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dc.contributor.authorBajaj, Jasmohan S.
dc.contributor.authorFagan, Andrew
dc.contributor.authorGavis, Edith A.
dc.contributor.authorLiu, Eric
dc.contributor.authorCox, I. Jane
dc.contributor.authorKheradman, Raffi
dc.contributor.authorHeuman, Douglas
dc.contributor.authorWang, Jessica
dc.contributor.authorWilliams, Roger
dc.contributor.authorSikaroodi, Masoumeh
dc.contributor.authorFuchs, Michael
dc.contributor.authorJohn, Binu
dc.contributor.authorThacker, Leroy R.
dc.contributor.authorRiva, Antonio
dc.contributor.authorSmith, Mark
dc.contributor.authorTaylor-Robinson, Simon D.
dc.contributor.authorGillevet, Patrick M
dc.contributor.authorKassam, Zain
dc.contributor.authorGurry, Thomas Jerome
dc.contributor.authorAlm, Eric J
dc.date.accessioned2019-01-04T15:22:02Z
dc.date.available2019-01-04T15:22:02Z
dc.date.issued2017-06
dc.date.submitted2017-05
dc.identifier.issn0270-9139
dc.identifier.urihttp://hdl.handle.net/1721.1/119850
dc.description.abstractRecurrent hepatic encephalopathy (HE) is a leading cause of readmission despite standard of care (SOC) associated with microbial dysbiosis. Fecal microbiota transplantation (FMT) may improve dysbiosis; however, it has not been studied in HE. We aimed to define whether FMT using a rationally derived stool donor is safe in recurrent HE compared to SOC alone. An open-label, randomized clinical trial with a 5-month follow-up in outpatient men with cirrhosis with recurrent HE on SOC was conducted with 1:1 randomization. FMT-randomized patients received 5 days of broad-spectrum antibiotic pretreatment, then a single FMT enema from the same donor with the optimal microbiota deficient in HE. Follow-up occurred on days 5, 6, 12, 35, and 150 postrandomization. The primary outcome was safety of FMT compared to SOC using FMT-related serious adverse events (SAEs). Secondary outcomes were adverse events, cognition, microbiota, and metabolomic changes. Participants in both arms were similar on all baseline criteria and were followed until study end. FMT with antibiotic pretreatment was well tolerated. Eight (80%) SOC participants had a total of 11 SAEs compared to 2 (20%) FMT participants with SAEs (both FMT unrelated; P = 0.02). Five SOC and no FMT participants developed further HE (P = 0.03). Cognition improved in the FMT, but not the SOC, group. Model for End-Stage Liver Disease (MELD) score transiently worsened postantibiotics, but reverted to baseline post-FMT. Postantibiotics, beneficial taxa, and microbial diversity reduction occurred with Proteobacteria expansion. However, FMT increased diversity and beneficial taxa. SOC microbiota and MELD score remained similar throughout. Conclusion: FMT from a rationally selected donor reduced hospitalizations, improved cognition, and dysbiosis in cirrhosis with recurrent HE. Keywords: Cirrhosis; Dysbiosis; Hospitalizations; Metabolomics; Stroop Appen_US
dc.publisherWileyen_US
dc.relation.isversionofhttp://dx.doi.org/10.1002/HEP.29306en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleFecal microbiota transplant from a rational stool donor improves hepatic encephalopathy: A randomized clinical trialen_US
dc.typeArticleen_US
dc.identifier.citationBajaj, Jasmohan S., Zain Kassam, Andrew Fagan, Edith A. Gavis, Eric Liu, I. Jane Cox, Raffi Kheradman, et al. “Fecal Microbiota Transplant from a Rational Stool Donor Improves Hepatic Encephalopathy: A Randomized Clinical Trial.” Hepatology 66, no. 6 (October 30, 2017): 1727–1738.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.mitauthorKassam, Zain
dc.contributor.mitauthorGurry, Thomas Jerome
dc.contributor.mitauthorAlm, Eric J
dc.relation.journalHepatologyen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2018-12-19T15:51:20Z
dspace.orderedauthorsBajaj, Jasmohan S.; Kassam, Zain; Fagan, Andrew; Gavis, Edith A.; Liu, Eric; Cox, I. Jane; Kheradman, Raffi; Heuman, Douglas; Wang, Jessica; Gurry, Thomas; Williams, Roger; Sikaroodi, Masoumeh; Fuchs, Michael; Alm, Eric; John, Binu; Thacker, Leroy R.; Riva, Antonio; Smith, Mark; Taylor-Robinson, Simon D.; Gillevet, Patrick Men_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-8639-1860
dc.identifier.orcidhttps://orcid.org/0000-0001-8294-9364
mit.licenseOPEN_ACCESS_POLICYen_US


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