Publication:
Association of MEFV Gene Mutations with Rheumatoid Factor Levels in Patients with Rheumatoid Arthritis

dc.authorscopusid22934499300
dc.authorscopusid12805499100
dc.authorscopusid24781203900
dc.authorscopusid7003318655
dc.authorscopusid25655269800
dc.contributor.authorInanir, A.
dc.contributor.authorYigit, S.
dc.contributor.authorKarakuş, N.
dc.contributor.authorTeki̇n, S.
dc.contributor.authorRüstemoǧlu, A.
dc.date.accessioned2025-12-10T22:32:54Z
dc.date.issued2013
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Inanir] Ahmet, Department of Physical Therapy and Rehabilitation, Tokat Gaziosmanpaşa Üniversitesi, Tokat, Turkey; [Yigit] Serbulent, Department of Medical Biology, Tokat Gaziosmanpaşa Üniversitesi, Tokat, Turkey; [Karakuş] Nevin, Department of Medical Biology, Tokat Gaziosmanpaşa Üniversitesi, Tokat, Turkey, Department of Medical Biology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Teki̇n] Şaban, Department of Biology, Tokat Gaziosmanpaşa Üniversitesi, Tokat, Turkey; [Rüstemoǧlu] Aydin, Department of Medical Biology, Tokat Gaziosmanpaşa Üniversitesi, Tokat, Turkeyen_US
dc.description.abstractPurpose: 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. Copyright © 2013 by The American Federation for Medical Research.en_US
dc.identifier.doi10.2310/JIM.0b013e318280a96e
dc.identifier.endpage596en_US
dc.identifier.issn1081-5589
dc.identifier.issn1708-8267
dc.identifier.issue3en_US
dc.identifier.pmid23360841.0
dc.identifier.scopus2-s2.0-84877902234
dc.identifier.scopusqualityQ2
dc.identifier.startpage593en_US
dc.identifier.urihttps://doi.org/10.2310/JIM.0b013e318280a96e
dc.identifier.urihttps://hdl.handle.net/20.500.12712/35198
dc.identifier.volume61en_US
dc.identifier.wosqualityQ2
dc.language.isoenen_US
dc.publisherBMJ Publishing Groupen_US
dc.relation.ispartofJournal of Investigative Medicineen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAutoimmune Diseaseen_US
dc.subjectMEFV Geneen_US
dc.subjectMutationen_US
dc.subjectRheumatoid Arthritisen_US
dc.titleAssociation of MEFV Gene Mutations with Rheumatoid Factor Levels in Patients with Rheumatoid Arthritisen_US
dc.typeArticleen_US
dspace.entity.typePublication

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