ACE2 (Angiotensin-Converting Enzyme 2), COVID-19, and ACE Inhibitor and Ang II (Angiotensin II) Receptor Blocker Use During the Pandemic: The Pediatric Perspective.
Identifieur interne : 000314 ( Main/Curation ); précédent : 000313; suivant : 000315ACE2 (Angiotensin-Converting Enzyme 2), COVID-19, and ACE Inhibitor and Ang II (Angiotensin II) Receptor Blocker Use During the Pandemic: The Pediatric Perspective.
Auteurs : Andrew M. South [États-Unis] ; Tammy M. Brady ; Joseph T. FlynnSource :
- Hypertension (Dallas, Tex. : 1979) [ 1524-4563 ] ; 2020.
Descripteurs français
- KwdFr :
- Antagonistes des récepteurs aux angiotensines (pharmacologie), Betacoronavirus (physiologie), Comorbidité (MeSH), Enfant (MeSH), Humains (MeSH), Hypertension artérielle (métabolisme), Hypertension artérielle (traitement médicamenteux), Hypertension artérielle (épidémiologie), Infections à coronavirus (métabolisme), Infections à coronavirus (virologie), Infections à coronavirus (épidémiologie), Inhibiteurs de l'enzyme de conversion de l'angiotensine (pharmacologie), Pandémies (MeSH), Peptidyl-Dipeptidase A (métabolisme), Pneumopathie virale (métabolisme), Pneumopathie virale (virologie), Pneumopathie virale (épidémiologie), Système rénine-angiotensine (effets des médicaments et des substances chimiques), Système rénine-angiotensine (physiologie).
- MESH :
- effets des médicaments et des substances chimiques : Système rénine-angiotensine.
- métabolisme : Hypertension artérielle, Infections à coronavirus, Peptidyl-Dipeptidase A, Pneumopathie virale.
- pharmacologie : Antagonistes des récepteurs aux angiotensines, Inhibiteurs de l'enzyme de conversion de l'angiotensine.
- physiologie : Betacoronavirus, Système rénine-angiotensine.
- traitement médicamenteux : Hypertension artérielle.
- virologie : Infections à coronavirus, Pneumopathie virale.
- épidémiologie : Hypertension artérielle, Infections à coronavirus, Pneumopathie virale.
- Comorbidité, Enfant, Humains, Pandémies.
English descriptors
- KwdEn :
- Angiotensin Receptor Antagonists (pharmacology), Angiotensin-Converting Enzyme Inhibitors (pharmacology), Betacoronavirus (physiology), Child (MeSH), Comorbidity (MeSH), Coronavirus Infections (epidemiology), Coronavirus Infections (metabolism), Coronavirus Infections (virology), Humans (MeSH), Hypertension (drug therapy), Hypertension (epidemiology), Hypertension (metabolism), Pandemics (MeSH), Peptidyl-Dipeptidase A (metabolism), Pneumonia, Viral (epidemiology), Pneumonia, Viral (metabolism), Pneumonia, Viral (virology), Renin-Angiotensin System (drug effects), Renin-Angiotensin System (physiology).
- MESH :
- chemical , metabolism : Peptidyl-Dipeptidase A.
- chemical , pharmacology : Angiotensin Receptor Antagonists, Angiotensin-Converting Enzyme Inhibitors.
- drug effects : Renin-Angiotensin System.
- drug therapy : Hypertension.
- epidemiology : Coronavirus Infections, Hypertension, Pneumonia, Viral.
- metabolism : Coronavirus Infections, Hypertension, Pneumonia, Viral.
- physiology : Betacoronavirus, Renin-Angiotensin System.
- virology : Coronavirus Infections, Pneumonia, Viral.
- Child, Comorbidity, Humans, Pandemics.
Abstract
Potential but unconfirmed risk factors for coronavirus disease 2019 (COVID-19) in adults and children may include hypertension, cardiovascular disease, and chronic kidney disease, as well as the medications commonly prescribed for these conditions, ACE (angiotensin-converting enzyme) inhibitors, and Ang II (angiotensin II) receptor blockers. Coronavirus binding to ACE2 (angiotensin-converting enzyme 2), a crucial component of the renin-angiotensin-aldosterone system, underlies much of this concern. Children are uniquely impacted by the coronavirus, but the reasons are unclear. This review will highlight the relationship of COVID-19 with hypertension, use of ACE inhibitors and Ang II receptor blockers, and lifetime risk of cardiovascular disease from the pediatric perspective. We briefly summarize the renin-angiotensin-aldosterone system and comprehensively review the literature pertaining to the ACE 2/Ang-(1-7) pathway in children and the clinical evidence for how ACE inhibitors and Ang II receptor blockers affect this important pathway. Given the importance of the ACE 2/Ang-(1-7) pathway and the potential differences between adults and children, it is crucial that children are included in coronavirus-related research, as this may shed light on potential mechanisms for why children are at decreased risk of severe COVID-19.
