Evidence map›Paper›PMID 39248279›Full record

ArticleJournal of the American Heart Association2024

Gut Dysbiosis in Patients With Fontan Circulation.

Hideo Ohuchi, Ryotaro Asano, Aki Mori, Tomohiko Ishibashi, Daisuke Motooka, Michikazu Nakai, Yoshikazu Nakaoka

Abstract read
In one paragraph

Article in Journal of the American Heart Association, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Fontan-Associated Liver Disease.Seminars in liver disease · 2025
    Review
  14. Review
  15. Article
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

7 authors.

Hideo OhuchiDepartment of Pediatric Cardiology National Cerebral and Cardiovascular Center Suita Japan.ORCID 0000-0001-7092-4792
Ryotaro AsanoDepartment of Vascular Physiology National Cerebral and Cardiovascular Center Research Institute Suita Japan.ORCID 0000-0003-0303-6546
Aki MoriDepartment of Pediatric Cardiology National Cerebral and Cardiovascular Center Suita Japan.
Tomohiko IshibashiDepartment of Vascular Physiology National Cerebral and Cardiovascular Center Research Institute Suita Japan.ORCID 0000-0003-1953-5016
Daisuke MotookaDepartment of Infection Metagenomics, Research Institute for Microbial Diseases Osaka University Suita Japan.ORCID 0000-0002-4616-9608
Michikazu NakaiClinical Research Support Center University of Miyazaki Hospital Miyazaki Japan.ORCID 0000-0003-2240-1510
Yoshikazu NakaokaDepartment of Vascular Physiology National Cerebral and Cardiovascular Center Research Institute Suita Japan.ORCID 0000-0002-8404-2587

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe process underlying Fontan pathophysiology is multifactorial and may include gut dysbiosis (GD). We investigated the presence of GD and elucidated its correlation with Fontan pathophysiology. METHODS AND

resultsGut microbiomes of 155 consecutive patients with Fontan pathophysiology and 44 healthy individuals were analyzed using 16S rRNA sequencing of bacterial DNA extracted from fecal samples. GD was evaluated on the basis of α and ß diversities of the gut microbiome and was compared with natural log-transformed C-reactive protein, hemodynamics, von Willebrand factor antigen (a bacterial translocation marker), Mac-2 binding protein glycosylation isomer (a liver fibrosis indicator), peak oxygen uptake, and heart failure hospitalization. Patients with Fontan exhibited GD in terms of α and ß diversities as compared with controls (

conclusionsPatients with Fontan pathophysiology exhibited GD compared with healthy individuals, and GD was linked to failed hemodynamics and systemic inflammation with a poor prognosis. Therefore, GD may play a pivotal role in a failing Fontan status, including Fontan-associated liver disease, through GD-associated systemic inflammation.

Indexed as

DysbiosisFontan ProcedureGastrointestinal MicrobiomeAdolescentAdultBiomarkersCase-Control StudiesChildFecesFemaleHeart Defects, CongenitalHemodynamicsHumansMaleYoung AdultBiomarkersFontanFontan‐associated liver diseasegut dysbiosisheart failurehemodynamics

Identifiers

PMID39248279
PMCPMC11935625

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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 Socratic graph.