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Impact of diabetes on COVID-19 prognosis beyond comorbidity burden: the CORONADO initiative

AIMS/HYPOTHESIS: Diabetes has been recognised as a pejorative prognostic factor in coronavirus disease 2019 (COVID-19). Since diabetes is typically a disease of advanced age, it remains unclear whether diabetes remains a COVID-19 risk factor beyond advanced age and associated comorbidities. We desig...

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Autores principales: Cariou, Bertrand, Wargny, Matthieu, Boureau, Anne-Sophie, Smati, Sarra, Tramunt, Blandine, Desailloud, Rachel, Lebeault, Maylis, Amadou, Coralie, Ancelle, Deborah, Balkau, Beverley, Bordier, Lyse, Borot, Sophie, Bourgeon, Muriel, Bourron, Olivier, Cosson, Emmanuel, Eisinger, Martin, Gonfroy-Leymarie, Céline, Julla, Jean-Baptiste, Marchand, Lucien, Meyer, Laurent, Seret-Bégué, Dominique, Simon, Dominique, Sultan, Ariane, Thivolet, Charles, Vambergue, Anne, Vatier, Camille, Winiszewski, Patrice, Saulnier, Pierre-Jean, Bauduceau, Bernard, Gourdy, Pierre, Hadjadj, Samy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9197674/
https://www.ncbi.nlm.nih.gov/pubmed/35701673
http://dx.doi.org/10.1007/s00125-022-05734-1
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author Cariou, Bertrand
Wargny, Matthieu
Boureau, Anne-Sophie
Smati, Sarra
Tramunt, Blandine
Desailloud, Rachel
Lebeault, Maylis
Amadou, Coralie
Ancelle, Deborah
Balkau, Beverley
Bordier, Lyse
Borot, Sophie
Bourgeon, Muriel
Bourron, Olivier
Cosson, Emmanuel
Eisinger, Martin
Gonfroy-Leymarie, Céline
Julla, Jean-Baptiste
Marchand, Lucien
Meyer, Laurent
Seret-Bégué, Dominique
Simon, Dominique
Sultan, Ariane
Thivolet, Charles
Vambergue, Anne
Vatier, Camille
Winiszewski, Patrice
Saulnier, Pierre-Jean
Bauduceau, Bernard
Gourdy, Pierre
Hadjadj, Samy
author_facet Cariou, Bertrand
Wargny, Matthieu
Boureau, Anne-Sophie
Smati, Sarra
Tramunt, Blandine
Desailloud, Rachel
Lebeault, Maylis
Amadou, Coralie
Ancelle, Deborah
Balkau, Beverley
Bordier, Lyse
Borot, Sophie
Bourgeon, Muriel
Bourron, Olivier
Cosson, Emmanuel
Eisinger, Martin
Gonfroy-Leymarie, Céline
Julla, Jean-Baptiste
Marchand, Lucien
Meyer, Laurent
Seret-Bégué, Dominique
Simon, Dominique
Sultan, Ariane
Thivolet, Charles
Vambergue, Anne
Vatier, Camille
Winiszewski, Patrice
Saulnier, Pierre-Jean
Bauduceau, Bernard
Gourdy, Pierre
Hadjadj, Samy
author_sort Cariou, Bertrand
collection PubMed
description AIMS/HYPOTHESIS: Diabetes has been recognised as a pejorative prognostic factor in coronavirus disease 2019 (COVID-19). Since diabetes is typically a disease of advanced age, it remains unclear whether diabetes remains a COVID-19 risk factor beyond advanced age and associated comorbidities. We designed a cohort study that considered age and comorbidities to address this question. METHODS: The Coronavirus SARS-CoV-2 and Diabetes Outcomes (CORONADO) initiative is a French, multicentric, cohort study of individuals with (exposed) and without diabetes (non-exposed) admitted to hospital with COVID-19, with a 1:1 matching on sex, age (±5 years), centre and admission date (10 March 2020 to 10 April 2020). Comorbidity burden was assessed by calculating the updated Charlson comorbidity index (uCCi). A predefined composite primary endpoint combining death and/or invasive mechanical ventilation (IMV), as well as these two components separately, was assessed within 7 and 28 days following hospital admission. We performed multivariable analyses to compare clinical outcomes between patients with and without diabetes. RESULTS: A total of 2210 pairs of participants (diabetes/no-diabetes) were matched on age (mean±SD 69.4±13.2/69.5±13.2 years) and sex (36.3% women). The uCCi was higher in individuals with diabetes. In unadjusted analysis, the primary composite endpoint occurred more frequently in the diabetes group by day 7 (29.0% vs 21.6% in the no-diabetes group; HR 1.43 [95% CI 1.19, 1.72], p<0.001). After multiple adjustments for age, BMI, uCCi, clinical (time between onset of COVID-19 symptoms and dyspnoea) and biological variables (eGFR, aspartate aminotransferase, white cell count, platelet count, C-reactive protein) on admission to hospital, diabetes remained associated with a higher risk of primary composite endpoint within 7 days (adjusted HR 1.42 [95% CI 1.17, 1.72], p<0.001) and 28 days (adjusted HR 1.30 [95% CI 1.09, 1.55], p=0.003), compared with individuals without diabetes. Using the same adjustment model, diabetes was associated with the risk of IMV, but not with risk of death, within 28 days of admission to hospital. CONCLUSIONS/INTERPRETATION: Our results demonstrate that diabetes status was associated with a deleterious COVID-19 prognosis irrespective of age and comorbidity status. TRIAL REGISTRATION: ClinicalTrials.gov NCT04324736 GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version of this article (10.1007/s00125-022-05734-1) contains peer-reviewed but unedited supplementary material.
