Is colchicine an effective treatment in periodic fever, aphtous stomatitis, pharyngitis, cervical adenitis (PFAPA) syndrome?

被引:42
作者
Dusser, Perrine [1 ,2 ]
Hentgen, Veronique [2 ,3 ]
Neven, Benedicte [4 ]
Kone-Paut, Isabelle [1 ,2 ]
机构
[1] CHU Kremlin Bicetre, AP HP, Serv Rhumatol Pediat, 78 Rue Gen Leclerc, F-94270 Le Kremlin Bicetre, France
[2] Ctr Reference Malad Autoinflammatoires MAI, Rue Gen Leclerc, F-94270 Le Kremlin Bicetre, France
[3] Hop Andre Mignot, Serv Pediat Gen, Ctr Hosp, Ctr Hosp Versailles, F-78150 Le Chesnay, France
[4] Hop Necker Enfants Malad, CHU Paris, AP HP, Unite Immunol Hematol & Rhumatol Pediat, F-75015 Paris, France
关键词
PFAPA; Marshall syndrome; Children; Recurrent fever; Colchicine; Treatment; Autoinflammatory diseases; FAMILIAL MEDITERRANEAN FEVER; APHTHOUS STOMATITIS; ADENOPATHY SYNDROME; AUTOINFLAMMATORY DISEASES; CHILDREN; ACTIVATION; MEFV;
D O I
10.1016/j.jbspin.2015.08.017
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: PFAPA syndrome is the most frequent periodic fever syndrome in non-Mediterranean patients. The pathogenesis is unclear and the treatment is purely symptomatic and not standardized. The aim of this study was to assess colchicine's efficacy as prophylactic treatment in PFAPA syndrome and to identify factors able to predict response to treatment. Methods: We performed a retrospective, multicentric, cohort study of PFAPA patients under colchicine prophylaxis. PFAPA diagnosis was established according to Feder's criteria. Medical records were reviewed and analyzed for demographic, clinical and laboratory data. We distinguished one responder's group, defined as patients who had no more or twice fewer crises under colchicine and another one of non-responders. Subgroup analyses were performed using non-parametric Mann-Whitney test for quantitative data and calculating odds ratio and confidence interval for qualitative data. Difference between the two groups was considered significant for P-value < 0.05 or a confidence interval different from 1. Results-conclusion: Twenty children, 65% of whom were boys, were analyzed. Their mean age at disease onset was 2.3 +/- 1.5 years. Among the nine responder patients, five were MEFV (71%) heterozygotes: M694V mutation in four and V726A once. Heterozygous MEW gene mutation tended to be more frequent in the responders group (71% versus 43%; OR = 0.3 [0.03-2.7]). Non-responder patients had more chronic fatigue (82% versus 33%; OR= 9 [1,14-71]) and had more oral aphtosis (82% versus 11%; OR = 36 [1,7-141]) than the responders ones. Although not significant, colchicine treatment appeared more effective in patients with less complete PFAPA phenotype and MEFV heterozygosity. (C) 2016 Societe francaise de rhumatologie. Published by Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:406 / 411
页数:6
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