Clinical and immunological features for early differentiation between primary immune thrombocytopenia and connective tissue disease in children.
10.7499/j.issn.1008-8830.2411121
- Author:
Fu-Rong KANG
1
;
Mei YAN
1
;
Ying-Bin YUE
1
;
Hailiguli NURIDDIN
1
;
Yong-Feng CHENG
1
;
Yu LIU
1
Author Information
1. Pediatric Center, The First Affiliated Hospital of Xinjiang Medical University, Urumqi 830054, China.
- Publication Type:Journal Article
- Keywords:
Child;
Connective tissue disease;
Primary immune thrombocytopenia;
Thrombocytopenia
- MeSH:
Purpura, Thrombocytopenic, Idiopathic/immunology*;
Diagnosis, Differential;
Connective Tissue Diseases/immunology*;
Retrospective Studies;
Early Diagnosis;
Age of Onset;
Leukocyte Count;
Complement C4/immunology*;
C-Reactive Protein/immunology*;
Immunoglobulin E/immunology*;
Immunoglobulin M/immunology*;
Humans;
Male;
Female;
Infant;
Child, Preschool;
Child;
Adolescent;
Biomarkers/blood*
- From:
Chinese Journal of Contemporary Pediatrics
2025;27(8):974-981
- CountryChina
- Language:Chinese
-
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.
