Fecal microbiota transplantation for ulcerative colitis: a prospective clinical study

Fecal microbiota transplantation may contribute to disease remission in ulcerative colitis; however, the factors that determine the effects of treatment remain unknown. The aim of the present study was to prospectively investigate the clinical efficacy of fecal microbiota transplantation in patients...

Full description

Saved in:
Bibliographic Details
Published inBMC gastroenterology Vol. 19; no. 1; pp. 116 - 12
Main Authors Tian, Yan, Zhou, Yan, Huang, Sisi, Li, Jun, Zhao, Kui, Li, Xiaohui, Wen, Xiangchen, Li, Xiao-an
Format Journal Article
LanguageEnglish
Published England BioMed Central Ltd 04.07.2019
BioMed Central
BMC
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Fecal microbiota transplantation may contribute to disease remission in ulcerative colitis; however, the factors that determine the effects of treatment remain unknown. The aim of the present study was to prospectively investigate the clinical efficacy of fecal microbiota transplantation in patients with ulcerative colitis and identify the bacterial signatures associated with clinical remission. A total of 20 patients with ulcerative colitis were included in this prospective and uncontrolled study. All patients underwent gastroscopy five times, once every 3 weeks. Clinical indices were used to assess the efficacy of fecal microbiota transplantation, as well as the Mayo score, a score used to evaluate the extent of intestinal mucosal lesions in patients with ulcerative colitis. The changes in intestinal flora were detected by 16S ribosomal RNA-sequencing, and the relationship between ulcerative colitis and intestinal flora was analyzed. After treatment, clinical index scores for diarrhea, abdominal pain, and blood stool decreased significantly (p < 0.05). Erythrocyte sedimentation rate and C-reactive protein levels had not changed significantly; however, the clinical index score for intestinal mucosal lesions and the Mayo score decreased significantly. In addition, 16S ribosomal RNA-sequencing revealed that the intestinal flora in patients diagnosed with ulcerative colitis was different from that of donors. Fecal microbiota transplantation has a potential therapeutic value for the treatment of ulcerative colitis as it changes the abundance of bacterial flora and improves the scores for diarrhea, abdominal pain, and mucous membrane lesions in patients with this disease. The clinical trial was retrospectively registered with ClinicalTrials.gov ( NCT03016780 ) on January 11th, 2017.
AbstractList Abstract Background Fecal microbiota transplantation may contribute to disease remission in ulcerative colitis; however, the factors that determine the effects of treatment remain unknown. The aim of the present study was to prospectively investigate the clinical efficacy of fecal microbiota transplantation in patients with ulcerative colitis and identify the bacterial signatures associated with clinical remission. Methods A total of 20 patients with ulcerative colitis were included in this prospective and uncontrolled study. All patients underwent gastroscopy five times, once every 3 weeks. Clinical indices were used to assess the efficacy of fecal microbiota transplantation, as well as the Mayo score, a score used to evaluate the extent of intestinal mucosal lesions in patients with ulcerative colitis. The changes in intestinal flora were detected by 16S ribosomal RNA-sequencing, and the relationship between ulcerative colitis and intestinal flora was analyzed. Results After treatment, clinical index scores for diarrhea, abdominal pain, and blood stool decreased significantly (p < 0.05). Erythrocyte sedimentation rate and C-reactive protein levels had not changed significantly; however, the clinical index score for intestinal mucosal lesions and the Mayo score decreased significantly. In addition, 16S ribosomal RNA-sequencing revealed that the intestinal flora in patients diagnosed with ulcerative colitis was different from that of donors. Conclusion Fecal microbiota transplantation has a potential therapeutic value for the treatment of ulcerative colitis as it changes the abundance of bacterial flora and improves the scores for diarrhea, abdominal pain, and mucous membrane lesions in patients with this disease. Trial registration The clinical trial was retrospectively registered with ClinicalTrials.gov (NCT03016780) on January 11th, 2017.
