4.8 Article

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

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ELIFE
卷 10, 期 -, 页码 -

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eLIFE SCIENCES PUBL LTD
DOI: 10.7554/eLife.61700

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资金

  1. Microsoft Research
  2. George Mason University Emergent Ventures Program
  3. National Science Foundation [DGE - 1656518]
  4. National Institute of Arthritis and Musculoskeletal and Skin Diseases [T32AR048522]
  5. Burroughs Wellcome Fund
  6. National Institute of Mental Health [R01MH115487]
  7. National Cancer Institute [5K08CA230179, 1U01CA247576]
  8. Swedish Research Council [2019-01059]
  9. Swedish Heart-Lung Foundation

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Research shows that the use of α-AR antagonists can reduce the risk of mechanical ventilation and death in patients with pneumonia and acute respiratory distress syndrome. These results suggest that prophylactic use of α-AR antagonists may help reduce inflammation and mortality rates, warranting further prospective trials.
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 (a,-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 alpha(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 a,-AR antagonists ameliorates lower respiratory tract infection-associated hyperinflammation and death, as observed in COVID-19.

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