Characterization of microbiota in systemic-onset juvenile idiopathic arthritis with different disease severities

被引:13
|
作者
Dong, Yan-Qing [1 ,2 ]
Wang, Wei [1 ,2 ]
Li, Ji [1 ,2 ]
Ma, Ming-Sheng [1 ,2 ]
Zhong, Lin-Qing [1 ,2 ]
Wei, Qi-Jiao [1 ,2 ]
Song, Hong-Mei [1 ,2 ]
机构
[1] Chinese Acad Med Sci, Peking Union Med Coll Hosp, Dept Pediat, 1 Shuaifuyuan Rd, Beijing 100730, Peoples R China
[2] Peking Union Med Coll, 1 Shuaifuyuan Rd, Beijing 100730, Peoples R China
关键词
Microbiota; Systemic-onset juvenile idiopathic arthritis; Disease activity; Dysbiosis; GUT MICROBIOME; PERMEABILITY; EXPOSURE;
D O I
10.12998/wjcc.v7.i18.2734
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Systemic-onset juvenile idiopathic arthritis (SoJIA) is one of most serious subtypes of juvenile idiopathic arthritis. Although the pathogenesis of SoJIA remains unclear, several studies have suggested a correlation between gut dysbiosis and JIA. Further understanding of the intestinal microbiome may help to establish alternative ways to treat, or even prevent, the disease. AIM To explore alterations in fecal microbiota profiles in SoJIA patients and to evaluate the correlations between microbiota and clinical parameters. METHODS We conducted an observational single-center study at the Pediatric Department of Peking Union Medical College Hospital. Children who were diagnosed with SoJIA at our institution and followed for a minimum period of six months after diagnosis were recruited for the study. Healthy children were recruited as a control group (HS group) during the same period. Clinical data and stool samples were collected from SoJIA patients when they visited the hospital. RESULTS The SoJIA group included 17 active and 15 inactive consecutively recruited children; the control group consisted of 32 children. Firmicutes and Bacteroidetes were the two most abundant phyla among the total sample of SoJIA children and controls. There was a significant difference among the three groups in observed species, which was the highest in the Active-SoJIA group, followed by the Inactive-SoJIA group and then HS group (Active-SoJIA vs HS: P = 0.000; and Inactive-SoJIA vs HS: P = 0.005). We observed a lower Firmicutes/Bacteroidetes ratio in SoJIA patients (3.28 +/- 4.47 in Active-SoJIA, 5.36 +/- 8.39 in Inactive-SoJIA, and 5.67 +/- 3.92 in HS). We also observed decreased abundances of Ruminococcaceae (14.9% in Active-SoJIA, 17.3% in Inactive-SoJIA, and 22.8% in HS; Active-SoJIA vs HS: P = 0.005) and Faecalibacterium (5.1% in Active-SoJIA, 9.9% in Inactive-SoJIA, and 13.0% in HS; Active-SoJIA vs HS: P = 0.000) in SoJIA compared with HS. By contrast, the abundance of Bacteroidaceae was the highest in the Active-SoJIA group, followed by the Inactive-SoJIA and HS groups (16.5% in Active-SoJIA, 12.8% in Inactive-SoJIA, and 9.7% in HS; Active-SoJIA vs HS: P = 0.03). The Spearman correlation analysis revealed a negative correlation between Proteobacteria or Enterobacteriaceae and juvenile arthritis disease activity score on 27 joints (JADAS-27). CONCLUSION The composition of the intestinal microbiota is different in SoJIA patients compared with healthy children. The dysbiosis presents partial restoration in inactive status patients.
引用
收藏
页码:2734 / 2745
页数:12
相关论文
共 50 条
  • [1] Characterization of microbiota in systemic-onset juvenile idiopathic arthritis with different disease severities
    Yan-Qing Dong
    Wei Wang
    Ji Li
    Ming-Sheng Ma
    Lin-Qing Zhong
    Qi-Jiao Wei
    Hong-Mei Song
    World Journal of Clinical Cases, 2019, (18) : 2734 - 2745
  • [2] Systemic-onset juvenile idiopathic arthritis
    Cimaz, Rolando
    AUTOIMMUNITY REVIEWS, 2016, 15 (09) : 931 - 934
  • [3] Still's disease (Systemic-Onset Juvenile Idiopathic Arthritis)
    Quartier, P.
    ARCHIVES DE PEDIATRIE, 2008, 15 (05): : 865 - 866
  • [4] Systemic-onset juvenile idiopathic arthritis: the changing life of a rare disease
    Cimaz, Rolando
    Von Scheven, Annette
    Hofer, Michael
    SWISS MEDICAL WEEKLY, 2012, 142
  • [5] Does systemic-onset juvenile idiopathic arthritis belong under juvenile idiopathic arthritis?
    Ramanan, AV
    Grom, AA
    RHEUMATOLOGY, 2005, 44 (11) : 1350 - 1353
  • [6] Anankinra in systemic-onset juvenile idiopathic arthritis and adult onset Still's disease
    Quartier, P.
    Lequerre, T.
    Rosellini, D.
    Sibilia, J.
    Debandt, M.
    Kone-Paut, I.
    Job-Deslandre, C.
    ANNALS OF THE RHEUMATIC DISEASES, 2006, 65 : 107 - 107
  • [7] ASSOCIATION OF SYSTEMIC-ONSET JUVENILE IDIOPATHIC ARTHRITIS AND CELIAC DISEASE - A CASE REPORT
    Michelin, Cintia Maria
    Aikawa, Nadia Emi
    Diniz, Joao Carlos
    Jesus, Adriana Almeida
    Ling Koda, Yu Kar
    Silva, Clovis Artur
    ACTA REUMATOLOGICA PORTUGUESA, 2011, 36 (04): : 404 - 407
  • [8] Systemic-onset juvenile idiopathic arthritis or incomplete Kawasaki disease: a diagnostic challenge
    Sahin, S.
    Adrovic, A.
    Barut, K.
    Kasapcopur, O.
    CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, 2017, 35 (02) : S10 - S10
  • [9] Effect of etanercept on refractory systemic-onset juvenile idiopathic arthritis
    Xiao Hu
    Fang Yuan
    Jian Zhang
    Lei Yin
    Bi-Ru Li
    Yan-Liang Jin
    World Journal of Pediatrics, 2016, 12 : 96 - 102
  • [10] Communicating Calf Swelling in Systemic-Onset Juvenile Idiopathic Arthritis
    Durga, Dulasi K.
    Gupta, Aditya
    Kandasamy, Devasenathipathy
    Bagri, Narendra Kumar
    JCR-JOURNAL OF CLINICAL RHEUMATOLOGY, 2021, 27 (8S) : S729 - S731