Skin Autofluorescence Assessment of Advanced Glycation End Products in Rheumatic Diseases

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-75
SponsorBursa City Hospital

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Age between 18 and 75 years

Diagnosis of an inflammatory rheumatic disease (including rheumatoid arthritis, ankylosing spondylitis, psoriatic arthritis, reactive arthritis, connective tissue diseases, Behçet disease, familial Mediterranean fever, or crystal arthropathies), confirmed by a rheumatologist

Healthy volunteers without a history of rheumatic or chronic inflammatory disease (for the control group)

Ability to undergo non-invasive skin autofluorescence measurement

Disqualifiers

Diagnosis of diabetes mellitus (type 1 or type 2)

Chronic kidney disease with estimated glomerular filtration rate (eGFR) < 60 mL/min/1.73 m²

Active malignancy or history of malignancy within the past 5 years

Presence of acute infection or acute inflammatory condition at the time of assessment

Trial population

The study population consists of adult patients aged 18 to 75 years diagnosed with inflammatory rheumatic diseases who are followed at a tertiary rheumatology outpatient clinic, as well as age- and sex-matched healthy volunteers without a history of rheumatic or chronic inflammatory disease. All participants will undergo a single, non-invasive skin autofluorescence measurement to assess advanced glycation end-product (AGE) accumulation.

Trial design

Design model

Case-control

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

300 Participants
are grouped into 2 trial groups
Group A: Rheumatic Diseases Group
Group B: Healthy Control Group

Trial outcomes

Primary outcomes

1

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)

Secondary outcomes

1

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)
2

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

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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