Rheumatic diseases are chronic inflammatory conditions that can lead to long-term tissue damage and increased cardiovascular and metabolic risk. Advanced glycation end products (AGEs) are harmful molecules that accumulate in the body over time and are known to promote inflammation and oxidative stress. Increased AGE burden has been implicated in several chronic diseases; however, its role in rheumatic diseases has not been fully clarified. This observational, cross-sectional study aims to evaluate the accumulation of AGEs in patients with various rheumatic diseases compared with healthy individuals. AGE levels will be assessed non-invasively using skin autofluorescence measurements. By comparing AGE burden between patients and healthy controls, this study seeks to improve understanding of the potential role of AGEs in the pathophysiology of rheumatic diseases and to explore their usefulness as a non-invasive biomarker in clinical practice.
Study Type
OBSERVATIONAL
Enrollment
300
Skin Autofluorescence-Derived Advanced Glycation End Product Level
Advanced glycation end-product (AGE) accumulation assessed non-invasively by skin autofluorescence measurement using a validated AGE Reader device, expressed in arbitrary units (AU).
Time frame: Baseline (single study visit)
Comparison of AGE Levels Between Rheumatic Disease Subtypes
Comparison of skin autofluorescence-derived advanced glycation end-product (AGE) levels among different rheumatic disease subgroups and healthy controls.
Time frame: Baseline (single study visit)
Association Between AGE Levels and Inflammatory Markers
Association between skin autofluorescence-derived AGE levels and systemic inflammatory markers, including C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR).
Time frame: Baseline
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