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Performance of Tel-Hashomer, Livneh, pediatric and new Eurofever/PRINTO classification criteria for familial Mediterranean fever in a referral center

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Abstract

Until now, the diagnosis of familial Mediterranean fever (FMF) was based on validated subsets of clinical criteria, but recently new Eurofever/PRINTO classification criteria concerning genetic analyses were proposed. The study aimed to compare the performances of three validated diagnostic criteria (Tel-Hashomer, Livneh, pediatric criteria) and new Eurofever/PRINTO classification criteria. The medical charts of study and control groups were reviewed retrospectively. Patients were evaluated for three diagnostic criteria and new Eurofever/PRINTO classification criteria. Control group consists of patients with other autoinflammatory diseases. A total of 1291 patients were classified into three groups according to their mutations: group 1: 447 patients with homozygous mutations; group 2: 429 patients with compound heterozygous mutations; and group 3: 415 patients with one heterozygous mutation. Similar diagnostic utility was found according to Livneh criteria between groups. But, proportion of patients fulfilling Tel-Hashomer and pediatric criteria was higher in groups 1 and 2. According to Eurofever/PRINTO criteria, 98.2% of patients with homozygous mutations, 94.2% of patients with compound heterozygous mutations and 80.2% of patients with heterozygous mutations were classified as FMF. In control group, 99.2% of them fulfilled the Livneh criteria, 66.9% met the pediatric criteria and 0.8% satisfied the Tel-Hashomer criteria, while none of control patients met the Eurofever/PRINTO classification criteria. Performances of three validated diagnostic criteria and new Eurofever/PRINTO classification criteria for FMF were similar and provide high utility in diagnosing/classifying patients with homozygous and compound heterozygous mutations. However, both Eurofever/PRINTO classification criteria and Tel-Hashomer criteria had significantly lower performance in heterozygous patients.

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References

  1. Sohar E, Gafni J, Pras M, Heller H (1967) Familial Mediterranean fever. A survey of 470 cases and review of the literature. Am J Med 43:227–253

    Article  CAS  Google Scholar 

  2. Soriano A, Manna R (2012) Familial Mediterranean fever: new phenotypes. Autoimmun Rev 12:31–37

    Article  Google Scholar 

  3. Booty MG, Chae JJ, Masters SL et al (2009) Familial Mediterranean fever with a single MEFV mutation: where is the second hit? Arthritis Rheumatol 60:1851–1861

    Article  CAS  Google Scholar 

  4. Kone-Paut I, Hentgen V, Guillaume-Czitrom S, Compeyrot-Lacassagne S, Tran TA, Touitou I (2009) The clinical spectrum of 94 patients carrying a single mutated MEFV allele. Rheumatology (Oxford) 48:840–842

    Article  CAS  Google Scholar 

  5. Lachmann HJ, Sengul B, Yavuzsen TU et al (2006) Clinical and subclinical inflammation in patients with familial Mediterranean fever and in heterozygous carriers of MEFV mutations. Rheumatology (Oxford) 45:746–750

    Article  CAS  Google Scholar 

  6. Lidar M, Livneh A (2007) Familial Mediterranean fever: clinical, molecular and management advancements. Neth J Med 65:318–324

    CAS  PubMed  Google Scholar 

  7. Ozen S (2009) Changing concepts in familial Mediterranean fever: is it possible to have an autosomal-recessive disease with only one mutation? Arthritis Rheumatol 60:1575–1577

    Article  CAS  Google Scholar 

  8. Livneh A, Langevitz P, Zemer D, Zaks N, Kees S, Lidar T, Migdal A, Padeh S, Pras M (1997) Criteria for the diagnosis of familial Mediterranean fever. Arthritis Rheumatol 40:1879–1885

    Article  CAS  Google Scholar 

  9. Yalcinkaya F, Ozen S, Ozcakar ZB et al (2009) A new set of criteria for the diagnosis of familial Mediterranean fever in childhood. Rheumatology (Oxford) 48:395–398

    Article  Google Scholar 

  10. Gattorno M, Hofer M, Federici S et al (2019) Classification criteria for autoinflammatory recurrent fevers. Ann Rheum Dis 78:1025–1032

    Article  CAS  Google Scholar 

  11. Marshall GS, Edwards KM, Butler J, Lawton AR (1987) Syndrome of periodic fever, pharyngitis, and aphthous stomatitis. J Pediatr 110:43–46

