Evidence map›Paper›PMID 24354889›Full record

Trial reportBritish journal of clinical pharmacology2014

Relationship between inflammation and infliximab pharmacokinetics in rheumatoid arthritis.

David Ternant, Emilie Ducourau, Aleth Perdriger, Anca Corondan, Benoît Le Goff, Valérie Devauchelle-Pensec, Elisabeth Solau-Gervais, Hervé Watier, Philippe Goupille, Gilles Paintaud and 1 more

2 registry-linked trialsOpen access · bronzeAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in British journal of clinical pharmacology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
4.0field-weighted citation impact, top 7% 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.

NCT00840957 completednot on this map

Pharmaco Kinetic and Pharmacokinetic-Pharmacodynamic Variability of Infliximab

TypeobservationalSponsorUniversity Hospital, ToursRan2007 to 2009Enrolled84ConditionsRheumatoid ArthritisArmsinfliximab
NCT04731831 unknown statusnot on this mapstarted 2020, after this paper: background citation

Characterization of Immunogenicity of Tumor Necrosis Factor Inhibitors in Arthritis Patients With Poorer Treatment Response Due to Gender, Obesity and Smoking Status.

TypeobservationalSponsorAalborg University HospitalRan2020 to 2025Enrolled120ConditionsArthritis, Rheumatoid, Arthritis, Psoriatic, Spondylitis, Ankylosing
3 · Its place in the literature

Who cites it

50 citing papers in PubMed, 81 citations in OpenAlex.

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  14. Pharmacogenomics of TNF inhibitors.Frontiers in immunology · 2025
    Review
  15. [Sex-specific aspects in rheumatology].Zeitschrift fur Rheumatologie · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 9 institutions in 1 country.

David TernantUniversité François Rabelais de Tours, GICC, Tours, France; CNRS, UMR 7293, Tours, France; CHRU de Tours, Tours, France.
Emilie Ducourau
Aleth Perdriger
Anca Corondan
Benoît Le Goff
Valérie Devauchelle-Pensec
Elisabeth Solau-Gervais
Hervé Watier
Philippe Goupille
Gilles Paintaud
Denis Mulleman
Université de Tours · FRCentre hospitalier régional d'Orléans · FRCentre Hospitalier Régional Universitaire de Brest · FRCentre Hospitalier Universitaire de Rennes · FRCentre Hospitalier Universitaire de Tours · FRCentre National de la Recherche Scientifique · FRInserm · FRLaboratoire de Thermique et Energie de Nantes · FRUniversité de Poitiers · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsInfliximab, an anti-tumour necrosis factor-α monoclonal antibody, is indicated in rheumatoid arthritis (RA). Our objective was to evaluate the influence of the sources of infliximab pharmacokinetic variability in RA.

methodsEighty-four patients treated with infliximab for RA were included in a prospective noncomparative study. They were analysed between two consecutive infliximab infusions. Infliximab concentrations were measured before the infusion, 2 h, 1 and 4 weeks after the infusion and immediately before the next infusion. Infliximab concentrations were described using a two-compartment population pharmacokinetic model.

resultsThe mean (interindividual standard deviation) estimated central volume of distribution was 2.3 l (36%) and systemic clearance was 0.019 l h(-1) (37%). The central volume of distribution increased with bodyweight; it was doubled between 50 and 90 kg. Systemic clearance increased with pre-infusion C-reactive protein concentration by 20%, varying from 3 to 14 mg l(-) 1, and was decreased by 30% when methotrexate was coadministered.

conclusionsThe influence of methotrexate and inflammation on infliximab clearance suggests that individual adjustment of infliximab doses according to disease activity may be useful in RA.

Indexed as

AdultAgedAged, 80 and overAntibodies, MonoclonalAntirheumatic AgentsArthritis, RheumatoidC-Reactive ProteinDrug Therapy, CombinationFemaleHumansInflammationInfliximabMaleMethotrexateMiddle AgedModels, BiologicalAntibodies, MonoclonalAntirheumatic AgentsC-Reactive ProteinInfliximabMethotrexatePrednisoneinflammationinfliximabmonoclonal antibodiespharmacokineticsrheumatoid arthritis

Identifiers

PMID24354889
PMCPMC4168386
OpenAlexW1516626166

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.