Identification of Key Biomarkers in Systemic Lupus Erythematosus by a Multi-Cohort Analysis

被引:1
作者
Wei, Meilin [1 ]
Dong, Qiguan [2 ]
Chen, Shaoqiu [3 ]
Wang, Junlong [3 ]
Yang, Hua [4 ]
Xiong, Qin [5 ]
机构
[1] Nanchang Univ, Affiliated Hosp 2, Dept Endocrinol & Metab, Jiangxi, Peoples R China
[2] Gen Hosp Fushun Min Bur, Liaoning Hlth Ind Grp, Dept Oncol, Fushun, Peoples R China
[3] Univ Hawaii Manoa, Coll Trop Agr & Human Resources, Mol Biosci & Bioengn Program, Honolulu, HI USA
[4] Chaminade Univ Honolulu, Honolulu, HI USA
[5] Nanchang Univ, Affiliated Hosp 1, Dept Endocrinol & Metab, Jiangxi, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2022年 / 13卷
关键词
SLE; transcriptome; diagnosis; immune cells; multi-cohort; ANTIBODIES; GENE;
D O I
10.3389/fimmu.2022.928623
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Systemic lupus erythematosus (SLE) is an autoimmune disease that affects multiple body systems with heterogeneous clinical manifestations. Since gene expression analyses have been accomplished on diverse types of samples to specify SLE-related genes, single-cohort transcriptomics have not produced reliable results. Using an integrated multi-cohort analysis framework, we analyzed whole blood cells from SLE patients from three transcriptomics cohorts (n=1222) and identified a five-gene signature that distinguished SLE patients from controls. We validated the diagnostic performance of this five-gene signature in six independent validation cohorts (n= 469), with an area under the receiver operating characteristic curve of 0.88 [95% CI 0.7 - 0.96]. This five-gene signature may be associated with the proportion of SLE immune cells, and generalizable across ages and sample types with real diagnostic value for clinical application.
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页数:6
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