Evidence map›Paper›PMID 38431763›Full record

ArticleBone marrow transplantation2024

Clostridium butyricum MIYAIRI 588 contributes to the maintenance of intestinal microbiota diversity early after haematopoietic cell transplantation.

Kentaro Fukushima, Hayami Kudo, Kentaro Oka, Atsushi Hayashi, Makoto Onizuka, Shinsuke Kusakabe, Akihisa Hino, Motomichi Takahashi, Kiyoshi Takeda, Masaki Mori and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Bone marrow transplantation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 10 citations in OpenAlex.

  1. Oncology research · 2025
    Trial
  2. Clinical analysis of 16 patients withNew microbes and new infections · 2026
    Article
  3. Review
  4. Synergistic effects ofmSystems · 2026
    Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Opportunistic Features of Non-Pathogens (Basel, Switzerland) · 2024
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

Kentaro FukushimaDepartment of Haematology and Oncology, Osaka University Graduate School of Medicine, Suita, 565-0871, Japan. kfukushi@bldon.med.osaka-u.ac.jp.ORCID 0000-0002-8003-2584
Hayami KudoR&D Division, Central Research Institute, Miyarisan Pharmaceutical Co., Ltd., Saitama, 331-0804, Japan.
Kentaro OkaR&D Division, Central Research Institute, Miyarisan Pharmaceutical Co., Ltd., Saitama, 331-0804, Japan.
Atsushi HayashiR&D Division, Central Research Institute, Miyarisan Pharmaceutical Co., Ltd., Saitama, 331-0804, Japan.ORCID 0000-0003-4060-2383
Makoto OnizukaDepartment of Hematology/Oncology, Tokai University School of Medicine, Isehara, 259-1193, Japan.ORCID 0000-0003-3864-0823
Shinsuke KusakabeDepartment of Haematology and Oncology, Osaka University Graduate School of Medicine, Suita, 565-0871, Japan.ORCID 0000-0002-9814-7611
Akihisa HinoDepartment of Haematology and Oncology, Osaka University Graduate School of Medicine, Suita, 565-0871, Japan.
Motomichi TakahashiR&D Division, Central Research Institute, Miyarisan Pharmaceutical Co., Ltd., Saitama, 331-0804, Japan.
Kiyoshi TakedaLaboratory of Immune Regulation, Department of Microbiology and Immunology, Graduate School of Medicine, Osaka University, Suita, 565-0871, Japan.
Masaki MoriFaculty of Medicine, Tokai University School of Medicine, Isehara, 259-1193, Japan.
Kiyoshi AndoDepartment of Hematology/Oncology, Tokai University School of Medicine, Isehara, 259-1193, Japan.
Naoki HosenDepartment of Haematology and Oncology, Osaka University Graduate School of Medicine, Suita, 565-0871, Japan.ORCID 0000-0001-9570-0947
The University of Osaka · JPTokai University · JPOsaka International University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In patients undergoing haematopoietic stem-cell transplantation (HSCT), the intestinal microbiota plays an important role in prognosis, transplant outcome, and complications such as graft-versus-host disease (GVHD). Our prior research revealed that patients undergoing HSCT substantially differed from healthy controls. In this retrospective study, we showed that administering Clostridium butyricum MIYAIRI 588 (CBM588) as a live biotherapeutic agent is associated with maintaining intestinal microbiota in the early post-HSCT period. Alpha diversity, which reflects species richness, declined considerably in patients who did not receive CBM588, whereas it remained consistent in those who received CBM588. In addition, β-diversity analysis revealed that CBM588 did not alter the gut microbiota structure at 7-21 days post-HSCT. Patients who developed GVHD showed structural changes in their microbiota from the pre-transplant period, which was noticeable on day 14 before developing GVHD. Enterococcus was significantly prevalent in patients with GVHD after HSCT, and the population of Bacteroides was maintained from the pre-HSCT period through to the post-HSCT period. Patients who received CBM588 exhibited a contrasting trend, with lower relative abundances of both genera Enterococcus and Bacteroides. These results suggest that preoperative treatment with CBM588 could potentially be beneficial in maintaining intestinal microbiota balance.

Indexed as

Clostridium butyricumGastrointestinal MicrobiomeHematopoietic Stem Cell TransplantationAdultAgedFemaleGraft vs Host DiseaseHumansMaleMiddle AgedRetrospective Studies

Identifiers

PMID38431763
PMCPMC11161410
OpenAlexW4392348879

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.