Alveolar Nitric Oxide as a Biomarker of COVID-19 Lung Sequelae: A Pivotal Study.
Paolo CameliElena BargagliLaura BergantiniMiriana d'AlessandroBruna GiugnoFrancesco GentiliPiersante SestiniPublished in: Antioxidants (Basel, Switzerland) (2021)
Since SARS-CoV-2 emerged in 2019, strict monitoring of post-COVID-19 patients in order to ensure the early detection of sequelae and/or chronic organ damage that could been associated with the infection has been essential. Potential involvement of the NO pathway in the development of post-COVID-19 lung fibrotic alterations is feasible, since the majority of respiratory cells can produce NO, and fractional exhaled NO (FeNO) represents a biomarker of airway inflammation. The aim of this study was to investigate the potential utility of multiple-flow FeNO parameters in a post-COVID-19 population and to compare it with other indicators of lung damage proposed in the literature. We enrolled 20 patients hospitalized for COVID-19, who underwent clinical, respiratory functional (including PFTs and FeNO) and radiological follow-up after discharge. Compared with age- and sex-matched healthy controls, post-COVID-19 patients showed significantly higher FeNO 350 mL/s and CaNO levels. Moreover, among the parameters included in the follow-up, CaNO showed the best accuracy in indicating predominant fibrotic changes and GGO at CT scan. To our knowledge, this preliminary study has investigated for the first time multiple-flow FeNO parameters in a post-COVID-19 population. The evidence of increased CaNO values may imply the persistence of alveolar and bronchiolar inflammation and/or a mild impairment of the alveolar-capillary membrane in these patients.
Keyphrases
- sars cov
- coronavirus disease
- end stage renal disease
- respiratory syndrome coronavirus
- nitric oxide
- ejection fraction
- newly diagnosed
- chronic kidney disease
- peritoneal dialysis
- computed tomography
- idiopathic pulmonary fibrosis
- risk assessment
- magnetic resonance imaging
- patient reported outcomes
- signaling pathway
- cell cycle arrest
- single molecule
- pet ct
- hydrogen peroxide
- human health
- drug induced