The receptor for advanced glycation end product (RAGE) pathway in COVID-19

Biomarkers. 2021 Mar;26(2):114-118. doi: 10.1080/1354750X.2020.1861099. Epub 2021 Jan 13.

Abstract

Introduction: Coronavirus disease-2019 (COVID-19) with lung involvement frequently causes morbidity and mortality. Advanced age appears to be the most important risk factor. The receptor for advanced glycation end-product (RAGE) pathway is considered to play important roles in the physiological aging and pathogenesis of lung diseases. This study aimed to investigate the possible relationship between COVID-19 and RAGE pathway.

Materials and methods: This study included 23 asymptomatic patients and 35 patients with lung involvement who were diagnosed with COVID-19 as well as 22 healthy volunteers. Lung involvement was determined using computed tomography. Serum soluble-RAGE (sRAGE) levels were determined using enzyme-linked immunosorbent assay.

Results: The sRAGE levels were significantly higher in the asymptomatic group than in the control group. Age, fibrinogen, C-reactive protein, and ferritin levels were higher and the sRAGE level was lower in the patients with lung involvement than in the asymptomatic patients.

Conclusions: In this study, patients with high sRAGE levels were younger and had asymptomatic COVID-19. Patients with low sRAGE levels were elderly patients with lung involvement, which indicates that the RAGE pathway plays an important role in the aggravation of COVID-19.

Keywords: COVID-19; aging; co-morbidity; infection; inflammation; the receptor for advanced glycation end product (RAGE).

MeSH terms

  • Adult
  • Aged
  • Aging
  • Antigens, Neoplasm / metabolism*
  • COVID-19 / complications
  • COVID-19 / physiopathology*
  • Case-Control Studies
  • Cross-Sectional Studies
  • Female
  • Humans
  • Lung / diagnostic imaging
  • Male
  • Middle Aged
  • Mitogen-Activated Protein Kinases / metabolism*
  • Pneumonia / diagnostic imaging
  • Pneumonia / etiology
  • Signal Transduction*
  • Tomography, X-Ray Computed

Substances

  • Antigens, Neoplasm
  • MOK protein, human
  • Mitogen-Activated Protein Kinases