FMF50评估疾病活动性评分和急性期反应物在预测秋水草碱反应中的应用:一项家族性地中海热儿童的回顾性队列研究

IF 2.8 3区 医学 Q2 RHEUMATOLOGY
Clinical Rheumatology Pub Date : 2025-09-01 Epub Date: 2025-07-14 DOI:10.1007/s10067-025-07567-w
Eda Nur Dizman, Feray Kaya, Elif Kucuk, Lutfiye Koru, Zelal Aydin, Hatice Kubra Dursun, Merve Ozen Balci, Fatih Haslak, Kubra Ozturk
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引用次数: 0

摘要

目的:监测家族性地中海热(FMF)患者的疾病活动可能具有挑战性,主要是由于伴随的炎症状况。本研究利用自身炎症性疾病活动性指数(AIDAI)、Pras、more、FMF国际严重程度评分(ISSF)和FMF50评分,评估FMF儿童的疾病活动性和秋水草碱反应,并检测其急性期反应物(APR)对FMF50反应的预测价值。方法:纳入符合欧洲热/PRINTO标准且接受秋水仙碱治疗≥6个月的FMF患者。没有外显子10突变和依从性差的患者被排除在外。采用AIDAI、Pras、more和ISSF评分评估疾病活动性,FMF50评估治疗反应。使用Cohen's和Fleiss's Kappa分析活动得分之间的一致性。患者分为FMF50应答者和无应答者。Logistic回归确定了FMF50反应预测因子。结果:共纳入117例儿童FMF患者,其中女性44.4%。无应答者的ISSF、AIDAI和Pras评分明显高于应答者(p结论:ISSF、AIDAI评分和CRP可以提前3个月预测FMF50应答,并建议对无应答者进行进一步治疗的早期评估。•本研究是文献中唯一评估所有疾病活动度评分并检查这些评分与APRs之间相关性的研究。•作为第二项利用FMF50评分来评估秋水仙碱反应的研究,它对具有更大患者队列的文献有重要贡献。•升高的CRP值,以及第3个月时较高的ISSF和AIDAI评分,在预测第6个月时的FMF50反应中起关键作用,表明早期评估高级治疗方案的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Utilization of disease activity scores and acute phase reactants in predicting colchicine response assessed by FMF50: a retrospective cohort study in children with Familial Mediterranean Fever.

Objectives: Monitoring disease activity in Familial Mediterranean Fever (FMF) patients might be challenging, mainly due to accompanying inflammatory conditions. This study assessed disease activity and colchicine response in children with FMF, using Auto-Inflammatory Diseases Activity Index (AIDAI), Pras, Mor, International Severity Score for FMF (ISSF), and FMF50 scores, and examined their acute phase reactant (APR) predictive value for FMF50 response.

Methods: FMF patients meeting Eurofever/PRINTO criteria and receiving colchicine for ≥ 6 months were included. Patients without exon 10 mutations and with poor adherence were excluded. Disease activity was assessed using AIDAI, Pras, Mor, and ISSF scores, while FMF50 evaluated treatment response. Concordance among activity scores was analyzed using Cohen's and Fleiss's Kappa. Patients were grouped as FMF50 responders or non-responders. Logistic regression identified FMF50 response predictors.

Results: A total of 117 pediatric FMF patients (44.4% female) were included. ISSF, AIDAI, and Pras scores were significantly higher in non-responders compared to responders (p < 0.001). Elevated CRP (OR 1.035, 95% CI 1.002-1.070, p < 0.05), ISSF (OR 1.703, 95% CI 1.135-2.557, p < 0.05), and AIDAI scores (OR 1.253, 95% CI 1.053-1.491, p < 0.05) at 3 months predicted FMF50 non-response at 6 months. Multivariate analysis identified high ISSF (OR 1.745, 95% CI 1.129-2.698, p < 0.05) and AIDAI scores (OR 1.265, 95% CI 1.056-1.514, p < 0.05) as independent predictors. APRs were correlated with ISSF, Pras, and AIDAI scores. Kappa analyses revealed poor agreement among activity scores (Kappa values 0.157 to - 0.048).

Conclusion: ISSF, AIDAI scores, and CRP can predict FMF50 response three months in advance and recommend earlier evaluation of further therapies in non-responders. Key Points • This study is the only investigation in the literature that evaluates all disease activity scores and examines the correlations between these scores and APRs. • As the second study to utilize the FMF50 score in assessing colchicine response, it contributes significantly to the literature with a larger patient cohort. • Elevated CRP values, along with high ISSF and AIDAI scores at the third month, play a critical role in predicting the FMF50 response at the sixth month, indicating the necessity for early evaluation of advanced treatment options.

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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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