Gut Microbiota Changes in Inflammatory Bowel Diseases and Ankylosing Spondylitis

被引:14
|
作者
Cardoneanu, Anca [1 ]
Mihai, Catalina [2 ]
Rezus, Elena [1 ]
Burlui, Alexandra [1 ]
Popa, Iolanda [2 ]
Prelipcean, Cristina Cijevschi [2 ]
机构
[1] Grigore T Popa Univ Med & Pharm, Rehabil Clin Hosp, Iasi, Romania
[2] Grigore T Popa Univ Med & Pharm, Sf Spiridon Emergency Hosp, Inst Gastroenterol & Hepatol, Iasi, Romania
关键词
microbiota; inflammatory bowel disease; ankylosing spondylitis; gut dysbiosis; FAECALIBACTERIUM-PRAUSNITZII; FECAL MICROBIOTA; DYSBIOSIS; PATHOGENESIS; IMBALANCES; MICROFLORA; DIVERSITY; PROFILES;
D O I
10.15403/jgld-2823
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Both inflammatory bowel diseases (IBD) and ankylosing spondylitis (AS) can be considered chronic immune disorders sharing common etiopathogenetic mechanisms. Changes in the composition of the intestinal microbiota, which can lead to an abnormal mucosal response, could be the missing link between these two diseases. Our study evaluate the composition of intestinal microbiota and to characterize gut dysbiosis in patients with IBD and AS. Methods: We conducted a prospective case-control study that enrolled 124 patients [20 Crohn's disease (CD), 27 ulcerative colitis (UC), 28 AS, 17 IBD + AS and 32 controls). Intestinal microbiota analysis was performed by real-time polymerase chain reaction in stool samples. Results: The total quantity of bacteria was decreased in all investigated groups compared to the control group. In studied groups, we noticed an increased percentage of Bacteroides and Escherichia coli (E.coli) and a decreased percentage of Clostridium coccoides, Clostridium leptum, and Faecalibacterium prausnitzii compared to the control group. The percentages of Bifidobacterium (p=0.010) as well as Lactobacillus group (p=0.023) were higher in the L3 form of CD patients. In the E2 form of UC, the quantity of Bacteroides was much higher compared to the E3 form (p=0.004). In AS patients, significant correlations were observed only for the Bifidobacterium species, significantly increased in the axial form compared to peripheral disease (p=0.035). Statistically significant correlations were demonstrated between the Crohn Disease Activity Index score and the total bacterial group (p=0.023, r=-0.507), respectively Bacteroides (p=0.021, r=-0.511) and between the Mayo score and Lactobacillus (p=0.001), respectively E. coli (p=0.001). In IBD + AS group, the Crohn Disease Activity Index score was inversely correlated with the total bacterial group (p=0.010) and directly correlated with Lactobacillus (p=0.047). Conclusions: Intestinal dysbiosis is associated with both IBD and AS. In the association of IBD with AS, dysbiosis is intermediate, but it is associated with the more severe articular disease. Bifidobacterium and Lactobacillus (commonly used as probiotics!) were found to be increased in the association between active IBD and active AS. Further studies are needed to understand how dysbiosis regulates the gut immune system and contributes to intestinal and articular inflammation.
引用
收藏
页码:46 / 54
页数:9
相关论文
共 50 条
  • [41] Gut Fungal Microbiota: The Yin and Yang of Inflammatory Bowel Disease
    Richard, Mathias L.
    Lamas, Bruno
    Liguori, Giuseppina
    Hoffmann, Thomas W.
    Sokol, Harry
    INFLAMMATORY BOWEL DISEASES, 2015, 21 (03) : 656 - 665
  • [42] Modulation of inflammatory response and gut microbiota in ankylosing spondylitis mouse model by bioactive peptide IQW
    Liu, G.
    Ma, Y.
    Yang, Q.
    Deng, S.
    JOURNAL OF APPLIED MICROBIOLOGY, 2020, 128 (06) : 1669 - 1677
  • [43] Gut microbiota in pathophysiology, diagnosis, and therapeutics of inflammatory bowel disease
    Pandey, Himani
    Jain, Dheeraj
    Tang, Daryl W. T.
    Wong, Sunny H.
    Lal, Devi
    INTESTINAL RESEARCH, 2024, 22 (01) : 15 - 43
  • [44] A distinct gut microbiota composition in patients with ankylosing spondylitis is associated with increased levels of fecal calprotectin
    Eva Klingberg
    Maria K. Magnusson
    Hans Strid
    Anna Deminger
    Arne Ståhl
    Johanna Sundin
    Magnus Simrén
    Hans Carlsten
    Lena Öhman
    Helena Forsblad-d’Elia
    Arthritis Research & Therapy, 21
  • [45] Restoring the gut microbiome for the treatment of inflammatory bowel diseases
    Allegretti, Jessica R.
    Hamilton, Matthew J.
    WORLD JOURNAL OF GASTROENTEROLOGY, 2014, 20 (13) : 3468 - 3474
  • [46] Gut microbiota in inflammatory bowel disease: a target for therapy not to be missed
    Larussa, Tiziana
    Abenavoli, Ludovico
    Fabiano, Giulia
    Mancuso, Maria A.
    Polimeni, Natale
    Dumitrascu, Dan L.
    Luzza, Francesco
    MINERVA GASTROENTEROLOGY, 2021, 67 (04): : 357 - 368
  • [47] Interactions between Diet, Bile Acid Metabolism, Gut Microbiota, and Inflammatory Bowel Diseases
    Devkota, Suzanne
    Chang, Eugene B.
    DIGESTIVE DISEASES, 2015, 33 (03) : 351 - 356
  • [48] Diet, gut microbes, and the pathogenesis of inflammatory bowel diseases
    Dolan, Kyle T.
    Chang, Eugene B.
    MOLECULAR NUTRITION & FOOD RESEARCH, 2017, 61 (01)
  • [49] Terminal Restriction Fragment Length Polymorphism Analysis of the Gut Microbiota Profiles of Pediatric Patients with Inflammatory Bowel Disease
    Aomatsu, Tomoki
    Imaeda, Hirotsugu
    Fujimoto, Takehide
    Takahashi, Kenichiro
    Yoden, Atsushi
    Tamai, Hiroshi
    Fujiyama, Yoshihide
    Andoh, Akira
    DIGESTION, 2012, 86 (02) : 129 - 135
  • [50] Enteroendocrine Cells: Sensing Gut Microbiota and Regulating Inflammatory Bowel Diseases
    Yu, Yanbo
    Yang, Wenjing
    Li, Yanqing
    Cong, Yingzi
    INFLAMMATORY BOWEL DISEASES, 2020, 26 (01) : 11 - 20