Residential College | false |
Status | 已發表Published |
Alterations of Gut Microbiome, Metabolome, and Lipidome in Takayasu Arteritis | |
Luyun Fan1; Junru Chen2; Lili Pan3; Xiaohong Xin4; Bin Geng1; Lirui Yang5; Qian Wang4; Wenjun Ma1; Ying Lou1; Jin Bian1; Xiao Cui6; Jing Li7; Lu Wang1; Zhenzhen Chen1; Wenjie Wang1; Changting Cui1; Shuangyue Li1; Qiannan Gao1; Qirui Song1; Yue Deng1; Jiali Fan1; Jiachen Yu1; Huimin Zhang1![]() ![]() ![]() | |
2022-08-23 | |
Source Publication | Arthritis & Rheumatology
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ISSN | 2326-5191 |
Volume | 75Issue:2Pages:266-278 |
Abstract | Objective: Mounting evidence has linked microbiome and metabolome to systemic autoimmunity and cardiovascular diseases (CVDs). Takayasu arteritis (TAK) is a rare disease that shares features of immune-related inflammatory diseases and CVDs, about which there is relatively limited information. This study was undertaken to characterize gut microbial dysbiosis and its crosstalk with phenotypes in TAK. Methods: To address the discriminatory signatures, we performed shotgun sequencing of fecal metagenome across a discovery cohort (n = 97) and an independent validation cohort (n = 75) including TAK patients, healthy controls, and controls with Behçet's disease (BD). Interrogation of untargeted metabolomics and lipidomics profiling of plasma and fecal samples were also used to refine features mediating associations between microorganisms and TAK phenotypes. Results: A combined model of bacterial species, including unclassified Escherichia, Veillonella parvula, Streptococcus parasanguinis, Dorea formicigenerans, Bifidobacterium adolescentis, Lachnospiraceae bacterium 7 1 58FAA, Escherichia coli, Streptococcus salivarius, Klebsiella pneumoniae, Bifidobacterium longum, and Lachnospiraceae Bacterium 5 1 63FAA, distinguished TAK patients from controls with areas under the curve (AUCs) of 87.8%, 85.9%, 81.1%, and 71.1% in training, test, and validation sets including healthy or BD controls, respectively. Diagnostic species were directly or indirectly (via metabolites or lipids) correlated with TAK phenotypes of vascular involvement, inflammation, discharge medication, and prognosis. External validation against publicly metagenomic studies (n = 184) on hypertension, atrial fibrillation, and healthy controls, confirmed the diagnostic accuracy of the model for TAK. Conclusion: This study first identifies the discriminatory gut microbes in TAK. Dysbiotic microbes are also linked to TAK phenotypes directly or indirectly via metabolic and lipid modules. Further explorations of the microbiome–metagenome interface in TAK subtype prediction and pathogenesis are suggested. |
Keyword | Criteria Phospholipids Modulation Features Disease |
DOI | 10.1002/art.42331 |
URL | View the original |
Indexed By | SCIE |
Language | 英語English |
WOS Research Area | Rheumatology |
WOS Subject | Rheumatology |
WOS ID | WOS:000899020100001 |
Publisher | WILEY,111 RIVER ST, HOBOKEN 07030-5774, NJ |
Scopus ID | 2-s2.0-85139294299 |
Fulltext Access | |
Citation statistics | |
Document Type | Journal article |
Collection | Institute of Chinese Medical Sciences THE STATE KEY LABORATORY OF QUALITY RESEARCH IN CHINESE MEDICINE (UNIVERSITY OF MACAU) |
Corresponding Author | Huimin Zhang; Yafeng Li; Jun Cai |
Affiliation | 1.State Key Laboratory of Cardiovascular Disease, National Center for Cardiovascular Diseases, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China 2.State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Taipa, Macao, China, and Reproductive and Genetic Hospital of CITIC-Xiangya, Changsha, China 3.Department of Rheumatology and Immunology, Beijing Anzhen Hospital, Capital Medical University, Beijing, China 4.Department of Nephrology, Precision Medicine Center, The Affiliated People's Hospital of Shanxi Medical University, Shanxi Provincial People's Hospital, Taiyuan, China 5.Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University, Beijing, China 6.Department of Cardiology, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China 7.Heart Center, Beijing Chaoyang Hospital, Capital Medical University, Beijing Key Laboratory of Hypertension, Beijing, China 8.Department of Nephrology, Shanxi Provincial People's Hospital (Fifth Hospital) of Shanxi Medical University, Core Laboratory, Shanxi Provincial Key Laboratory of Kidney Disease, and Academy of Microbial Ecology, Shanxi Medical University, Taiyuan, China |
Recommended Citation GB/T 7714 | Luyun Fan,Junru Chen,Lili Pan,et al. Alterations of Gut Microbiome, Metabolome, and Lipidome in Takayasu Arteritis[J]. Arthritis & Rheumatology, 2022, 75(2), 266-278. |
APA | Luyun Fan., Junru Chen., Lili Pan., Xiaohong Xin., Bin Geng., Lirui Yang., Qian Wang., Wenjun Ma., Ying Lou., Jin Bian., Xiao Cui., Jing Li., Lu Wang., Zhenzhen Chen., Wenjie Wang., Changting Cui., Shuangyue Li., Qiannan Gao., Qirui Song., ...& Jun Cai (2022). Alterations of Gut Microbiome, Metabolome, and Lipidome in Takayasu Arteritis. Arthritis & Rheumatology, 75(2), 266-278. |
MLA | Luyun Fan,et al."Alterations of Gut Microbiome, Metabolome, and Lipidome in Takayasu Arteritis".Arthritis & Rheumatology 75.2(2022):266-278. |
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