Evidence map›Paper›PMID 29516410›Full record

ArticleAdvances in therapy2018

Adalimumab Reduces Extraintestinal Manifestations in Patients with Crohn's Disease: A Pooled Analysis of 11 Clinical Studies.

Edouard J Louis, Walter Reinisch, David A Schwartz, Robert Löfberg, Anne M Robinson, Sofie Berg, Anthony W Wang, Jen-Fue Maa, Bidan Huang, Brandee Pappalardo

Open access · hybridAbstract read
In one paragraph

Article in Advances in therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

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  7. Positioning biologics in the treatment of IBD: A practical guideCurrent research in pharmacology and drug discovery · 2022
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  13. Pulmonary Extraintestinal Manifestation of Crohn's Disease Treated Successfully with Adalimumab.The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi · 2018
    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

10 authors at 5 institutions in 5 countries.

Edouard J LouisUniversity Hospital CHU of Liège, Liège, Belgium. edouard.louis@ulg.ac.be.
Walter ReinischMcMaster University, Hamilton, ON, Canada.
David A SchwartzVanderbilt University, Nashville, TN, USA.
Robert LöfbergKarolinska Institutet, Sophiahemmet, Stockholm, Sweden.
Anne M RobinsonAbbVie Inc., North Chicago, IL, USA.
Sofie BergAbbVie Inc., North Chicago, IL, USA.
Anthony W WangAbbVie Inc., North Chicago, IL, USA.
Jen-Fue MaaAbbVie Inc., North Chicago, IL, USA.
Bidan HuangAbbVie Inc., North Chicago, IL, USA.
Brandee PappalardoAbbVie Inc., North Chicago, IL, USA.
AbbVie (United States) · USCentre Hospitalier Universitaire de Liège · BEKarolinska Institutet · SEMedical University of Vienna · ATVanderbilt University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionExtraintestinal manifestations (EIMs) in patients with Crohn's disease (CD) are common and associated with additional morbidity. This study aimed to evaluate the effect of adalimumab therapy on EIM resolution and identify potential predictors of EIM resolution in adult and pediatric patients with moderate to severe CD.

methodsEIM data were pooled from 11 induction, maintenance, and open-label extension studies of adalimumab. Resolution of EIMs was evaluated at approximately 6 months and 1 year. Median time to initial EIM resolution and first EIM recurrence (reflecting durable resolution) of any EIM and specific categories of EIMs (arthritis/arthralgia, ocular, cutaneous) were calculated. A Cox model was used to determine predictors of initial and durable EIM resolution.

resultsAt baseline, 54% (1137/2094) of patients receiving adalimumab and 51% (297/586) receiving placebo had EIMs. EIM resolution occurred in a significantly greater proportion of adalimumab versus placebo patients at 6 months (54% vs 31%; P < .001) and 1 year (60% vs 42%; P = .008). Median time to initial resolution of any EIM, arthritis/arthralgia, and cutaneous EIMs was significantly shorter in patients receiving adalimumab versus placebo. Durable resolution of any EIM and arthritis/arthralgia was significantly longer for patients receiving adalimumab versus placebo. Clinically meaningful predictors of EIM resolution included adalimumab treatment, male sex, and moderate (versus severe) disease activity at baseline.

conclusionAdalimumab is effective for achieving initial and durable resolution of any EIM and, in particular, arthritis/arthralgia in patients with moderate to severe CD. Predictors of EIM resolution included adalimumab treatment and moderate disease severity.

fundingAbbVie.

Indexed as

AdalimumabArthritisChronic DiseaseCrohn DiseaseEye DiseasesHumansSkin DiseasesAdalimumabAdalimumabArthralgiaArthritisCDAICrohn’s diseaseExtraintestinal manifestationGastroenterologyInflammatory bowel disease

Identifiers

PMID29516410
PMCPMC5910478
OpenAlexW2790983276

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.