Evidence map›Paper›PMID 39657589›Full record

ArticleJournal of Crohn's & colitis2025

Diverse Phenotypes, Consistent Treatment: A Study of 30 997 South Asian and White Inflammatory Bowel Disease Patients Using the UK Inflammatory Bowel Disease BioResource.

Sharmili Balarajah, Laura Martinez-Gili, James Leslie Alexander, Benjamin Harvey Mullish, Robert William Perry, Jia V Li, Julian Roberto Marchesi, Miles Parkes, Timothy Robin Orchard, Lucy Charlotte Hicks and 1 more

Abstract read
In one paragraph

Article in Journal of Crohn's & colitis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Observational
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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

11 authors.

Sharmili BalarajahDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.ORCID 0000-0003-0229-8528
Laura Martinez-GiliDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
James Leslie AlexanderDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.ORCID 0000-0001-8542-327X
Benjamin Harvey MullishDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.ORCID 0000-0001-6300-3100
Robert William PerryDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
Jia V LiDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
Julian Roberto MarchesiDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
Miles ParkesDepartment of Medicine, University of Cambridge, Cambridge, UK.
Timothy Robin OrchardDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
Lucy Charlotte HicksDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
Horace Richard Timothy WilliamsDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.

Funding

Bowel Research UKImperial Biomedical Research CentreNational Institute for Health Research
6 · The paper itself

Abstract

backgroundStudies in the UK and North America have suggested a distinct disease profile in South Asians compared to that of White populations. Disparities in the medical and surgical management of IBD in minority ethnic groups (including Black Americans and Asians) in the US have been shown, while data from Europe, including the UK, have been lacking. This study sought to evaluate South Asian (SA) and White (WH) inflammatory bowel disease (IBD) phenotypes, and to explore treatment approach variations between these cohorts in the UK using the IBD BioResource database.

designDifferences between WH and SA IBD patients were analysed using demographic, phenotypic and outcome data. Drug utilisation patterns and surgical outcomes were assessed in propensity score-matched (PSM) cohorts with multivariable logistic regression, Cox regression and Kaplan-Meier analysis.

results30,997 eligible patients were included. UC was the predominant disease subtype in SA (p<0.001). SA were younger at diagnosis (p<0.001), had a male preponderance (p<0.001), and were less likely to have a smoking history at diagnosis. The SA CD phenotype differed from WH, with less ileal (SA 30.3%, WH 38.4%, p=0.008) and stricturing (SA 16.9%, WH 25.6%, p<0.001) disease, but more perianal disease (SA 38.5%, WH 32.2%, p=0.009). More SA UC patients had extensive disease (SA 41.7%, WH 34.1%, p<0.001). In PSM cohorts, comparing treatments, there were no differences in 5-aminosalicylate, corticosteroid, thiopurine, anti-TNF or vedolizumab use. Survival analysis in matched cohorts showed no difference in time to surgery (CD) or colectomy (UC), and SA ethnicity was not associated with a difference in risk of surgery/colectomy.

conclusionDemographic and phenotypic differences exist between UK SA and WH IBD patients, highlighting distinct ethnicity-related variance, and the need for a research focus on under-represented populations. In comparing matched SA and WH patients, no disparity in medical and surgical IBD therapy in UK healthcare has been demonstrated: treatment is consistent regardless of ethnicity.

Indexed as

Colitis, UlcerativeCrohn DiseaseInflammatory Bowel DiseasesSouth Asian PeopleWhite PeopleAdultAntibodies, Monoclonal, HumanizedFemaleHumansMaleMiddle AgedPhenotypeUnited KingdomAntibodies, Monoclonal, HumanizedCrohn’s diseaseethnicityIBD BioResourcephenotypeSouth Asiantreatmentulcerative colitis

Identifiers

PMID39657589
PMCPMC11737890

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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.