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Gut-microbiota-based ensemble model predicts prognosis of pediatric inflammatory bowel disease.

作者信息

Ha Sung Min, Lee Kihyun, Kim Gun-Ha, Hurych Jakub, Cinek Ondřej, Shim Jung Ok

机构信息

Department of Integrative Biology and Physiology, UCLA, Los Angeles, CA 957246, USA.

CJ Bioscience, Seoul 04527, Republic of Korea.

出版信息

iScience. 2024 Nov 22;27(12):111442. doi: 10.1016/j.isci.2024.111442. eCollection 2024 Dec 20.


DOI:10.1016/j.isci.2024.111442
PMID:39691780
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11650326/
Abstract

Developing microbiome-based markers for pediatric inflammatory bowel disease (PIBD) is challenging. Here, we evaluated the diagnostic and prognostic potential of the gut microbiome in PIBD through a case-control study and cross-cohort analyses. In a Korean PIBD cohort (24 patients with PIBD, 43 controls), we observed that microbial diversity and composition shifted in patients with active PIBD versus controls and recovered at remission. We employed a differential abundance meta-analysis approach to identify microbial markers consistently associated with active inflammation and remission across seven PIBD cohorts from six countries ( = 1,670) including our dataset. Finally, we trained and tested various machine learning models for their ability to predict a patient's future remission based on baseline bacterial composition. An ensemble model trained with the amplicon sequence variants effectively predicted future remission of PIBD. This research highlights the gut microbiome's potential to guide precision therapy for PIBD.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/552c/11650326/3d9d67b7725b/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/552c/11650326/695e79e5849d/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/552c/11650326/16aa410c0adc/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/552c/11650326/f7e7f73a2344/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/552c/11650326/f90c040636da/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/552c/11650326/8573153ac770/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/552c/11650326/da2db02fc493/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/552c/11650326/3d9d67b7725b/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/552c/11650326/695e79e5849d/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/552c/11650326/16aa410c0adc/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/552c/11650326/f7e7f73a2344/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/552c/11650326/f90c040636da/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/552c/11650326/8573153ac770/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/552c/11650326/da2db02fc493/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/552c/11650326/3d9d67b7725b/gr6.jpg

相似文献

[1]
Gut-microbiota-based ensemble model predicts prognosis of pediatric inflammatory bowel disease.

iScience. 2024-11-22

[2]
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[3]
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[4]
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[5]
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[6]
Identification of FCN1 as a novel macrophage infiltration-associated biomarker for diagnosis of pediatric inflammatory bowel diseases.

J Transl Med. 2023-3-17

[7]
Medical Management of Pediatric Inflammatory Bowel Disease (PIBD) in the Asia Pacific Region: A Position Paper by the Asian Pan-Pacific Society for Pediatric Gastroenterology, Hepatology, and Nutrition (APPSPGHAN) PIBD Working Group.

J Gastroenterol Hepatol. 2022-12-27

[8]
Management and monitoring of pediatric inflammatory bowel disease in the Asia-Pacific region: A position paper by the Asian Pan-Pacific Society for Pediatric Gastroenterology, Hepatology, and Nutrition (APPSPGHAN) PIBD Working Group: Surgical management, disease monitoring, and special considerations.

J Gastroenterol Hepatol. 2023-4

[9]
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[10]
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Inflamm Bowel Dis. 2024-1-5

引用本文的文献

[1]
Human DNA levels in feces reflect gut inflammation and associate with presence of gut species in IBD patients across the age spectrum.

Res Sq. 2025-7-7

[2]
Evolution of inflammatory bowel disease in Korea: a 60-year perspective on clinical and research development.

Intest Res. 2025-7

本文引用的文献

[1]
, a butyrate-producing bacterium capable of metabolizing 5-fluorouracil.

mSphere. 2024-4-23

[2]
Faecal Bacteriome and Metabolome Profiles Associated with Decreased Mucosal Inflammatory Activity Upon Anti-TNF Therapy in Paediatric Crohn's Disease.

J Crohns Colitis. 2024-1-27

[3]
Gut Bacterial Dysbiosis in Irritable Bowel Syndrome: a Case-Control Study and a Cross-Cohort Analysis Using Publicly Available Data Sets.

Microbiol Spectr. 2023-2-14

[4]
Klebsiella pneumoniae Induces Inflammatory Bowel Disease Through Caspase-11-Mediated IL18 in the Gut Epithelial Cells.

Cell Mol Gastroenterol Hepatol. 2023

[5]
Population structure discovery in meta-analyzed microbial communities and inflammatory bowel disease using MMUPHin.

Genome Biol. 2022-10-3

[6]
Intercontinental Gut Microbiome Variances in IBD.

Int J Mol Sci. 2022-9-17

[7]
Quantitative Fecal Microbiota Profiles Relate to Therapy Response During Induction With Tumor Necrosis Factor α Antagonist Infliximab in Pediatric Inflammatory Bowel Disease.

Inflamm Bowel Dis. 2023-1-5

[8]
Butyrate-producing Eubacterium rectale suppresses lymphomagenesis by alleviating the TNF-induced TLR4/MyD88/NF-κB axis.

Cell Host Microbe. 2022-8-10

[9]
Treatment patterns of anti-tumour necrosis factor-alpha and prognosis of paediatric and adult-onset inflammatory bowel disease in Korea: a nationwide population-based study.

Aliment Pharmacol Ther. 2022-9

[10]
Machine Learning Based Microbiome Signature to Predict Inflammatory Bowel Disease Subtypes.

Front Microbiol. 2022-5-17

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