Serveur d'exploration sur la COVID en France

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Highly sensitive quantification of plasma SARS-CoV-2 RNA shelds light on its potential clinical value.

Identifieur interne : 000E30 ( Main/Exploration ); précédent : 000E29; suivant : 000E31

Highly sensitive quantification of plasma SARS-CoV-2 RNA shelds light on its potential clinical value.

Auteurs : David Veyer [France] ; Solen Kernéis [France] ; Geoffroy Poulet [France] ; Maxime Wack [France] ; Nicolas Robillard [France] ; Valérie Taly [France] ; Anne-Sophie L'Honneur [France] ; Flore Rozenberg [France] ; Pierre Laurent-Puig [France] ; Laurent Bélec [France] ; Jérôme Hadjadj [France] ; Benjamin Terrier [France] ; Hélène Péré [France]

Source :

RBID : pubmed:32803231

Abstract

BACKGROUND

Coronavirus disease 2019 (COVID-19) is a global public health problem that has already caused more than 662,000 deaths worldwide. Although the clinical manifestations of COVID-19 are dominated by respiratory symptoms, some patients present other severe damage such as cardiovascular, renal and liver injury or/and multiple organ failure, suggesting a spread of the SARS-CoV-2 in blood. Recent ultrasensitive polymerase chain reaction (PCR) technology now allows absolute quantification of nucleic acids in plasma. We herein intended to use the droplet-based digital PCR technology to obtain sensitive detection and precise quantification of plasma SARS-CoV-2 viral load (SARS-CoV-2 RNAaemia) in hospitalized COVID-19 patients.

METHODS

Fifty-eight consecutive COVID-19 patients with pneumonia 8 to 12 days after onset of symptoms and 12 healthy controls were analyzed. Disease severity was categorized as mild-to-moderate in 17 patients, severe in 16 patients and critical in 26 patients. Plasma SARS-CoV-2 RNAaemia was quantified by droplet digital Crystal Digital PCR™ next-generation technology (Stilla Technologies, Villejuif, France).

RESULTS

Overall, SARS-CoV-2 RNAaemia was detected in 43 (74.1%) patients. Prevalence of positive SARS-CoV-2 RNAaemia correlated with disease severity, ranging from 53% in mild-to-moderate patients to 88% in critically ill patients (p=0.036). Levels of SARS-CoV-2 RNAaemia were associated with severity (p=0.035). Among nine patients who experienced clinical deterioration during follow-up, eight had positive SARS-CoV-2 RNAaemia at baseline while only one critical patient with undetectable SARS-CoV-2 RNAaemia at the time of analysis died at day 27.

CONCLUSION

SARS-CoV-2 RNAaemia measured by droplet-based digital PCR constitutes a promising prognosis biomarker in COVID-19 patients.


DOI: 10.1093/cid/ciaa1196
PubMed: 32803231
PubMed Central: PMC7454373


Affiliations:


