Literature DB >> 32101664

Microbiota as Predictor of Mortality in Allogeneic Hematopoietic-Cell Transplantation.

Jonathan U Peled1, Antonio L C Gomes1, Sean M Devlin1, Eric R Littmann1, Ying Taur1, Anthony D Sung1, Daniela Weber1, Daigo Hashimoto1, Ann E Slingerland1, John B Slingerland1, Molly Maloy1, Annelie G Clurman1, Christoph K Stein-Thoeringer1, Kate A Markey1, Melissa D Docampo1, Marina Burgos da Silva1, Niloufer Khan1, André Gessner1, Julia A Messina1, Kristi Romero1, Meagan V Lew1, Amy Bush1, Lauren Bohannon1, Daniel G Brereton1, Emily Fontana1, Luigi A Amoretti1, Roberta J Wright1, Gabriel K Armijo1, Yusuke Shono1, Míriam Sanchez-Escamilla1, Nerea Castillo Flores1, Ana Alarcon Tomas1, Richard J Lin1, Lucrecia Yáñez San Segundo1, Gunjan L Shah1, Christina Cho1, Michael Scordo1, Ioannis Politikos1, Kasumi Hayasaka1, Yuta Hasegawa1, Boglarka Gyurkocza1, Doris M Ponce1, Juliet N Barker1, Miguel-Angel Perales1, Sergio A Giralt1, Robert R Jenq1, Takanori Teshima1, Nelson J Chao1, Ernst Holler1, Joao B Xavier1, Eric G Pamer1, Marcel R M van den Brink1.   

Abstract

BACKGROUND: Relationships between microbiota composition and clinical outcomes after allogeneic hematopoietic-cell transplantation have been described in single-center studies. Geographic variations in the composition of human microbial communities and differences in clinical practices across institutions raise the question of whether these associations are generalizable.
METHODS: The microbiota composition of fecal samples obtained from patients who were undergoing allogeneic hematopoietic-cell transplantation at four centers was profiled by means of 16S ribosomal RNA gene sequencing. In an observational study, we examined associations between microbiota diversity and mortality using Cox proportional-hazards analysis. For stratification of the cohorts into higher- and lower-diversity groups, the median diversity value that was observed at the study center in New York was used. In the analysis of independent cohorts, the New York center was cohort 1, and three centers in Germany, Japan, and North Carolina composed cohort 2. Cohort 1 and subgroups within it were analyzed for additional outcomes, including transplantation-related death.
RESULTS: We profiled 8767 fecal samples obtained from 1362 patients undergoing allogeneic hematopoietic-cell transplantation at the four centers. We observed patterns of microbiota disruption characterized by loss of diversity and domination by single taxa. Higher diversity of intestinal microbiota was associated with a lower risk of death in independent cohorts (cohort 1: 104 deaths among 354 patients in the higher-diversity group vs. 136 deaths among 350 patients in the lower-diversity group; adjusted hazard ratio, 0.71; 95% confidence interval [CI], 0.55 to 0.92; cohort 2: 18 deaths among 87 patients in the higher-diversity group vs. 35 deaths among 92 patients in the lower-diversity group; adjusted hazard ratio, 0.49; 95% CI, 0.27 to 0.90). Subgroup analyses identified an association between lower intestinal diversity and higher risks of transplantation-related death and death attributable to graft-versus-host disease. Baseline samples obtained before transplantation already showed evidence of microbiome disruption, and lower diversity before transplantation was associated with poor survival.
CONCLUSIONS: Patterns of microbiota disruption during allogeneic hematopoietic-cell transplantation were similar across transplantation centers and geographic locations; patterns were characterized by loss of diversity and domination by single taxa. Higher diversity of intestinal microbiota at the time of neutrophil engraftment was associated with lower mortality. (Funded by the National Cancer Institute and others.).
Copyright © 2020 Massachusetts Medical Society.

