Evidence map›Paper›PMID 37318072›Full record

Observational studyUnited European gastroenterology journal2023

How many biomarker measurements are needed to predict prognosis in Crohn's disease patients under infliximab?-A prospective study.

Fernando Magro, Maria Manuela Estevinho, Gaia Catalano, Marta Patita, Bruno Arroja, Paula Lago, Isadora Rosa, Helena Tavares de Sousa, Paula Ministro, Irina Mocanu and 16 more

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study in United European gastroenterology journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. UEG Journal and Impact on Clinical Practice.United European gastroenterology journal · 2024
    Article
  7. Article
  8. Biomarkers in inflammatory bowel disease: a practical guide.Therapeutic advances in gastroenterology · 2024
    Review
  9. Observational
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

26 authors.

Fernando MagroDepartment of Biomedicine, Unit of Pharmacology and Therapeutics, Faculty of Medicine, University of Porto, Porto, Portugal.ORCID 0000-0003-2634-9668
Maria Manuela EstevinhoDepartment of Biomedicine, Unit of Pharmacology and Therapeutics, Faculty of Medicine, University of Porto, Porto, Portugal.ORCID 0000-0001-7171-0139
Gaia CatalanoDepartment of Biomedicine, Unit of Pharmacology and Therapeutics, Faculty of Medicine, University of Porto, Porto, Portugal.
Marta PatitaDepartment of Gastroenterology, Garcia da Orta Hospital, Almada, Portugal.
Bruno ArrojaDepartment of Gastroenterology, Braga Hospital, Braga, Portugal.
Paula LagoDepartment of Gastroenterology, Porto Hospital University Centre, Porto, Portugal.
Isadora RosaDepartment of Gastroenterology, IPOLFG, EPE, Lisbon, Portugal.ORCID 0000-0002-2953-5987
Helena Tavares de SousaDepartment of Gastroenterology, Algarve Hospital University Centre - Portimão Unit, Portimão, Portugal.ORCID 0000-0002-6626-205X
Paula MinistroDepartment of Gastroenterology, Viseu-Tondela Hospital Centre, Viseu, Portugal.
Irina MocanuDepartment of Gastroenterology, Garcia da Orta Hospital, Almada, Portugal.
Ana VieiraDepartment of Gastroenterology, Garcia da Orta Hospital, Almada, Portugal.
Joana CastelaDepartment of Gastroenterology, IPOLFG, EPE, Lisbon, Portugal.
Joana MoleiroDepartment of Gastroenterology, IPOLFG, EPE, Lisbon, Portugal.
Joana RoseiraDepartment of Gastroenterology, Algarve Hospital University Centre - Portimão Unit, Portimão, Portugal.ORCID 0000-0002-5098-8729
Eugénia CancelaDepartment of Gastroenterology, Viseu-Tondela Hospital Centre, Viseu, Portugal.
Paula SousaDepartment of Gastroenterology, Viseu-Tondela Hospital Centre, Viseu, Portugal.
Francisco PortelaDepartment of Gastroenterology, Coimbra Hospital University Centre, Coimbra, Portugal.
Luís CorreiaDepartment of Gastroenterology, Northern Lisbon University Hospital Centre, Lisbon, Portugal.
Paula MoreiraUnidade de Farmacologia Clínica, São João Hospital University Centre, Porto, Portugal.
Mafalda SantiagoCenter for Health Technology and Services Research (CINTESIS), Porto, Portugal.
Sandra DiasPortuguese Group of Studies in Inflammatory Bowel Disease (Grupo de Estudos da Doença Inflamatória Intestinal - GEDII), Porto, Portugal.
Joana AfonsoDepartment of Biomedicine, Unit of Pharmacology and Therapeutics, Faculty of Medicine, University of Porto, Porto, Portugal.
Silvio DaneseDepartment of Biomedical Sciences, Humanitas University, Milan, Italy.
Laurent Peyrin-BirouletDepartment of Gastroenterology and Inserm NGERE U1256, University Hospital of Nancy, University of Lorraine, Nancy, France.ORCID 0000-0003-2536-6618
Cláudia Camila DiasCenter for Health Technology and Services Research (CINTESIS), Porto, Portugal.
GEDII (Grupo de Estudos da Doença Inflamatória Intestinal)

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTimely stratification of Crohn's disease (CD) is essential for patients' management. The use of noninvasive accurate biomarkers is key to monitor treatment and to pursue mucosal healing, the ultimate treatment endpoint in CD.

objectiveWe aimed to evaluate the performance of readily available biomarkers and develop risk matrices to predict CD progression.

methodsData from 289 CD patients receiving infliximab (IFX) maintenance therapy for 2 years was collected; those patients were included in DIRECT, a prospective multicenter observational study. Disease progression was evaluated using two composite outcomes incorporating clinical and drug-related factors, the first including IFX dose and/or frequency adjustments. Univariate and multivariable logistic regressions were used to calculate the odds ratios (OR) and to develop risk matrices.

resultsThe isolated presence of anemia at least once during follow-up was a significant predictor of disease progression (OR 2.436 and 3.396 [p ≤ 0.001] for composite outcomes 1 and 2, respectively) regardless of confounding factors. Isolated highly elevated C-reactive protein (CRP; >10.0 mg/L) and fecal calprotectin (FC; >500.0 μg/g) in at least one visit were also significant predictors, while milder elevations (3.1-10.0 mg/L and 250.1-500.0 μg/g) were only relevant when detected in at least two visits (consecutive or not). The combination of biomarkers in risk matrices had good ability to predict progression; patients simultaneously presenting anemia, highly elevated CRP and FC at least once had 42%-63% probability of achieving the composite outcomes.

conclusionThe combined evaluation of hemoglobin, CRP, and FC in at least one time point and their incorporation into risk matrices seems to be the optimal strategy for CD management, as data from additional visits did not meaningfully influence the predictions and may delay decision-making.

Indexed as

Crohn DiseaseBiomarkersDisease ProgressionHumansInfliximabPrognosisProspective StudiesBiomarkersInfliximabbiomarkerscalprotectinCrohn's diseaseinfliximab

Identifiers

PMID37318072
PMCPMC10337732

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.