儿童家族性地中海热的不同关节炎类型:关注外显子10双等位基因致病性基因型

IF 3.8 3区 医学 Q1 RHEUMATOLOGY
Eray Tunce, Sıla Atamyildiz Uçar, Betül Sözeri
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引用次数: 0

摘要

目的:本研究旨在评估具有MEFV外显子10双等位基因致病性突变的儿童家族性地中海热(FMF)患者关节炎的患病率和特征,并评估轴向关节受损伤对疾病进展的影响。方法:本横断面研究纳入808例双等位基因外显子10突变的儿童FMF患者,随访至少12个月。分析了人口统计学、临床特征、基因变异和治疗反应的数据。根据关节炎的存在、持续时间和轴关节受累情况对患者进行分组,以进行比较分析。结果:关节炎占19.2%,急性关节炎占17.9%,慢性关节炎占6.4%。M694V等位基因频率在关节炎组显著高于(82%)。结论:我们的研究强调了双等位基因致病性基因型的儿童FMF患者关节炎的不同表现。M694V等位基因在关节炎组中更为普遍,这表明存在潜在的遗传联系。具体而言,关节炎患者常见FMF发作症状(如发烧和腹痛)的频率降低表明,这可能导致诊断延迟。轴向受累的慢性关节炎与较高的秋水仙碱耐药性相关,更需要先进的治疗。这些发现强调了针对儿童FMF合并关节炎患者量身定制的治疗策略和长期随访以优化预后的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Different arthritis patterns in pediatric familial Mediterranean fever: Focus on exon 10 biallelic pathogenic genotypes

Objectives

This study aimed to evaluate the prevalence and characteristics of arthritis in pediatric familial Mediterranean fever (FMF) patients with biallelic pathogenic MEFV mutations on exon 10 and to assess the impact of axial joint involvement on disease progression.

Methods

This cross-sectional study included 808 pediatric FMF patients with biallelic exon 10 mutations, followed for at least 12 months. Data on demographics, clinical features, genetic variants, and treatment responses were analyzed. Patients were grouped based on arthritis presence, duration, and axial joint involvement for comparative analysis.

Results

Arthritis was observed in 19.2% of patients, with acute and chronic arthritis in 17.9% and 6.4%, respectively. The M694V allele frequency was significantly higher in the arthritis group (82%, P < 0.01), with a predominance of the M694V/M694V genotype (70.3%). In contrast, V726A and R761H alleles were less frequent. Chronic arthritis with axial involvement was associated with older age at diagnosis (P < 0.01), increased polyarticular involvement (P < 0.01), and elevated colchicine resistance (22.6%, P < 0.01). The most frequently affected joints included the knee and sacroiliac joints. HLA-B27 positivity was higher in axial arthritis cases, but the need for advanced therapies did not differ significantly.

Conclusions

Our study highlights the diverse arthritis presentations in pediatric FMF patients with biallelic pathogenic genotypes. The M694V allele was more prevalent in the arthritis group, suggesting a potential genetic link. Specifically, the reduced frequency of common FMF attack symptoms, such as fever and abdominal pain, in patients with arthritis suggests that this may lead to diagnostic delays. Chronic arthritis with axial involvement was associated with higher colchicine resistance and a greater need for advanced treatments. These findings emphasize the importance of tailored management strategies and long-term follow-up in pediatric FMF patients with arthritis to optimize outcomes.
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来源期刊
Joint Bone Spine
Joint Bone Spine 医学-风湿病学
CiteScore
4.50
自引率
11.90%
发文量
184
审稿时长
25 days
期刊介绍: Bimonthly e-only international journal, Joint Bone Spine publishes in English original research articles and all the latest advances that deal with disorders affecting the joints, bones, and spine and, more generally, the entire field of rheumatology. All submitted manuscripts to the journal are subjected to rigorous peer review by international experts: under no circumstances does the journal guarantee publication before the editorial board makes its final decision. (Surgical techniques and work focusing specifically on orthopedic surgery are not within the scope of the journal.)Joint Bone Spine is indexed in the main international databases and is accessible worldwide through the ScienceDirect and ClinicalKey platforms.
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