Systematic Review: The Gut Microbiome and Its Potential Clinical Application in Inflammatory Bowel Disease

被引:102
作者
Aldars-Garcia, Laila [1 ,2 ]
Chaparro, Maria [1 ,2 ]
Gisbert, Javier P. [1 ,2 ]
机构
[1] Univ Autonoma Madrid, Hosp Univ La Princesa, Inst Invest Sanitaria Princesa IIS IP, Madrid 28006, Spain
[2] Ctr Invest Biomed Red Enfermedades Hepat & Digest, Madrid 28006, Spain
关键词
gut microbiome; inflammatory bowel disease; Crohn's disease; ulcerative colitis; biomarkers; MUCOSA-ASSOCIATED MICROBIOTA; BUTYRATE-PRODUCING BACTERIA; DOMINANT FECAL MICROBIOTA; ULCERATIVE-COLITIS PATIENTS; CROHNS-DISEASE; FAECALIBACTERIUM-PRAUSNITZII; TRANSCRIPTIONAL ACTIVITY; LONGITUDINAL ANALYSES; METAGENOMIC ANALYSIS; RELEVANT DYSBIOSIS;
D O I
10.3390/microorganisms9050977
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Inflammatory bowel disease (IBD) is a chronic relapsing-remitting systemic disease of the gastrointestinal tract. It is well established that the gut microbiome has a profound impact on IBD pathogenesis. Our aim was to systematically review the literature on the IBD gut microbiome and its usefulness to provide microbiome-based biomarkers. A systematic search of the online bibliographic database PubMed from inception to August 2020 with screening in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines was conducted. One-hundred and forty-four papers were eligible for inclusion. There was a wide heterogeneity in microbiome analysis methods or experimental design. The IBD intestinal microbiome was generally characterized by reduced species richness and diversity, and lower temporal stability, while changes in the gut microbiome seemed to play a pivotal role in determining the onset of IBD. Multiple studies have identified certain microbial taxa that are enriched or depleted in IBD, including bacteria, fungi, viruses, and archaea. The two main features in this sense are the decrease in beneficial bacteria and the increase in pathogenic bacteria. Significant differences were also present between remission and relapse IBD status. Shifts in gut microbial community composition and abundance have proven to be valuable as diagnostic biomarkers. The gut microbiome plays a major role in IBD, yet studies need to go from casualty to causality. Longitudinal designs including newly diagnosed treatment-naive patients are needed to provide insights into the role of microbes in the onset of intestinal inflammation. A better understanding of the human gut microbiome could provide innovative targets for diagnosis, prognosis, treatment and even cure of this relevant disease.
引用
收藏
页数:43
相关论文
共 178 条
  • [1] Al-Bayati L, 2018, ARCH IRAN MED, V21, P578
  • [2] Microbial imbalance in inflammatory bowel disease patients at different taxonomic levels
    Alam, Mohammad Tauqeer
    Amos, Gregory C. A.
    Murphy, Andrew R. J.
    Murch, Simon
    Wellington, Elizabeth M. H.
    Arasaradnam, Ramesh P.
    [J]. GUT PATHOGENS, 2020, 12 (01)
  • [3] Gut mucosal-associated microbiota better discloses inflammatory bowel disease differential patterns than faecal microbiota
    Altomare, Annamaria
    Putignani, Lorenza
    Del Chierico, Federica
    Cocca, Silvia
    Angeletti, Silvia
    Ciccozzi, Massimo
    Tripiciano, Costanza
    Piccola, Bruno Dalla
    Cicala, Michele
    Guarino, Michele Pier Luca
    [J]. DIGESTIVE AND LIVER DISEASE, 2019, 51 (05) : 648 - 656
  • [4] Faecal microbiota profile of Crohn's disease determined by terminal restriction fragment length polymorphism analysis
    Andoh, A.
    Tsujikawa, T.
    Sasaki, M.
    Mitsuyama, K.
    Suzuki, Y.
    Matsui, T.
    Matsumoto, T.
    Benno, Y.
    Fujiyama, Y.
    [J]. ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2009, 29 (01) : 75 - 82
  • [5] Terminal restriction fragment length polymorphism analysis of the diversity of fecal microbiota in patients with ulcerative colitis
    Andoh, Akira
    Sakata, Shinji
    Koizumi, Yuhsuke
    Mitsuyama, Keiichi
    Fujiyoma, Yoshihide
    Benno, Yoshimi
    [J]. INFLAMMATORY BOWEL DISEASES, 2007, 13 (08) : 955 - 962
  • [6] Terminal restriction fragment polymorphism analyses of fecal microbiota in five siblings including two with ulcerative colitis
    Andoh A.
    Ida S.
    Tsujikawa T.
    Benno Y.
    Fujiyama Y.
    [J]. Clinical Journal of Gastroenterology, 2009, 2 (5) : 343 - 345
  • [7] Characterization of gut microbiota profiles by disease activity in patients with Crohn's disease using data mining analysis of terminal restriction fragment length polymorphisms
    Andoh, Akira
    Kobayashi, Toshio
    Kuzuoka, Hiroyuki
    Tsujikawa, Tomoyuki
    Suzuki, Yasuo
    Hirai, Fumihito
    Matsui, Toshiyuki
    Nakamura, Shiro
    Matsumoto, Takayuki
    Fujiyama, Yoshihide
    [J]. BIOMEDICAL REPORTS, 2014, 2 (03) : 370 - 373
  • [8] Multicenter analysis of fecal microbiota profiles in Japanese patients with Crohn's disease
    Andoh, Akira
    Kuzuoka, Hiroyuki
    Tsujikawa, Tomoyuki
    Nakamura, Shiro
    Hirai, Fumihito
    Suzuki, Yasuo
    Matsui, Toshiyuki
    Fujiyama, Yoshihide
    Matsumoto, Takayuki
    [J]. JOURNAL OF GASTROENTEROLOGY, 2012, 47 (12) : 1298 - 1307
  • [9] Comparison of the fecal microbiota profiles between ulcerative colitis and Crohn's disease using terminal restriction fragment length polymorphism analysis
    Andoh, Akira
    Imaeda, Hirotsugu
    Aomatsu, Tomoki
    Inatomi, Osamu
    Bamba, Shigeki
    Sasaki, Masaya
    Saito, Yasuharu
    Tsujikawa, Tomoyuki
    Fujiyama, Yoshihide
    [J]. JOURNAL OF GASTROENTEROLOGY, 2011, 46 (04) : 479 - 486
  • [10] Defining a Healthy Human Gut Microbiome: Current Concepts, Future Directions, and Clinical Applications
    Backhed, Fredrik
    Fraser, Claire M.
    Ringel, Yehuda
    Sanders, Mary Ellen
    Sartor, R. Balfour
    Sherman, Philip M.
    Versalovic, James
    Young, Vincent
    Finlay, B. Brett
    [J]. CELL HOST & MICROBE, 2012, 12 (05) : 611 - 622