Fecal microbiota transplantation may contribute to disease remission in ulcerative colitis; however, the factors that determine the effects of treatment remain unknown. The aim of the present study was to prospectively investigate the clinical efficacy of fecal microbiota transplantation in patients with ulcerative colitis and identify the bacterial signatures associated with clinical remission. A total of 20 patients with ulcerative colitis were included in this prospective and uncontrolled study. All patients underwent gastroscopy five times, once every 3 weeks. Clinical indices were used to assess the efficacy of fecal microbiota transplantation, as well as the Mayo score, a score used to evaluate the extent of intestinal mucosal lesions in patients with ulcerative colitis. The changes in intestinal flora were detected by 16S ribosomal RNA-sequencing, and the relationship between ulcerative colitis and intestinal flora was analyzed. After treatment, clinical index scores for diarrhea, abdominal pain, and blood stool decreased significantly (p < 0.05). Erythrocyte sedimentation rate and C-reactive protein levels had not changed significantly; however, the clinical index score for intestinal mucosal lesions and the Mayo score decreased significantly. In addition, 16S ribosomal RNA-sequencing revealed that the intestinal flora in patients diagnosed with ulcerative colitis was different from that of donors. Fecal microbiota transplantation has a potential therapeutic value for the treatment of ulcerative colitis as it changes the abundance of bacterial flora and improves the scores for diarrhea, abdominal pain, and mucous membrane lesions in patients with this disease.
Fecal microbiota transplantation may contribute to disease remission in ulcerative colitis; however, the factors that determine the effects of treatment remain unknown. The aim of the present study was to prospectively investigate the clinical efficacy of fecal microbiota transplantation in patients with ulcerative colitis and identify the bacterial signatures associated with clinical remission. A total of 20 patients with ulcerative colitis were included in this prospective and uncontrolled study. All patients underwent gastroscopy five times, once every 3 weeks. Clinical indices were used to assess the efficacy of fecal microbiota transplantation, as well as the Mayo score, a score used to evaluate the extent of intestinal mucosal lesions in patients with ulcerative colitis. The changes in intestinal flora were detected by 16S ribosomal RNA-sequencing, and the relationship between ulcerative colitis and intestinal flora was analyzed. After treatment, clinical index scores for diarrhea, abdominal pain, and blood stool decreased significantly (p < 0.05). Erythrocyte sedimentation rate and C-reactive protein levels had not changed significantly; however, the clinical index score for intestinal mucosal lesions and the Mayo score decreased significantly. In addition, 16S ribosomal RNA-sequencing revealed that the intestinal flora in patients diagnosed with ulcerative colitis was different from that of donors. Fecal microbiota transplantation has a potential therapeutic value for the treatment of ulcerative colitis as it changes the abundance of bacterial flora and improves the scores for diarrhea, abdominal pain, and mucous membrane lesions in patients with this disease. The clinical trial was retrospectively registered with ClinicalTrials.gov ( NCT03016780 ) on January 11th, 2017.
Fecal microbiota transplantation may contribute to disease remission in ulcerative colitis; however, the factors that determine the effects of treatment remain unknown. The aim of the present study was to prospectively investigate the clinical efficacy of fecal microbiota transplantation in patients with ulcerative colitis and identify the bacterial signatures associated with clinical remission.BACKGROUNDFecal microbiota transplantation may contribute to disease remission in ulcerative colitis; however, the factors that determine the effects of treatment remain unknown. The aim of the present study was to prospectively investigate the clinical efficacy of fecal microbiota transplantation in patients with ulcerative colitis and identify the bacterial signatures associated with clinical remission.A total of 20 patients with ulcerative colitis were