Blood Growth Factor Levels in Patients with Systemic Lupus Erythematosus: High Neuregulin-1 Is Associated with

Evgeny A Ermakov1,2, Mark M Melamud1, Anastasiia S Boiko3

  • 1Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, Russia.

Life (Basel, Switzerland)
|October 26, 2024
PubMed

Insights

Systemic lupus erythematosus (SLE) patients show higher levels of nerve growth factor beta (NGFβ) and neuregulin-1 beta (NRG-1β). Elevated NRG-1β is linked to cardiovascular diseases (CVDs) in SLE patients, suggesting a potential biomarker.

Area of Science:

  • Immunology
  • Cardiology
  • Biochemistry

Background:

  • Systemic lupus erythematosus (SLE) patients frequently experience cardiovascular diseases (CVDs).
  • While cytokines are studied in SLE pathogenesis, growth factors remain less explored.
  • Understanding growth factor roles is crucial for managing SLE comorbidities.

Purpose of the Study:

  • To investigate serum growth factor levels in SLE patients.
  • To determine the association between growth factors and comorbid CVDs in SLE.
  • To evaluate specific growth factors: GM-CSF, NGFβ, GDNF, and NRG-1β.

Main Methods:

  • Serum concentrations of four growth factors were measured using a Luminex multiplex assay.
  • Samples were collected from SLE patients (n=35) and healthy controls (n=38).
  • Statistical analysis compared growth factor levels between groups and correlated them with CVD presence.

Main Results:

  • NGFβ and NRG-1β levels were significantly higher in SLE patients compared to healthy individuals.
  • GM-CSF and GDNF levels did not show significant differences between groups.
  • Elevated NRG-1β levels were strongly associated with the presence of CVDs in SLE patients (AUC = 0.67).

Conclusions:

  • Altered growth factor levels, particularly NRG-1β, may be linked to CVDs in SLE.
  • NRG-1β shows potential as a biomarker for cardiovascular comorbidity in SLE.
  • Further research into growth factor involvement in SLE pathogenesis and CVD is warranted.