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Differentially Abundant Bacterial Taxa Associated with Prognostic Variables of Crohn's Disease: Results from the IMPACT Study.
Park, Soo-Kyung; Kim, Han-Na; Choi, Chang Hwan; Im, Jong Pil; Cha, Jae Myung; Eun, Chang Soo; Kim, Tae-Oh; Kang, Sang-Bum; Bang, Ki Bae; Kim, Hyun Gun; Jung, Yunho; Yoon, Hyuk; Han, Dong-Soo-; Lee, Chil-Woo; Ahn, Kwangsung; Kim, Hyung-Lae; Park, Dong Il.
Affiliation
  • Park SK; Division of Gastroenterology, Department of Internal Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul 03181, Korea.
  • Kim HN; Medical Research Institute, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul 03181, Korea.
  • Choi CH; Inflammatory Bowel Disease Study Group of the Korean Association for the Study of Intestinal Diseases, Seoul 06193, Korea.
  • Im JP; Medical Research Institute, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul 03181, Korea.
  • Cha JM; Department of Clinical Research Design and Evaluation, SAIHST, Sungkyunkwan University, Seoul 03063, Korea.
  • Eun CS; Inflammatory Bowel Disease Study Group of the Korean Association for the Study of Intestinal Diseases, Seoul 06193, Korea.
  • Kim TO; Department of Internal Medicine, Chung-Ang University College of Medicine, Seoul 06973, Korea.
  • Kang SB; Inflammatory Bowel Disease Study Group of the Korean Association for the Study of Intestinal Diseases, Seoul 06193, Korea.
  • Bang KB; Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul 03080, Korea.
  • Kim HG; Department of Internal Medicine, Kyung Hee University Hospital at Gang Dong, Kyung Hee University School of Medicine, Seoul 02447, Korea.
  • Jung Y; Department of Internal Medicine, Hanyang University Guri Hospital, Guri 11923, Korea.
  • Yoon H; Inflammatory Bowel Disease Study Group of the Korean Association for the Study of Intestinal Diseases, Seoul 06193, Korea.
  • Han DS; Division of Gastroenterology, Department of Internal Medicine, Inje University Haeundae Paik Hospital, Busan 48108, Korea.
  • Lee CW; Division of Gastroenterology, Department of Internal medicine, Daejeon St. Mary's Hospital, The Catholic University of Korea, Daejeon 34943, Korea.
  • Ahn K; Department of Internal Medicine, Dankook University College of Medicine, Cheonan 31116, Korea.
  • Kim HL; Division of Gastroenterology, Department of Internal Medicine, Soonchunhyang University College of Medicine, Seoul Hospital, Seoul 04401, Korea.
  • Park DI; Division of Gastroenterology, Department of Internal Medicine, Soonchunhyang University College of Medicine, Cheonan Hospital, Cheonan 31151, Korea.
J Clin Med ; 9(6)2020 Jun 05.
Article de En | MEDLINE | ID: mdl-32516912
ABSTRACT
Limited studies have examined the intestinal microbiota composition in relation to Crohn's disease (CD) prognosis. We analyzed the differences in microbial communities and relevant metabolic pathways associated with prognostic variables in patients with CD. We applied 16S rRNA gene sequencing to analyze a cohort of 1110 CD and healthy control (HC) fecal samples. We categorized patients with CD into good (CD-G), intermediate (CD-I) and poor (CD-P) prognosis groups, according to the history of using biologics and intestinal resection. Microbiota α-diversity decreased more in CD-P than CD-G and CD-I. Microbiota ß-diversity in CD-P differed from that in CD-G and CD-I. Thirteen genera and 10 species showed differential abundance between CD-G and CD-P groups. Escherichia coli (p = 0.001) and species Producta (p = 0.01) and genera Lactobacillus (p = 0.003) and Coprococcus (p = 0.01) consistently showed differences between CD-G and CD-P groups after adjusting for confounding variables. Functional profiling suggested that the microbial catabolic pathways and pathways related to enterobacterial common antigen and lipopolysaccharide biosynthesis were better represented in the CD-P group than in the CD-G group, and E. coli were the top contributors to these pathways. CD prognosis is associated with altered microbiota composition and decreased diversity, and E. coli might be causally involved in CD progression, and may have adapted to live in inflammatory environments.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Incidence_studies / Prognostic_studies / Risk_factors_studies Langue: En Journal: J Clin Med Année: 2020 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Incidence_studies / Prognostic_studies / Risk_factors_studies Langue: En Journal: J Clin Med Année: 2020 Type de document: Article