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土耳其 FMF 患儿继发淀粉样变性发生率降低:我们做得更好了吗?

Decrease in the rate of secondary amyloidosis in Turkish children with FMF: are we doing better?

机构信息

Department of Pediatrics, Hacettepe University, Ankara 06100, Turkey.

出版信息

Eur J Pediatr. 2010 Aug;169(8):971-4. doi: 10.1007/s00431-010-1158-y. Epub 2010 Feb 24.

Abstract

Familial Mediterranean fever (FMF) is the most common autoinflammatory disease in the world. The most serious complication of FMF is the development of secondary amyloidosis. Besides genetic factors, environment has been implicated in the development of this complication. The main objective of this study is to analyze whether there has been a substantial decrease of secondary amyloidosis in Turkey and possible effective factors. For this purpose, clinical features of the patients diagnosed with secondary amyloidosis between the years 1978 and 1990 were compared with those diagnosed between 2000 and 2009. Severity scores were determined by the use of a scoring system modified for children. Median ages of the group diagnosed between 1978 and 1990 (n = 115; 12.1% among a total of 947 renal biopsies) and diagnosed after 2000 (n = 19; 2% among a total of 974 renal biopsies) were 12 and 13 years, respectively. There were no significant differences between the two patient groups according to gender, age, age of onset, disease duration, and disease severity. There was, however, a clear decrease in the percentage of biopsies with secondary amyloidosis from 12.1% (1978-1990) to 2% (after 2000; p < 0.001). Our results have shown that there has been a significant decrease in the rate of secondary amyloidosis in Turkey. The main reason for this decrease is better medical care with increased awareness and treatment of the disease. However, we suggest that the improvement of infectious milieu may possibly have had a positive effect on the course of this monogenic disease, since inflammatory pathways related to innate immunity are deregulated.

摘要

家族性地中海热(FMF)是世界上最常见的自身炎症性疾病。FMF 的最严重并发症是继发性淀粉样变性的发展。除遗传因素外,环境也与这种并发症的发展有关。本研究的主要目的是分析土耳其继发性淀粉样变性是否有实质性减少,以及可能的有效因素。为此,比较了 1978 年至 1990 年和 2000 年至 2009 年诊断为继发性淀粉样变性的患者的临床特征。使用针对儿童的改良评分系统确定严重程度评分。1978 年至 1990 年(947 例肾活检中占 12.1%)和 2000 年后诊断的(974 例肾活检中占 2%)组的中位年龄分别为 12 岁和 13 岁。两组患者的性别、年龄、发病年龄、病程和疾病严重程度无显著差异。然而,继发性淀粉样变性活检的百分比从 12.1%(1978-1990 年)降至 2%(2000 年后;p<0.001),这一变化非常明显。我们的结果表明,土耳其继发性淀粉样变性的发生率显著下降。这种下降的主要原因是更好的医疗保健,提高了对疾病的认识和治疗。然而,我们认为,感染环境的改善可能对这种单基因疾病的病程产生了积极影响,因为与先天免疫相关的炎症途径失调。

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