PREDICT-crFMF score: A novel model for predicting colchicine resistance in children with familial Mediterranean fever

Author:

Aktay Ayaz Nuray1ORCID,Demirkan Fatma Gül1,Coşkuner Taner2,Demir Ferhat3,Tanatar Ayşe1,Çakan Mustafa2,Karadağ Şerife Gül1,Yener Gülçin Otar4,Öztürk Kübra5,Bağlan Esra6,Çakmak Figen1,Çağlayan Şengül2,Özdel Semanur6,Ulu Kadir2,Sözeri Betül2,Sönmez Hafize Emine7

Affiliation:

1. Department of Pediatric Rheumatology, Istanbul Faculty of Medicine, Istanbul University , Istanbul, Turkey

2. Department of Pediatric Rheumatology, University of Health Sciences, Umraniye Research and Training Hospital , Istanbul, Turkey

3. Department of Pediatric Rheumatology, Acıbadem Healthcare Group , Istanbul, Turkey

4. Department of Pediatric Rheumatology, Sanliurfa Training and Research Hospital , Sanliurfa, Turkey

5. Department of Pediatric Rheumatology, Istanbul Medeniyet University, School of Medicine, Goztepe Research and Training Hospital , Istanbul, Turkey

6. Department of Pediatric Rheumatology, University of Health Sciences, Dr. Sami Ulus Obstetrics and Gynecology, Pediatric Health and Disease Training and Research Hospital , Ankara, Turkey

7. Department of Pediatric Rheumatology, Kocaeli University, Kocaeli School of Medicine , Kocaeli, Turkey

Abstract

ABSTRACT Objectives To develop a novel scoring system to predict colchicine resistance in Familial Mediterranean fever (FMF) based on the initial features of the patients. Methods The medical records of patients were analyzed prior to the initiation of colchicine. After generating a predictive score in the initial cohort, it was applied to an independent cohort for external validation of effectiveness and reliability. Results Among 1418 patients with FMF, 56 (3.9%) were colchicine resistant (cr) and 1312 (96.1%) were colchicine responsive. Recurrent arthritis (4 points), protracted febrile myalgia (8 points), erysipelas-like erythema (2 points), exertional leg pain (2 points), and carrying M694V homozygous mutation (4 points) were determined as the parameters for predicting cr-FMF in the logistic regression model. The cut-off value of 9 was 87% sensitive and 82% specific to foresee the risk of cr-FMF in the receiver operating characteristic. Validation of the scoring system with an independent group (cr-FMF = 107, colchicine responsive = 1935) revealed that the cut-off value was 82% sensitive and 79% specific to identify the risk of cr-FMF. Conclusions By constructing this reliable and predictor tool, we enunciate that predicting cr-FMF at the initiation of the disease and interfering timely before the emergence of complications will be possible.

Publisher

Oxford University Press (OUP)

Subject

Rheumatology

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