Abstract | BACKGROUND:
Coronavirus disease 2019 (COVID-19) is an acute respiratory disease; approximately 5% of patients developing severe COVID-19. It is known that cytokine release is associated with disease severity, but the relationship between the different clinical phenotypes and inflammatory endotypes is not well understood. OBJECTIVE: This study investigated the association between inflammatory biomarker-based endotypes and severe COVID-19 phenotypes. METHODS: RESULTS: Significantly higher blood levels of the eight inflammatory markers were noted in patients who developed acute respiratory distress syndrome (ARDS) than in those who did not develop ARDS (non-ARDS). Using a cluster analysis, the patient groups were classified into four clusters, of which two had patients with high IL-6 and CRP levels. In the cluster with high levels of Type 1 (T1) inflammatory markers such as CXCL9 and IL-18, 85% of the patients had ARDS, 65% of the patients developed acute kidney injury (AKI), and 78% of the patients developed pulmonary fibrosis. CONCLUSIONS: In the cluster with high levels of T1 inflammatory markers, the patients frequently suffered from tissue damage, manifested as ARDS and AKI. Our findings identified distinct T1 inflammatory endotypes of COVID-19 and suggest the importance of controlling inflammation by monitoring T1 biomarkers and treating accordingly to limit the severity of the disease.
|
Authors | Takehiro Hasegawa, Atsushi Nakagawa, Kohjin Suzuki, Kazuto Yamashita, Saya Yamashita, Niina Iwanaga, Eiya Tamada, Kenta Noda, Keisuke Tomii |
Journal | Cytokine
(Cytokine)
Vol. 148
Pg. 155618
(12 2021)
ISSN: 1096-0023 [Electronic] England |
PMID | 34127355
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Copyright | Copyright © 2021 The Author(s). Published by Elsevier Ltd.. All rights reserved. |
Chemical References |
|
Topics |
- Aged
- Biomarkers
(blood)
- COVID-19
(blood, complications, physiopathology, virology)
- Cluster Analysis
- Disease Progression
- Female
- Humans
- Inflammation
(blood, complications, pathology)
- Lung Compliance
- Male
- Middle Aged
- Pulmonary Fibrosis
(blood, complications, physiopathology)
- Respiratory Distress Syndrome
(blood, complications)
- SARS-CoV-2
(physiology)
|