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Could Skin Autofluorescence Be a Useful Biomarker in Systemic Lupus Erythematosus? A Systematic Review
Teodor Salmen1, Claudia Cobilinschi2,3, Andrei Mihăilescu2,3
1Doctoral School, "Carol Davila" University of Medicine and Pharmacy, 050474 Bucharest, Romania.
Skin autofluorescence (SAF), a measure of advanced glycation end products (AGEs), may serve as a useful biomarker for systemic lupus erythematosus (SLE) severity and activity. Higher AGEs and lower soluble RAGE (sRAGE) were observed in SLE patients, suggesting potential for diagnostic development.
Area of Science:
- Rheumatology and Immunology
- Biomarker Discovery
- Oxidative Stress Research
Background:
- Systemic lupus erythematosus (SLE) is a complex autoimmune disease with varied organ involvement.
- Reliable biomarkers for SLE severity and activity are still under investigation.
- Advanced glycation end products (AGEs) and their receptor (RAGE) are implicated in chronic inflammatory conditions.
Purpose of the Study:
- To systematically review the utility of skin autofluorescence (SAF) as a biomarker in SLE.
- To assess SAF's correlation with disease severity, activity, and impact in SLE patients.
- To evaluate the role of the AGEs-RAGE axis in SLE pathophysiology.
Main Methods:
- Systematic review conducted following PRISMA guidelines.
- Analysis of six studies evaluating SAF, circulating AGEs, and soluble RAGE (sRAGE) in SLE patients.
- Comparison of biomarker levels and correlations with clinical features between SLE patients and healthy controls.
Main Results:
- Elevated AGE levels were consistently found in SLE patients compared to controls.
- Higher SAF and AGE levels correlated with increased SLE disease activity (SLEDAI scores), organ involvement, and damage indices.
- Lower sRAGE levels were observed in SLE patients, potentially due to consumption by AGEs.
Conclusions:
- The AGEs-RAGE axis, particularly SAF, shows promise as a non-invasive biomarker for SLE.
- SAF may help assess disease severity and activity in SLE patients.
- Further large-scale longitudinal studies are required to validate the clinical utility of SAF in SLE management.
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