Familial Mediterranean fever in children from central-southern Italy: a multicentric retrospective cohort study.

IF 2.9 3区 医学 Q2 RHEUMATOLOGY
Saverio La Bella, Roberta Loconte, Marina Attanasi, Mario Muselli, Giulia Di Donato, Armando Di Ludovico, Marco Natale, Violetta Mastrorilli, Andrea Giugno, Santi Papa, Rossella Ferrante, Carlotta Buccolini, Ivana Antonucci, Francesco Chiarelli, Stefano Necozione, Patrizia Barone, Francesco La Torre, Luciana Breda
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引用次数: 0

Abstract

Introduction: Although familial Mediterranean fever (FMF) is a relevant disease in countries surrounding the Mediterranean Sea, there are still few reports from Italy.

Methods: We retrospectively evaluated patients with FMF diagnosed according to the EuroFever/PRINTO classification criteria in three pediatric rheumatology referral centers in central-southern Italy. Logistic regression analysis assessed the associations between age at disease onset and symptoms.

Results: Overall, 48 patients were enrolled (28 females, 20 males), with a median age at onset of 3.3 [3.1] years, and a median follow-up period of 5.1 [10.8] years. The most common MEFV genotype was M694V/- (11 patients, 22.9%), followed by M694V/M694V (6 patients, 12.5%). At onset, recurrent fever was observed in 47 patients (97.9%), with a median time between attacks of 18 [11] days. Overall, recurrent fever was observed in all patients, abdominal pain in 44 (91.7%), and chest pain in 18 (37.5%). At the last follow-up visit, 24 patients were on colchicine (50%), 2 on biologic (4.2%), and 6 on both (12.5%). Canakinumab was the most used biologic drug, in 6 (12.5%) patients. MEFV genotype was associated with disease severity (p = 0.007) and the use of a biological drug (p = 0.01). FMF prevalence in the Abruzzo region was found highly than expected (at least 1:45,000). Differently, we found a relevant gap among FMF patients expected and observed in the Apulia and Sicily regions.

Conclusions: FMF is a relevant issue in central-southern Italy. A large epidemiologic study should be performed to better define its prevalence in the country. Key Points • Italian children with familial Mediterranean fever tend to have an early age of onset, primarily manifesting with recurrent fever and characteristic associated symptoms. • Many MEFV gene variants are present in Italian children with familial Mediterranean fever, and these patients are most often heterozygous, exhibiting a mild to moderate phenotype. • The prevalence of familial Mediterranean fever in Italy is still unknown but recently estimated to be around 1:60,000, probably higher in central and southern Italy. • According to our cohort, the prevalence of FMF in the Abruzzo region is at least 1:45,000, higher than expected. Differently, we found lower prevalence rates of the disease in Apulia and Sicily.

意大利中南部儿童家族性地中海热:一项多中心回顾性队列研究。
简介:尽管家族性地中海热(FMF)是地中海周边国家的一种常见疾病,但意大利的报道仍然很少:尽管家族性地中海热(FMF)是地中海周边国家的一种相关疾病,但意大利的相关报道仍然很少:我们对意大利中南部三家儿科风湿病转诊中心根据欧洲热/PRINTO分类标准确诊的FMF患者进行了回顾性评估。逻辑回归分析评估了发病年龄与症状之间的关联:共有 48 名患者(28 名女性,20 名男性)参与研究,中位发病年龄为 3.3 [3.1] 岁,中位随访时间为 5.1 [10.8] 年。最常见的 MEFV 基因型是 M694V/-(11 名患者,22.9%),其次是 M694V/M694V(6 名患者,12.5%)。发病时,47 名患者(97.9%)出现反复发热,中位间隔时间为 18 [11] 天。总体而言,所有患者均出现反复发热,44 名患者(91.7%)出现腹痛,18 名患者(37.5%)出现胸痛。在最后一次随访中,24 名患者服用秋水仙碱(50%),2 名患者服用生物制剂(4.2%),6 名患者同时服用两种药物(12.5%)。卡那单抗是使用最多的生物制剂药物,有6名患者(12.5%)使用了卡那单抗。MEFV 基因型与疾病的严重程度(p = 0.007)和生物制剂的使用(p = 0.01)有关。阿布鲁佐地区的 FMF 患病率高于预期(至少为 1:45,000)。与此不同的是,我们发现在阿普利亚和西西里地区,预期的 FMF 患者与观察到的 FMF 患者之间存在相关差距:结论:FMF 是意大利中南部的一个相关问题。结论:FMF 是意大利中南部地区的一个重要问题,应开展大规模流行病学研究,以更好地确定其在该国的发病率。要点--意大利儿童家族性地中海热的发病年龄往往较早,主要表现为反复发热和特征性相关症状。- 家族性地中海热的意大利儿童中存在许多 MEFV 基因变异,这些患者多为杂合子,表现为轻度至中度表型。- 家族性地中海热在意大利的发病率尚不清楚,但最近估计约为 1:60000,意大利中部和南部的发病率可能更高。- 根据我们的队列,阿布鲁佐地区的家族性地中海热发病率至少为 1:45,000,高于预期。不同的是,我们发现阿普利亚和西西里的患病率较低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical Rheumatology
Clinical Rheumatology 医学-风湿病学
CiteScore
6.90
自引率
2.90%
发文量
441
审稿时长
3 months
期刊介绍: Clinical Rheumatology is an international English-language journal devoted to publishing original clinical investigation and research in the general field of rheumatology with accent on clinical aspects at postgraduate level. The journal succeeds Acta Rheumatologica Belgica, originally founded in 1945 as the official journal of the Belgian Rheumatology Society. Clinical Rheumatology aims to cover all modern trends in clinical and experimental research as well as the management and evaluation of diagnostic and treatment procedures connected with the inflammatory, immunologic, metabolic, genetic and degenerative soft and hard connective tissue diseases.
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