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Dynamics of circulating calprotectin accurately predict the outcome of moderate COVID-19 patients.
Chapuis, Nicolas; Ibrahimi, Nusaibah; Belmondo, Thibaut; Goulvestre, Claire; Berger, Anne-Emmanuelle; Mariaggi, Alice-Andrée; Andrieu, Muriel; Chenevier-Gobeaux, Camille; Bayle, Arnaud; Campos, Lydia; Cheurfa, Cherifa; Chocron, Richard; Diehl, Jean-Luc; Doumenc, Benoît; Duchemin, Jérôme; Duprat, Manon; François, Fabien; Gendron, Nicolas; Mirault, Tristant; Pène, Frédéric; Philippe, Aurélien; Pommeret, Fanny; Sanchez, Olivier; Smadja, David M; Szwebel, Tali-Anne; Silvin, Aymeric; Ginhoux, Florent; Lacroix, Ludovic; Jules-Clément, Gérôme; Rapeteramana, Sarobidy; Mavier, Colette; Steller, Laura; Perniconi, Barbara; André, Fabrice; Drubay, Damien; Fontenay, Michaela; Hüe, Sophie; Paul, Stéphane; Solary, Eric.
  • Chapuis N; Laboratory of Hematology, Assistance Publique-Hôpitaux de Paris, Cochin Hospital, Paris, France; Université de Paris, Institut Cochin, CNRS UMR8104, INSERM U1016, Paris, France.
  • Ibrahimi N; Department of Biostatistics and Epidemiology, Gustave Roussy Cancer Center, Villejuif, France; Université Paris-Saclay, INSERM U1018, Gustave Roussy Cancer Center, Villejuif, France.
  • Belmondo T; Laboratory of Immunology, Assistance Publique-Hôpitaux de Paris, Groupe Hospitalier Henri Mondor, Créteil, France.
  • Goulvestre C; Laboratory of Immunology, Assistance Publique-Hôpitaux de Paris, Cochin Hospital, Paris, France.
  • Berger AE; Department of Immunology, University Hospital of Saint Etienne, CIC1408, GIMAP EA3064, Saint Etienne, France.
  • Mariaggi AA; Université de Paris, Institut Cochin, CNRS UMR8104, INSERM U1016, Paris, France; Assistance Publique-Hôpitaux de Paris, Laboratory of Virology, Cochin hospital, Paris, France.
  • Andrieu M; Université de Paris, Institut Cochin, CNRS UMR8104, INSERM U1016, Paris, France.
  • Chenevier-Gobeaux C; Department of automated biological diagnosis, Assistance Publique-Hôpitaux de Paris, Cochin Hospital, Paris, France.
  • Bayle A; Department of Biostatistics and Epidemiology, Gustave Roussy Cancer Center, Villejuif, France; Université Paris-Saclay, INSERM U1018, Gustave Roussy Cancer Center, Villejuif, France; Drug Development Department, Gustave Roussy Cancer Center, Villejuif, France.
  • Campos L; Department of Hematology, University Hospital of Saint Etienne, Saint Etienne, France.
  • Cheurfa C; Department of Anesthesiology and Intensive care, Assistance Publique-Hôpitaux de Paris, Cochin hospital, Paris, France.
  • Chocron R; Department of Emergency, Assistance Publique-Hôpitaux de Paris, European Georges Pompidou Hospital, Paris, France; Paris Cardiovascular Research Center (PARCC), Université de Paris, INSERM U970, European Georges Pompidou Hospital, Paris, France.
  • Diehl JL; Medical Intensive Care Department and Biosurgical Research Lab (Carpentier Foundation), Assistance Publique-Hôpitaux de Paris, Georges Pompidou European Hospital, Paris, France; Université de Paris, Innovative Therapies in Haemostasis, INSERM U1140, Paris France.
  • Doumenc B; Department of Emergencies, Assistance Publique-Hôpitaux de Paris, Cochin Hospital, Paris, France.
  • Duchemin J; Laboratory of Hematology, Assistance Publique-Hôpitaux de Paris, Cochin Hospital, Paris, France.
  • Duprat M; Department of Immunology, University Hospital of Saint Etienne, CIC1408, GIMAP EA3064, Saint Etienne, France.
  • François F; Department of Immunology, University Hospital of Saint Etienne, CIC1408, GIMAP EA3064, Saint Etienne, France.
  • Gendron N; Université de Paris, Innovative Therapies in Haemostasis, INSERM U1140, Paris France; Department of Emergencies, Assistance Publique-Hôpitaux de Paris, Cochin Hospital, Paris, France.
  • Mirault T; Paris Cardiovascular Research Center (PARCC), Université de Paris, INSERM U970, European Georges Pompidou Hospital, Paris, France.
  • Pène F; Université de Paris, Institut Cochin, CNRS UMR8104, INSERM U1016, Paris, France; Assistance Publique-Hôpitaux de Paris, Medical Intensive Care, Cochin hospital, Paris, France.
  • Philippe A; Université de Paris, Innovative Therapies in Haemostasis, INSERM U1140, Paris France; Department of Biological Hematology, Assistance Publique-Hôpitaux de Paris, Georges Pompidou European Hospital, Paris France; Laboratory of Hematology and Biosurgical Research (Carpentier Foundation)Assistance Publ
  • Pommeret F; Medical Oncology Department, Gustave Roussy Cancer Center, Villejuif, France.
  • Sanchez O; Université de Paris, Innovative Therapies in Haemostasis, INSERM U1140, Paris France; Department of Pneumology and Intensive Care, Assistance Publique-Hôpitaux de Paris, European Georges Pompidou Hospital, Paris, France.
  • Smadja DM; Université de Paris, Innovative Therapies in Haemostasis, INSERM U1140, Paris France; Department of Biological Hematology, Assistance Publique-Hôpitaux de Paris, Georges Pompidou European Hospital, Paris France.
  • Szwebel TA; Internal Medicine Department, Assistance Publique-Hôpitaux de Paris, Cochin hospital, Paris, France.
  • Silvin A; University Paris-Saclay, INSERM U1015, Gustave Roussy Cancer Center, Villejuif, France.
  • Ginhoux F; University Paris-Saclay, INSERM U1015, Gustave Roussy Cancer Center, Villejuif, France.
  • Lacroix L; Department of Biopathology, Gustave Roussy Cancer Center, Villejuif, France.
  • Jules-Clément G; Gustave Roussy Cancer Center, Bioinformatics platform, Université Paris-Saclay, INSERM US23, CNRS UMS 3655, Villejuif, France.
  • Rapeteramana S; Gustave Roussy Cancer Center, Bioinformatics platform, Université Paris-Saclay, INSERM US23, CNRS UMS 3655, Villejuif, France.
  • Mavier C; Thermofisher immunodiagnostics, Dardilly, France.
  • Steller L; Thermo Fisher Scientific ImmunoDiagnostics, Phadia GmbH, Freiburg, Germany.
  • Perniconi B; CerbaXpert Alliance, Saint Ouen L'Aumone, France.
  • André F; Medical Oncology Department, Gustave Roussy Cancer Center, Villejuif, France.
  • Drubay D; Department of Biostatistics and Epidemiology, Gustave Roussy Cancer Center, Villejuif, France; Université Paris-Saclay, INSERM U1018, Gustave Roussy Cancer Center, Villejuif, France.
  • Fontenay M; Laboratory of Hematology, Assistance Publique-Hôpitaux de Paris, Cochin Hospital, Paris, France; Université de Paris, Institut Cochin, CNRS UMR8104, INSERM U1016, Paris, France; Laboratory of Immunology, Assistance Publique-Hôpitaux de Paris, Cochin Hospital, Paris, France.
  • Hüe S; Laboratory of Immunology, Assistance Publique-Hôpitaux de Paris, Groupe Hospitalier Henri Mondor, Créteil, France.
  • Paul S; Department of Immunology, University Hospital of Saint Etienne, CIC1408, GIMAP EA3064, Saint Etienne, France.
  • Solary E; Université Paris-Saclay, INSERM U1287, Gustave Roussy Cancer Center, 114 rue Edouard Vaillant, Villejuif 94805, France; Department of Hematology, Gustave Roussy Cancer Center, Villejuif, France. Electronic address: eric.solary@gustaveroussy.fr.
EBioMedicine ; 80: 104077, 2022 Jun.
Article in English | MEDLINE | ID: covidwho-1867076
ABSTRACT

