Article Text

Association of MEFV Gene Mutations With Rheumatoid Factor Levels in Patients With Rheumatoid Arthritis
  1. Ahmet Inanir, MD*,
  2. Serbulent Yigit, PhD,
  3. Nevin Karakus, PhD†‡,
  4. Saban Tekin, PhD§,
  5. Aydin Rustemoglu, PhD
  1. From the *Department of Physical Therapy and Rehabilitation, Faculty of Medicine, Gaziosmanpasa University, Tokat, Turkey; †Department of Medical Biology, Faculty of Medicine, Gaziosmanpasa University, Tokat, Turkey; ‡Department of Medical Biology, Faculty of Medicine, Ondokuz Mayis University, Samsun, Turkey; and §Department of Biology, Faculty of Science, Gaziosmanpasa University, Tokat, Turkey.
  1. Received September 7, 2012, and in revised form November 21, 2012.
  2. Accepted for publication November 22, 2012.
  3. Reprints: Ahmet Inanir, MD, Department of Physical Therapy and Rehabilitation, Faculty of Medicine, Gaziosmapasa University, 60100, Tokat/Turkey. E-mail: inanira{at}
  4. Supported by Gaziosmanpasa University (Project No. 2011/54).


Purpose Rheumatoid arthritis (RA) is a systemic autoimmune disease primarily affecting the joints. Arthritis disorders are associated with mutations of the Mediterranean fever (MEFV) gene. This gene has already been identified as being responsible for familial Mediterranean fever. The aim of this study was to explore the frequency and clinical significance of MEFV gene mutations in a cohort of Turkish patients with RA.

Methods The study included 101 patients with RA and 110 healthy controls. Genomic DNA was isolated and genotyped using polymerase chain reaction and restriction fragment length polymorphism for the 5 MEFV gene mutations (M694V, M680I, V726A, E148Q, and P369S).

Results Carrier rates of MEFV gene mutations were 31 (30.7%) of 101 and 26 (23.6%) of 110 in the RA and healthy control groups, respectively (P > 0.05; odds ratio, 1.4; 95% CI, 0.77–2.65). Whereas deformed joint count was relatively higher in the mutation carrier group than those of the noncarrier group, the rheumatoid factor levels were significantly higher in the carrier group of patients with RA (P = 0.001).

Conclusions The results of this study suggest that MEFV gene mutations are not positively associated with a predisposition to develop RA but might increase the severity of RA. Further research is needed to determine the actual pathogenic role of MEFV mutations in this disease.

Key Words
  • rheumatoid arthritis
  • MEFV gene
  • mutation
  • autoimmune disease

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