Identifying clinical subgroups in IgG4-related disease patients using cluster analysis and IgG4-RD composite score

被引:17
|
作者
Li, Jieqiong [1 ]
Peng, Yu [1 ]
Zhang, Yuelun [2 ]
Zhang, Panpan [1 ]
Liu, Zheng [1 ]
Lu, Hui [1 ]
Peng, Linyi [1 ]
Zhu, Liang [3 ]
Xue, Huadan [3 ]
Zhao, Yan [1 ]
Zeng, Xiaofeng [1 ]
Fei, Yunyun [1 ]
Zhang, Wen [1 ]
机构
[1] Peking Union Med Coll Hosp, Clin Immunol Ctr, Dept Rheumatol, Beijing, Peoples R China
[2] Peking Union Med Coll Hosp, Cent Res Lab, Beijing, Peoples R China
[3] Peking Union Med Coll Hosp, Dept Radiol, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
IgG4-related disease; Laboratory test; Organs involved; Cluster analysis; IgG4-RD CS; IMMUNOGLOBULIN G4-RELATED DISEASE; ORGAN INVOLVEMENT; CELLS; SIALADENITIS; MAINTENANCE; REMISSION; EXPANSION; RITUXIMAB; DIAGNOSIS; BIOMARKER;
D O I
10.1186/s13075-019-2090-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background To explore the clinical patterns of patients with IgG4-related disease (IgG4-RD) based on laboratory tests and the number of organs involved. Methods Twenty-two baseline variables were obtained from 154 patients with IgG4-RD. Based on principal component analysis (PCA), patients with IgG4-RD were classified into different subgroups using cluster analysis. Additionally, IgG4-RD composite score (IgG4-RD CS) as a comprehensive score was calculated for each patient by principal component evaluation. Multiple linear regression was used to establish the "IgG4-RD CS" prediction model for the comprehensive assessment of IgG4-RD. To evaluate the value of the IgG4-RD CS in the assessment of disease severity, patients in different IgG4-RD CS groups and in different IgG4-RD responder index (RI) groups were compared. Results PCA indicated that the 22 baseline variables of IgG4-RD patients mainly consisted of inflammation, high serum IgG4, multi-organ involvement, and allergy-related phenotypes. Cluster analysis classified patients into three groups: cluster 1, inflammation and immunoglobulin-dominant group; cluster 2, internal organs-dominant group; and cluster 3, inflammation and immunoglobulin-low with superficial organs-dominant group. Moreover, there were significant differences in serum and clinical characteristics among subgroups based on the CS and RI scores. IgG4-RD CS had a similar ability to assess disease severity as RI. The "IgG4-RD CS" prediction model was established using four independent variables including lymphocyte count, eosinophil count, IgG levels, and the total number of involved organs. Conclusion Our study indicated that newly diagnosed IgG4-RD patients could be divided into three subgroups. We also showed that the IgG4-RD CS had the potential to be complementary to the RI score, which can help assess disease severity.
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页数:13
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