RISS 학술연구정보서비스

검색
다국어 입력

http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.

변환된 중국어를 복사하여 사용하시면 됩니다.

예시)
  • 中文 을 입력하시려면 zhongwen을 입력하시고 space를누르시면됩니다.
  • 北京 을 입력하시려면 beijing을 입력하시고 space를 누르시면 됩니다.
닫기
    인기검색어 순위 펼치기

    RISS 인기검색어

      KCI등재 SCOPUS

      Relationship between the gut microbiota and bile acid composition in the ileal mucosa of Crohn’s disease

      한글로보기

      https://www.riss.kr/link?id=A108204555

      • 0

        상세조회
      • 0

        다운로드
      서지정보 열기
      • 내보내기
      • 내책장담기
      • 공유하기
      • 오류접수

      부가정보

      다국어 초록 (Multilingual Abstract)

      Background/Aims: Crosstalk between the gut microbiota and bile acid plays an important role in the pathogenesis of gastrointestinal disorders. We investigated the relationship between microbial structure and bile acid metabolism in the ileal mucosa of...

      Background/Aims: Crosstalk between the gut microbiota and bile acid plays an important role in the pathogenesis of gastrointestinal disorders. We investigated the relationship between microbial structure and bile acid metabolism in the ileal mucosa of Crohn’s disease (CD).Methods: Twelve non-CD controls and 38 CD patients in clinical remission were enrolled. Samples were collected from the distal ileum under balloon-assisted enteroscopy. Bile acid composition was analyzed by liquid chromatography-mass spectrometry. The gut microbiota was analyzed by 16S rRNA gene sequencing.Results: The Shannon evenness index was significantly lower in endoscopically active lesions than in non-CD controls. β-Diversity, evaluated by the UniFrac metric, revealed a significant difference between the active lesions and non-CD controls (<i>P</i>=0.039). The relative abundance of <i>Escherichia</i> was significantly higher and that of <i>Faecalibacterium</i> and <i>Roseburia</i> was significantly lower in CD samples than in non-CD controls. The increased abundance of <i>Escherichia</i> was more prominent in active lesions than in inactive lesions. The proportion of conjugated bile acids was significantly higher in CD patients than in non-CD controls, but there was no difference in the proportion of primary or secondary bile acids. The genera <i>Escherichia</i> and <i>Lactobacillus</i> were positively correlated with the proportion of conjugated bile acids. On the other hand, <i>Roseburia</i>, <i>Intestinibacter</i>, and <i>Faecalibacterium</i> were negatively correlated with the proportion of conjugated bile acids.Conclusions: Mucosa-associated dysbiosis and the alteration of bile acid composition were identified in the ileum of CD patients. These may play a role in the pathophysiology of ileal lesions in CD patients.

      더보기

      참고문헌 (Reference)

      1 Kaplan GG, "Understanding and preventing the global increase of inflammatory bowel disease" 152 : 313-321, 2017

      2 Goldsmith JR, "The role of diet on intestinal microbiota metabolism: downstream impacts on host immune function and health, and therapeutic implications" 49 : 785-798, 2014

      3 Sheehan D, "The microbiota in inflammatory bowel disease" 50 : 495-507, 2015

      4 Begley M, "The interaction between bacteria and bile" 29 : 625-651, 2005

      5 Mak WY, "The epidemiology of inflammatory bowel disease : east meets west" 35 : 380-389, 2020

      6 Nagayama M, "TH1 cell-inducing Escherichia coli strain identified from the small intestinal mucosa of patients with Crohn’s disease" 12 : 1788898-, 2020

      7 Shoda J, "Similarity of unusual bile acids in human umbilical cord blood and amniotic fluid from newborns and in sera and urine from adult patients with cholestatic liver diseases" 29 : 847-858, 1988

      8 Nagalingam NA, "Role of the microbiota in inflammatory bowel diseases" 18 : 968-984, 2012

      9 Hasegawa M, "Regulation of the gut microbiota by the mucosal immune system in mice" 26 : 481-487, 2014

      10 Takahashi K, "Reduced abundance of butyrate-producing bacteria species in the fecal microbial community in Crohn’s disease" 93 : 59-65, 2016

      1 Kaplan GG, "Understanding and preventing the global increase of inflammatory bowel disease" 152 : 313-321, 2017

      2 Goldsmith JR, "The role of diet on intestinal microbiota metabolism: downstream impacts on host immune function and health, and therapeutic implications" 49 : 785-798, 2014

