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Recognition of Epidermal Transglutaminase by IgA and Tissue Transglutaminase 2 Antibodies in a Rare Case of Rhesus Dermatitis
Published on: December 15, 2011
Antigliadin antibodies in psoriasis
Sheikh Javeed Sultan1, Qazi Masood Ahmad, Sheikh Tariq Sultan
1Department of Dermatology, STDs and Leprosy, Government Medical College, Srinagar, Kashmir, India. sjsultan@gmail.com
The Australasian Journal of Dermatology
|January 5, 2011
Summary
Elevated antigliadin antibodies (AGA) are not more common in Kashmiri psoriasis patients than in healthy individuals. This study found no association between AGA and psoriasis severity or joint symptoms.
Area of Science:
- Immunodermatology
- Autoimmune disease research
- Gastroenterology
Background:
- Antigliadin antibodies (AGA) are associated with celiac disease but also elevated in various autoimmune disorders.
- Previous studies suggest a link between psoriasis and AGA, with some patients improving on a gluten-free diet.
- The prevalence of AGA in Kashmiri psoriasis patients remains uninvestigated.
Purpose of the Study:
- To investigate the prevalence of elevated antigliadin antibodies (AGA) in patients with psoriasis in Kashmir.
- To determine if there is an association between AGA levels and psoriasis severity, onset, or joint involvement.
Main Methods:
- A case-control study involving 120 Kashmiri patients with psoriasis and 120 age- and sex-matched controls.
- Testing for IgA and IgG antigliadin antibodies (AGA) using enzyme-linked immunosorbent assay (ELISA).
Main Results:
- No statistically significant difference in AGA prevalence was found between psoriasis patients and controls.
- Mean AGA levels did not differ significantly between the two groups.
- No significant association was observed between AGA levels and psoriasis severity, joint involvement, age of onset, or arthritis.
Conclusions:
- Antigliadin antibodies (AGA) are not elevated in Kashmiri psoriasis patients compared to the general population.
- There is no evidence of an association between AGA and psoriasis, including its onset, severity, or associated joint symptoms.
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