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Compositional changes in fecal microbiota associated with clinical phenotypes and prognosis in Korean patients with inflammatory bowel disease.
Shin, Seung Yong; Kim, Young; Kim, Won-Seok; Moon, Jung Min; Lee, Kang-Moon; Jung, Sung-Ae; Park, Hyesook; Huh, Eun Young; Kim, Byung Chang; Lee, Soo Chan; Choi, Chang Hwan.
Affiliation
  • Shin SY; Department of Internal Medicine, Chung-Ang University College of Medicine, Seoul, Korea.
  • Kim Y; Department of Internal Medicine, Chung-Ang University College of Medicine, Seoul, Korea.
  • Kim WS; Department of Internal Medicine, Chung-Ang University College of Medicine, Seoul, Korea.
  • Moon JM; Department of Internal Medicine, Chung-Ang University College of Medicine, Seoul, Korea.
  • Lee KM; Department of Internal Medicine, St. Vincent's Hospital, College of Medicine, The Catholic University of Korea, Suwon, Korea.
  • Jung SA; Department of Internal Medicine, Graduate Program in System Health Science and Engineering, Ewha Womans University College of Medicine, Seoul, Korea.
  • Park H; Department of Preventive Medicine, Graduate Program in System Health Science and Engineering, Ewha Womans University College of Medicine, Seoul, Korea.
  • Huh EY; South Texas Center of Emerging Infectious Diseases (STCEID) and Department of Molecular Microbiology and Immunology, The University of Texas at San Antonio, San Antonio, TX, USA.
  • Kim BC; Division of Gastroenterology, Center for Colorectal Cancer, Research Institute and Hospital, National Cancer Center, Goyang, Korea.
  • Lee SC; South Texas Center of Emerging Infectious Diseases (STCEID) and Department of Molecular Microbiology and Immunology, The University of Texas at San Antonio, San Antonio, TX, USA.
  • Choi CH; Department of Internal Medicine, Chung-Ang University College of Medicine, Seoul, Korea.
Intest Res ; 21(1): 148-160, 2023 Jan.
Article in En | MEDLINE | ID: mdl-35692191
BACKGROUND/AIMS: The fecal microbiota of Korean patients with inflammatory bowel disease (IBD) was investigated with respect to disease phenotypes and taxonomic biomarkers for diagnosis and prognosis of IBD. METHODS: Fecal samples from 70 ulcerative colitis (UC) patients, 39 Crohn's disease (CD) patients, and 100 healthy control individuals (HC) were collected. The fecal samples were amplified via polymerase chain reaction and sequenced using Illumina MiSeq. The relationships between fecal bacteria and clinical phenotypes were analyzed using the EzBioCloud database and 16S microbiome pipeline. RESULTS: The alpha-diversity of fecal bacteria was significantly lower in UC and CD (P<0.05) compared to that in HC. Bacterial community compositions in UC and CD were significantly different from that of HC according to Bray-Curtis dissimilarities, and there was also a difference between community composition in UC and CD (P=0.01). In UC, alpha-diversity was further decreased when the disease was more severe and the extent of disease was greater, and community composition significantly differed depending on the extent of the disease. We identified 9 biomarkers of severity and 6 biomarkers of the extent of UC. We also identified 5 biomarkers of active disease and 3 biomarkers of ileocolonic involvement in CD. Lachnospiraceae and Ruminococcus gnavus were biomarkers for better prognosis in CD. CONCLUSIONS: The fecal microbiota profiles of IBD patients were different from those of HC, and several bacterial taxa may be used as biomarkers to determine disease phenotypes and prognosis. These data may also help discover new therapeutic targets for IBD.
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Full text: 1 Database: MEDLINE Type of study: Prognostic_studies / Risk_factors_studies Language: En Journal: Intest Res Year: 2023 Type: Article

Full text: 1 Database: MEDLINE Type of study: Prognostic_studies / Risk_factors_studies Language: En Journal: Intest Res Year: 2023 Type: Article