Evidence map›Paper›PMID 33709340›Full record

Observational studyPaediatric drugs2021

Is It Useful to Monitor Thiopurine Metabolites in Pediatric Patients with Crohn's Disease on Combination Therapy? A Multicenter Prospective Observational Study.

Kristyna Pospisilova, Jitka Siroka, Eva Karaskova, Ondrej Hradsky, Tereza Lerchova, Kristyna Zarubova, Ivana Copova, Lucie Gonsorcikova, Maria Velganova-Veghova, Irena Francova and 4 more

Abstract readMulticenter StudyObservational Study
PubMed Publisher
In one paragraph

Observational study in Paediatric drugs, 2021. 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, top 97% 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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. Review
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

14 authors at 4 institutions in 1 country.

Kristyna PospisilovaDepartment of Pediatrics, 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital, V Uvalu 84, 150 06, Prague 5, Czech Republic. potuznikovakris@gmail.com.
Jitka SirokaLaboratory of Growth Regulators, Palacky University Olomouc and Institute of Experimental Botany AS CR, Slechtitelu 27, 783 71, Olomouc, Czech Republic.
Eva KaraskovaDepartment of Pediatrics, Faculty of Medicine and Dentistry, Palacky University and University Hospital, I.P. Pavlova 185/6, 779 00, Olomouc, Czech Republic.
Ondrej HradskyDepartment of Pediatrics, 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital, V Uvalu 84, 150 06, Prague 5, Czech Republic.
Tereza LerchovaDepartment of Pediatrics, 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital, V Uvalu 84, 150 06, Prague 5, Czech Republic.
Kristyna ZarubovaDepartment of Pediatrics, 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital, V Uvalu 84, 150 06, Prague 5, Czech Republic.
Ivana CopovaDepartment of Pediatrics, 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital, V Uvalu 84, 150 06, Prague 5, Czech Republic.
Lucie GonsorcikovaDepartment of Pediatrics, 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital, V Uvalu 84, 150 06, Prague 5, Czech Republic.
Maria Velganova-VeghovaDepartment of Pediatrics, Faculty of Medicine and Dentistry, Palacky University and University Hospital, I.P. Pavlova 185/6, 779 00, Olomouc, Czech Republic.
Irena FrancovaInstitute of Medical Biochemistry and Laboratory Diagnosis, General University Hospital and 1st Faculty of Medicine, Charles University in Prague, Na Bojisti 3, Prague 2, 121 08, Prague, Czech Republic.
Lubor UrbanekLaboratory of Growth Regulators, Palacky University Olomouc and Institute of Experimental Botany AS CR, Slechtitelu 27, 783 71, Olomouc, Czech Republic.
Milos GerykDepartment of Pediatrics, Faculty of Medicine and Dentistry, Palacky University and University Hospital, I.P. Pavlova 185/6, 779 00, Olomouc, Czech Republic.
Vladimir MihalDepartment of Pediatrics, Faculty of Medicine and Dentistry, Palacky University and University Hospital, I.P. Pavlova 185/6, 779 00, Olomouc, Czech Republic.
Jiri BronskyDepartment of Pediatrics, 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital, V Uvalu 84, 150 06, Prague 5, Czech Republic.
Palacký University Olomouc · CZUniversity Hospital in Motol · CZCharles University · CZCzech Academy of Sciences, Institute of Experimental Botany · CZ

Funding

Ministerstvo Zdravotnictví Ceské Republiky 00064203Ministerstvo Zdravotnictví Ceské Republiky 0098892OP VVV ENOCH CZ.02.1.01/0.0/0.0/16_019/0000868
6 · The paper itself

Abstract

backgroundThe additional value of azathioprine concomitant treatment on infliximab pharmacokinetics in children is not well described yet.

aimsIn the present study, we aimed to describe the relationship between thiopurine metabolite levels, infliximab trough levels, anti-IFX antibody formation, and clinical and laboratory markers of disease activity in pediatric patients with Crohn's disease, and to assess non-adherence.

methodsData were collected prospectively during repeated visits from pediatric patients followed for Crohn's disease in two Czech pediatric inflammatory bowel disease centers between January 2016 and June 2017. Thiopurine metabolites (6-thioguanine and 6-methylmercaptopurine) were measured by high-performance liquid chromatography. Infliximab trough levels and anti-IFX antibody serum levels were measured routinely by ELISA. The risk of loss of response to infliximab therapy was also assessed.

resultsA significant association between infliximab serum levels and 6-thioguanine erythrocyte levels was observed when tested as categorical variables (63 patients, 321 observations). To predict infliximab levels > 5 µg/mL, we propose a 6-thioguanine cutoff of 278 pmol/8 × 10

conclusionThiopurine metabolite monitoring in pediatric patients with Crohn's disease is useful when optimizing combination therapy. Pediatric patients with undetectable 6-thioguanine levels are more likely to lose response to infliximab therapy. When targeting optimal infliximab levels, the 6-thioguanine cutoff levels in children appear to be higher than in adults.

Indexed as

AdolescentAzathioprineBiomarkersChildCrohn DiseaseDrug Therapy, CombinationFemaleHumansImmunologic FactorsInfliximabLongitudinal StudiesMaleMercaptopurineProspective Studies6-methylthiopurineAzathioprineBiomarkersImmunologic FactorsInfliximabMercaptopurine

Identifiers

PMID33709340
OpenAlexW3135562039

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Registered trials

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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.