Mortality and microbial diversity after allogeneic hematopoietic stem cell transplantation: secondary analysis of a randomized nutritional intervention trial
Abstract Gut 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 p...
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doaj-506291e3837948b684d37c1e58ee93fd2021-06-06T11:40:15ZengNature Publishing GroupScientific Reports2045-23222021-06-0111111210.1038/s41598-021-90976-zMortality and microbial diversity after allogeneic hematopoietic stem cell transplantation: secondary analysis of a randomized nutritional intervention trialKristin J. Skaarud0Johannes R. Hov1Simen H. Hansen2Martin Kummen3Jørgen Valeur4Ingebjørg Seljeflot5Asta Bye6Vemund Paulsen7Knut E. A. Lundin8Marius Trøseid9Geir E. Tjønnfjord10Per Ole Iversen11Department of Haematology, Oslo University HospitalSection of Gastroenterology, Department of Transplantation Medicine, Oslo University HospitalInstitute of Clinical Medicine, University of OsloInstitute of Clinical Medicine, University of OsloDepartment of Gastroenterology, Oslo University HospitalInstitute of Clinical Medicine, University of OsloRegional Advisory Unit for Palliative Care, Department of Oncology, Oslo University HospitalSection of Gastroenterology, Department of Transplantation Medicine, Oslo University HospitalSection of Gastroenterology, Department of Transplantation Medicine, Oslo University HospitalInstitute of Clinical Medicine, University of OsloDepartment of Haematology, Oslo University HospitalDepartment of Haematology, Oslo University HospitalAbstract Gut 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. ClinicalTrials.gov (NCT01181076).https://doi.org/10.1038/s41598-021-90976-z |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Kristin J. Skaarud Johannes R. Hov Simen H. Hansen Martin Kummen Jørgen Valeur Ingebjørg Seljeflot Asta Bye Vemund Paulsen Knut E. A. Lundin Marius Trøseid Geir E. Tjønnfjord Per Ole Iversen |
spellingShingle |
Kristin J. Skaarud Johannes R. Hov Simen H. Hansen Martin Kummen Jørgen Valeur Ingebjørg Seljeflot Asta Bye Vemund Paulsen Knut E. A. Lundin Marius Trøseid Geir E. Tjønnfjord Per Ole Iversen Mortality and microbial diversity after allogeneic hematopoietic stem cell transplantation: secondary analysis of a randomized nutritional intervention trial Scientific Reports |
author_facet |
Kristin J. Skaarud Johannes R. Hov Simen H. Hansen Martin Kummen Jørgen Valeur Ingebjørg Seljeflot Asta Bye Vemund Paulsen Knut E. A. Lundin Marius Trøseid Geir E. Tjønnfjord Per Ole Iversen |
author_sort |
Kristin J. Skaarud |
title |
Mortality and microbial diversity after allogeneic hematopoietic stem cell transplantation: secondary analysis of a randomized nutritional intervention trial |
title_short |
Mortality and microbial diversity after allogeneic hematopoietic stem cell transplantation: secondary analysis of a randomized nutritional intervention trial |
title_full |
Mortality and microbial diversity after allogeneic hematopoietic stem cell transplantation: secondary analysis of a randomized nutritional intervention trial |
title_fullStr |
Mortality and microbial diversity after allogeneic hematopoietic stem cell transplantation: secondary analysis of a randomized nutritional intervention trial |
title_full_unstemmed |
Mortality and microbial diversity after allogeneic hematopoietic stem cell transplantation: secondary analysis of a randomized nutritional intervention trial |
title_sort |
mortality and microbial diversity after allogeneic hematopoietic stem cell transplantation: secondary analysis of a randomized nutritional intervention trial |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2021-06-01 |
description |
Abstract Gut 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. ClinicalTrials.gov (NCT01181076). |
url |
https://doi.org/10.1038/s41598-021-90976-z |
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