Antioxidants (Jun 2022)

Effect of Low-Dose Radiotherapy on the Circulating Levels of Paraoxonase-1-Related Variables and Markers of Inflammation in Patients with COVID-19 Pneumonia

  • Elisabet Rodríguez-Tomàs,
  • Johana C. Acosta,
  • Laura Torres-Royo,
  • Gabriel De Febrer,
  • Gerard Baiges-Gaya,
  • Helena Castañé,
  • Andrea Jiménez,
  • Carlos Vasco,
  • Pablo Araguas,
  • Junior Gómez,
  • Bárbara Malave,
  • Miguel Árquez,
  • David Calderón,
  • Berta Piqué,
  • Manel Algara,
  • Ángel Montero,
  • Josep M. Simó,
  • Xavier Gabaldó-Barrios,
  • Sebastià Sabater,
  • Jordi Camps,
  • Jorge Joven,
  • Meritxell Arenas

DOI
https://doi.org/10.3390/antiox11061184
Journal volume & issue
Vol. 11, no. 6
p. 1184

Abstract

Read online

The aim of our study was to investigate the changes produced by low-dose radiotherapy (LDRT) in the circulating levels of the antioxidant enzyme paraoxonase-1 (PON1) and inflammatory markers in patients with COVID-19 pneumonia treated with LDRT and their interactions with clinical and radiological changes. Data were collected from the IPACOVID prospective clinical trial (NCT04380818). The study included 30 patients treated with a whole-lung dose of 0.5 Gy. Clinical follow-up, as well as PON1-related variables, cytokines, and radiological parameters were analyzed before LDRT, at 24 h, and 1 week after treatment. Twenty-five patients (83.3%) survived 1 week after LDRT. Respiratory function and radiological images improved in survivors. Twenty-four hours after LDRT, PON1 concentration significantly decreased, while transforming growth factor beta 1 (TGF-β1) increased with respect to baseline. One week after LDRT, patients had increased PON1 activities and lower PON1 and TGF-β1 concentrations compared with 24 h after LDRT, PON1 specific activity increased, lactate dehydrogenase (LDH), and C-reactive protein (CRP) decreased, and CD4+ and CD8+ cells increased after one week. Our results highlight the benefit of LDRT in patients with COVID-19 pneumonia and it might be mediated, at least in part, by an increase in serum PON1 activity at one week and an increase in TGF-β1 concentrations at 24 h.

Keywords