    Article  CAS  Google Scholar 

  12. Pras E, Livneh A, Balow JE Jr, Pras E, Kastner DL, Pras M, Langevitz P (1998) Clinical differences between North African and Iraqi Jews with familial Mediterranean fever. Am J Med Genet 75:216–219

    Article  CAS  Google Scholar 

  13. Ozen S, Aktay N, Lainka E, Duzova A, Bakkaloglu A, Kallinich T (2009) Disease severity in children and adolescents with familial Mediterranean fever: a comparative study to explore environmental effects on a monogenic disease. Ann Rheum Dis 68:246–248

    Article  CAS  Google Scholar 

  14. Ozen S, Demirkaya E, Erer B et al (2016) EULAR recommendations for the management of familial Mediterranean fever. Ann Rheum Dis 75:644–651

    Article  CAS  Google Scholar 

  15. Kallinich T, Haffner D, Niehues T et al (2007) Colchicine use in children and adolescents with familial Mediterranean fever: literature review and consensus statement. Pediatrics 119:e474–e483

    Article  Google Scholar 

  16. Demirkaya E, Saglam C, Turker T et al (2016) Performance of different diagnostic criteria for familial mediterranean fever in children with periodic fevers: results from a multicenter international registry. J Rheumatol 43:154–160

    Article  CAS  Google Scholar 

  17. Eisenstein EM, Berkun Y, Ben-Chetrit E (2013) Familial Mediterranean fever: a critical digest of the 2012–2013 literature. Clin Exp Rheumatol 31:103–107

    PubMed  Google Scholar 

  18. Sag E, Demirel D, Demir S, Atalay E, Akca U, Bilginer Y, Ozen S (2019) Performance of the new ‘Eurofever/PRINTO classification criteria’ in FMF patients. Semin Arthritis Rheum. https://doi.org/10.1016/j.semarthrit.2019.08.004

    Article  PubMed  Google Scholar 

  19. Daniels M, Shohat T, Brenner-Ullman A, Shohat M (1995) Familial Mediterranean fever: high gene frequency among the non-Ashkenazic and Ashkenazic Jewish populations in Israel. Am J Med Genet 55:311–314

    Article  CAS  Google Scholar 

  20. Yilmaz E, Ozen S, Balci B et al (2001) Mutation frequency of Familial Mediterranean Fever and evidence for a high carrier rate in the Turkish population. Eur J Hum Genet 9:553–555

    Article  CAS  Google Scholar 

  21. Sarkisian T, Ajrapetian H, Beglarian A, Shahsuvarian G, Egiazarian A (2008) Familial Mediterranean fever in Armenian population. Georgian Med News 156:105–111

    Google Scholar 

  22. Jeru I, Hentgen V, Cochet E et al (2013) The risk of familial Mediterranean fever in MEFV heterozygotes: a statistical approach. PLoS One ​ 8:68431

    Article  Google Scholar 

  23. Hentgen V, Grateau G, Stankovic-Stojanovic K, Amselem S, Jeru I (2013) Familial Mediterranean fever in heterozygotes: are we able to accurately diagnose the disease in very young children? Arthritis Rheum 65:1654–1662

    Article  Google Scholar 

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AT conceptualized and designed the study, drafted the initial manuscript, and had full access to all the data in the study; HES designed the study, conducted the data analyses, drafted the initial manuscript, and had full access to all the data in the study; ŞGK, FÇ and MÇ drafted the initial manuscript; NAA conceptualized and designed the study, drafted the final manuscript, and had full access to all the data in the study and all authors reviewed and revised the manuscript and approved the final manuscript as submitted and agree to be accountable for all aspects of the work.

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Correspondence to Nuray Aktay Ayaz.

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The study was reviewed and approved by the ethical review committee of Kanuni Sultan Süleyman Training and Research Hospital (Ethics approval number: KAEK/2018.12.65).

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All participants and parents provided written informed consent.

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Tanatar, A., Sönmez, H.E., Karadağ, Ş.G. et al. Performance of Tel-Hashomer, Livneh, pediatric and new Eurofever/PRINTO classification criteria for familial Mediterranean fever in a referral center. Rheumatol Int 40, 21–27 (2020). https://doi.org/10.1007/s00296-019-04463-w

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  • DOI: https://doi.org/10.1007/s00296-019-04463-w

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