Levels of sCD163 in women rheumatoid arthritis: Relationship with cardiovascular risk markers

Oscar Zaragoza-García1, Olivia Briceño2, José Rafael Villafan-Bernal3

  • 1Laboratory of Multidisciplinary Research and Biomedical Innovation, Universidad Autónoma de Guerrero, Chilpancingo, Guerrero, Mexico.

Insights

Soluble CD163 (sCD163) levels indicate higher cardiovascular risk and disease activity in rheumatoid arthritis (RA) patients. This marker may serve as a predictor for cardiovascular complications in RA.

Area of Science:

  • Rheumatology
  • Cardiology
  • Biomarkers

Background:

  • Soluble scavenger receptor differentiation antigen 163 (sCD163) is a marker of monocyte/macrophage activation.
  • Elevated sCD163 levels are linked to cardiovascular mortality in the general population.

Purpose of the Study:

  • To investigate the association between serum sCD163 levels and cardiovascular risk indicators in rheumatoid arthritis (RA).
  • To evaluate sCD163 as a potential biomarker for cardiovascular risk and disease activity in RA patients.

Main Methods:

  • Cross-sectional study involving 80 women with RA.
  • Cardiovascular risk assessed via lipid profile, metabolic syndrome, and QRISK3 calculator.
  • RA disease activity measured by DAS28-ESR; serum sCD163 quantified using ELISA.
  • Logistic regression and ROC curve analysis employed to determine associations and predictive values.

Main Results:

  • Higher sCD163 levels correlated significantly with adverse lipid ratios, atherogenic index, cardiometabolic index (CMI), and high RA disease activity (DAS28-ESR).
  • Multivariate analysis revealed sCD163 levels (≥1107.3ng/mL) were independently associated with high CHR, CMI, unfavorable cholesterol ratios, and high DAS28-ESR.
  • Serum sCD163 demonstrated predictive value for high CHR, unfavorable cholesterol ratios, and high DAS28-ESR.

Conclusions:

  • Serum sCD163 levels can serve as a surrogate marker for cardiovascular risk in RA patients.
  • sCD163 may also reflect clinical disease activity in rheumatoid arthritis.
Abstract

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