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Performance of Tel-Hashomer, Livneh, pediatric and new Eurofever/PRINTO classification criteria for familial Mediterranean fever in a referral center.
- Source :
-
Rheumatology international [Rheumatol Int] 2020 Jan; Vol. 40 (1), pp. 21-27. Date of Electronic Publication: 2019 Oct 23. - Publication Year :
- 2020
-
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.
- Subjects :
- Adolescent
Arthritis physiopathology
Case-Control Studies
Chest Pain physiopathology
Child
Child, Preschool
Colchicine therapeutic use
Consanguinity
Drug Resistance
Exons genetics
Familial Mediterranean Fever classification
Familial Mediterranean Fever genetics
Familial Mediterranean Fever physiopathology
Female
Hereditary Autoinflammatory Diseases classification
Hereditary Autoinflammatory Diseases diagnosis
Humans
Male
Mutation
Reproducibility of Results
Retrospective Studies
Severity of Illness Index
Tubulin Modulators therapeutic use
Familial Mediterranean Fever diagnosis
Heterozygote
Homozygote
Pyrin genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1437-160X
- Volume :
- 40
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Rheumatology international
- Publication Type :
- Academic Journal
- Accession number :
- 31646357
- Full Text :
- https://doi.org/10.1007/s00296-019-04463-w