>
<term>Sujet âgé (MeSH)</term>
<term>Sujet âgé de 80 ans ou plus (MeSH)</term>
<term>Techniques de génotypage (MeSH)</term>
<term>Études cas-témoins (MeSH)</term>
</keywords>
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<term>Peptidyl-Dipeptidase A</term>
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<term>Spain</term>
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<term>Hypercholesterolemia</term>
<term>Hypertension</term>
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<term>Pneumonia, Viral</term>
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<term>Hypercholestérolémie</term>
<term>Hypertension artérielle</term>
<term>Infections à coronavirus</term>
<term>Peptidyl-Dipeptidase A</term>
<term>Pneumopathie virale</term>
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<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Betacoronavirus</term>
<term>Case-Control Studies</term>
<term>Female</term>
<term>Genotyping Techniques</term>
<term>Humans</term>
<term>INDEL Mutation</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Pandemics</term>
<term>Polymorphism, Single Nucleotide</term>
<term>Risk Factors</term>
<term>Young Adult</term>
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<div type="abstract" xml:lang="en">The Angiotensin system is implicated in the pathogenesis of COVID-19. First, ACE2 is the cellular receptor for SARS-CoV-2, and expression of the ACE2 gene could regulate the individuaĺs susceptibility to infection. In addition, the balance between ACE1 and ACE2 activity has been implicated in the pathogenesis of respiratory diseases and could play a role in the severity of COVID-19. Functional ACE1/ACE2 gene polymorphisms have been associated with the risk of cardiovascular and pulmonary diseases, and could thus also contribute to the outcome of COVID-19. We studied 204 COVID-19 patients (137 non-severe and 67 severe-ICU cases) and 536 age-matched controls. The ACE1 insertion/deletion and ACE2 rs2285666 polymorphism were determined. Variables frequencies were compared between the groups by logistic regression. We also sequenced the ACE2 coding nucleotides in a group of patients. Severe COVID-19 was associated with hypertension male gender (p < 0.001), hypertension (p = 0.006), hypercholesterolaemia (p = 0.046), and the ACE1-DD genotype (p = 0.049). In the multiple logistic regression hypertension (p = 0.02, OR = 2.26, 95%CI = 1.12-4.63) and male gender (p = 0.002; OR = 3.15, 95%CI = 1.56-6.66) remained as independent significant predictors of severity. The ACE2 polymorphism was not associated with the disease outcome. The ACE2 sequencing showed no coding sequence variants that could explain an increased risk of developing COVID-19. In conclusion, an adverse outcome of COVID-19 was associated with male gender, hypertension, hypercholesterolemia and the ACE1 genotype. Our work suggested that the ACE1-I/D might influence COVID-19 severity, but the effect was dependent on the hypertensive status. This result requires further validation in other large cohorts.</div>
</front>
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<Year>2020</Year>
<Month>10</Month>
<Day>01</Day>
</DateCompleted>
<DateRevised>
<Year>2020</Year>
<Month>10</Month>
<Day>01</Day>
</DateRevised>
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<ISSN IssnType="Electronic">1879-0038</ISSN>
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<Volume>762</Volume>
<PubDate>
<Year>2020</Year>
<Month>Dec</Month>
<Day>15</Day>
</PubDate>
</JournalIssue>
<Title>Gene</Title>
<ISOAbbreviation>Gene</ISOAbbreviation>
</Journal>
<ArticleTitle>Angiotensin-converting enzymes (ACE, ACE2) gene variants and COVID-19 outcome.</ArticleTitle>
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<AbstractText>The Angiotensin system is implicated in the pathogenesis of COVID-19. First, ACE2 is the cellular receptor for SARS-CoV-2, and expression of the ACE2 gene could regulate the individuaĺs susceptibility to infection. In addition, the balance between ACE1 and ACE2 activity has been implicated in the pathogenesis of respiratory diseases and could play a role in the severity of COVID-19. Functional ACE1/ACE2 gene polymorphisms have been associated with the risk of cardiovascular and pulmonary diseases, and could thus also contribute to the outcome of COVID-19. We studied 204 COVID-19 patients (137 non-severe and 67 severe-ICU cases) and 536 age-matched controls. The ACE1 insertion/deletion and ACE2 rs2285666 polymorphism were determined. Variables frequencies were compared between the groups by logistic regression. We also sequenced the ACE2 coding nucleotides in a group of patients. Severe COVID-19 was associated with hypertension male gender (p < 0.001), hypertension (p = 0.006), hypercholesterolaemia (p = 0.046), and the ACE1-DD genotype (p = 0.049). In the multiple logistic regression hypertension (p = 0.02, OR = 2.26, 95%CI = 1.12-4.63) and male gender (p = 0.002; OR = 3.15, 95%CI = 1.56-6.66) remained as independent significant predictors of severity. The ACE2 polymorphism was not associated with the disease outcome. The ACE2 sequencing showed no coding sequence variants that could explain an increased risk of developing COVID-19. In conclusion, an adverse outcome of COVID-19 was associated with male gender, hypertension, hypercholesterolemia and the ACE1 genotype. Our work suggested that the ACE1-I/D might influence COVID-19 severity, but the effect was dependent on the hypertensive status. This result requires further validation in other large cohorts.</AbstractText>
<CopyrightInformation>Copyright © 2020 Elsevier B.V. All rights reserved.</CopyrightInformation>
</Abstract>
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<LastName>Gómez</LastName>
<ForeName>Juan</ForeName>
<Initials>J</Initials>
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<LastName>Albaiceta</LastName>
<ForeName>Guillermo M</ForeName>
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<ForeName>Pablo</ForeName>
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<ForeName>Victoria</ForeName>
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