Serveur d'exploration sur la COVID chez les séniors

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Lung involvement in macrophage activation syndrome and severe COVID-19: results from a cross-sectional study to assess clinical, laboratory and artificial intelligence-radiological differences.

Identifieur interne : 000443 ( Main/Exploration ); précédent : 000442; suivant : 000444

Lung involvement in macrophage activation syndrome and severe COVID-19: results from a cross-sectional study to assess clinical, laboratory and artificial intelligence-radiological differences.

Auteurs : Piero Ruscitti [Italie] ; Federico Bruno [Italie] ; Onorina Berardicurti [Italie] ; Chiara Acanfora [Italie] ; Viktoriya Pavlych [Italie] ; Pierpaolo Palumbo [Italie] ; Alessandro Conforti [Italie] ; Francesco Carubbi [Italie] ; Ilenia Di Cola [Italie] ; Paola Di Benedetto [Italie] ; Paola Cipriani [Italie] ; Davide Grassi [Italie] ; Carlo Masciocchi [Italie] ; Annamaria Iagnocco [Oman] ; Antonio Barile [Italie] ; Roberto Giacomelli [Italie]

Source :

RBID : pubmed:32719039

Descripteurs français

English descriptors

Abstract

OBJECTIVES

To evaluate the clinical pictures, laboratory tests and imaging of patients with lung involvement, either from severe COVID-19 or macrophage activation syndrome (MAS), in order to assess how similar these two diseases are.

METHODS

The present work has been designed as a cross-sectional single-centre study to compare characteristics of patients with lung involvement either from MAS or severe COVID-19. Chest CT scans were assessed by using an artificial intelligence (AI)-based software.

RESULTS

Ten patients with MAS and 47 patients with severe COVID-19 with lung involvement were assessed. Although all patients showed fever and dyspnoea, patients with MAS were characterised by thrombocytopaenia, whereas patients with severe COVID-19 were characterised by lymphopaenia and neutrophilia. Higher values of H-score characterised patients with MAS when compared with severe COVID-19. AI-reconstructed images of chest CT scan showed that apical, basal, peripheral and bilateral distributions of ground-glass opacities (GGOs), as well as apical consolidations, were more represented in severe COVID-19 than in MAS. C reactive protein directly correlated with GGOs extension in both diseases. Furthermore, lymphopaenia inversely correlated with GGOs extension in severe COVID-19.

CONCLUSIONS

Our data could suggest laboratory and radiological differences between MAS and severe COVID-19, paving the way for further hypotheses to be investigated in future confirmatory studies.


DOI: 10.1136/annrheumdis-2020-218048
PubMed: 32719039
PubMed Central: PMC7456556


Affiliations:


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<keywords scheme="KwdEn" xml:lang="en">
<term>Aged (MeSH)</term>
<term>Artificial Intelligence (MeSH)</term>
<term>Betacoronavirus (MeSH)</term>
<term>Coronavirus Infections (diagnostic imaging)</term>
<term>Coronavirus Infections (pathology)</term>
<term>Coronavirus Infections (virology)</term>
<term>Cross-Sectional Studies (MeSH)</term>
<term>Female (MeSH)</term>
<term>Humans (MeSH)</term>
<term>Lung (diagnostic imaging)</term>
<term>Lung (pathology)</term>
<term>Lung (virology)</term>
<term>Macrophage Activation Syndrome (diagnostic imaging)</term>
<term>Macrophage Activation Syndrome (pathology)</term>
<term>Male (MeSH)</term>
<term>Middle Aged (MeSH)</term>
<term>Pandemics (MeSH)</term>
<term>Pneumonia, Viral (diagnostic imaging)</term>
<term>Pneumonia, Viral (pathology)</term>
<term>Pneumonia, Viral (virology)</term>
<term>Retrospective Studies (MeSH)</term>
<term>Tomography, X-Ray Computed (methods)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Adulte d'âge moyen (MeSH)</term>
<term>Betacoronavirus (MeSH)</term>
<term>Femelle (MeSH)</term>
<term>Humains (MeSH)</term>
<term>Infections à coronavirus (anatomopathologie)</term>
<term>Infections à coronavirus (imagerie diagnostique)</term>
<term>Infections à coronavirus (virologie)</term>
<term>Intelligence artificielle (MeSH)</term>
<term>Mâle (MeSH)</term>
<term>Pandémies (MeSH)</term>
<term>Pneumopathie virale (anatomopathologie)</term>
<term>Pneumopathie virale (imagerie diagnostique)</term>
<term>Pneumopathie virale (virologie)</term>
<term>Poumon (anatomopathologie)</term>
<term>Poumon (imagerie diagnostique)</term>
<term>Poumon (virologie)</term>
<term>Sujet âgé (MeSH)</term>
<term>Syndrome d'activation macrophagique (anatomopathologie)</term>
<term>Syndrome d'activation macrophagique (imagerie diagnostique)</term>
<term>Tomodensitométrie (méthodes)</term>
<term>Études rétrospectives (MeSH)</term>
<term>Études transversales (MeSH)</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr">
<term>Infections à coronavirus</term>
<term>Pneumopathie virale</term>
<term>Poumon</term>
<term>Syndrome d'activation macrophagique</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnostic imaging" xml:lang="en">
<term>Coronavirus Infections</term>
<term>Lung</term>
<term>Macrophage Activation Syndrome</term>
<term>Pneumonia, Viral</term>
</keywords>
<keywords scheme="MESH" qualifier="imagerie diagnostique" xml:lang="fr">
<term>Infections à coronavirus</term>
<term>Pneumopathie virale</term>
<term>Poumon</term>
<term>Syndrome d'activation macrophagique</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en">
<term>Tomography, X-Ray Computed</term>
</keywords>
<keywords scheme="MESH" qualifier="méthodes" xml:lang="fr">
<term>Tomodensitométrie</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en">
<term>Coronavirus Infections</term>
<term>Lung</term>
<term>Macrophage Activation Syndrome</term>
<term>Pneumonia, Viral</term>
</keywords>
<keywords scheme="MESH" qualifier="virologie" xml:lang="fr">
<term>Infections à coronavirus</term>
<term>Pneumopathie virale</term>
<term>Poumon</term>
</keywords>
<keywords scheme="MESH" qualifier="virology" xml:lang="en">
<term>Coronavirus Infections</term>
<term>Lung</term>
<term>Pneumonia, Viral</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Aged</term>
<term>Artificial Intelligence</term>
<term>Betacoronavirus</term>
<term>Cross-Sectional Studies</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Pandemics</term>
<term>Retrospective Studies</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Adulte d'âge moyen</term>
<term>Betacoronavirus</term>
<term>Femelle</term>
<term>Humains</term>
<term>Intelligence artificielle</term>
<term>Mâle</term>
<term>Pandémies</term>
<term>Sujet âgé</term>
<term>Études rétrospectives</term>
<term>Études transversales</term>
</keywords>
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<front>
<div type="abstract" xml:lang="en">
<p>
<b>OBJECTIVES</b>
</p>
<p>To evaluate the clinical pictures, laboratory tests and imaging of patients with lung involvement, either from severe COVID-19 or macrophage activation syndrome (MAS), in order to assess how similar these two diseases are.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>METHODS</b>
</p>
<p>The present work has been designed as a cross-sectional single-centre study to compare characteristics of patients with lung involvement either from MAS or severe COVID-19. Chest CT scans were assessed by using an artificial intelligence (AI)-based software.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>Ten patients with MAS and 47 patients with severe COVID-19 with lung involvement were assessed. Although all patients showed fever and dyspnoea, patients with MAS were characterised by thrombocytopaenia, whereas patients with severe COVID-19 were characterised by lymphopaenia and neutrophilia. Higher values of H-score characterised patients with MAS when compared with severe COVID-19. AI-reconstructed images of chest CT scan showed that apical, basal, peripheral and bilateral distributions of ground-glass opacities (GGOs), as well as apical consolidations, were more represented in severe COVID-19 than in MAS. C reactive protein directly correlated with GGOs extension in both diseases. Furthermore, lymphopaenia inversely correlated with GGOs extension in severe COVID-19.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSIONS</b>
</p>
<p>Our data could suggest laboratory and radiological differences between MAS and severe COVID-19, paving the way for further hypotheses to be investigated in future confirmatory studies.</p>
</div>
</front>
</TEI>
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<Year>2020</Year>
<Month>09</Month>
<Day>08</Day>
</DateCompleted>
<DateRevised>
<Year>2020</Year>
<Month>09</Month>
<Day>08</Day>
</DateRevised>
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<Journal>
<ISSN IssnType="Electronic">1468-2060</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>79</Volume>
<Issue>9</Issue>
<PubDate>
<Year>2020</Year>
<Month>09</Month>
</PubDate>
</JournalIssue>
<Title>Annals of the rheumatic diseases</Title>
<ISOAbbreviation>Ann Rheum Dis</ISOAbbreviation>
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<ArticleTitle>Lung involvement in macrophage activation syndrome and severe COVID-19: results from a cross-sectional study to assess clinical, laboratory and artificial intelligence-radiological differences.</ArticleTitle>
