Serveur d'exploration sur le Covid à Stanford

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Blood Biomarkers for Detection of Brain Injury in COVID-19 Patients.

Identifieur interne : 000099 ( Main/Exploration ); précédent : 000098; suivant : 000100

Blood Biomarkers for Detection of Brain Injury in COVID-19 Patients.

Auteurs : Steven T. Dekosky [États-Unis] ; Patrick M. Kochanek [États-Unis] ; Alex B. Valadka [États-Unis] ; Robert S B. Clark [États-Unis] ; Sherry H-Y Chou [États-Unis] ; Alicia K. Au [États-Unis] ; Christopher Horvat [États-Unis] ; Ruchira M. Jha [États-Unis] ; Rebekah Mannix [États-Unis] ; Stephen R. Wisniewski [États-Unis] ; Max Wintermark [États-Unis] ; Susan E. Rowell [États-Unis] ; Robert D. Welch [États-Unis] ; Lawrence Lewis [États-Unis] ; Stacey House [États-Unis] ; Rudolph E. Tanzi [États-Unis] ; Darci R. Smith [États-Unis] ; Amy Y. Vittor [États-Unis] ; Nancy D. Denslow [États-Unis] ; Michael D. Davis [États-Unis] ; Olena Y. Glushakova [États-Unis] ; Ronald L. Hayes [États-Unis]

Source :

RBID : pubmed:33115334

Descripteurs français

English descriptors

Abstract

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus attacks multiple organs of coronavirus disease 2019 (COVID-19) patients, including the brain. There are worldwide descriptions of neurological deficits in COVID-19 patients. Central nervous system (CNS) symptoms can be present early in the course of the disease. As many as 55% of hospitalized COVID-19 patients have been reported to have neurological disturbances three months after infection by SARS-CoV-2. The mutability of the SARS-COV-2 virus and its potential to directly affect the CNS highlight the urgency of developing technology to diagnose, manage, and treat brain injury in COVID-19 patients. The pathobiology of CNS infection by SARS-CoV-2 and the associated neurological sequelae of this infection remain poorly understood. In this review, we outline the rationale for the use of blood biomarkers (BBs) for diagnosis of brain injury in COVID-19 patients, the research needed to incorporate their use into clinical practice, and the improvements in patient management and outcomes that can result. BBs of brain injury could potentially provide tools for detection of brain injury in COVID-19 patients. Elevations of BBs have been reported in cerebrospinal fluid (CSF) and blood of COVID-19 patients. BB proteins have been analyzed in CSF to detect CNS involvement in patients with infectious diseases, including human immunodeficiency virus and tuberculous meningitis. BBs are approved by the U.S. Food and Drug Administration for diagnosis of mild versus moderate traumatic brain injury and have identified brain injury after stroke, cardiac arrest, hypoxia, and epilepsy. BBs, integrated with other diagnostic tools, could enhance understanding of viral mechanisms of brain injury, predict severity of neurological deficits, guide triage of patients and assignment to appropriate medical pathways, and assess efficacy of therapeutic interventions in COVID-19 patients.

DOI: 10.1089/neu.2020.7332
PubMed: 33115334
PubMed Central: PMC7757533


Affiliations:


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Le document en format XML

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<name sortKey="Davis, Michael D" sort="Davis, Michael D" uniqKey="Davis M" first="Michael D" last="Davis">Michael D. Davis</name>
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<name sortKey="Glushakova, Olena Y" sort="Glushakova, Olena Y" uniqKey="Glushakova O" first="Olena Y" last="Glushakova">Olena Y. Glushakova</name>
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<nlm:affiliation>University of Virginia Cancer Center, Charlottesville, Virginia, USA.</nlm:affiliation>
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<region type="state">Virginie</region>
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<name sortKey="Hayes, Ronald L" sort="Hayes, Ronald L" uniqKey="Hayes R" first="Ronald L" last="Hayes">Ronald L. Hayes</name>
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<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Critical Care Medicine, University of Pittsburgh School of Medicine, Division of Pediatric Critical Care, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania</wicri:regionArea>
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<region type="state">Pennsylvanie</region>
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<name sortKey="Jha, Ruchira M" sort="Jha, Ruchira M" uniqKey="Jha R" first="Ruchira M" last="Jha">Ruchira M. Jha</name>
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<nlm:affiliation>Departments of Critical Care Medicine, Neurology, Neurological Surgery, Clinical and Translational Science Institute, Safar Center for Resuscitation Research, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
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<name sortKey="Mannix, Rebekah" sort="Mannix, Rebekah" uniqKey="Mannix R" first="Rebekah" last="Mannix">Rebekah Mannix</name>
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<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Pediatrics and Emergency Medicine, Harvard Medical School, Department of Medicine, Division of Emergency Medicine, Boston Children's Hospital, Boston, Massachusetts</wicri:regionArea>
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<region type="state">Massachusetts</region>
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<nlm:affiliation>University of Pittsburgh, Pittsburgh, Pennsylvania, USA.</nlm:affiliation>
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<wicri:regionArea>University of Pittsburgh, Pittsburgh, Pennsylvania</wicri:regionArea>
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<region type="state">Pennsylvanie</region>
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<wicri:regionArea>Department of Emergency Medicine, Wayne State University School of Medicine, Detroit Receiving Hospital/University Health Center, Detroit, Michigan</wicri:regionArea>
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<name sortKey="Lewis, Lawrence" sort="Lewis, Lawrence" uniqKey="Lewis L" first="Lawrence" last="Lewis">Lawrence Lewis</name>
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<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Emergency Medicine, Washington University in St. Louis, St. Louis, Missouri</wicri:regionArea>
<placeName>
<region type="state">Missouri (État)</region>
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<orgName type="university">Université Washington de Saint-Louis</orgName>
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<name sortKey="House, Stacey" sort="House, Stacey" uniqKey="House S" first="Stacey" last="House">Stacey House</name>
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<region type="state">Missouri (État)</region>
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<orgName type="university">École de médecine (Université Washington de Saint-Louis)</orgName>
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<name sortKey="Tanzi, Rudolph E" sort="Tanzi, Rudolph E" uniqKey="Tanzi R" first="Rudolph E" last="Tanzi">Rudolph E. Tanzi</name>
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<country xml:lang="fr">États-Unis</country>
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<region type="state">Maryland</region>
</placeName>
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<name sortKey="Vittor, Amy Y" sort="Vittor, Amy Y" uniqKey="Vittor A" first="Amy Y" last="Vittor">Amy Y. Vittor</name>
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<region type="state">Floride</region>
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<author>
<name sortKey="Davis, Michael D" sort="Davis, Michael D" uniqKey="Davis M" first="Michael D" last="Davis">Michael D. Davis</name>
