Evidence map›Paper›PMID 37158577›Full record

Observational studyInflammatory bowel diseases2024

Higher Ustekinumab Levels in Maintenance Therapy are Associated with Greater Mucosal Healing and Mucosal Response in Crohn's Disease: An Experience of 2 IBD Centers.

Ciarán McDonald, Hilary Kerr, Eimear Gibbons, Tincymol Lukose, Danny Cheriyan, Gavin Harewood, Stephen Patchett, Aoibhlinn O'Toole, Orlaith Kelly, Karen Boland

Open access · hybridAbstract readObservational Study
In one paragraph

Observational study in Inflammatory bowel diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
6.6field-weighted citation impact, top 3% of its field
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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Guideline
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  9. Key Interleukins in Inflammatory Bowel Disease-A Review of Recent Studies.International journal of molecular sciences · 2024
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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

10 authors at 2 institutions in 1 country.

Ciarán McDonaldDepartment of Gastroenterology, Beaumont Hospital, RCSI Hospital Group, Dublin 9, Ireland.ORCID 0000-0001-8597-0222
Hilary KerrDepartment of Gastroenterology, James Connolly Hospital, RCSI Hospital Group, Dublin 15, Ireland.
Eimear GibbonsDepartment of Gastroenterology, James Connolly Hospital, RCSI Hospital Group, Dublin 15, Ireland.
Tincymol LukoseDepartment of Gastroenterology, Beaumont Hospital, RCSI Hospital Group, Dublin 9, Ireland.
Danny CheriyanDepartment of Gastroenterology, Beaumont Hospital, RCSI Hospital Group, Dublin 9, Ireland.
Gavin HarewoodDepartment of Gastroenterology, Beaumont Hospital, RCSI Hospital Group, Dublin 9, Ireland.
Stephen PatchettDepartment of Gastroenterology, Beaumont Hospital, RCSI Hospital Group, Dublin 9, Ireland.
Aoibhlinn O'TooleDepartment of Gastroenterology, Beaumont Hospital, RCSI Hospital Group, Dublin 9, Ireland.
Orlaith KellyDepartment of Gastroenterology, James Connolly Hospital, RCSI Hospital Group, Dublin 15, Ireland.
Karen BolandDepartment of Gastroenterology, Beaumont Hospital, RCSI Hospital Group, Dublin 9, Ireland.
Beaumont Hospital · IEConnolly Hospital Blanchardstown · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundUstekinumab (UST), a human monoclonal antibody that binds the p40 subunit of interleukin 12 (IL-12) and IL-23, is licensed for induction and maintenance therapy of moderate to severe inflammatory bowel disease (IBD). To date, there is limited data published on any potential association between ustekinumab serum trough levels and mucosal healing in order to guide treatment strategies and appropriate dosing.

aimThis study aims to identify a relationship between maintenance ustekinumab serum trough levels and mucosal healing and/or response in patients with Crohn's disease in an observational cohort study.

methodsUstekinumab serum trough levels and antibody titres were analyzed in patients on maintenance drug using an ELISA drug-tolerant assay. Mucosal response (MR) was defined as ≥50% reduction in fecal calprotectin level (FC) and/or ≥50% reduction in the Simple Endoscopic Score for Crohn's Disease (SES-CD score). Mucosal healing (MH) was defined as FC ≤150 µg/mL and/or global SES-CD score ≤5. Median trough levels were analyzed using the Kruskal-Wallis test, and logistic regression was used to determine sensitivity and specificity of levels predicting mucosal response.

resultsForty-seven patients on maintenance ustekinumab for Crohn's disease were included in this study. The majority were female (66%), with a median age of 40 years (21-78 years). The majority of patients were biologic-experienced (89.4%, n = 42). Patients with histologically confirmed Crohn's disease represented 100% (n = 47) of the cohort. Over one-third of patients (n = 18, 38.3%) were on higher than standard dosing of 90 mg every 8 weeks. Patients with mucosal healing (n = 30) had significantly higher mean serum ustekinumab levels (5.7 µg/mL, SD 6.4) compared with those with no response (1.1 µg/mL, SD 0.52; n = 7, P < .0001). A serum ustekinumab trough level greater than 2.3 µg/mL was associated with MH, with a sensitivity of 100% and specificity of 90.6% (likelihood ratio 10.7). Similarly, for patients with MR (n = 40), we observed a higher mean serum ustekinumab trough level (5.1 µg/mL, SD 6.1) compared with those with no response (1.1 µg/mL, SD 0.52; n = 7, P < .0001). Furthermore, a serum ustekinumab trough level greater than 2.3 µg/mL was associated with a 10-fold increased likelihood of mucosal response vs mucosal nonresponse (sensitivity 100%, specificity 90.5%, likelihood ratio 10.5).

conclusionThis study demonstrates that higher ustekinumab serum trough levels are associated with a greater likelihood of achieving mucosal healing and mucosal response in patients with Crohn's disease regardless of prior biologic exposure. Further prospective studies are required to correlate target maintenance trough levels and the optimal time to dose-escalate in order to improve patient outcomes.

Indexed as

Biological ProductsCrohn DiseaseInflammatory Bowel DiseasesAdultFemaleHumansInterleukin-12Leukocyte L1 Antigen ComplexMaleUstekinumabBiological ProductsInterleukin-12Leukocyte L1 Antigen ComplexUstekinumabCrohn’s diseaseinflammatory bowel diseasemucosal healingmucosal responsetherapeutic drug monitoringustekinumab

Identifiers

PMID37158577
PMCPMC10906356
OpenAlexW4375956223

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.