幼年银屑病关节炎的发病特点

S. Chebysheva, N. Geppe, I. Korsunskaya, V. Sobolev, A. V. Polyanskaya, L. Khachatryan, M. Nikolaeva, E. Afonina
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To analyze the data, universal nonparametric (randomization-permutation) algorithms for constructing confidence intervals (CI) and statistical comparisons based on the bootstrap and Monte Carlo methods were used.Results. It was possible to identify a relationship between the onset variant and the gender of the child. The incidence of asymmetric oligoarthritis in boys and girls at onset was approximately the same, 68% and 59%, respectively, and did not differ significantly. At onset, girls had a higher incidence of rheumatoid-like arthritis (37%) (p<0.005), and boys had a higher incidence of spondyloarthritis (26%) (p<0.005). A relationship was also revealed between the onset, gender and age of the child. Girls aged 0–6 years most often debuted with asymmetric oligoarthritis (90%) (p<0.005), and at the age of 11–15 years — with the rheumatoid-like (polyarticular) variant (73%) (p<0.005). 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引用次数: 0

摘要

青少年银屑病关节炎是一种外周关节、脊柱关节和内膜的慢性炎症性疾病,在银屑病患者中的发病率为10%-25%。研究幼年银屑病关节炎的首发特征将提高早期诊断率,并有助于避免残疾、使儿童社会化和融入社会。确定幼年银屑病关节炎的发病与患儿年龄和性别之间的关系,追溯我们的患者从发病到病重期间关节综合征的性质。研究对象为155名确诊为幼年银屑病关节炎的患者。在分析数据时,使用了基于引导法和蒙特卡罗法的通用非参数(随机化-畸变)算法来构建置信区间(CI)和进行统计比较。结果表明,发病变异与儿童性别之间存在关系。男孩和女孩发病时的非对称性少关节炎发病率大致相同,分别为68%和59%,没有显著差异。发病时,女孩类风湿关节炎的发病率较高(37%)(P<0.005),男孩脊柱关节炎的发病率较高(26%)(P<0.005)。儿童的发病、性别和年龄之间也存在一定的关系。0-6岁的女孩最常见的是不对称少关节炎(90%)(p<0.005),11-15岁的女孩则是类风湿(多关节)变异型(73%)(p<0.005)。在0-6岁和7-10岁的男孩中,非对称性少关节炎占多数(分别为100%和100%)(p<0.005),而在11-15岁的男孩中,脊柱关节炎伴有外周关节损伤的情况更为常见(73%)(p<0.005)。研究还发现了关节综合征的转变:如果说发病时最常见的是非对称少关节炎(63%),那么在发病5年后,40.7%的被观察儿童出现了类风湿样(多关节)变异。结论:幼年银屑病关节炎的病程可能受儿童性别和发病年龄的影响;幼年银屑病关节炎从少关节炎到多关节炎(类风湿样)变异型的病程有一定的规律可循。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Features of the onset of juvenile psoriatic arthritis
Juvenile psoriatic arthritis is a chronic inflammatory disease of the peripheral joints, spinal joints and entheses, which occurs in 10–25% of patients with psoriasis. Studying the features of the juvenile psoriatic arthritis debut will increase early diagnosis and will help to avoid disability, socialize and integrate the child into society.Purpose. To identify the relationship between the onset of juvenile psoriatic arthritis and the age and gender of the child, to trace the nature of the articular syndrome in our patients from the onset to the height of the disease.Methods. 155 patients with an established diagnosis of juvenile psoriatic arthritis were examined. To analyze the data, universal nonparametric (randomization-permutation) algorithms for constructing confidence intervals (CI) and statistical comparisons based on the bootstrap and Monte Carlo methods were used.Results. It was possible to identify a relationship between the onset variant and the gender of the child. The incidence of asymmetric oligoarthritis in boys and girls at onset was approximately the same, 68% and 59%, respectively, and did not differ significantly. At onset, girls had a higher incidence of rheumatoid-like arthritis (37%) (p<0.005), and boys had a higher incidence of spondyloarthritis (26%) (p<0.005). A relationship was also revealed between the onset, gender and age of the child. Girls aged 0–6 years most often debuted with asymmetric oligoarthritis (90%) (p<0.005), and at the age of 11–15 years — with the rheumatoid-like (polyarticular) variant (73%) (p<0.005). In boys aged 0–6 and 7–10 years, asymmetric oligoarthritis predominated (100% and 100%, respectively) (p <0.005), and at the age of 11–15 years, spondyloarthritis with damage to peripheral joints was more common (73%) (p<0.005). A transformation of the articular syndrome was revealed: if at the onset of the disease asymmetric oligoarthritis was most common (63%), then 5 years from the onset of the disease, 40.7% of the observed children had a rheumatoid-like (polyarticular) variant of the disease.Conclusion. The course of juvenile psoriatic arthritis may be influenced by the gender and age of the child at onset; a certain pattern of the course of juvenile psoriatic arthritis from oligoarthritis to the polyarticular (rheumatoid-like) variant has been identified.
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