included in this prospective and uncontrolled study. All patients underwent gastroscopy five times, once every 3 weeks. Clinical indices were used to assess the efficacy of fecal microbiota transplantation, as well as the Mayo score, a score used to evaluate the extent of intestinal mucosal lesions in patients with ulcerative colitis. The changes in intestinal flora were detected by 16S ribosomal RNA-sequencing, and the relationship between ulcerative colitis and intestinal flora was analyzed.METHODSA total of 20 patients with ulcerative colitis were included in this prospective and uncontrolled study. All patients underwent gastroscopy five times, once every 3 weeks. Clinical indices were used to assess the efficacy of fecal microbiota transplantation, as well as the Mayo score, a score used to evaluate the extent of intestinal mucosal lesions in patients with ulcerative colitis. The changes in intestinal flora were detected by 16S ribosomal RNA-sequencing, and the relationship between ulcerative colitis and intestinal flora was analyzed.After treatment, clinical index scores for diarrhea, abdominal pain, and blood stool decreased significantly (p < 0.05). Erythrocyte sedimentation rate and C-reactive protein levels had not changed significantly; however, the clinical index score for intestinal mucosal lesions and the Mayo score decreased significantly. In addition, 16S ribosomal RNA-sequencing revealed that the intestinal flora in patients diagnosed with ulcerative colitis was different from that of donors.RESULTSAfter treatment, clinical index scores for diarrhea, abdominal pain, and blood stool decreased significantly (p < 0.05). Erythrocyte sedimentation rate and C-reactive protein levels had not changed significantly; however, the clinical index score for intestinal mucosal lesions and the Mayo score decreased significantly. In addition, 16S ribosomal RNA-sequencing revealed that the intestinal flora in patients diagnosed with ulcerative colitis was different from that of donors.Fecal microbiota transplantation has a potential therapeutic value for the treatment of ulcerative colitis as it changes the abundance of bacterial flora and improves the scores for diarrhea, abdominal pain, and mucous membrane lesions in patients with this disease.CONCLUSIONFecal microbiota transplantation has a potential therapeutic value for the treatment of ulcerative colitis as it changes the abundance of bacterial flora and improves the scores for diarrhea, abdominal pain, and mucous membrane lesions in patients with this disease.The clinical trial was retrospectively registered with ClinicalTrials.gov ( NCT03016780 ) on January 11th, 2017.TRIAL REGISTRATIONThe clinical trial was retrospectively registered with ClinicalTrials.gov ( NCT03016780 ) on January 11th, 2017.
Background Fecal microbiota transplantation may contribute to disease remission in ulcerative colitis; however, the factors that determine the effects of treatment remain unknown. The aim of the present study was to prospectively investigate the clinical efficacy of fecal microbiota transplantation in patients with ulcerative colitis and identify the bacterial signatures associated with clinical remission. Methods A total of 20 patients with ulcerative colitis were included in this prospective and uncontrolled study. All patients underwent gastroscopy five times, once every 3 weeks. Clinical indices were used to assess the efficacy of fecal microbiota transplantation, as well as the Mayo score, a score used to evaluate the extent of intestinal mucosal lesions in patients with ulcerative colitis. The changes in intestinal flora were detected by 16S ribosomal RNA-sequencing, and the relationship between ulcerative colitis and intestinal flora was analyzed. Results After treatment, clinical index scores for diarrhea, abdominal pain, and blood stool decreased significantly (p < 0.05). Erythrocyte sedimentation rate and C-reactive protein levels had not changed significantly; however, the clinical index score for intestinal mucosal lesions and the Mayo score decreased significantly. In addition, 16S ribosomal RNA-sequencing revealed that the intestinal flora in patients diagnosed with ulcerative colitis was different from that of donors. Conclusion Fecal microbiota transplantation has a potential therapeutic value for the treatment of ulcerative colitis as it changes the abundance of bacterial flora and improves the scores for diarrhea, abdominal pain, and mucous membrane lesions in patients with this disease. Trial registration The clinical trial was retrospectively registered with ClinicalTrials.gov (NCT03016780) on January 11th, 2017. Keywords: Fecal microbiota transplantation, Intestinal flora, Intestinal microorganisms, Ulcerative colitis