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<nlm:affiliation>Department of Pediatrics, Wells Center for Pediatric Research/Pulmonology, Allergy, and Sleep Medicine, Riley Hospital for Children at Indiana University, Indianapolis, Indiana, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Pediatrics, Wells Center for Pediatric Research/Pulmonology, Allergy, and Sleep Medicine, Riley Hospital for Children at Indiana University, Indianapolis, Indiana</wicri:regionArea>
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<region type="state">Indiana</region>
</placeName>
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<name sortKey="Glushakova, Olena Y" sort="Glushakova, Olena Y" uniqKey="Glushakova O" first="Olena Y" last="Glushakova">Olena Y. Glushakova</name>
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<nlm:affiliation>University of Virginia Cancer Center, Charlottesville, Virginia, USA.</nlm:affiliation>
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<wicri:regionArea>University of Virginia Cancer Center, Charlottesville, Virginia</wicri:regionArea>
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<region type="state">Virginie</region>
</placeName>
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<name sortKey="Hayes, Ronald L" sort="Hayes, Ronald L" uniqKey="Hayes R" first="Ronald L" last="Hayes">Ronald L. Hayes</name>
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<nlm:affiliation>Banyan Biomarkers Inc., Alachua, Florida, USA.</nlm:affiliation>
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<wicri:regionArea>Banyan Biomarkers Inc., Alachua, Florida</wicri:regionArea>
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</placeName>
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<title level="j">Journal of neurotrauma</title>
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<term>Biomarkers (blood)</term>
<term>Brain (metabolism)</term>
<term>Brain (pathology)</term>
<term>Brain Injuries (blood)</term>
<term>Brain Injuries (diagnosis)</term>
<term>Brain Injuries (etiology)</term>
<term>COVID-19 (blood)</term>
<term>COVID-19 (complications)</term>
<term>COVID-19 (diagnosis)</term>
<term>Humans (MeSH)</term>
<term>Nervous System Diseases (blood)</term>
<term>Nervous System Diseases (diagnosis)</term>
<term>Nervous System Diseases (etiology)</term>
<term>Prospective Studies (MeSH)</term>
<term>Retrospective Studies (MeSH)</term>
</keywords>
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<term>Encéphale (anatomopathologie)</term>
<term>Encéphale (métabolisme)</term>
<term>Humains (MeSH)</term>
<term>Lésions encéphaliques (diagnostic)</term>
<term>Lésions encéphaliques (sang)</term>
<term>Lésions encéphaliques (étiologie)</term>
<term>Maladies du système nerveux (diagnostic)</term>
<term>Maladies du système nerveux (sang)</term>
<term>Maladies du système nerveux (étiologie)</term>
<term>Marqueurs biologiques (sang)</term>
<term>Études prospectives (MeSH)</term>
<term>Études rétrospectives (MeSH)</term>
</keywords>
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<term>Brain Injuries</term>
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<term>Nervous System Diseases</term>
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<term>COVID-19</term>
<term>Nervous System Diseases</term>
</keywords>
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<term>Lésions encéphaliques</term>
<term>Maladies du système nerveux</term>
</keywords>
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<term>Brain Injuries</term>
<term>Nervous System Diseases</term>
</keywords>
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<term>Brain</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr">
<term>Encéphale</term>
</keywords>
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<term>Brain</term>
</keywords>
<keywords scheme="MESH" qualifier="sang" xml:lang="fr">
<term>Lésions encéphaliques</term>
<term>Maladies du système nerveux</term>
<term>Marqueurs biologiques</term>
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<term>Lésions encéphaliques</term>
<term>Maladies du système nerveux</term>
</keywords>
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<term>Humans</term>
<term>Prospective Studies</term>
<term>Retrospective Studies</term>
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<div type="abstract" xml:lang="en">The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus attacks multiple organs of coronavirus disease 2019 (COVID-19) patients, including the brain. There are worldwide descriptions of neurological deficits in COVID-19 patients. Central nervous system (CNS) symptoms can be present early in the course of the disease. As many as 55% of hospitalized COVID-19 patients have been reported to have neurological disturbances three months after infection by SARS-CoV-2. The mutability of the SARS-COV-2 virus and its potential to directly affect the CNS highlight the urgency of developing technology to diagnose, manage, and treat brain injury in COVID-19 patients. The pathobiology of CNS infection by SARS-CoV-2 and the associated neurological sequelae of this