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Year:  2020        PMID: 32101664      PMCID: PMC7534690          DOI: 10.1056/NEJMoa1900623

Source DB:  PubMed          Journal:  N Engl J Med        ISSN: 0028-4793            Impact factor:   91.245


  44 in total

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Journal:  Am J Respir Crit Care Med       Date:  2016-08-15       Impact factor: 21.405

2.  Intestinal Blautia Is Associated with Reduced Death from Graft-versus-Host Disease.

Authors:  Robert R Jenq; Ying Taur; Sean M Devlin; Doris M Ponce; Jenna D Goldberg; Katya F Ahr; Eric R Littmann; Lilan Ling; Asia C Gobourne; Liza C Miller; Melissa D Docampo; Jonathan U Peled; Nicholas Arpaia; Justin R Cross; Tatanisha K Peets; Melissa A Lumish; Yusuke Shono; Jarrod A Dudakov; Hendrik Poeck; Alan M Hanash; Juliet N Barker; Miguel-Angel Perales; Sergio A Giralt; Eric G Pamer; Marcel R M van den Brink
Journal:  Biol Blood Marrow Transplant       Date:  2015-05-11       Impact factor: 5.742

3.  The effects of intestinal tract bacterial diversity on mortality following allogeneic hematopoietic stem cell transplantation.

Authors:  Ying Taur; Robert R Jenq; Miguel-Angel Perales; Eric R Littmann; Sejal Morjaria; Lilan Ling; Daniel No; Asia Gobourne; Agnes Viale; Parastoo B Dahi; Doris M Ponce; Juliet N Barker; Sergio Giralt; Marcel van den Brink; Eric G Pamer
Journal:  Blood       Date:  2014-06-17       Impact factor: 22.113

4.  Variability of nutritional practices in peritransplant period after allogeneic hematopoietic stem cell transplantation: a survey by the Complications and Quality of Life Working Party of the EBMT.

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Authors:  Paul I Costea; Falk Hildebrand; Manimozhiyan Arumugam; Fredrik Bäckhed; Martin J Blaser; Frederic D Bushman; Willem M de Vos; S Dusko Ehrlich; Claire M Fraser; Masahira Hattori; Curtis Huttenhower; Ian B Jeffery; Dan Knights; James D Lewis; Ruth E Ley; Howard Ochman; Paul W O'Toole; Christopher Quince; David A Relman; Fergus Shanahan; Shinichi Sunagawa; Jun Wang; George M Weinstock; Gary D Wu; Georg Zeller; Liping Zhao; Jeroen Raes; Rob Knight; Peer Bork
Journal:  Nat Microbiol       Date:  2017-12-18       Impact factor: 17.745

6.  Microbiota Disruption Induced by Early Use of Broad-Spectrum Antibiotics Is an Independent Risk Factor of Outcome after Allogeneic Stem Cell Transplantation.

Authors:  Daniela Weber; Robert R Jenq; Jonathan U Peled; Ying Taur; Andreas Hiergeist; Josef Koestler; Katja Dettmer; Markus Weber; Daniel Wolff; Joachim Hahn; Eric G Pamer; Wolfgang Herr; André Gessner; Peter J Oefner; Marcel R M van den Brink; Ernst Holler
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7.  Assessment of variation in microbial community amplicon sequencing by the Microbiome Quality Control (MBQC) project consortium.

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Journal:  Nat Biotechnol       Date:  2017-10-02       Impact factor: 54.908

8.  Vancomycin-resistant enterococcal colonization appears associated with increased mortality among allogeneic hematopoietic stem cell transplant recipients.

Authors:  A Zirakzadeh; D A Gastineau; J N Mandrekar; J P Burke; P B Johnston; R Patel
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9.  Structure, function and diversity of the healthy human microbiome.

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10.  Compositional Flux Within the Intestinal Microbiota and Risk for Bloodstream Infection With Gram-negative Bacteria.

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  119 in total

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3.  Functional and phylogenetic alterations in gut microbiome are linked to graft-versus-host disease severity.

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Review 4.  The role of the thymus in allogeneic bone marrow transplantation and the recovery of the peripheral T-cell compartment.

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6.  Low diversity of gut microbiota in the early phase of post-bone marrow transplantation increases the risk of chronic graft-versus-host disease.

Authors:  Tatsuya Konishi; Shinsuke Kusakabe; Akihisa Hino; Kyoko Inamoto; Kota Yoshifuji; Yuko Kiridoshi; Kozue Takeshita; Satoshi Sasajima; Takashi Toya; Aiko Igarashi; Yuho Najima; Takeshi Kobayashi; Noriko Doki; Daisuke Motooka; Shota Nakamura; Masahiro Suyama; Wataru Suda; Atsushi Shiota; Koji Atarashi; Masahira Hattori; Kenya Honda; Takafumi Yokota; Kazuteru Ohashi; Hirohiko Shibayama; Kentaro Fukushima; Kazuhiko Kakihana
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7.  Early antibiotic use is associated with CMV risk and outcomes following allogeneic hematopoietic cell transplantation.

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