ArticleNumber 116
Audience Academic
Author Li, Jun
Zhou, Yan
Li, Xiao-an
Wen, Xiangchen
Zhao, Kui
Li, Xiaohui
Tian, Yan
Huang, Sisi
Author_xml – sequence: 1
  givenname: Yan
  surname: Tian
  fullname: Tian, Yan
– sequence: 2
  givenname: Yan
  surname: Zhou
  fullname: Zhou, Yan
– sequence: 3
  givenname: Sisi
  surname: Huang
  fullname: Huang, Sisi
– sequence: 4
  givenname: Jun
  surname: Li
  fullname: Li, Jun
– sequence: 5
  givenname: Kui
  surname: Zhao
  fullname: Zhao, Kui
– sequence: 6
  givenname: Xiaohui
  surname: Li
  fullname: Li, Xiaohui
– sequence: 7
  givenname: Xiangchen
  surname: Wen
  fullname: Wen, Xiangchen
– sequence: 8
  givenname: Xiao-an
  surname: Li
  fullname: Li, Xiao-an
BackLink https://www.ncbi.nlm.nih.gov/pubmed/31272391$$D View this record in MEDLINE/PubMed
BookMark eNp9Uk1rFTEUDVKx7dMf4EYG3LiZms9J4kIoRW2h4EbBXcgkd54peZNnMlPovzfj1NJXRLJIcnPuuTf3nFN0NKYREHpN8BkhqntfCFWyazHRLcEEt_wZOiFckpYy_OPo0fkYnZZygzGRirIX6JgRKinT5AR9_wzOxmYXXE59SJNtpmzHso92nOwU0tgMKTdzdJDr9RYal2KYQvnQ2GafU9mDW8MxjGFhKtPs716i54ONBV7d75ta59O3i8v2-uuXq4vz69YJrabWUiGd873weugGjbUTYB2WtrdKaum5Vx1nPQOHe06E1BykFBqwYMxpqdkGXa28Ptkbs89hZ_OdSTaYP4GUt8bmKbgIBltHAHpQndfcc6t74F0tM3AJvcaqcn1cufZzvwPvYKyTiAekhy9j-Gm26dZ0HcFLnxv07p4gp18zlMnsQnEQ6yghzcVQKhhVdfCyQt-u0K2trYVxSJXRLXBzLjTVVR8lKursH6i6PFS9qhWGUOMHCW8ef-Gh979yVwBZAVXtUjIMDxCCzWIps1rKVEuZxVJm-ZZ8kuPCao3aTYj_yfwNAKLQyA
CitedBy_id crossref_primary_10_3390_foods11192961
crossref_primary_10_1177_15353702211006044
crossref_primary_10_5217_ir_2023_00080
crossref_primary_10_1016_j_matchemphys_2022_126460
crossref_primary_10_14309_ctg_0000000000000568
crossref_primary_10_2174_1381612826666200420144128
crossref_primary_10_3390_cells9051234
crossref_primary_10_3389_fimmu_2023_1235827
crossref_primary_10_3390_biomedicines10092236
crossref_primary_10_33073_pjm_2023_025
crossref_primary_10_3892_etm_2020_8512
crossref_primary_10_3748_wjg_v29_i14_2078
crossref_primary_10_3390_microorganisms11061427
crossref_primary_10_3390_microorganisms11051223
crossref_primary_10_1016_j_phrs_2020_104954
crossref_primary_10_1016_j_medmic_2020_100026
crossref_primary_10_1016_j_jaut_2023_103062
crossref_primary_10_1016_j_medmic_2020_100028
crossref_primary_10_3390_microorganisms10112146
crossref_primary_10_1111_1751_2980_12933
crossref_primary_10_1186_s40169_019_0251_8
crossref_primary_10_3390_jcm9061650
crossref_primary_10_1016_j_fochx_2023_101102
crossref_primary_10_1007_s00394_021_02627_8
crossref_primary_10_1053_j_gastro_2020_11_041
crossref_primary_10_3390_jcm9061757
crossref_primary_10_3390_microorganisms11092238
crossref_primary_10_1016_j_jsbmb_2020_105663
crossref_primary_10_3390_cells11121903
crossref_primary_10_3390_biomedicines12040800
crossref_primary_10_3390_pathogens10020152
crossref_primary_10_3390_cells9102283
crossref_primary_10_3168_jds_2022_21877
crossref_primary_10_1002_14651858_CD012774_pub3
crossref_primary_10_7717_peerj_12293
crossref_primary_10_1016_j_iotech_2020_11_001
crossref_primary_10_1371_journal_pone_0238910
crossref_primary_10_1007_s11104_024_06610_0
crossref_primary_10_1097_MD_0000000000029790
crossref_primary_10_1016_j_lfs_2022_120719
crossref_primary_10_1016_j_amolm_2024_100056
crossref_primary_10_1093_ecco_jcc_jjae137
crossref_primary_10_1016_j_phanu_2022_100303
crossref_primary_10_3390_jcm10112466
crossref_primary_10_1016_j_ebiom_2022_104088
Cites_doi 10.1097/MIB.0b013e31829ea325
10.1586/egh.11.71
10.1038/ajg.2013.257
10.1038/s41564-017-0089-z
10.1038/ajg.2012.93
10.1016/j.autrev.2013.06.004
10.1128/AEM.00434-18
10.1016/j.cgh.2018.09.034
10.3748/wjg.14.5020
10.1111/1751-2980.12603
10.1136/bmjopen-2018-021987
10.1080/08923973.2018.1469144
10.1038/nrgastro.2012.152
10.1016/j.chom.2018.09.009
10.1097/MD.0000000000006479
10.1038/ajg.2012.60
10.1038/nri.2017.7
10.1073/pnas.1322269111
10.1053/j.gastro.2014.02.009
10.1136/gutjnl-2014-307410
10.3389/fimmu.2018.02211
ContentType Journal Article
Copyright COPYRIGHT 2019 BioMed Central Ltd.