infection remain poorly understood. In this review, we outline the rationale for the use of blood biomarkers (BBs) for diagnosis of brain injury in COVID-19 patients, the research needed to incorporate their use into clinical practice, and the improvements in patient management and outcomes that can result. BBs of brain injury could potentially provide tools for detection of brain injury in COVID-19 patients. Elevations of BBs have been reported in cerebrospinal fluid (CSF) and blood of COVID-19 patients. BB proteins have been analyzed in CSF to detect CNS involvement in patients with infectious diseases, including human immunodeficiency virus and tuberculous meningitis. BBs are approved by the U.S. Food and Drug Administration for diagnosis of mild versus moderate traumatic brain injury and have identified brain injury after stroke, cardiac arrest, hypoxia, and epilepsy. BBs, integrated with other diagnostic tools, could enhance understanding of viral mechanisms of brain injury, predict severity of neurological deficits, guide triage of patients and assignment to appropriate medical pathways, and assess efficacy of therapeutic interventions in COVID-19 patients.</div>
</front>
</TEI>
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<DateCompleted>
<Year>2021</Year>
<Month>01</Month>
<Day>19</Day>
</DateCompleted>
<DateRevised>
<Year>2021</Year>
<Month>01</Month>
<Day>19</Day>
</DateRevised>
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<Journal>
<ISSN IssnType="Electronic">1557-9042</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>38</Volume>
<Issue>1</Issue>
<PubDate>
<Year>2021</Year>
<Month>01</Month>
<Day>01</Day>
</PubDate>
</JournalIssue>
<Title>Journal of neurotrauma</Title>
<ISOAbbreviation>J Neurotrauma</ISOAbbreviation>
</Journal>
<ArticleTitle>Blood Biomarkers for Detection of Brain Injury in COVID-19 Patients.</ArticleTitle>
<Pagination>
<MedlinePgn>1-43</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1089/neu.2020.7332</ELocationID>
<Abstract>
<AbstractText>The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus attacks multiple organs of coronavirus disease 2019 (COVID-19) patients, including the brain. There are worldwide descriptions of neurological deficits in COVID-19 patients. Central nervous system (CNS) symptoms can be present early in the course of the disease. As many as 55% of hospitalized COVID-19 patients have been reported to have neurological disturbances three months after infection by SARS-CoV-2. The mutability of the SARS-COV-2 virus and its potential to directly affect the CNS highlight the urgency of developing technology to diagnose, manage, and treat brain injury in COVID-19 patients. The pathobiology of CNS infection by SARS-CoV-2 and the associated neurological sequelae of this infection remain poorly understood. In this review, we outline the rationale for the use of blood biomarkers (BBs) for diagnosis of brain injury in COVID-19 patients, the research needed to incorporate their use into clinical practice, and the improvements in patient management and outcomes that can result. BBs of brain injury could potentially provide tools for detection of brain injury in COVID-19 patients. Elevations of BBs have been reported in cerebrospinal fluid (CSF) and blood of COVID-19 patients. BB proteins have been analyzed in CSF to detect CNS involvement in patients with infectious diseases, including human immunodeficiency virus and tuberculous meningitis. BBs are approved by the U.S. Food and Drug Administration for diagnosis of mild versus moderate traumatic brain injury and have identified brain injury after stroke, cardiac arrest, hypoxia, and epilepsy. BBs, integrated with other diagnostic tools, could enhance understanding of viral mechanisms of brain injury, predict severity of neurological deficits, guide triage of patients and assignment to appropriate medical pathways, and assess efficacy of therapeutic interventions in COVID-19 patients.</AbstractText>
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<LastName>DeKosky</LastName>
<ForeName>Steven T</ForeName>
<Initials>ST</Initials>
<AffiliationInfo>
<Affiliation>McKnight Brain Institute, University of Florida College of Medicine, Gainesville, Florida, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Kochanek</LastName>
<ForeName>Patrick M</ForeName>
<Initials>PM</Initials>
<AffiliationInfo>
<Affiliation>Department of Critical Care Medicine, Department of Anesthesiology, Pediatrics, Bioengineering, and Clinical and Translational Science, Safar Center for Resuscitation Research, University of Pittsburgh School of Medicine, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.</Affiliation>
</AffiliationInfo>
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<LastName>Valadka</LastName>
<ForeName>Alex B</ForeName>
<Initials>AB</Initials>
<AffiliationInfo>