      3 Sheehan D, "The microbiota in inflammatory bowel disease" 50 : 495-507, 2015

      4 Begley M, "The interaction between bacteria and bile" 29 : 625-651, 2005

      5 Mak WY, "The epidemiology of inflammatory bowel disease : east meets west" 35 : 380-389, 2020

      6 Nagayama M, "TH1 cell-inducing Escherichia coli strain identified from the small intestinal mucosa of patients with Crohn’s disease" 12 : 1788898-, 2020

      7 Shoda J, "Similarity of unusual bile acids in human umbilical cord blood and amniotic fluid from newborns and in sera and urine from adult patients with cholestatic liver diseases" 29 : 847-858, 1988

      8 Nagalingam NA, "Role of the microbiota in inflammatory bowel diseases" 18 : 968-984, 2012

      9 Hasegawa M, "Regulation of the gut microbiota by the mucosal immune system in mice" 26 : 481-487, 2014

      10 Takahashi K, "Reduced abundance of butyrate-producing bacteria species in the fecal microbial community in Crohn’s disease" 93 : 59-65, 2016

      11 Lloyd-Price J, "Multi-omics of the gut microbial ecosystem in inflammatory bowel diseases" 569 : 655-662, 2019

      12 Sartor RB, "Microbial influences in inflammatory bowel diseases" 134 : 577-594, 2008

      13 Schloss PD, "Introducing mothur: open-source, platform-independent, community-supported software for describing and comparing microbial communities" 75 : 7537-7541, 2009

      14 Baumgart DC, "Inflammatory bowel disease : clinical aspects and established and evolving therapies" 369 : 1641-1657, 2007

      15 Johansson ME, "Immunological aspects of intestinal mucus and mucins" 16 : 639-649, 2016

      16 Lavelle A, "Gut microbiota-derived metabolites as key actors in inflammatory bowel disease" 17 : 223-237, 2020

      17 Nishida A, "Gut microbiota in the pathogenesis of inflammatory bowel disease" 11 : 1-10, 2018

      18 Franzosa EA, "Gut microbiome structure and metabolic activity in inflammatory bowel disease" 4 : 293-305, 2019

      19 Ananthakrishnan AN, "Epidemiology and risk factors for IBD" 12 : 205-217, 2015

      20 Litvak Y, "Dysbiotic Proteobacteria expansion : a microbial signature of epithelial dysfunction" 39 : 1-6, 2017

      21 Sinha SR, "Dysbiosis-induced secondary bile acid deficiency promotes intestinal inflammation" 27 : 659-670, 2020

      22 Frank DN, "Disease phenotype and genotype are associated with shifts in intestinal-associated microbiota in inflammatory bowel diseases" 17 : 179-184, 2011

      23 Best WR, "Development of a Crohn’s disease activity index. National Cooperative Crohn’s Disease Study" 70 : 439-444, 1976

      24 Murakami M, "Detection of gut dysbiosis due to reduced Clostridium subcluster XIVa using the fecal or serum bile acid profile" 24 : 1035-1044, 2018

      25 Ridlon JM, "Consequences of bile salt biotransformations by intestinal bacteria" 7 : 22-39, 2016

      26 Duboc H, "Connecting dysbiosis, bile-acid dysmetabolism and gut inflammation in inflammatory bowel disease" 62 : 531-539, 2013

      27 Litvak Y, "Colonocyte metabolism shapes the gut microbiota" 362 : eaat9076-, 2018

      28 Jia W, "Bile acid-microbiota crosstalk in gastrointestinal inflammation and carcinogenesis" 15 : 111-128, 2018

      29 Costello EK, "Bacterial community variation in human body habitats across space and time" 326 : 1694-1697, 2009

      30 Nishino K, "Analysis of endoscopic brush samples identified mucosa-associated dysbiosis in inflammatory bowel disease" 53 : 95-106, 2018

      더보기

      분석정보

      View

      상세정보조회

      0

      Usage

      원문다운로드

      0

      대출신청

      0

      복사신청

      0

      EDDS신청

      0

      동일 주제 내 활용도 TOP

      더보기

      주제

      연도별 연구동향

      연도별 활용동향

      연관논문

      연구자 네트워크맵

      공동연구자 (7)

      유사연구자 (20) 활용도상위20명

      인용정보 인용지수 설명보기

      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2015-03-30 학회명변경 영문명 : 미등록 -> KASID KCI등재
      2015-03-30 학회명변경 영문명 : KASID -> Korean Association for the Study of Intestinal Disease KCI등재
      2015-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2011-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2010-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2008-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
      더보기

      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.54 0.54 0.46
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.4 0.35 0.652 0.08
      더보기

      이 자료와 함께 이용한 RISS 자료

      나만을 위한 추천자료

      해외이동버튼