The Author(s). 2019
Copyright_xml – notice: COPYRIGHT 2019 BioMed Central Ltd.
– notice: The Author(s). 2019
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7X8
5PM
DOA
DOI 10.1186/s12876-019-1010-4
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
PubMed Central (Full Participant titles)
Directory of Open Access Journals (DOAJ)
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList

MEDLINE
MEDLINE - Academic

Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 3
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1471-230X
EndPage 12
ExternalDocumentID oai_doaj_org_article_0ac1eebe86d94d4a9be46a87f47eb908
PMC6610864
A592931285
31272391
10_1186_s12876_019_1010_4
Genre Clinical Trial, Phase II
Clinical Trial, Phase I
Randomized Controlled Trial
Journal Article
GeographicLocations China
GeographicLocations_xml – name: China
GrantInformation_xml – fundername: Foundation of the First Affiliated Hospital of Chengdu Medical College
  grantid: ZYFY2017XH04
– fundername: Natural Science Foundation of Science and Technology Department of Sichuan Province
  grantid: 2016JY0090
– fundername: Natural Science Foundation of Education Department of Sichuan Province
  grantid: 16ZA0280
– fundername: Science and Technology Project of The Health Planning Committee of Sichuan
  grantid: 17ZD012
– fundername: Foundation of the Medical Association of Sichuan Province
  grantid: S16019
– fundername: Innovative Group Foundation of Education Department of Sichuan Province
  grantid: 16TD0028
– fundername: ;
  grantid: 16TD0028
– fundername: ;
  grantid: S16019
– fundername: ;
  grantid: ZYFY2017XH04
– fundername: ;
  grantid: 2016JY0090
– fundername: ;
  grantid: 17ZD012
– fundername: ;
  grantid: 16ZA0280
GroupedDBID ---
0R~
23N
2WC
53G
5VS
6J9
6PF
7X7
88E
8FI
8FJ
AAFWJ
AAJSJ
AASML
AAWTL
AAYXX
ABDBF
ABUWG
ACGFO
ACGFS
ACIHN
ACIWK
ACPRK
ACUHS
ADBBV
ADRAZ
ADUKV
AEAQA
AENEX
AFKRA
AFPKN
AHBYD
AHMBA
AHYZX
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AMKLP
AMTXH
AOIJS
BAPOH
BAWUL
BCNDV
BENPR
BFQNJ
BMC
BPHCQ
BVXVI
C6C
CCPQU
CITATION
CS3
DIK
E3Z
EAD
EAP
EAS
EBD
EBLON
EBS
EJD
EMB
EMK
EMOBN
ESX
F5P
FYUFA
GROUPED_DOAJ
GX1
HMCUK
HYE
IAO
IHR
INH
INR
ITC
KQ8
M1P
M48
M~E
O5R
O5S
OK1
OVT
P2P
PHGZM
PHGZT
PIMPY
PQQKQ
PROAC
PSQYO
RBZ
RNS
ROL
RPM
RSV
SMD
SOJ
SV3
TR2
TUS
UKHRP
W2D
WOQ
WOW
XSB
CGR
CUY
CVF
ECM
EIF
NPM
PJZUB
PPXIY
PMFND
7X8
5PM
PUEGO
ID FETCH-LOGICAL-c598t-a257ccdb5d9f6f909c5eac07aba8797d4d8643b3ec0b415794e7759e0533c9793
IEDL.DBID M48
ISSN 1471-230X
IngestDate Wed Aug 27 01:15:38 EDT 2025
Thu Aug 21 18:09:51 EDT 2025
Fri Jul 11 05:13:35 EDT 2025
Tue Jun 17 21:33:41 EDT 2025
Tue Jun 10 20:47:28 EDT 2025
Tue Jul 29 01:37:20 EDT 2025
Tue Jul 01 04:12:03 EDT 2025
Thu Apr 24 23:01:23 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 1
Keywords Intestinal microorganisms
