Integration of metabolomics and lipidomics reveals serum biomarkers for systemic lupus erythematosus with different organs involvement

被引:14
|
作者
Zhang, Wenqian [1 ]
Zhao, Hongjun [2 ]
Du, Pei [3 ,4 ]
Cui, Haobo [1 ]
Lu, Shuang [3 ,4 ]
Xiang, Zhongyuan [5 ]
Lu, Qianjin [6 ,7 ]
Jia, Sujie [1 ]
Zhao, Ming [3 ,4 ]
机构
[1] Cent South Univ, Xiangya Hosp 3, Dept Pharm, Changsha 410013, Peoples R China
[2] Cent South Univ, Xiangya Hosp, Dept Rheumatol, Changsha 410008, Peoples R China
[3] Cent South Univ, Xiangya Hosp 2, Dept Dermatol, Hunan Key Lab Med Epigen, Changsha 410011, Peoples R China
[4] Chinese Acad Med Sci, Res Unit Key Technol Diag & Treatment Immune Rela, Changsha 410011, Peoples R China
[5] Cent South Univ, Dept Clin Lab, Xiangya Hosp 2, Changsha 410011, Peoples R China
[6] Chinese Acad Med Sci & Peking Union Med Coll, Inst Dermatol, Nanjing, Peoples R China
[7] Chinese Acad Med Sci, Key Lab Basic & Translat Res Immune Mediated Skin, Nanjing, Peoples R China
基金
中国国家自然科学基金;
关键词
SLE; Metabolomics; Lipidomics; Biomarkers; PROFILING REVEALS; DISEASE-ACTIVITY; FATTY-ACIDS; DEHYDROEPIANDROSTERONE; EXPRESSION; LYSOPHOSPHATIDYLCHOLINE; PATHOGENESIS; PATHWAYS; ENRICHES; DHA;
D O I
10.1016/j.clim.2022.109057
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 a chronic autoimmune disease that affects various organs or systems. We performed metabolomic and lipidomic profiles analyses of 133 SLE patients and 30 HCs. Differential metabolites and lipids were integrated, and then the biomarker panel was identified using binary logistic regression. We found that a combination of four metabolites or lipids could distinguish SLE from HC with an AUC of 0.998. Three lipids were combined to differentiate inactive SLE and active SLE. The AUC was 0.767. In addition, we also identified the biomarkers for different organ phenotypes of SLE. The AUCs for diagnosing SLE patients with only kidney involvement, skin involvement, blood system involvement, and multisystem involvement were 0.766, 0.718, 0.951, and 0.909, respectively. Our study succeeded in identifying biomarkers associated with different clinical phenotypes in SLE patients, which could facilitate a more precise diagnosis and assessment of disease progression in SLE.
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页数:10
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