Associations of gut microbiota with disease development, disease activity, and therapeutic effects in patients with systemic lupus erythematosus

被引:0
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作者
Nishio, Junko [1 ,2 ]
Sato, Hiroshi [1 ]
Watanabe, Eri [1 ]
Masuoka, Hiroaki [3 ]
Aoki, Kotaro [4 ]
Kawazoe, Mai [1 ]
Wakiya, Risa [5 ]
Yamada, Soichi [1 ]
Muraoka, Sei [1 ]
Masuoka, Shotaro [1 ]
Hayashi, Tomoki [6 ]
Mizutani, Satoshi [1 ]
Yamada, Zento [1 ]
Koshiba, Keiko [1 ]
Irita, Izumi [1 ]
Kanaji, Miwa [1 ]
Furukawa, Karin [1 ]
Yajima, Nobuyuki [6 ]
Dobashi, Hiroaki [5 ]
Hirose, Wataru [7 ]
Ishii, Yoshikazu [4 ]
Suda, Wataru [3 ]
Nanki, Toshihiro [1 ]
机构
[1] Toho Univ, Sch Med, Dept Internal Med, Div Rheumatol, 6-11-1 Omori Nishi,Ota Ku, Tokyo 1438541, Japan
[2] Toho Univ, Sch Med, Dept Immunopathol & Immunoregulat, 5-21-16 Omori Nishi,Ota Ku, Tokyo 1438540, Japan
[3] RIKEN Ctr Integrat Med Sci, 1-7-22 Suehiro Cho,Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
[4] Toho Univ, Sch Med, Dept Microbiol & Infect Dis, 5-21-16 Omori nishi,Ota Ku, Tokyo 1438540, Japan
[5] Kagawa Univ, Fac Med, Dept Internal Med, Div Hematol Rheumatol & Resp Med, 1750-1 Ikenobe,Miki Cho, Kita, Kagawa 7610793, Japan
[6] Showa Univ, Dept Med, Div Rheumatol, 2-14-19 Nishinakanobu,Shinagawa Ku, Tokyo 1420054, Japan
[7] Hirose Clin Rheumatol, 2-14-7 Midoricho, Tokorozawa, Saitama 3591111, Japan
来源
SCIENTIFIC REPORTS | 2024年 / 14卷 / 01期
关键词
Systemic lupus erythematosus; Gut microbiota; Butyrate-producing bacteria; <italic>[Eubacterium] rectale</italic>; <italic>Hungatella effluvii</italic>; <italic>Streptococcus</italic>; CHAIN FATTY-ACIDS;
D O I
10.1038/s41598-024-83835-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Altered gut microbiota is linked to systemic lupus erythematosus (SLE), but its association with disease development, disease activity, and post-intervention changes remains unclear. We compared new-onset SLE (NOSLE, n = 25), SLE in remission (RemSLE, n = 30), and healthy controls (HC, n = 30) cross-sectionally and conducted the first longitudinal analysis of NOSLE patients (n = 22) from pre-intervention to remission over 12 months. Significant beta-diversity differences were observed in both NOSLE and RemSLE compared to HC, but not between NOSLE and RemSLE. Only four operational taxonomic units (OTUs) were enriched in NOSLE versus HC. However, 26 OTUs, including butyrate-producing bacteria (BPB), were depleted, and seven (including five BPBs) remained depleted in RemSLE compared to HC. OTUs positively and negatively correlated with disease activity were also identified. Longitudinal analysis revealed a reversal of several OTUs altered at onset and an increase in Streptococci, unrelated to the disease. Significant beta-diversity differences were observed in patients with anti-SSA or anti-RNP antibodies and those with complement reduction compared to their counterparts. Our study identified gut microbiota alterations, including BPB depletion, in SLE regardless of onset or remission status, bacteria linked to disease activity, and a reversal of disease-associated bacteria along with the enrichment of Streptococci through intervention.
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页数:16
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