Intestinal flora
Fecal microbiota transplantation
Ulcerative colitis
Language English
License Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c598t-a257ccdb5d9f6f909c5eac07aba8797d4d8643b3ec0b415794e7759e0533c9793
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
OpenAccessLink http://journals.scholarsportal.info/openUrl.xqy?doi=10.1186/s12876-019-1010-4
PMID 31272391
PQID 2253282727
PQPubID 23479
PageCount 12
ParticipantIDs doaj_primary_oai_doaj_org_article_0ac1eebe86d94d4a9be46a87f47eb908
pubmedcentral_primary_oai_pubmedcentral_nih_gov_6610864
proquest_miscellaneous_2253282727
gale_infotracmisc_A592931285
gale_infotracacademiconefile_A592931285
pubmed_primary_31272391
crossref_primary_10_1186_s12876_019_1010_4
crossref_citationtrail_10_1186_s12876_019_1010_4
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2019-07-04
PublicationDateYYYYMMDD 2019-07-04
PublicationDate_xml – month: 07
  year: 2019
  text: 2019-07-04
  day: 04
PublicationDecade 2010
PublicationPlace England
PublicationPlace_xml – name: England
– name: London
PublicationTitle BMC gastroenterology
PublicationTitleAlternate BMC Gastroenterol
PublicationYear 2019
Publisher BioMed Central Ltd
BioMed Central
BMC
Publisher_xml – name: BioMed Central Ltd
– name: BioMed Central
– name: BMC
References C Manichanh (1010_CR6) 2012; 9
JS Barrett (1010_CR12) 2008; 14
PK Kump (1010_CR21) 2013; 19
M Jitsumura (1010_CR16) 2018; 8
A Geremia (1010_CR1) 2014; 13
SC Ng (1010_CR7) 2015; 64
I D'Odorico (1010_CR13) 2018; 19
S Angelberger (1010_CR14) 2013; 108
A Uygun (1010_CR18) 2017; 96
M Schirmer (1010_CR11) 2018; 24
LJ Brandt (1010_CR20) 2012; 107
S Khan (1010_CR2) 2018; 29
M Levy (1010_CR4) 2017; 17
M Schirmer (1010_CR22) 2018; 3
PV Chang (1010_CR8) 2014; 111
AD Kostic (1010_CR5) 2014; 146
Jordan E. Axelrad (1010_CR10) 2019; 17
TJ Borody (1010_CR19) 2011; 5
Christian L. Hvas (1010_CR3) 2018; 40
1010_CR9
HP Sham (1010_CR17) 2018; 9
CJ Damman (1010_CR15) 2012; 107
References_xml – volume: 19
  start-page: 2155
  issue: 10
  year: 2013
  ident: 1010_CR21
  publication-title: Inflamm Bowel Dis
  doi: 10.1097/MIB.0b013e31829ea325
– volume: 29
  start-page: 1
  year: 2018
  ident: 1010_CR2
  publication-title: Crit Rev Clin Lab Sci
– volume: 5
  start-page: 653
  issue: 6
  year: 2011
  ident: 1010_CR19
  publication-title: Expert Rev Gastroenterol Hepatol
  doi: 10.1586/egh.11.71
– volume: 108
  start-page: 1620
  issue: 10
  year: 2013
  ident: 1010_CR14
  publication-title: Am J Gastroenterol
  doi: 10.1038/ajg.2013.257
– volume: 3
  start-page: 337
  issue: 3
  year: 2018
  ident: 1010_CR22
  publication-title: Nat Microbiol
  doi: 10.1038/s41564-017-0089-z
– volume: 107
  start-page: 1452
  issue: 10
  year: 2012
  ident: 1010_CR15
  publication-title: Am J Gastroenterol
