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dc.contributor.authorSkaarud, Kristin Aneta Joan
dc.contributor.authorHov, Johannes Espolin Roksund
dc.contributor.authorHansen, Simen Hyll
dc.contributor.authorKummen, Martin
dc.contributor.authorValeur, Jørgen
dc.contributor.authorSeljeflot, Ingebjørg
dc.contributor.authorBye, Asta
dc.contributor.authorPaulsen, Vemund
dc.contributor.authorLundin, Knut Erik Aslaksen
dc.contributor.authorTrøseid, Marius
dc.contributor.authorTjønnfjord, Geir Erland
dc.contributor.authorIversen, Per Ole
dc.date.accessioned2021-06-24T12:52:48Z
dc.date.available2021-06-24T12:52:48Z
dc.date.created2021-06-03T14:22:21Z
dc.date.issued2021-06-02
dc.identifier.citationScientific Reports. 2021, 11, (1-11).en_US
dc.identifier.issn2045-2322
dc.identifier.urihttps://hdl.handle.net/11250/2761177
dc.description.abstractGut mucosal barrier injury is common following allogeneic hematopoietic stem cell transplantation (allo-HSCT) and associated with poor clinical outcomes. Diet is critical for microbial diversity, but whether nutritional support affects microbiota and outcome after allo-HSCT is unknown. We present a secondary analysis of a randomized controlled nutritional intervention trial during allo-HSCT. We investigated if the intervention influenced gut microbiota, short-chain fatty acids (SCFAs), and markers of gut barrier functions, and if these parameters were associated with clinical outcomes. Fecal specimens were available from 47 recipients, and subjected to 16S rRNA gene sequencing. We found no significant differences between the intervention group and controls in investigated parameters. We observed a major depletion of microbiota, SCFAs, and altered markers of gut barrier function from baseline to 3 weeks post-transplant. One-year mortality was significantly higher in patients with lower diversity at 3 weeks post-HSCT, but not related to diversity at baseline. The relative abundance of Blautia genus at 3 weeks was higher in survivors. Fecal propionic acid was associated with survival. Markers of gut barrier functions were less strongly associated with clinical outcomes. Possibly, other strategies than dietary intervention are needed to prevent negative effects of gut microbiota and clinical outcomes after allo-HSCT.en_US
dc.description.sponsorshipThe study was supported by Oslo University Hospital, Larvik Cancer Society, Norwegian Nurses Organization and the Throne Holst Foundation, Norway. The tube feeding was provided by Nutricia, Norway.en_US
dc.language.isoengen_US
dc.publisherNature Researchen_US
dc.relation.ispartofseriesScientific Reports;11:11593
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectMortalityen_US
dc.subjectMicrobial diversitiesen_US
dc.subjectStem cellsen_US
dc.subjectTransplantationen_US
dc.subjectNutritional intervention trialsen_US
dc.titleMortality and microbial diversity after allogenic hematopoietic stem cell transplantation: secondary analysis of a randomized nutritional intervention trialen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© The Author(s) 2021.en_US
dc.source.articlenumber11593en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doihttps://doi.org/10.1038/s41598-021-90976-z
dc.identifier.cristin1913594
dc.source.journalScientific Reportsen_US
dc.source.volume11en_US
dc.source.pagenumber11en_US


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