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<Abstract>
<AbstractText Label="OBJECTIVES">To evaluate the clinical pictures, laboratory tests and imaging of patients with lung involvement, either from severe COVID-19 or macrophage activation syndrome (MAS), in order to assess how similar these two diseases are.</AbstractText>
<AbstractText Label="METHODS">The present work has been designed as a cross-sectional single-centre study to compare characteristics of patients with lung involvement either from MAS or severe COVID-19. Chest CT scans were assessed by using an artificial intelligence (AI)-based software.</AbstractText>
<AbstractText Label="RESULTS">Ten patients with MAS and 47 patients with severe COVID-19 with lung involvement were assessed. Although all patients showed fever and dyspnoea, patients with MAS were characterised by thrombocytopaenia, whereas patients with severe COVID-19 were characterised by lymphopaenia and neutrophilia. Higher values of H-score characterised patients with MAS when compared with severe COVID-19. AI-reconstructed images of chest CT scan showed that apical, basal, peripheral and bilateral distributions of ground-glass opacities (GGOs), as well as apical consolidations, were more represented in severe COVID-19 than in MAS. C reactive protein directly correlated with GGOs extension in both diseases. Furthermore, lymphopaenia inversely correlated with GGOs extension in severe COVID-19.</AbstractText>
<AbstractText Label="CONCLUSIONS">Our data could suggest laboratory and radiological differences between MAS and severe COVID-19, paving the way for further hypotheses to be investigated in future confirmatory studies.</AbstractText>
<CopyrightInformation>© Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.</CopyrightInformation>
</Abstract>
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<LastName>Ruscitti</LastName>
<ForeName>Piero</ForeName>
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<Affiliation>Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Abruzzo, Italy.</Affiliation>
</AffiliationInfo>
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<LastName>Bruno</LastName>
<ForeName>Federico</ForeName>
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<Affiliation>Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Abruzzo, Italy.</Affiliation>
</AffiliationInfo>
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<ForeName>Onorina</ForeName>
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<AffiliationInfo>
<Affiliation>Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Abruzzo, Italy.</Affiliation>
</AffiliationInfo>
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<Affiliation>Department of Medicine, ASL 1 Avezzano Sulmona L'Aquila, L'Aquila, Abruzzo, Italy.</Affiliation>
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<LastName>Di Cola</LastName>
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<Affiliation>Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Abruzzo, Italy.</Affiliation>
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<Affiliation>Department of Life, Health, and Environmental Sciences, University of L'Aquila, L'Aquila, Abruzzo, Italy.</Affiliation>
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<LastName>Masciocchi</LastName>
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<Affiliation>Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Abruzzo, Italy.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Iagnocco</LastName>
<ForeName>Annamaria</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Dipartimento Scienze Cliniche e Biologiche, Università degli Studi di Torino, Torino, Piemonte, Italy annamaria.iagnocco1@gmail.com.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Barile</LastName>
<ForeName>Antonio</ForeName>
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<AffiliationInfo>
<Affiliation>Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Abruzzo, Italy.</Affiliation>
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</Author>
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<LastName>Giacomelli</LastName>
<ForeName>Roberto</ForeName>
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<Identifier Source="ORCID">0000-0003-0670-9638</Identifier>
<AffiliationInfo>
<Affiliation>Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Abruzzo, Italy.</Affiliation>
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<Month>07</Month>
<Day>21</Day>
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<Keyword MajorTopicYN="Y">inflammation</Keyword>
<Keyword MajorTopicYN="Y">still's disease, adult-onset</Keyword>
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<CoiStatement>Competing interests: None declared.</CoiStatement>
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<name sortKey="Di Cola, Ilenia" sort="Di Cola, Ilenia" uniqKey="Di Cola I" first="Ilenia" last="Di Cola">Ilenia Di Cola</name>
<name sortKey="Giacomelli, Roberto" sort="Giacomelli, Roberto" uniqKey="Giacomelli R" first="Roberto" last="Giacomelli">Roberto Giacomelli</name>
<name sortKey="Grassi, Davide" sort="Grassi, Davide" uniqKey="Grassi D" first="Davide" last="Grassi">Davide Grassi</name>
<name sortKey="Masciocchi, Carlo" sort="Masciocchi, Carlo" uniqKey="Masciocchi C" first="Carlo" last="Masciocchi">Carlo Masciocchi</name>
<name sortKey="Palumbo, Pierpaolo" sort="Palumbo, Pierpaolo" uniqKey="Palumbo P" first="Pierpaolo" last="Palumbo">Pierpaolo Palumbo</name>
<name sortKey="Pavlych, Viktoriya" sort="Pavlych, Viktoriya" uniqKey="Pavlych V" first="Viktoriya" last="Pavlych">Viktoriya Pavlych</name>
</country>
<country name="Oman">
<noRegion>
<name sortKey="Iagnocco, Annamaria" sort="Iagnocco, Annamaria" uniqKey="Iagnocco A" first="Annamaria" last="Iagnocco">Annamaria Iagnocco</name>
</noRegion>
</country>
</tree>
</affiliations>
</record>

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{{Explor lien
   |wiki=    Sante
   |area=    CovidSeniorV1
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
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   |texte=   Lung involvement in macrophage activation syndrome and severe COVID-19: results from a cross-sectional study to assess clinical, laboratory and artificial intelligence-radiological differences.
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Pour générer des pages wiki

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Data generation: Thu Oct 15 09:49:45 2020. Site generation: Wed Jan 27 17:10:23 2021