Author: 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
Title: Alpha-1 adrenergic receptor antagonists to prevent hyperinflammation and death from lower respiratory tract infection Cord-id: vcl2p1p0 Document date: 2021_6_11
ID: vcl2p1p0
Snippet: 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 (âº(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 w
Document: 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 (âº(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 âº(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 âº(1)-AR antagonists ameliorates lower respiratory tract infection-associated hyperinflammation and death, as observed in COVID-19.
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