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Familial Mediterranean fever (FMF) is a hereditary autoinflammatory disease characterized by recurrent self-limiting fever and serositis that mainly affects Mediterranean populations. Many patients with FMF have been reported in Japan due to increasing recognition of this condition and the availability of genetic analysis for the gene responsible,  MEFV . The present study was performed to elucidate the clinical characteristics of Japanese FMF patients and to examine the precise genotype-phenotype correlation in a large cohort of Japanese FMF patients.    Methods  We analyzed the  MEFV  genotypes and clinical manifestations in 116 patients clinically diagnosed as having FMF and with at least one mutation.    Results  The most frequent mutation in Japanese patients was E148Q (40.2%), followed by M694I (21.0%), L110P (18.8%), P369S (5.4%), and R408Q (5.4%). In contrast, common mutations seen in Mediterranean patients, such as M694V, V726A, and M680I, were not detected in this population. The clinical features with M694I were associated with more severe clinical course compared to those seen with E148Q. P369S/R408Q showed variable phenotypes with regard to both clinical manifestations and severity. Patients with M694I showed a very favorable response to colchicine therapy, while those with P369S and R408Q did not.    Conclusions  Clinical features and efficacy of treatment in Japanese FMF patients vary widely according to the specific  MEFV  gene mutation, and therefore genetic analysis should be performed for diagnosis in cases of Japanese FMF.    Electronic supplementary material  The online version of this article (doi:10.1186/s13075-014-0439-7) contains supplementary material, which is available to authorized users.

arthritis research and therapy

Genotype-phenotype correlation in Japanese patients with familial Mediterranean fever: differences in genotype and clinical features between Japanese and Mediterranean populations