BACKGROUND:

Severe COVID-19 is associated with a high circulating level of calprotectin, the S100A8/S100A9 alarmin heterodimer. Baseline calprotectin amount measured in peripheral blood at diagnosis correlates with disease severity. The optimal use of this biomarker along COVID-19 course remains to be delineated.

METHODS:

We focused on patients with a WHO-defined moderate COVID-19 requiring hospitalization in a medical ward. We collected plasma and serum from three independent cohorts (N = 626 patients) and measured calprotectin amount at admission. We performed longitudinal measures of calprotectin in 457 of these patients (1461 samples) and used a joint latent class mixture model in which classes were defined by age, body mass index and comorbidities to identify calprotectin trajectories predicting the risk of transfer into an intensive care unit or death.

FINDINGS:

After adjustment for age, sex, body mass index and comorbidities, the predictive value of baseline calprotectin in patients with moderate COVID19 could be refined by serial monitoring of the biomarker. We discriminated three calprotectin trajectories associated with low, moderate, and high risk of poor outcome, and we designed an algorithm available as online software (https//calpla.gustaveroussy.fr8443/) to monitor the probability of a poor outcome in individual patients with moderate COVID-19.

INTERPRETATION:

These results emphasize the clinical interest of serial monitoring of calprotectin amount in the peripheral blood to anticipate the risk of poor outcomes in patients with moderate COVID-19 hospitalized in a standard care unit.

FUNDING:

The study received support (research grants) from ThermoFisher immunodiagnostics (France) and Gustave Roussy Foundation.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Leukocyte L1 Antigen Complex / COVID-19 Type of study: Cohort study / Diagnostic study / Observational study / Prognostic study Limits: Humans Language: English Journal: EBioMedicine Year: 2022 Document Type: Article Affiliation country: J.ebiom.2022.104077

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Leukocyte L1 Antigen Complex / COVID-19 Type of study: Cohort study / Diagnostic study / Observational study / Prognostic study Limits: Humans Language: English Journal: EBioMedicine Year: 2022 Document Type: Article Affiliation country: J.ebiom.2022.104077