<p>Age is a well-known risk factor to develop severe viral respiratory infections, including severe COVID-19. This study aimed to identify the biological alterations linked to severe disease in elderly patients with COVID-19. For this purpose, we employed a derivation cohort with 450 SARS-CoV-2 infected and unvaccinated patients admitted to hospital wards and a validation cohort with 244 SARS-CoV-2 infected and unvaccinated patients admitted to hospital Intensive Care&#xa0;Unit (ICU). Twenty-one biomarkers were measured in plasma samples from patients upon admission, including SARS-CoV-2 RNA, IgG antibodies, and protein biomarkers. Patient cohorts were divided into two groups based on age: adult (≤ 70&#xa0;years old) and elderly (&gt; 70&#xa0;years old) patients. In the derivation cohort, 90-day mortality rate observed in the adult group was 6.0% whereas in the elderly group it rises to 31.6%, same trend was noticed regarding the validation cohort, with 11.2% versus 40.3% 90-day mortality rates for adult and elderly groups, respectively. The machine-learning framework XGBoost-SHAP, fed with the plasma biomarkers information, was used to profile an age-related host response to SARS-CoV-2 infection. Based on SHAP plot, elderly patients had a strong thrombo-inflammatory response profile (significantly elevated plasma levels of: lipocalin-2, endothelin-1, D-dimer) combined with deficient adaptive and cytotoxic antiviral responses. Model performance evaluated with the validation cohort confirmed the robustness and generalizability of the model developed (AUC = 0.710). In conclusion, the machine learning approach we built allowed us to identify the presence of a deranged host response in elderly patients with COVID-19 linked to poor viral control and increased mortality.</p> Graphical Abstract <p></p>

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Key factors of the deranged antiviral response in elderly patients with COVID-19: a machine-learning analysis

  • Tamara Postigo-Casado,
  • Alicia Ortega,
  • Alejandro Álvaro-Meca,
  • Daniel Vélez-Serrano,
  • Nadia García-Mateo,
  • Ana P. Tedim,
  • Raquel Almansa,
  • Jose María Eiros,
  • David de Gonzalo-Calvo,
  • Anna Moncusí-Moix,
  • Clara Gort-Paniello,
  • Manel Perez-Pons,
  • Marta Molinero,
  • Marta Dominguez-Gil,
  • Amanda de la Fuente,
  • Laura González-González,
  • Tania Luis-García,
  • Fátima Rodríguez-Jara,
  • Noelia Jorge,
  • Jessica González,
  • Gerard Torres,
  • Oliver Norberto Gutiérrez-Pérez,
  • María José Villegas,
  • Sonia Campo,
  • Eva Ayllón,
  • Tomás Ruiz Albi,
  • Julio de Frutos Arribas,
  • Ainhoa Arroyo Domingo,
  • Jessica Abadia-Otero,
  • Julia Gómez Barquero,
  • Wysali Trapiello,
  • Luis Javier García Frade,
  • Luis Inglada,
  • Félix del Campo,
  • Ferrán Barbé,
  • Antoni Torres,
  • Raúl López-Izquierdo,
  • Jesús F. Bermejo-Martin,
  • Luis Jorge Valdivia,
  • Juan López Messa,
  • Pablo Vidal-Cortés,
  • Nieves Carbonell,
  • Elena Bustamante-Munguira,
  • María del Carmen De la Torre,
  • Caridad Martín López,
  • Milagros González Rivera,
  • Ruth Noemí Jorge García,
  • Alejandro Úbeda Iglesias,
  • Elena Gallego Curto,
  • Lorenzo Socias,
  • Jesús Caballero,
  • Ángel Estella,
  • Víctor Sagredo Meneses,
  • María Cruz Martín Delgado,
  • Amalia Martínez de la Gándara,
  • Emilio Maseda,
  • Ignacio Martínez Varela,
  • Sandra Campos-Fernández,
  • Felipe Pérez-García,
  • Luis Tamayo,
  • Ana Loza Vázquez,
  • Salvador Resino,
  • Isidoro Martínez,
  • Anna Motos,
  • Laia Fernández-Barat,
  • Adrián Ceccato

摘要

Age is a well-known risk factor to develop severe viral respiratory infections, including severe COVID-19. This study aimed to identify the biological alterations linked to severe disease in elderly patients with COVID-19. For this purpose, we employed a derivation cohort with 450 SARS-CoV-2 infected and unvaccinated patients admitted to hospital wards and a validation cohort with 244 SARS-CoV-2 infected and unvaccinated patients admitted to hospital Intensive Care Unit (ICU). Twenty-one biomarkers were measured in plasma samples from patients upon admission, including SARS-CoV-2 RNA, IgG antibodies, and protein biomarkers. Patient cohorts were divided into two groups based on age: adult (≤ 70 years old) and elderly (> 70 years old) patients. In the derivation cohort, 90-day mortality rate observed in the adult group was 6.0% whereas in the elderly group it rises to 31.6%, same trend was noticed regarding the validation cohort, with 11.2% versus 40.3% 90-day mortality rates for adult and elderly groups, respectively. The machine-learning framework XGBoost-SHAP, fed with the plasma biomarkers information, was used to profile an age-related host response to SARS-CoV-2 infection. Based on SHAP plot, elderly patients had a strong thrombo-inflammatory response profile (significantly elevated plasma levels of: lipocalin-2, endothelin-1, D-dimer) combined with deficient adaptive and cytotoxic antiviral responses. Model performance evaluated with the validation cohort confirmed the robustness and generalizability of the model developed (AUC = 0.710). In conclusion, the machine learning approach we built allowed us to identify the presence of a deranged host response in elderly patients with COVID-19 linked to poor viral control and increased mortality.

Graphical Abstract