[Clinical and immunological features for early differentiation between primary immune thrombocytopenia and connective tissue disease in children].

Q3 Medicine
Fu-Rong Kang, Mei Yan, Ying-Bin Yue, Hailiguli Nuriddin, Yong-Feng Cheng, Yu Liu
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引用次数: 0

Abstract

Objectives: To investigate the clinical and immunological features of children with primary immune thrombocytopenia (pITP) or connective tissue disease (CTD) with thrombocytopenia as the initial manifestation at initial diagnosis, and to provide a basis for early differentiation.

Methods: A retrospective study was performed on 236 children with pITP (pITP group) or CTD with thrombocytopenia as the initial manifestation (CTD-TP group) who were admitted from January 2019 to August 2024. Clinical and immunological indicators were compared between the two groups to identify potential influencing factors for early differentiation and their discriminative validity.

Results: Compared with the pITP group, the CTD-TP group had a significantly older age of onset and significantly lower leukocyte count, eosinophil count, lymphocyte count, and complement C4 level (P<0.05), as well as significantly higher levels of C-reactive protein, IgE, and IgM (P<0.05). The logistic regression analysis showed that age, IgE, IgM, total B cells, and complement C4 were predictive factors for early differentiation between pITP and CTD-TP (P<0.05). The receiver operating characteristic curve analysis showed that a combination of these five factors had a good discriminative validity, with an area under the curve of 0.944. The correlation analysis showed a negative correlation between IgG and platelet count in the pITP group (rs=-0.363, P<0.05) and a positive correlation between NK cells and platelet count in the CTD-TP group (rs=0.713, P<0.05).

Conclusions: There is heterogeneity in the clinical and immunological indicators between children with pITP and CTD-TP at initial diagnosis, and these research findings can help with the early differentiation between the two diseases.

【儿童原发性免疫性血小板减少症与结缔组织病早期鉴别的临床及免疫学特点】。
目的:探讨以血小板减少为首发表现的原发性免疫性血小板减少症(pITP)或结缔组织病(CTD)患儿的临床及免疫学特点,为早期鉴别提供依据。方法:对2019年1月至2024年8月住院的236例pITP (pITP组)或以血小板减少为首发表现的CTD (CTD- tp组)患儿进行回顾性研究。比较两组临床及免疫学指标,探讨早期分化的潜在影响因素及其判别效度。结果:与pITP组相比,CTD-TP组发病年龄明显变大,白细胞计数、嗜酸性粒细胞计数、淋巴细胞计数、补体C4水平明显降低(PPPrs=-0.363, pr =0.713, p)。结论:初诊pITP患儿与CTD-TP患儿在临床及免疫学指标上存在异质性,这些研究结果有助于两种疾病的早期鉴别。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
中国当代儿科杂志
中国当代儿科杂志 Medicine-Pediatrics, Perinatology and Child Health
CiteScore
1.50
自引率
0.00%
发文量
5006
期刊介绍: The Chinese Journal of Contemporary Pediatrics (CJCP) is a peer-reviewed open access periodical in the field of pediatrics that is sponsored by the Central South University/Xiangya Hospital of Central South University and under the auspices of the Ministry of Education of China. It is cited as a source in the scientific and technological papers of Chinese journals, the Chinese Science Citation Database (CSCD), and is one of the core Chinese periodicals in the Peking University Library. CJCP has been indexed by MEDLINE/PubMed/PMC of the American National Library, American Chemical Abstracts (CA), Holland Medical Abstracts (EM), Western Pacific Region Index Medicus (WPRIM), Scopus and EBSCO. It is a monthly periodical published on the 15th of every month, and is distributed both at home and overseas. The Chinese series publication number is CN 43-1301/R;ISSN 1008-8830. The tenet of CJCP is to “reflect the latest advances and be open to the world”. The periodical reports the most recent advances in the contemporary pediatric field. The majority of the readership is pediatric doctors and researchers.
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