Evidence map›Paper›PMID 39187879›Full record

ArticleGut pathogens2024

Dynamic changes in the gut microbiota composition during adalimumab therapy in patients with ulcerative colitis: implications for treatment response prediction and therapeutic targets.

Han Na Oh, Seung Yong Shin, Jong-Hwa Kim, Jihye Baek, Hyo Jong Kim, Kang-Moon Lee, Soo Jung Park, Seok-Young Kim, Hyung-Kyoon Choi, Wonyong Kim and 2 more

Abstract read
In one paragraph

Article in Gut pathogens, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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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

12 authors.

Han Na Oh *Department of Systems Biotechnology, Chung-Ang University, Anseong, 17546, Republic of Korea.
Seung Yong Shin *Department of Internal Medicine, Chung-Ang University College of Medicine, 102 Heukseok-Ro, Dongjak-Gu, Seoul, Republic of Korea, 06973.
Jong-Hwa Kim *Department of Microbiology, Chung-Ang University College of Medicine, Seoul, Republic of Korea.
Jihye BaekDepartment of Microbiology, Chung-Ang University College of Medicine, Seoul, Republic of Korea.
Hyo Jong KimDepartment of Gastroenterology, Kyung Hee University Hospital, Seoul, Republic of Korea.
Kang-Moon LeeDepartment of Gastroenterology, The Catholic University of Korea St. Vincent's Hospital, Suwon, Republic of Korea.
Soo Jung ParkDepartment of Internal Medicine and Institute of Gastroenterology, Yonsei University College of Medicine, Seoul, Republic of Korea.
Seok-Young KimCollege of Pharmacy, Chung-Ang University, Seoul, Republic of Korea.
Hyung-Kyoon ChoiCollege of Pharmacy, Chung-Ang University, Seoul, Republic of Korea.
Wonyong KimDepartment of Microbiology, Chung-Ang University College of Medicine, Seoul, Republic of Korea.
Woo Jun SulDepartment of Systems Biotechnology, Chung-Ang University, Anseong, 17546, Republic of Korea. sulwj@cau.ac.kr.
Chang Hwan ChoiDepartment of Internal Medicine, Chung-Ang University College of Medicine, 102 Heukseok-Ro, Dongjak-Gu, Seoul, Republic of Korea, 06973. gicch@cau.ac.kr.

Funding

AbbVie and the National Research Foundation of Korea (NRF) NRF-2017R1D1A1B03031924
6 · The paper itself

Abstract

backgroundWhile significant research exists on gut microbiota changes after anti-tumor necrosis factor-alpha (anti TNF-α) therapy for ulcerative colitis, little is known about the longitudinal changes related to the effects of anti TNF-α. This study aimed to investigate the dynamics of gut microbiome changes during anti TNF-α (adalimumab) therapy in patients with ulcerative colitis (UC).

resultsThe microbiota composition was affected by the disease severity and extent in patients with UC. Regardless of clinical remission status at each time point, patients with UC exhibited microbial community distinctions from healthy controls. Distinct amplicon sequence variants (ASVs) differences were identified throughout the course of Adalimumab (ADA) treatment at each time point. A notable reduction in gut microbiome dissimilarity was observed only in remitters. Remitters demonstrated a decrease in the relative abundances of Burkholderia-Caballeronia-Paraburkholderia and Staphylococcus as the treatment progressed. Additionally, there was an observed increase in the relative abundances of Bifidobacterium and Dorea. Given the distribution of the 48 ASVs with high or low relative abundances in the pre-treatment samples according to clinical remission at week 8, a clinical remission at week 8 with a sensitivity and specificity of 72.4% and 84.3%, respectively, was predicted on the receiver operating characteristic curve (area under the curve, 0.851).

conclusionsThe gut microbiota undergoes diverse changes according to the treatment response during ADA treatment. These changes provide insights into predicting treatment responses to ADA and offer new therapeutic targets for UC.

Indexed as

MicrobiomeTumor necrosis factor inhibitorUlcerative colitis

Identifiers

PMID39187879
PMCPMC11346184

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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.