Evidence map›Paper›PMID 39846163›Full record

ReviewArteriosclerosis, thrombosis, and vascular biology2025

Gut Microbiota Alterations in Patients With Kawasaki Disease.

Prasant K Jena, Moshe Arditi, Magali Noval Rivas

Abstract readReview
In one paragraph

Review in Arteriosclerosis, thrombosis, and vascular biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
–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

14 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  8. Recent advances in the positive role ofFrontiers in immunology · 2026
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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

3 authors.

Prasant K JenaDepartment of Pediatrics, Division of Pediatric Infectious Diseases, Guerin Children's (P.K.J., M.A., M.N.R.), Cedars-Sinai Medical Center, Los Angeles, CA.ORCID 0000-0002-6729-5881
Moshe Arditi *Department of Pediatrics, Division of Pediatric Infectious Diseases, Guerin Children's (P.K.J., M.A., M.N.R.), Cedars-Sinai Medical Center, Los Angeles, CA.ORCID 0000-0001-9042-2909
Magali Noval Rivas *Department of Pediatrics, Division of Pediatric Infectious Diseases, Guerin Children's (P.K.J., M.A., M.N.R.), Cedars-Sinai Medical Center, Los Angeles, CA.ORCID 0000-0001-5570-8928

Funding

Role of intestinal microbiome and gut permeability in the development of Kawasaki Disease vasculitisR01HL139766 · NHLBI · CEDARS-SINAI MEDICAL CENTER · PI Magali Noval Rivas · 2018 to 2026
$3.4M
Role of neutrophils and eosinophils in bacterial ligand-induced vasculitisR01AI157274 · NIAID · CEDARS-SINAI MEDICAL CENTER · PI ARDITI, MOSHE, NOVAL RIVAS, MAGALI · 2020 to 2024
$3.2M
RNA-Mediated Inter-Organelle Communication in AtherosclerosisR01HL149972 · NHLBI · CEDARS-SINAI MEDICAL CENTER · PI ARDITI, MOSHE · 2020 to 2023
$2.0M
Role of Sex in Immune Stromal cell Interactions driving cardiovascular lesions in Kawasaki Disease vasculitisR01HL170580 · NHLBI · CEDARS-SINAI MEDICAL CENTER · PI Moshe Arditi · 2024 to 2026
$1.7M
Targeting the Sirt-1 pathway to modulate inflammation during murine Kawasaki Disease vasculitisR01HL159297 · NHLBI · CEDARS-SINAI MEDICAL CENTER · PI NOVAL RIVAS, MAGALI · 2021 to 2024
$1.7M
NHLBI NIH HHS R01 HL139766NHLBI NIH HHS R01 HL149972NHLBI NIH HHS R01 HL159297NHLBI NIH HHS R01 HL170580NIAID NIH HHS R01 AI157274
6 · The paper itself

Abstract

The intestinal microbiota influences many host biological processes, including metabolism, intestinal barrier functions, and immune responses in the gut and distant organs. Alterations in its composition have been associated with the development of inflammatory disorders and cardiovascular diseases, including Kawasaki disease (KD). KD is an acute pediatric vasculitis of unknown etiology and the leading cause of acquired heart disease in children in the United States. The presence of gastrointestinal symptoms in the acute phase of KD has been associated with an increased risk of treatment resistance and the development of coronary artery aneurysms. Studies report alterations in fecal bacterial communities of patients with KD, characterized by the blooming of pathogenic bacteria and decreased relative abundance of short-chain fatty acid-producing bacteria. However, causality and functionality cannot be established from these observational patient cohorts of KD. This highlights the need for more advanced and rigorous studies to establish causality and functionality in both experimental models of KD vasculitis and patient cohorts. Here, we review the evidence linking an altered gut microbiota composition to the development of KD, assess the potential mechanisms involved in this process, and discuss the potential therapeutic value of these observations.

Indexed as

BacteriaGastrointestinal MicrobiomeIntestinesMucocutaneous Lymph Node SyndromeAnimalsDysbiosisHumansantibacterial agentscoronary vesselsmetagenomicsmicrobiotamucocutaneous lymph node syndrome

Identifiers

PMID39846163
PMCPMC11998981

What OpenQuestion holds

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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 OpenQuestion graph.