• Sanne de Bruin, Lieuwe D Bos, Marian A van Roon, Anita M Tuip-de Boer, Alex R Schuurman, Marleen J A Koel-Simmelinck, Harm Jan Bogaard, Pieter Roel Tuinman, Michiel A van Agtmael, Jörg Hamann, Charlotte E Teunissen, W Joost Wiersinga, A H Koos Zwinderman, Matthijs C Brouwer, Diederik van de Beek, VlaarAlexander P JAPJFrom the Department of Intensive Care, University of Amsterdam, Amsterdam UMC, Amsterdam, The Netherlands., and Amsterdam UMC COVID-19 Biobank Investigators.
• From the Department of Intensive Care, University of Amsterdam, Amsterdam UMC, Amsterdam, The Netherlands.
• EBioMedicine. 2021 May 1; 67: 103378.

BackgroundMortality rates are high among hospitalized patients with COVID-19, especially in those intubated on the ICU. Insight in pathways associated with unfavourable outcome may lead to new treatment strategies.MethodsWe performed a prospective cohort study of patients with COVID-19 admitted to general ward or ICU who underwent serial blood sampling. To provide insight in the pathways involved in disease progression, associations were estimated between outcome risk and serial measurements of 64 biomarkers in potential important pathways of COVID-19 infection (inflammation, tissue damage, complement system, coagulation and fibrinolysis) using joint models combining Cox regression and linear mixed-effects models. For patients admitted to the general ward, the primary outcome was admission to the ICU or mortality (unfavourable outcome). For patients admitted to the ICU, the primary outcome was 12-week mortality.FindingsA total of 219 patients were included: 136 (62%) on the ward and 119 patients (54%) on the ICU; 36 patients (26%) were included in both cohorts because they were transferred from general ward to ICU. On the general ward, 54 of 136 patients (40%) had an unfavourable outcome and 31 (23%) patients died. On the ICU, 54 out of 119 patients (45%) died. Unfavourable outcome on the general ward was associated with changes in concentrations of IL-6, IL-8, IL-10, soluble Receptor for Advanced Glycation End Products (sRAGE), vascular cell adhesion molecule 1 (VCAM-1) and Pentraxin-3. Death on the ICU was associated with changes in IL-6, IL-8, IL-10, sRAGE, VCAM-1, Pentraxin-3, urokinase-type plasminogen activator receptor, IL-1-receptor antagonist, CD14, procalcitonin, tumor necrosis factor alfa, tissue factor, complement component 5a, Growth arrest-specific 6, angiopoietin 2, and lactoferrin. Pathway analysis showed that unfavourable outcome on the ward was mainly driven by chemotaxis and interleukin production, whereas death on ICU was associated with a variety of pathways including chemotaxis, cell-cell adhesion, innate host response mechanisms, including the complement system, viral life cycle regulation, angiogenesis, wound healing and response to corticosteroids.InterpretationClinical deterioration in patients with severe COVID-19 involves multiple pathways, including chemotaxis and interleukin production, but also endothelial dysfunction, the complement system, and immunothrombosis. Prognostic markers showed considerable overlap between general ward and ICU patients, but we identified distinct differences between groups that should be considered in the development and timing of interventional therapies in COVID-19.FundingAmsterdam UMC, Amsterdam UMC Corona Fund, and Dr. C.J. Vaillant Fonds.Copyright © 2021 The Author(s). Published by Elsevier B.V. All rights reserved.

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