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<name sortKey="Pere, Helene" sort="Pere, Helene" uniqKey="Pere H" first="Hélène" last="Péré">Hélène Péré</name>
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<name sortKey="Wack, Maxime" sort="Wack, Maxime" uniqKey="Wack M" first="Maxime" last="Wack">Maxime Wack</name>
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<name sortKey="Robillard, Nicolas" sort="Robillard, Nicolas" uniqKey="Robillard N" first="Nicolas" last="Robillard">Nicolas Robillard</name>
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<name sortKey="Taly, Valerie" sort="Taly, Valerie" uniqKey="Taly V" first="Valérie" last="Taly">Valérie Taly</name>
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</affiliation>
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<author>
<name sortKey="L Honneur, Anne Sophie" sort="L Honneur, Anne Sophie" uniqKey="L Honneur A" first="Anne-Sophie" last="L'Honneur">Anne-Sophie L'Honneur</name>
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<nlm:affiliation>Centre de Recherche des Cordeliers, Sorbonne Université, Inserm, Université de Paris, Information sciences to support medicine Paris, France.</nlm:affiliation>
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<wicri:regionArea>Centre de Recherche des Cordeliers, Sorbonne Université, Inserm, Université de Paris, Information sciences to support medicine Paris</wicri:regionArea>
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<author>
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<nlm:affiliation>Institut Pasteur, Epidemiology and Modelling of Antibiotic Evasion (EMAE), F-75015 Paris, France.</nlm:affiliation>
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<settlement type="city">Paris</settlement>
</placeName>
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<country xml:lang="fr">France</country>
<wicri:regionArea>Assistance Publique Hôpitaux de Paris-Centre (AP-HP.Centre), Service de Virologie, Hôpital Cochin, Paris</wicri:regionArea>
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<author>
<name sortKey="Belec, Laurent" sort="Belec, Laurent" uniqKey="Belec L" first="Laurent" last="Bélec">Laurent Bélec</name>
<affiliation wicri:level="3">
<nlm:affiliation>Assistance Publique Hôpitaux de Paris-Centre (AP-HP.Centre), Service de Microbiologie (Unité de virologie), Hôpital Européen Georges Pompidou, Paris, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
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<region type="region">Île-de-France</region>
<region type="old region">Île-de-France</region>
<settlement type="city">Paris</settlement>
</placeName>
</affiliation>
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<nlm:affiliation>Department of Internal Medicine, National Referral Center for Rare Systemic Autoimmune Diseases, AP-HP CUP, Paris, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>Department of Internal Medicine, National Referral Center for Rare Systemic Autoimmune Diseases, AP-HP CUP, Paris</wicri:regionArea>
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<region type="old region">Île-de-France</region>
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<author>
<name sortKey="Hadjadj, Jerome" sort="Hadjadj, Jerome" uniqKey="Hadjadj J" first="Jérôme" last="Hadjadj">Jérôme Hadjadj</name>
<affiliation wicri:level="3">
<nlm:affiliation>Assistance Publique Hôpitaux de Paris-Centre (AP-HP.Centre), Service de Biochimie, Hôpital Européen Georges Pompidou, Paris, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
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<region type="region">Île-de-France</region>
<region type="old region">Île-de-France</region>
<settlement type="city">Paris</settlement>
</placeName>
</affiliation>
<affiliation>
<nlm:affiliation>Imagine Institute, laboratory of Immunogenetics of Pediatric Autoimmune Diseases, INSERM UMR 1163.</nlm:affiliation>
<wicri:noCountry code="subField">INSERM UMR 1163</wicri:noCountry>
</affiliation>
</author>
<author>
<name sortKey="Terrier, Benjamin" sort="Terrier, Benjamin" uniqKey="Terrier B" first="Benjamin" last="Terrier">Benjamin Terrier</name>
<affiliation>
<nlm:affiliation>Imagine Institute, laboratory of Immunogenetics of Pediatric Autoimmune Diseases, INSERM UMR 1163.</nlm:affiliation>
<wicri:noCountry code="subField">INSERM UMR 1163</wicri:noCountry>
</affiliation>
<affiliation wicri:level="3">
<nlm:affiliation>Department of Internal Medicine, National Referral Center for Rare Systemic Autoimmune Diseases, AP-HP CUP, Paris, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>Department of Internal Medicine, National Referral Center for Rare Systemic Autoimmune Diseases, AP-HP CUP, Paris</wicri:regionArea>
<placeName>
<region type="region">Île-de-France</region>
<region type="old region">Île-de-France</region>
