Evidence map›Paper›PMID 41274279›Full record

ArticleInflammatory bowel diseases2026

Differences in Anti-αvβ6 Integrin Antibody Expression between U.S. and Japanese Cohorts in Inflammatory Bowel Disease.

Yoichi Kakuta, Dalin Li, Philip Debbas, Soshi Okazaki, Motoi Sawahashi, Shaohong Yang, Hideya Iwaki, Daisuke Okamoto, Hiroshi Nagai, Yusuke Shimoyama and 9 more

Abstract readComparative Study
In one paragraph

Article in Inflammatory bowel diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

19 authors.

Yoichi KakutaDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, 980-8574, Japan.ORCID 0000-0002-7042-009X
Dalin LiF. Widjaja Inflammatory Bowel Disease Institute, Cedars-Sinai Medical Center, Los Angeles, CA, 90048, United States.
Philip DebbasF. Widjaja Inflammatory Bowel Disease Institute, Cedars-Sinai Medical Center, Los Angeles, CA, 90048, United States.
Soshi OkazakiDepartment of Rheumatology, Tohoku University Hospital, Sendai, 980-8574, Japan.
Motoi SawahashiDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, 980-8574, Japan.
Shaohong YangF. Widjaja Inflammatory Bowel Disease Institute, Cedars-Sinai Medical Center, Los Angeles, CA, 90048, United States.
Hideya IwakiDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, 980-8574, Japan.
Daisuke OkamotoDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, 980-8574, Japan.
Hiroshi NagaiDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, 980-8574, Japan.
Yusuke ShimoyamaDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, 980-8574, Japan.
Takeo NaitoDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, 980-8574, Japan.
Rintaro MoroiDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, 980-8574, Japan.
Masatake KurohaDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, 980-8574, Japan.
Hisashi ShigaDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, 980-8574, Japan.
Yoshitaka KinouchiStudent Healthcare Center, Institute for Excellence in Higher Education, Tohoku University, Sendai, 980-8576, Japan.
Tsuyoshi ShiraiDepartment of Rheumatology, Tohoku University Hospital, Sendai, 980-8574, Japan.ORCID 0000-0002-6295-3494
Hiroshi FujiiDepartment of Rheumatology, Tohoku University Hospital, Sendai, 980-8574, Japan.ORCID 0000-0002-6885-6492
Dermot P B McGovernF. Widjaja Inflammatory Bowel Disease Institute, Cedars-Sinai Medical Center, Los Angeles, CA, 90048, United States.
Atsushi MasamuneDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, 980-8574, Japan.

Funding

F. Widjaja Inflammatory Bowel Disease Institute of Cedars-Sinai Medical CenterIntractable Diseases from the Ministry of Health, Labour and Welfare of Japan U01DK062413Japan Society for the Promotion of ScienceJapan Society for the Promotion of Science 21K08469KAKENHI 21K08469Labor Sciences Research Grants for ResearchMedical & Biological Laboratories Co., Ltd.Tohoku University
6 · The paper itself

Abstract

backgroundInflammatory bowel diseases (IBDs), including ulcerative colitis (UC) and Crohn's disease (CD), have complex pathologies requiring precise diagnostic tools. We evaluated the clinical utility of anti-integrin αvβ6 antibodies in diagnosing UC, focusing on differences between a U.S. cohort (self-reported White) and a Japanese cohort, and additionally assessed whether combining anti-αvβ6 with anti-EPCR improved diagnostic performance.

methodsSerum anti-αvβ6 antibody levels were measured in 1138 participants (514 in the U.S. cohort, 624 in the Japanese cohort), including 1093 IBD cases and 45 healthy control subjects. Positivity rates and titers were compared between cohorts, and associations with clinical subphenotypes and anti-EPCR were examined.

resultsAnti-αvβ6 positivity was significantly higher in UC patients (85.4%) than in CD patients (16.4%) or control subjects (0%). Within UC, high positivity was observed across all disease extents, with only minor cohort differences. Longer disease duration was associated with lower positivity in both cohorts. In CD, the U.S. cohort showed higher positivity (23.4%) than the Japanese cohort (10.1%), particularly in colonic CD. Absence of ileal involvement, strictures, or perianal disease was associated with higher positivity. Anti-αvβ6 and anti-EPCR levels were strongly correlated, but their expression patterns differed in primary sclerosing cholangitis-associated IBD. Combining anti-αvβ6 and anti-EPCR improved UC diagnostic accuracy (area under the curve, 0.98; 95% confidence interval, 0.95-1.00) over either antibody alone (P = .00264).

conclusionsAnti-αvβ6 is a valuable biomarker for UC diagnosis. However, this study demonstrated differences in its behavior between U.S. and Japanese cohorts, particularly in CD. Cohort-informed interpretation and combined antibody testing may improve diagnostic precision and disease stratification in IBD.

Indexed as

Antigens, NeoplasmColitis, UlcerativeCrohn DiseaseIntegrinsAdultAgedBiomarkersCase-Control StudiesCohort StudiesFemaleHumansJapanMaleMiddle AgedUnited StatesYoung AdultAntigens, NeoplasmBiomarkersintegrin alphavbeta6Integrinsanti-EPCR antibodyanti-integrin αvβ6 antibodyCrohn’s diseaseulcerative colitis

Identifiers

PMID41274279
PMCPMC12759057

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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.