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Autoantibodies are not associated with familial mediterranean fever
Emel Guler1, Ece Kaptanoglu, Ozlem Sahin
1Kayseri Education and Research Hospital, Kayseri, Turkey.
Objective:
It has been suggested that Mediterranean fever (MEFV) gene mutations are also seen in certain autoimmune diseases and are related to severity of the disease activity. As most of the clinical symptoms of these inflammatory diseases are related to autoantibody positivity, we assessed autoantibody prevalence in patients with Familial Mediterranean fever (FMF) and investigated the relationship between clinical involvement of FMF and the autoantibodies. There are a few studies on this subject with conflicting results.
Patients And Methods:
Fifty patients with FMF without attack and 27 healthy controls were enrolled to the study. Clinical characteristics of the patient group were questioned. Rheumatoid factor (RF), anti-cyclic citrullinated peptide (anti-CCP) values, Fluorescent antinuclear antibody (ANA), extractable nuclear antigen (ENA) profile was studied in both groups.
Results:
No statistically significant difference was found in ANA, ENA profile, anti-CCP, and RF positivity between the groups (p>0.05). There was no relationship between the autoantibodies and the clinical status in patients with FMF. MEFV gene mutations were identified in 98% of the FMF patients.
Conclusion:
In conclusion, autoantibody positivity is similar to the healthy population in FMF. Although MEFV mutations affect clinical course in other autoantibody mediated diseases, it is not related to autoantibody formation in FMF.
Insights
Autoantibody positivity in Familial Mediterranean fever (FMF) patients mirrors the general population, with no link found between MEFV gene mutations and autoantibody formation. This suggests FMF
Area of Science:
- Rheumatology
- Genetics
- Immunology
Background:
- Familial Mediterranean fever (FMF) is an autoinflammatory disease.
- MEFV gene mutations are implicated in FMF pathogenesis.
- The role of autoantibodies in FMF and their association with MEFV mutations is unclear.
Purpose of the Study:
- To assess autoantibody prevalence in FMF patients.
- To investigate the relationship between FMF clinical activity and autoantibody positivity.
- To explore the association between MEFV gene mutations and autoantibody formation in FMF.
Main Methods:
- Fifty FMF patients and 27 healthy controls were enrolled.
- Autoantibody testing included antinuclear antibody (ANA), extractable nuclear antigen (ENA) profile, anti-cyclic citrullinated peptide (anti-CCP), and rheumatoid factor (RF).
- MEFV gene mutations were identified in FMF patients.
Main Results:
- No significant differences in ANA, ENA profile, anti-CCP, or RF positivity were observed between FMF patients and controls.
- No correlation was found between autoantibody status and clinical manifestations in FMF patients.
- MEFV gene mutations were present in 98% of FMF patients.
Conclusions:
- Autoantibody positivity in FMF patients is comparable to the healthy population.
- MEFV mutations do not appear to influence autoantibody formation in FMF.
- Findings suggest distinct mechanisms underlying FMF compared to other autoantibody-mediated diseases.
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