Viruses (Sep 2022)

CGRP Plasma Levels Correlate with the Clinical Evolution and Prognosis of Hospitalized Acute COVID-19 Patients

  • Manuela Rizzi,
  • Stelvio Tonello,
  • Francesca Morani,
  • Eleonora Rizzi,
  • Giuseppe Francesco Casciaro,
  • Erica Matino,
  • Martina Costanzo,
  • Erika Zecca,
  • Alessandro Croce,
  • Anita Pedrinelli,
  • Veronica Vassia,
  • Raffaella Landi,
  • Venkata Ramana Mallela,
  • Davide D’Onghia,
  • Rosalba Minisini,
  • Mattia Bellan,
  • Luigi Mario Castello,
  • Francesco Gavelli,
  • Gian Carlo Avanzi,
  • Filippo Patrucco,
  • Mario Pirisi,
  • Donato Colangelo,
  • Pier Paolo Sainaghi

DOI
https://doi.org/10.3390/v14102123
Journal volume & issue
Vol. 14, no. 10
p. 2123

Abstract

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SARS-CoV-2 is the etiological agent of COVID-19, an extremely heterogenous disease that can cause severe respiratory failure and critical illness. To date, reliable biomarkers allowing for early patient stratification according to disease severity are still lacking. Calcitonin gene-related peptide (CGRP) is a vasoactive neuropeptide involved in lung pathophysiology and immune modulation and is poorly investigated in the COVID-19 context. In this observational, prospective cohort study, we investigated the correlation between CGRP and clinical disease evolution in hospitalized moderate to severe COVID-19 patients. Between January and May 2021 (Italian third pandemic wave), 135 consecutive SARS-CoV-2 patients were diagnosed as being eligible for the study. Plasma CGRP level evaluation and routine laboratory tests were performed on blood samples collected at baseline and after 7 days of hospitalization. At baseline, the majority our patients had a moderate to severe clinical presentation, and higher plasma CGRP levels predicted a higher risk of in-hospital negative evolution (odds-ratio OR 2.84 [IQR 1.07–7.51]) and were correlated with pulmonary intravascular coagulopathy (OR 2.92 [IQR 1.19–7.17]). Finally, plasma CGRP levels were also correlated with plasma IP10 levels. Our data support a possible crosstalk between the lung and the neuroimmune axis, highlighting a crucial role for plasma CGRP in sustaining COVID-19-related hyperinflammation.

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