<settlement type="city">Paris</settlement>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Pere, Helene" sort="Pere, Helene" uniqKey="Pere H" first="Hélène" last="Péré">Hélène Péré</name>
<affiliation wicri:level="3">
<nlm:affiliation>Assistance Publique Hôpitaux de Paris-Centre (AP-HP.Centre), Service de Microbiologie (Unité de virologie), Hôpital Européen Georges Pompidou, Paris, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
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<placeName>
<region type="region">Île-de-France</region>
<region type="old region">Île-de-France</region>
<settlement type="city">Paris</settlement>
</placeName>
</affiliation>
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<nlm:affiliation>PARCC, Université de Paris, INSERM U970, Paris, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>PARCC, Université de Paris, INSERM U970, Paris</wicri:regionArea>
<placeName>
<region type="region">Île-de-France</region>
<region type="old region">Île-de-France</region>
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<series>
<title level="j">Clinical infectious diseases : an official publication of the Infectious Diseases Society of America</title>
<idno type="eISSN">1537-6591</idno>
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<date when="2020" type="published">2020</date>
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<div type="abstract" xml:lang="en">
<p>
<b>BACKGROUND</b>
</p>
<p>Coronavirus disease 2019 (COVID-19) is a global public health problem that has already caused more than 662,000 deaths worldwide. Although the clinical manifestations of COVID-19 are dominated by respiratory symptoms, some patients present other severe damage such as cardiovascular, renal and liver injury or/and multiple organ failure, suggesting a spread of the SARS-CoV-2 in blood. Recent ultrasensitive polymerase chain reaction (PCR) technology now allows absolute quantification of nucleic acids in plasma. We herein intended to use the droplet-based digital PCR technology to obtain sensitive detection and precise quantification of plasma SARS-CoV-2 viral load (SARS-CoV-2 RNAaemia) in hospitalized COVID-19 patients.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>METHODS</b>
</p>
<p>Fifty-eight consecutive COVID-19 patients with pneumonia 8 to 12 days after onset of symptoms and 12 healthy controls were analyzed. Disease severity was categorized as mild-to-moderate in 17 patients, severe in 16 patients and critical in 26 patients. Plasma SARS-CoV-2 RNAaemia was quantified by droplet digital Crystal Digital PCR™ next-generation technology (Stilla Technologies, Villejuif, France).</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>Overall, SARS-CoV-2 RNAaemia was detected in 43 (74.1%) patients. Prevalence of positive SARS-CoV-2 RNAaemia correlated with disease severity, ranging from 53% in mild-to-moderate patients to 88% in critically ill patients (p=0.036). Levels of SARS-CoV-2 RNAaemia were associated with severity (p=0.035). Among nine patients who experienced clinical deterioration during follow-up, eight had positive SARS-CoV-2 RNAaemia at baseline while only one critical patient with undetectable SARS-CoV-2 RNAaemia at the time of analysis died at day 27.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSION</b>
</p>
<p>SARS-CoV-2 RNAaemia measured by droplet-based digital PCR constitutes a promising prognosis biomarker in COVID-19 patients.</p>
</div>
</front>
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<DateRevised>
<Year>2020</Year>
<Month>09</Month>
<Day>01</Day>
</DateRevised>
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<Journal>
<ISSN IssnType="Electronic">1537-6591</ISSN>
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<PubDate>
<Year>2020</Year>
<Month>Aug</Month>
<Day>17</Day>
</PubDate>
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<Title>Clinical infectious diseases : an official publication of the Infectious Diseases Society of America</Title>
<ISOAbbreviation>Clin. Infect. Dis.</ISOAbbreviation>
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<ArticleTitle>Highly sensitive quantification of plasma SARS-CoV-2 RNA shelds light on its potential clinical value.</ArticleTitle>
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<ELocationID EIdType="doi" ValidYN="Y">10.1093/cid/ciaa1196</ELocationID>
