Evidence map›Paper›PMID 42630711›Full record

ArticleCrohn's & colitis 3602026

Serum leucine-rich α-2-glycoprotein and monocyte chemoattractant protein-1 as novel biomarkers for predicting vedolizumab response in patients with ulcerative colitis.

Takeo Yoshihara, Shinichiro Shinzaki, Tetsuji Naka, Hideki Iijima, Yoshito Hayashi, OGF study group, Kaori Ishiguro, Yuji Baba, Tetsuo Takehara, OGF study group

Abstract read
In one paragraph

Article in Crohn's & colitis 360, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Takeo YoshiharaDepartment of Gastroenterology and Hepatology, The University of Osaka, Graduate School of Medicine, Osaka 565-0871, Japan.ORCID https://orcid.org/0000-0003-0131-9294
Shinichiro ShinzakiDepartment of Gastroenterology, Hyogo Medical University School of Medicine, Hyogo 663-8501, Japan.ORCID https://orcid.org/0000-0002-7051-618X
Tetsuji NakaInstitute for Biomedical Sciences Molecular Pathophysiology, Iwate Medical University, Iwate 028-3694, Japan.
Hideki IijimaDepartment of Gastroenterology and Hepatology, The University of Osaka, Graduate School of Medicine, Osaka 565-0871, Japan.ORCID https://orcid.org/0000-0002-5423-3059
Yoshito HayashiDepartment of Gastroenterology and Hepatology, The University of Osaka, Graduate School of Medicine, Osaka 565-0871, Japan.ORCID https://orcid.org/0000-0003-4168-3322
OGF study group
Kaori IshiguroJapan Medical Office, Takeda Pharmaceutical Company Limited, Tokyo 103-8668, Japan.
Yuji BabaJapan Medical Office, Takeda Pharmaceutical Company Limited, Tokyo 103-8668, Japan.
Tetsuo TakeharaDepartment of Gastroenterology and Hepatology, The University of Osaka, Graduate School of Medicine, Osaka 565-0871, Japan.ORCID https://orcid.org/0000-0001-5036-3457
OGF study group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aims: Effective, minimally invasive biomarkers are needed to predict treatment outcomes in ulcerative colitis (UC). This multicenter observational study investigated predictive serum and genetic biomarkers for vedolizumab (VDZ) therapy in UC, including serum leucine-rich α-2-glycoprotein (LRG), cytokines, and differentially expressed genes (DEGs) in intestinal tissue. Methods: Eligible patients (18-80 years; moderately to severely active UC) received intravenous VDZ (300 mg; Weeks 0, 2, 6, then every 8 weeks through Week 54). Serum biomarkers were compared between those who did/did not achieve clinical remission (CR; full Mayo score ≤2, all subscores ≤1) or mucosal healing (MH; Mayo endoscopic subscore ≤1) at Week 14. Week 0 inflammatory tissue data were stratified by Week 14 VDZ effect (CR and complete-MH [Mayo endoscopic subscore = 0]) for DEGs. Results: Overall, 21 patients were included. Mean serum LRG was significantly lower in the CR ( Conclusions: Serum LRG and MCP-1 may be candidate biomarkers of VDZ treatment response in UC.

Indexed as

colitisinflammatory bowel diseaseleucine-rich α-2-glycoproteinulcerative

Identifiers

PMID42630711
PMCPMC13495107

What Socratic holds

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Registered trials

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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 Socratic graph.