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儿童系统性红斑狼疮中的自身抗体:种族分组、聚类分析及临床相关性

Autoantibodies in pediatric systemic lupus erythematosus: ethnic grouping, cluster analysis, and clinical correlations.

作者信息

Jurencák Roman, Fritzler Marvin, Tyrrell Pascal, Hiraki Linda, Benseler Susanne, Silverman Earl

机构信息

Division of Rheumatology, Hospital for Sick Children, 555 University Avenue, Toronto, Ontario M5G 1X8.

出版信息

J Rheumatol. 2009 Feb;36(2):416-21. doi: 10.3899/jrheum.080588. Epub 2009 Jan 22.

Abstract

OBJECTIVE

(1) To evaluate the spectrum of serum autoantibodies in pediatric-onset systemic lupus erythematosus (pSLE) with a focus on ethnic differences; (2) using cluster analysis, to identify patients with similar autoantibody patterns and to determine their clinical associations.

METHODS

A single-center cohort study of all patients with newly diagnosed pSLE seen over an 8-year period was performed. Ethnicity, clinical, and serological data were prospectively collected from 156/169 patients (92%). The frequencies of 10 selected autoantibodies among ethnic groups were compared. Cluster analysis identified groups of patients with similar autoantibody profiles. Associations of these groups with clinical and laboratory features of pSLE were examined.

RESULTS

Among our 5 ethnic groups, there were differences only in the prevalence of anti-U1RNP and anti-Sm antibodies, which occurred more frequently in non-Caucasian patients (p < 0.0001, p < 0.01, respectively). Cluster analysis revealed 3 autoantibody clusters. Cluster 1 consisted of anti-dsDNA antibodies. Cluster 2 consisted of anti-dsDNA, antichromatin, antiribosomal P, anti-U1RNP, anti-Sm, anti-Ro and anti-La autoantibody. Cluster 3 consisted of anti-dsDNA, anti-RNP, and anti-Sm autoantibody. The highest proportion of Caucasians was in cluster 1 (p < 0.05), which was characterized by a mild disease with infrequent major organ involvement compared to cluster 2, which had the highest frequency of nephritis, renal failure, serositis, and hemolytic anemia, or cluster 3, which was characterized by frequent neuropsychiatric disease and nephritis.

CONCLUSION

We observed ethnic differences in autoantibody profiles in pSLE. Autoantibodies tended to cluster together and these clusters were associated with different clinical courses.

摘要

目的

(1)评估儿童期起病的系统性红斑狼疮(pSLE)患者血清自身抗体谱,重点关注种族差异;(2)采用聚类分析,识别自身抗体模式相似的患者,并确定其临床关联。

方法

对8年间新诊断的所有pSLE患者进行单中心队列研究。前瞻性收集了156/169例患者(92%)的种族、临床和血清学数据。比较了10种选定自身抗体在不同种族群体中的频率。聚类分析确定了自身抗体谱相似的患者组。研究了这些组与pSLE临床和实验室特征的关联。

结果

在我们的5个种族群体中,仅抗U1RNP和抗Sm抗体的患病率存在差异,非白种人患者中出现的频率更高(分别为p < 0.0001,p < 0.01)。聚类分析揭示了3个自身抗体簇。簇1由抗双链DNA(dsDNA)抗体组成。簇2由抗dsDNA、抗染色质、抗核糖体P、抗U1RNP、抗Sm、抗Ro和抗La自身抗体组成。簇3由抗dsDNA、抗RNP和抗Sm自身抗体组成。白种人在簇1中的比例最高(p < 0.05),与簇2相比,其疾病较轻,主要器官受累较少,簇2中肾炎、肾衰竭、浆膜炎和溶血性贫血的发生率最高,而簇3的特征是频繁出现神经精神疾病和肾炎。

结论

我们观察到pSLE患者自身抗体谱存在种族差异。自身抗体倾向于聚集在一起,这些簇与不同的临床病程相关。

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