  doi: 10.1038/ajg.2012.93
– volume: 13
  start-page: 3
  issue: 1
  year: 2014
  ident: 1010_CR1
  publication-title: Autoimmun Rev
  doi: 10.1016/j.autrev.2013.06.004
– ident: 1010_CR9
  doi: 10.1128/AEM.00434-18
– volume: 17
  start-page: 1311-1322.e7
  issue: 7
  year: 2019
  ident: 1010_CR10
  publication-title: Clinical Gastroenterology and Hepatology
  doi: 10.1016/j.cgh.2018.09.034
– volume: 14
  start-page: 5020
  issue: 32
  year: 2008
  ident: 1010_CR12
  publication-title: World J Gastroenterol
  doi: 10.3748/wjg.14.5020
– volume: 19
  start-page: 322
  issue: 6
  year: 2018
  ident: 1010_CR13
  publication-title: J Dig Dis
  doi: 10.1111/1751-2980.12603
– volume: 8
  start-page: e021987
  issue: 10
  year: 2018
  ident: 1010_CR16
  publication-title: BMJ Open
  doi: 10.1136/bmjopen-2018-021987
– volume: 40
  start-page: 446
  issue: 6
  year: 2018
  ident: 1010_CR3
  publication-title: Immunopharmacology and Immunotoxicology
  doi: 10.1080/08923973.2018.1469144
– volume: 9
  start-page: 599
  issue: 10
  year: 2012
  ident: 1010_CR6
  publication-title: Nat Rev Gastroenterol Hepatol
  doi: 10.1038/nrgastro.2012.152
– volume: 24
  start-page: 600
  issue: 4
  year: 2018
  ident: 1010_CR11
  publication-title: Cell Host Microbe
  doi: 10.1016/j.chom.2018.09.009
– volume: 96
  start-page: e6479
  issue: 16
  year: 2017
  ident: 1010_CR18
  publication-title: Medicine (Baltimore)
  doi: 10.1097/MD.0000000000006479
– volume: 107
  start-page: 1079
  issue: 7
  year: 2012
  ident: 1010_CR20
  publication-title: Am J Gastroenterol
  doi: 10.1038/ajg.2012.60
– volume: 17
  start-page: 219
  issue: 4
  year: 2017
  ident: 1010_CR4
  publication-title: Nat Rev Immunol
  doi: 10.1038/nri.2017.7
– volume: 111
  start-page: 2247
  issue: 6
  year: 2014
  ident: 1010_CR8
  publication-title: Proc Natl Acad Sci U S A
  doi: 10.1073/pnas.1322269111
– volume: 146
  start-page: 1489
  year: 2014
  ident: 1010_CR5
  publication-title: Gastroenterology
  doi: 10.1053/j.gastro.2014.02.009
– volume: 64
  start-page: 1063
  issue: 7
  year: 2015
  ident: 1010_CR7
  publication-title: Gut
  doi: 10.1136/gutjnl-2014-307410
– volume: 9
  start-page: 2211
  year: 2018
  ident: 1010_CR17
  publication-title: Front Immunol
  doi: 10.3389/fimmu.2018.02211
SSID ssj0017823
Score 2.421419
Snippet Fecal microbiota transplantation may contribute to disease remission in ulcerative colitis; however, the factors that determine the effects of treatment remain...
Background Fecal microbiota transplantation may contribute to disease remission in ulcerative colitis; however, the factors that determine the effects of...
Abstract Background Fecal microbiota transplantation may contribute to disease remission in ulcerative colitis; however, the factors that determine the effects...