<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Coronavirus disease 2019 (COVID-19) is a global public health problem that has already caused more than 662,000 deaths worldwide. Although the clinical manifestations of COVID-19 are dominated by respiratory symptoms, some patients present other severe damage such as cardiovascular, renal and liver injury or/and multiple organ failure, suggesting a spread of the SARS-CoV-2 in blood. Recent ultrasensitive polymerase chain reaction (PCR) technology now allows absolute quantification of nucleic acids in plasma. We herein intended to use the droplet-based digital PCR technology to obtain sensitive detection and precise quantification of plasma SARS-CoV-2 viral load (SARS-CoV-2 RNAaemia) in hospitalized COVID-19 patients.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Fifty-eight consecutive COVID-19 patients with pneumonia 8 to 12 days after onset of symptoms and 12 healthy controls were analyzed. Disease severity was categorized as mild-to-moderate in 17 patients, severe in 16 patients and critical in 26 patients. Plasma SARS-CoV-2 RNAaemia was quantified by droplet digital Crystal Digital PCR™ next-generation technology (Stilla Technologies, Villejuif, France).</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Overall, SARS-CoV-2 RNAaemia was detected in 43 (74.1%) patients. Prevalence of positive SARS-CoV-2 RNAaemia correlated with disease severity, ranging from 53% in mild-to-moderate patients to 88% in critically ill patients (p=0.036). Levels of SARS-CoV-2 RNAaemia were associated with severity (p=0.035). Among nine patients who experienced clinical deterioration during follow-up, eight had positive SARS-CoV-2 RNAaemia at baseline while only one critical patient with undetectable SARS-CoV-2 RNAaemia at the time of analysis died at day 27.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">SARS-CoV-2 RNAaemia measured by droplet-based digital PCR constitutes a promising prognosis biomarker in COVID-19 patients.</AbstractText>
<CopyrightInformation>© The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.</CopyrightInformation>
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<LastName>Veyer</LastName>
<ForeName>David</ForeName>
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</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Centre de Recherche des Cordeliers, Sorbonne Université, Inserm, Université de Paris, Functional Genomics of Solid Tumors laboratory, équipe labellisée Ligue Nationale contre le Cancer, Labex OncoImmunology, Paris, France.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Kernéis</LastName>
<ForeName>Solen</ForeName>
<Initials>S</Initials>
<AffiliationInfo>
<Affiliation>Equipe Mobile d'Infectiologie, AP-HP, APHP.CUP, Hôpital Cochin, F-75014 Paris, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Université de Paris, INSERM, IAME, F-75006 Paris, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Institut Pasteur, Epidemiology and Modelling of Antibiotic Evasion (EMAE), F-75015 Paris, France.</Affiliation>
</AffiliationInfo>
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<LastName>Poulet</LastName>
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<LastName>Wack</LastName>
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</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Département d'Informatique Médicale, Biostatistiques et Santé Publique, Hôpital Européen Georges Pompidou, AP-HP CUP, Paris, France.</Affiliation>
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<AffiliationInfo>
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</AffiliationInfo>
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<AffiliationInfo>
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<LastName>Terrier</LastName>
<ForeName>Benjamin</ForeName>
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<Affiliation>Imagine Institute, laboratory of Immunogenetics of Pediatric Autoimmune Diseases, INSERM UMR 1163.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Internal Medicine, National Referral Center for Rare Systemic Autoimmune Diseases, AP-HP CUP, Paris, France.</Affiliation>
</AffiliationInfo>
</Author>
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<Affiliation>PARCC, Université de Paris, INSERM U970, Paris, France.</Affiliation>
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<name sortKey="Laurent Puig, Pierre" sort="Laurent Puig, Pierre" uniqKey="Laurent Puig P" first="Pierre" last="Laurent-Puig">Pierre Laurent-Puig</name>
<name sortKey="Pere, Helene" sort="Pere, Helene" uniqKey="Pere H" first="Hélène" last="Péré">Hélène Péré</name>
<name sortKey="Pere, Helene" sort="Pere, Helene" uniqKey="Pere H" first="Hélène" last="Péré">Hélène Péré</name>
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<name sortKey="Rozenberg, Flore" sort="Rozenberg, Flore" uniqKey="Rozenberg F" first="Flore" last="Rozenberg">Flore Rozenberg</name>
<name sortKey="Taly, Valerie" sort="Taly, Valerie" uniqKey="Taly V" first="Valérie" last="Taly">Valérie Taly</name>
<name sortKey="Terrier, Benjamin" sort="Terrier, Benjamin" uniqKey="Terrier B" first="Benjamin" last="Terrier">Benjamin Terrier</name>
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<name sortKey="Wack, Maxime" sort="Wack, Maxime" uniqKey="Wack M" first="Maxime" last="Wack">Maxime Wack</name>
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