DOI: 10.1161/HYPERTENSIONAHA.120.15291
PubMed: 32367746
PubMed Central: PMC7289676
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Andrew M. South<affiliation><nlm:affiliation>From the Section of Nephrology, Department of Pediatrics, Wake Forest School of Medicine and Brenner Children's Hospital (A.M.S.).</nlm:affiliation>
<wicri:noCountry code="subField">Wake Forest School of Medicine and Brenner Children's Hospital (A.M.S.).</wicri:noCountry>
</affiliation>
<affiliation wicri:level="2"><nlm:affiliation>Department of Surgery-Hypertension and Vascular Research (A.M.S.), Wake Forest School of Medicine, Winston Salem, NC.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<placeName><region type="state">Caroline du Nord</region>
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<affiliation><nlm:affiliation>Division of Nephrology, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD (T.M.B.).</nlm:affiliation>
<wicri:noCountry code="subField">MD (T.M.B.).</wicri:noCountry>
</affiliation>
<affiliation><nlm:affiliation>Department of Pediatrics, University of Washington School of Medicine and Division of Nephrology, Seattle Children's Hospital (J.T.F.).</nlm:affiliation>
<wicri:noCountry code="subField">Seattle Children's Hospital (J.T.F.).</wicri:noCountry>
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Le document en format XML
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<term>Child (MeSH)</term>
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<term>Coronavirus Infections (metabolism)</term>
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<term>Hypertension (epidemiology)</term>
<term>Hypertension (metabolism)</term>
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<term>Enfant (MeSH)</term>
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<front><div type="abstract" xml:lang="en">Potential but unconfirmed risk factors for coronavirus disease 2019 (COVID-19) in adults and children may include hypertension, cardiovascular disease, and chronic kidney disease, as well as the medications commonly prescribed for these conditions, ACE (angiotensin-converting enzyme) inhibitors, and Ang II (angiotensin II) receptor blockers. Coronavirus binding to ACE2 (angiotensin-converting enzyme 2), a crucial component of the renin-angiotensin-aldosterone system, underlies much of this concern. Children are uniquely impacted by the coronavirus, but the reasons are unclear. This review will highlight the relationship of COVID-19 with hypertension, use of ACE inhibitors and Ang II receptor blockers, and lifetime risk of cardiovascular disease from the pediatric perspective. We briefly summarize the renin-angiotensin-aldosterone system and comprehensively review the literature pertaining to the ACE 2/Ang-(1-7) pathway in children and the clinical evidence for how ACE inhibitors and Ang II receptor blockers affect this important pathway. Given the importance of the ACE 2/Ang-(1-7) pathway and the potential differences between adults and children, it is crucial that children are included in coronavirus-related research, as this may shed light on potential mechanisms for why children are at decreased risk of severe COVID-19.</div>
</front>
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<Abstract><AbstractText>Potential but unconfirmed risk factors for coronavirus disease 2019 (COVID-19) in adults and children may include hypertension, cardiovascular disease, and chronic kidney disease, as well as the medications commonly prescribed for these conditions, ACE (angiotensin-converting enzyme) inhibitors, and Ang II (angiotensin II) receptor blockers. Coronavirus binding to ACE2 (angiotensin-converting enzyme 2), a crucial component of the renin-angiotensin-aldosterone system, underlies much of this concern. Children are uniquely impacted by the coronavirus, but the reasons are unclear. This review will highlight the relationship of COVID-19 with hypertension, use of ACE inhibitors and Ang II receptor blockers, and lifetime risk of cardiovascular disease from the pediatric perspective. We briefly summarize the renin-angiotensin-aldosterone system and comprehensively review the literature pertaining to the ACE 2/Ang-(1-7) pathway in children and the clinical evidence for how ACE inhibitors and Ang II receptor blockers affect this important pathway. Given the importance of the ACE 2/Ang-(1-7) pathway and the potential differences between adults and children, it is crucial that children are included in coronavirus-related research, as this may shed light on potential mechanisms for why children are at decreased risk of severe COVID-19.</AbstractText>
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<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>South</LastName>
<ForeName>Andrew M</ForeName>
<Initials>AM</Initials>
<AffiliationInfo><Affiliation>From the Section of Nephrology, Department of Pediatrics, Wake Forest School of Medicine and Brenner Children's Hospital (A.M.S.).</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Department of Surgery-Hypertension and Vascular Research (A.M.S.), Wake Forest School of Medicine, Winston Salem, NC.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Division of Public Health Sciences, Department of Epidemiology and Prevention (A.M.S.), Wake Forest School of Medicine, Winston Salem, NC.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Cardiovascular Sciences Center (A.M.S.), Wake Forest School of Medicine, Winston Salem, NC.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Brady</LastName>
<ForeName>Tammy M</ForeName>
<Initials>TM</Initials>
<AffiliationInfo><Affiliation>Division of Nephrology, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD (T.M.B.).</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Flynn</LastName>
<ForeName>Joseph T</ForeName>
<Initials>JT</Initials>
<AffiliationInfo><Affiliation>Department of Pediatrics, University of Washington School of Medicine and Division of Nephrology, Seattle Children's Hospital (J.T.F.).</Affiliation>
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<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D000806">Angiotensin-Converting Enzyme Inhibitors</NameOfSubstance>
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<Chemical><RegistryNumber>EC 3.4.15.1</RegistryNumber>
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