Literature DB >> 25637003

Evidence-based provisional clinical classification criteria for autoinflammatory periodic fevers.

Silvia Federici1, Maria Pia Sormani2, Seza Ozen3, Helen J Lachmann4, Gayane Amaryan5, Patricia Woo6, Isabelle Koné-Paut7, Natacha Dewarrat8, Luca Cantarini9, Antonella Insalaco10, Yosef Uziel11, Donato Rigante12, Pierre Quartier13, Erkan Demirkaya14, Troels Herlin15, Antonella Meini16, Giovanna Fabio17, Tilmann Kallinich18, Silvana Martino19, Aviel Yonatan Butbul20, Alma Olivieri21, Jasmin Kuemmerle-Deschner22, Benedicte Neven13, Anna Simon23, Huri Ozdogan24, Isabelle Touitou25, Joost Frenkel26, Michael Hofer8, Alberto Martini27, Nicolino Ruperto1, Marco Gattorno1.   

Abstract

The objective of this work was to develop and validate a set of clinical criteria for the classification of patients affected by periodic fevers. Patients with inherited periodic fevers (familial Mediterranean fever (FMF); mevalonate kinase deficiency (MKD); tumour necrosis factor receptor-associated periodic fever syndrome (TRAPS); cryopyrin-associated periodic syndromes (CAPS)) enrolled in the Eurofever Registry up until March 2013 were evaluated. Patients with periodic fever, aphthosis, pharyngitis and adenitis (PFAPA) syndrome were used as negative controls. For each genetic disease, patients were considered to be 'gold standard' on the basis of the presence of a confirmatory genetic analysis. Clinical criteria were formulated on the basis of univariate and multivariate analysis in an initial group of patients (training set) and validated in an independent set of patients (validation set). A total of 1215 consecutive patients with periodic fevers were identified, and 518 gold standard patients (291 FMF, 74 MKD, 86 TRAPS, 67 CAPS) and 199 patients with PFAPA as disease controls were evaluated. The univariate and multivariate analyses identified a number of clinical variables that correlated independently with each disease, and four provisional classification scores were created. Cut-off values of the classification scores were chosen using receiver operating characteristic curve analysis as those giving the highest sensitivity and specificity. The classification scores were then tested in an independent set of patients (validation set) with an area under the curve of 0.98 for FMF, 0.95 for TRAPS, 0.96 for MKD, and 0.99 for CAPS. In conclusion, evidence-based provisional clinical criteria with high sensitivity and specificity for the clinical classification of patients with inherited periodic fevers have been developed. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

Entities:  

Keywords:  Familial Mediterranean Fever; Fever Syndromes; Inflammation

Mesh:

Year:  2015        PMID: 25637003     DOI: 10.1136/annrheumdis-2014-206580

Source DB:  PubMed          Journal:  Ann Rheum Dis        ISSN: 0003-4967            Impact factor:   19.103


  68 in total

1.  Autoinflammation. Management of hereditary recurrent fevers--SHARE experience.

Authors:  Guillaume Sarrabay; Isabelle Touitou
Journal:  Nat Rev Rheumatol       Date:  2015-08-18       Impact factor: 20.543

Review 2.  Lights and shadows in autoinflammatory syndromes from the childhood and adulthood perspective.

Authors:  Donato Rigante; Antonio Vitale; Marco Francesco Natale; Luca Cantarini
Journal:  Clin Rheumatol       Date:  2015-12-03       Impact factor: 2.980

Review 3.  Autoinflammatory Diseases with Periodic Fevers.

Authors:  Erdal Sag; Yelda Bilginer; Seza Ozen
Journal:  Curr Rheumatol Rep       Date:  2017-07       Impact factor: 4.592

4.  The diagnostic evaluation of patients with a suspected hereditary periodic fever syndrome: experience from a referral center in Italy.

Authors:  Antonio Vitale; Donato Rigante; Orso Maria Lucherini; Anna De Palma; Ida Orlando; Stefano Gentileschi; Jurgen Sota; Antonella Simpatico; Claudia Fabiani; Mauro Galeazzi; Bruno Frediani; Luca Cantarini
Journal:  Intern Emerg Med       Date:  2017-02-13       Impact factor: 3.397

Review 5.  [Role of genetics in familial Mediterranean fever].

Authors:  T Kallinich; B Orak; H Wittkowski
Journal:  Z Rheumatol       Date:  2017-05       Impact factor: 1.372

Review 6.  Current knowledge on procaspase-1 variants with reduced or abrogated enzymatic activity in autoinflammatory disease.

Authors:  Hella Luksch; Stefan Winkler; Michael C Heymann; Felix Schulze; Sigrun R Hofmann; Joachim Roesler; Angela Rösen-Wolff
Journal:  Curr Rheumatol Rep       Date:  2015-07       Impact factor: 4.592

7.  Inflammation: New classification criteria for autoinflammatory periodic fevers.

Authors:  Nicholas J Bernard
Journal:  Nat Rev Rheumatol       Date:  2015-02-17       Impact factor: 20.543

Review 8.  Familial Mediterranean fever and atherosclerosis in childhood and adolescence.

Authors:  Olga Vampertzi; Kyriaki Papadopoulou-Legbelou; Areti Triantafyllou; Stella Douma; Efimia Papadopoulou-Alataki
Journal:  Rheumatol Int       Date:  2019-11-08       Impact factor: 2.631

9.  Early Onset of Periodic Fever Syndrome in a Patient Carrying Both Tumor Necrosis Factor Receptor Superfamily 1A and Mediterranean Fever Mutations.

Authors:  Barbara Kraszewska-Głomba; Zofia Szymańska-Toczek; Leszek Szenborn
Journal:  Arch Rheumatol       Date:  2016-06-28       Impact factor: 1.472

Review 10.  Molecular genetic analysis for periodic fever syndromes: a supplemental role for the diagnosis of adult-onset Still's disease.

Authors:  Hongbin Li; Irina Abramova; Sandra Chesoni; Qingping Yao
Journal:  Clin Rheumatol       Date:  2018-06-17       Impact factor: 2.980

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