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spelling pubmed-91976742022-06-17 Impact of diabetes on COVID-19 prognosis beyond comorbidity burden: the CORONADO initiative Cariou, Bertrand Wargny, Matthieu Boureau, Anne-Sophie Smati, Sarra Tramunt, Blandine Desailloud, Rachel Lebeault, Maylis Amadou, Coralie Ancelle, Deborah Balkau, Beverley Bordier, Lyse Borot, Sophie Bourgeon, Muriel Bourron, Olivier Cosson, Emmanuel Eisinger, Martin Gonfroy-Leymarie, Céline Julla, Jean-Baptiste Marchand, Lucien Meyer, Laurent Seret-Bégué, Dominique Simon, Dominique Sultan, Ariane Thivolet, Charles Vambergue, Anne Vatier, Camille Winiszewski, Patrice Saulnier, Pierre-Jean Bauduceau, Bernard Gourdy, Pierre Hadjadj, Samy Diabetologia Article AIMS/HYPOTHESIS: Diabetes has been recognised as a pejorative prognostic factor in coronavirus disease 2019 (COVID-19). Since diabetes is typically a disease of advanced age, it remains unclear whether diabetes remains a COVID-19 risk factor beyond advanced age and associated comorbidities. We designed a cohort study that considered age and comorbidities to address this question. METHODS: The Coronavirus SARS-CoV-2 and Diabetes Outcomes (CORONADO) initiative is a French, multicentric, cohort study of individuals with (exposed) and without diabetes (non-exposed) admitted to hospital with COVID-19, with a 1:1 matching on sex, age (±5 years), centre and admission date (10 March 2020 to 10 April 2020). Comorbidity burden was assessed by calculating the updated Charlson comorbidity index (uCCi). A predefined composite primary endpoint combining death and/or invasive mechanical ventilation (IMV), as well as these two components separately, was assessed within 7 and 28 days following hospital admission. We performed multivariable analyses to compare clinical outcomes between patients with and without diabetes. RESULTS: A total of 2210 pairs of participants (diabetes/no-diabetes) were matched on age (mean±SD 69.4±13.2/69.5±13.2 years) and sex (36.3% women). The uCCi was higher in individuals with diabetes. In unadjusted analysis, the primary composite endpoint occurred more frequently in the diabetes group by day 7 (29.0% vs 21.6% in the no-diabetes group; HR 1.43 [95% CI 1.19, 1.72], p<0.001). After multiple adjustments for age, BMI, uCCi, clinical (time between onset of COVID-19 symptoms and dyspnoea) and biological variables (eGFR, aspartate aminotransferase, white cell count, platelet count, C-reactive protein) on admission to hospital, diabetes remained associated with a higher risk of primary composite endpoint within 7 days (adjusted HR 1.42 [95% CI 1.17, 1.72], p<0.001) and 28 days (adjusted HR 1.30 [95% CI 1.09, 1.55], p=0.003), compared with individuals without diabetes. Using the same adjustment model, diabetes was associated with the risk of IMV, but not with risk of death, within 28 days of admission to hospital. CONCLUSIONS/INTERPRETATION: Our results demonstrate that diabetes status was associated with a deleterious COVID-19 prognosis irrespective of age and comorbidity status. TRIAL REGISTRATION: ClinicalTrials.gov NCT04324736 GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version of this article (10.1007/s00125-022-05734-1) contains peer-reviewed but unedited supplementary material. Springer Berlin Heidelberg 2022-06-15 2022 /pmc/articles/PMC9197674/ /pubmed/35701673 http://dx.doi.org/10.1007/s00125-022-05734-1 Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Cariou, Bertrand
Wargny, Matthieu
Boureau, Anne-Sophie
Smati, Sarra
Tramunt, Blandine
Desailloud, Rachel
Lebeault, Maylis
Amadou, Coralie
Ancelle, Deborah
Balkau, Beverley
Bordier, Lyse
Borot, Sophie
Bourgeon, Muriel
Bourron, Olivier
Cosson, Emmanuel
Eisinger, Martin
Gonfroy-Leymarie, Céline
Julla, Jean-Baptiste
Marchand, Lucien
Meyer, Laurent
Seret-Bégué, Dominique
Simon, Dominique
Sultan, Ariane
Thivolet, Charles
Vambergue, Anne
Vatier, Camille
Winiszewski, Patrice
Saulnier, Pierre-Jean
Bauduceau, Bernard
Gourdy, Pierre
Hadjadj, Samy
Impact of diabetes on COVID-19 prognosis beyond comorbidity burden: the CORONADO initiative
title Impact of diabetes on COVID-19 prognosis beyond comorbidity burden: the CORONADO initiative
title_full Impact of diabetes on COVID-19 prognosis beyond comorbidity burden: the CORONADO initiative
title_fullStr Impact of diabetes on COVID-19 prognosis beyond comorbidity burden: the CORONADO initiative
title_full_unstemmed Impact of diabetes on COVID-19 prognosis beyond comorbidity burden: the CORONADO initiative
title_short Impact of diabetes on COVID-19 prognosis beyond comorbidity burden: the CORONADO initiative
title_sort impact of diabetes on covid-19 prognosis beyond comorbidity burden: the coronado initiative
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9197674/
https://www.ncbi.nlm.nih.gov/pubmed/35701673
http://dx.doi.org/10.1007/s00125-022-05734-1
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