SourceID doaj
pubmedcentral
proquest
gale
pubmed
crossref
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
StartPage 116
SubjectTerms Aged
Care and treatment
Colitis, Ulcerative - therapy
Fecal microbiota transplantation
Fecal Microbiota Transplantation - methods
Female
Gastrointestinal Microbiome
Health aspects
Humans
Intestinal flora
Intestinal microorganisms
Male
Microbiota (Symbiotic organisms)
Middle Aged
Prospective Studies
Remission Induction - methods
Treatment Outcome
Ulcerative colitis
SummonAdditionalLinks – databaseName: Directory of Open Access Journals (DOAJ)
  dbid: DOA
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Li9UwFA4yC3Ejvq2OEkEQhDLpNE93ozgMwrhyYHYhr-LAtSPe3v_vl6S93CLoxm2TNOnJeTbnfCHkbTaRsoP2E87LlifXtcZz3_Ymwlx6bUTMvwYuv8qLK_7lWlwfXPWVc8IqPHAl3AlzoUuYSctoeOTO-MSl02rgKnlTy3xh85Zgaj4_gN3r5zPMTsuTLbSwypGzgdqB4uErK1TA-v9UyQc2aZ0veWCAzh-Q-7PnSM_qih-SO2l8RO5ezmfjj8nVeQK96Y-bCq00OToV4PKNq9VFI4V_SnebkCrYNw0l9W37gTqKxSwll3SplaQFefYJ3vv526eLdr40oQ3C6Kl1kMEQohfRDHIwzAQB3cqU8yCaUZFHDSfE9ykwD-MNcUxKCZNviOiDgbQ-JUfj7ZieE8qjccMAD2XAkJDvJccuwqFKkmnMoRvCFiLaMCOK54stNrZEFlraSncLuudUMmZ5Q97vh_yscBp_6_wx78y-Y0bCLg_AH3bmD_sv_mjIu7yvNssrFhfcXHaAT8zIV_ZMwEHsMbVoyPGqJ-QsrJrfLJxhc1NOThvT7W5roRJ7RK7wBBvyrHLKfs0Yqk570zVErXho9VHrlvHme4H5hueEeJO_-B9UeEnunbJSrtYyfkyOpl-79Are1ORfF8H5DV9XHYw
  priority: 102
  providerName: Directory of Open Access Journals
Title Fecal microbiota transplantation for ulcerative colitis: a prospective clinical study
URI https://www.ncbi.nlm.nih.gov/pubmed/31272391
https://www.proquest.com/docview/2253282727
https://pubmed.ncbi.nlm.nih.gov/PMC6610864
https://doaj.org/article/0ac1eebe86d94d4a9be46a87f47eb908
Volume 19
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1bi9QwFA57AfFFvNt1HSIIglDNbNOkEUR2ZJdFmEUWBwZfQpKmujB23JkO6L_3S9qOW1zEl3mYJG0u5_Kd5lwIeRFUpBhD-uXGipR7M06V5TbNVAl1aQuVl-HTwPRcnM34x3k-3yF9eatuA9c3mnahntRstXj98-rXezD8u8jwhXizhoyVwS5WECoQK3yX7EMxyVDQYMr_XCpAGUZ_e8jjFMh73l1y3viIgZqK2fz_ltnXlNbQofKahjq9S-500JIet7Rwj-z4-j65Ne0uzx-Q2anHgdDvl23upcbQJmY2X5g2_KimALB0s3C-zQZOXfSNW7-lhmIyfUwm7YMpaUxN-xDPPfn84SztqiqkLldFkxowqXOlzUtViUox5XIIXyaNNYVUsuRlAZRiM--YhXYHv3opcxVKSGROgZ0fkb16WfsnhPJSmaoChKkwxIXC5ThmIC4vWIF3FAlh_SZq16UcD5UvFjqaHoXQ7b5r7HvwNWOaJ-TVdsiPNt_GvzpPwslsO4ZU2fGP5eqr7jhPM-PGHqRaiFLxkhtlPRdYasWlt4phki_DuepAYpicM11cApYYUmPp4xwIMsOr84QcDnqCEd2g-XlPGTo0Be-12i83aw2ZmcG0BVRMyOOWUrZzxlB5lKlxQuSAhgaLGrbUl99iHnBAKxik_OC_F_CU3D5iMWgtZfyQ7DWrjX8GTNXYEdmVczki-5OT808Xo_hlYhS5B78Xky-_AUwzIUs
linkProvider Scholars Portal
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Fecal+microbiota+transplantation+for+ulcerative+colitis%3A+a+prospective+clinical+study&rft.jtitle=BMC+gastroenterology&rft.au=Tian%2C+Yan&rft.au=Zhou%2C+Yan&rft.au=Huang%2C+Sisi&rft.au=Li%2C+Jun&rft.date=2019-07-04&rft.pub=BioMed+Central+Ltd&rft.issn=1471-230X&rft.eissn=1471-230X&rft.volume=19&rft.issue=1&rft_id=info:doi/10.1186%2Fs12876-019-1010-4&rft.externalDocID=A592931285
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1471-230X&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1471-230X&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1471-230X&client=summon