<Affiliation>Department of Neurosurgery, Virginia Commonwealth University, Richmond, Virginia, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Clark</LastName>
<ForeName>Robert S B</ForeName>
<Initials>RSB</Initials>
<AffiliationInfo>
<Affiliation>Department of Critical Care Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Chou</LastName>
<ForeName>Sherry H-Y</ForeName>
<Initials>SH</Initials>
<AffiliationInfo>
<Affiliation>Department of Critical Care Medicine, Neurology, and Neurosurgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.</Affiliation>
</AffiliationInfo>
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<ForeName>Alicia K</ForeName>
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<Affiliation>University of Pittsburgh, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.</Affiliation>
</AffiliationInfo>
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<LastName>Horvat</LastName>
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</AffiliationInfo>
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</AffiliationInfo>
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<LastName>Mannix</LastName>
<ForeName>Rebekah</ForeName>
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<Affiliation>Department of Pediatrics and Emergency Medicine, Harvard Medical School, Department of Medicine, Division of Emergency Medicine, Boston Children's Hospital, Boston, Massachusetts, USA.</Affiliation>
</AffiliationInfo>
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<LastName>Wisniewski</LastName>
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</AffiliationInfo>
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<LastName>Wintermark</LastName>
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</AffiliationInfo>
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<LastName>Lewis</LastName>
<ForeName>Lawrence</ForeName>
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<Affiliation>Department of Emergency Medicine, Washington University in St. Louis, St. Louis, Missouri, USA.</Affiliation>
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<LastName>House</LastName>
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<Affiliation>Genetics and Aging Research Unit, Massachusetts General Hospital, McCance Center for Brain Health, Massachusetts General Hospital, MassGeneral Institute for Neurodegenerative Diseases, Massachusetts General Hospital, Department of Neurology (Research), Massachusetts General Hospital, Department of Neurology, Harvard Medical School, Charlestown, Massachusetts, USA.</Affiliation>
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<LastName>Smith</LastName>
<ForeName>Darci R</ForeName>
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<Affiliation>Immunodiagnostics Department, Naval Medical Research Center, Biological Defense Research Directorate, Fort Detrick, Maryland, USA.</Affiliation>
</AffiliationInfo>
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<Affiliation>Division of Infectious Disease and Global Medicine, University of Florida, Emerging Pathogens Institute, Gainesville, Florida, USA.</Affiliation>
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<LastName>Denslow</LastName>
<ForeName>Nancy D</ForeName>
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<Affiliation>Departments of Physiological Sciences and Biochemistry and Molecular Biology, University of Florida, Center for Environmental and Human Toxicology, Gainesville, Florida.</Affiliation>
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<LastName>Davis</LastName>
<ForeName>Michael D</ForeName>
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<AffiliationInfo>
<Affiliation>Department of Pediatrics, Wells Center for Pediatric Research/Pulmonology, Allergy, and Sleep Medicine, Riley Hospital for Children at Indiana University, Indianapolis, Indiana, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Glushakova</LastName>
<ForeName>Olena Y</ForeName>
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<AffiliationInfo>
<Affiliation>University of Virginia Cancer Center, Charlottesville, Virginia, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Hayes</LastName>
<ForeName>Ronald L</ForeName>
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<Affiliation>Banyan Biomarkers Inc., Alachua, Florida, USA.</Affiliation>
</AffiliationInfo>
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<Grant>
<GrantID>P01 HL128192</GrantID>
<Acronym>HL</Acronym>
<Agency>NHLBI NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant>
<GrantID>K23 HD099331</GrantID>
<Acronym>HD</Acronym>
<Agency>NICHD NIH HHS</Agency>
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<MeshHeading>
<DescriptorName UI="D001921" MajorTopicYN="N">Brain</DescriptorName>
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<QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName>
<QualifierName UI="Q000209" MajorTopicYN="N">etiology</QualifierName>
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