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Alpha-1 adrenergic receptor antagonists to prevent hyperinflammation and death from lower respiratory tract infection.
Koenecke, Allison; Powell, Michael; Xiong, Ruoxuan; Shen, Zhu; Fischer, Nicole; Huq, Sakibul; Khalafallah, Adham M; Trevisan, Marco; Sparen, Pär; Carrero, Juan J; Nishimura, Akihiko; Caffo, Brian; Stuart, Elizabeth A; Bai, Renyuan; Staedtke, Verena; Thomas, David L; Papadopoulos, Nickolas; Kinzler, Ken W; Vogelstein, Bert; Zhou, Shibin; Bettegowda, Chetan; Konig, Maximilian F; Mensh, Brett D; Vogelstein, Joshua T; Athey, Susan.
  • Koenecke A; Institute for Computational & Mathematical Engineering, Stanford University, Stanford, United States.
  • Powell M; Department of Biomedical Engineering, Institute for Computational Medicine, The Johns Hopkins University, Baltimore, United States.
  • Xiong R; Management Science & Engineering, Stanford University, Stanford, United States.
  • Shen Z; Department of Statistics, Stanford University, Stanford, United States.
  • Fischer N; The Johns Hopkins University School of Medicine, Baltimore, United States.
  • Huq S; Department of Neurosurgery and Neurology, The Johns Hopkins University School of Medicine, Baltimore, United States.
  • Khalafallah AM; Department of Neurosurgery and Neurology, The Johns Hopkins University School of Medicine, Baltimore, United States.
  • Trevisan M; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Sweden, Solna, Sweden.
  • Sparen P; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Sweden, Solna, Sweden.
  • Carrero JJ; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Sweden, Solna, Sweden.
  • Nishimura A; Department of Biostatistics, Johns Hopkins Bloomberg School of Public Health at Johns Hopkins University, Baltimore, United States.
  • Caffo B; Department of Biostatistics, Johns Hopkins Bloomberg School of Public Health at Johns Hopkins University, Baltimore, United States.
  • Stuart EA; Department of Biostatistics, Johns Hopkins Bloomberg School of Public Health at Johns Hopkins University, Baltimore, United States.
  • Bai R; Department of Neurosurgery and Neurology, The Johns Hopkins University School of Medicine, Baltimore, United States.
  • Staedtke V; Department of Neurosurgery and Neurology, The Johns Hopkins University School of Medicine, Baltimore, United States.
  • Thomas DL; The Johns Hopkins University School of Medicine, Baltimore, United States.
  • Papadopoulos N; Ludwig Center, Lustgarten Laboratory, and the Howard Hughes Medical Institute at The Johns Hopkins Kimmel Cancer Center, Baltimore, United States.
  • Kinzler KW; Ludwig Center, Lustgarten Laboratory, and the Howard Hughes Medical Institute at The Johns Hopkins Kimmel Cancer Center, Baltimore, United States.
  • Vogelstein B; Ludwig Center, Lustgarten Laboratory, and the Howard Hughes Medical Institute at The Johns Hopkins Kimmel Cancer Center, Baltimore, United States.
  • Zhou S; Ludwig Center, Lustgarten Laboratory, and the Howard Hughes Medical Institute at The Johns Hopkins Kimmel Cancer Center, Baltimore, United States.
  • Bettegowda C; The Johns Hopkins University School of Medicine, Baltimore, United States.
  • Konig MF; Ludwig Center, Lustgarten Laboratory, and the Howard Hughes Medical Institute at The Johns Hopkins Kimmel Cancer Center, Baltimore, United States.
  • Mensh BD; Division of Rheumatology, Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, United States.
  • Vogelstein JT; Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, United States.
  • Athey S; Department of Biomedical Engineering, Institute for Computational Medicine, The Johns Hopkins University, Baltimore, United States.
Elife ; 102021 06 11.
Article in English | MEDLINE | ID: covidwho-1266916
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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Respiration, Artificial / Respiratory Distress Syndrome / Adrenergic alpha-1 Receptor Antagonists Type of study: Cohort study / Observational study / Prognostic study Limits: Aged / Humans / Male / Middle aged Country/Region as subject: North America / Europa Language: English Year: 2021 Document Type: Article Affiliation country: ELife.61700

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Respiration, Artificial / Respiratory Distress Syndrome / Adrenergic alpha-1 Receptor Antagonists Type of study: Cohort study / Observational study / Prognostic study Limits: Aged / Humans / Male / Middle aged Country/Region as subject: North America / Europa Language: English Year: 2021 Document Type: Article Affiliation country: ELife.61700