Alpha-1 adrenergic receptor antagonists to prevent hyperinflammation and death from lower respiratory tract infection

Author:

Koenecke Allison1ORCID,Powell Michael2ORCID,Xiong Ruoxuan3,Shen Zhu4,Fischer Nicole5,Huq Sakibul6,Khalafallah Adham M6,Trevisan Marco7,Sparen Pär7ORCID,Carrero Juan J7,Nishimura Akihiko8,Caffo Brian8,Stuart Elizabeth A8,Bai Renyuan6,Staedtke Verena6,Thomas David L5,Papadopoulos Nickolas9,Kinzler Ken W9,Vogelstein Bert9,Zhou Shibin9,Bettegowda Chetan59,Konig Maximilian F10ORCID,Mensh Brett D11,Vogelstein Joshua T28ORCID,Athey Susan12

Affiliation:

1. Institute for Computational & Mathematical Engineering, Stanford University

2. Department of Biomedical Engineering, Institute for Computational Medicine, The Johns Hopkins University

3. Management Science & Engineering, Stanford University

4. Department of Statistics, Stanford University

5. The Johns Hopkins University School of Medicine

6. Department of Neurosurgery and Neurology, The Johns Hopkins University School of Medicine

7. Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Sweden

8. Department of Biostatistics, Johns Hopkins Bloomberg School of Public Health at Johns Hopkins University

9. Ludwig Center, Lustgarten Laboratory, and the Howard Hughes Medical Institute at The Johns Hopkins Kimmel Cancer Center

10. Division of Rheumatology, Department of Medicine, The Johns Hopkins University School of Medicine

11. Janelia Research Campus, Howard Hughes Medical Institute

12. Stanford Graduate School of Business, Stanford University

Abstract

In severe viral pneumonia, including Coronavirus disease 2019 (COVID-19), the viral replication phase is often followed by hyperinflammation, which can lead to acute respiratory distress syndrome, multi-organ failure, and death. We previously demonstrated that alpha-1 adrenergic receptor (⍺1-AR) antagonists can prevent hyperinflammation and death in mice. Here, we conducted retrospective analyses in two cohorts of patients with acute respiratory distress (ARD, n = 18,547) and three cohorts with pneumonia (n = 400,907). Federated across two ARD cohorts, we find that patients exposed to ⍺1-AR antagonists, as compared to unexposed patients, had a 34% relative risk reduction for mechanical ventilation and death (OR = 0.70, p = 0.021). We replicated these methods on three pneumonia cohorts, all with similar effects on both outcomes. All results were robust to sensitivity analyses. These results highlight the urgent need for prospective trials testing whether prophylactic use of ⍺1-AR antagonists ameliorates lower respiratory tract infection-associated hyperinflammation and death, as observed in COVID-19.

Funder

Microsoft Research

George Mason University

National Science Foundation

National Institute of Arthritis and Musculoskeletal and Skin Diseases

Burroughs Wellcome Fund

National Institute of Mental Health

National Cancer Institute

Swedish Research Council

Swedish Heart-Lung Foundation

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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