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Increased Intestinal Permeability and Articular Involvement in Systemic Lupus Erythematosus Patients-A Mutually
Cristian-Mihai Ilie1,2, Cătălina-Anamaria Boromiz2, Irina Anna-Maria Stoian1
1Department of Functional Sciences I/Biochemistry, Carol Davila University of Medicine and Pharmacy, 050474 Bucharest, Romania.
Systemic lupus erythematosus (SLE) patients show higher gut leakage marker zonulin levels. However, zonulin did not correlate with disease activity or articular involvement in these patients.
Area of Science:
- Immunology
- Gastroenterology
- Rheumatology
Background:
- Systemic lupus erythematosus (SLE) is an autoimmune disease involving complex immune interactions.
- Increased intestinal permeability, a marker of gut leakage, is potentially linked to SLE.
- Zonulin is a key protein regulating intestinal permeability and a biomarker for gut leakage.
Purpose of the Study:
- To assess intestinal permeability in Caucasian SLE patients by measuring serum zonulin levels.
- To investigate the relationship between zonulin, SLE disease activity, and organ involvement.
Main Methods:
- Cross-sectional study design with 41 SLE patients and 29 controls.
- Plasma zonulin levels measured using indirect ELISA.
- Disease activity assessed using the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI).
Main Results:
- SLE patients exhibited significantly higher plasma zonulin levels compared to controls (7.566 ± 1.368 ng/mL vs. 2.306 ± 0.286 ng/mL, p < 0.01).
- Plasma zonulin levels did not correlate with SLE disease activity (SLEDAI).
- SLE patients with articular involvement showed paradoxically lower plasma zonulin levels than those without.
Conclusions:
- Elevated zonulin suggests increased intestinal permeability in Caucasian SLE patients.
- Zonulin levels are not associated with disease activity or articular manifestations in SLE.
- Findings support a potential inverse inflammatory relationship between the gut mucosa and synovium in SLE.
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