Evidence map›Paper›PMID 42503050›Full record

ArticleClinical pharmacokinetics2026

Pharmacometric Targets During Anti-TNF Induction and Their Association with Deep Remission in Pediatric Crohn's Disease.

Alexander Nasr, Tomoyuki Mizuno, Kei Irie, Jonathan R Dillman, Kimberly Jackson, Kimberly Lynch, Alexa Horrell, Thomas Aviles, Kelly Chun, Jane Yang and 5 more

Abstract readMulticenter Study
In one paragraph

Article in Clinical pharmacokinetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Alexander NasrDivision of Pediatric Gastroenterology, Hepatology and Nutrition, Cincinnati Children's Hospital Medical Center, MLC 2010, 3333 Burnet Avenue, Cincinnati, OH, 45229, USA.
Tomoyuki MizunoUniversity of Cincinnati College of Medicine, Cincinnati, OH, USA.
Kei IrieDivision of Clinical Pharmacology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Jonathan R DillmanUniversity of Cincinnati College of Medicine, Cincinnati, OH, USA.
Kimberly JacksonDivision of Pediatric Gastroenterology, Hepatology and Nutrition, Cincinnati Children's Hospital Medical Center, MLC 2010, 3333 Burnet Avenue, Cincinnati, OH, 45229, USA.
Kimberly LynchDivision of Pediatric Gastroenterology, Hepatology and Nutrition, Cincinnati Children's Hospital Medical Center, MLC 2010, 3333 Burnet Avenue, Cincinnati, OH, 45229, USA.
Alexa HorrellUniversity of Cincinnati College of Medicine, Cincinnati, OH, USA.
Thomas AvilesDivision of Pediatric Gastroenterology, Hepatology and Nutrition, Cincinnati Children's Hospital Medical Center, MLC 2010, 3333 Burnet Avenue, Cincinnati, OH, 45229, USA.
Kelly ChunEsoterix, LabCorp Specialty Lab, Calabasas, CA, USA.
Jane YangEsoterix, LabCorp Specialty Lab, Calabasas, CA, USA.
Brendan BoyleDivision of Pediatric Gastroenterology, Hepatology and Nutrition, Nationwide Children's Hospital, Columbus, OH, USA.
Jeffrey S HyamsDivision of Digestive Diseases and Nutrition, Connecticut Children's Medical Center, Hartford, CT, USA.
Joshua NoeDivision of Pediatric Gastroenterology, Medical College of Wisconsin, Milwaukee, WI, USA.
Lee A DensonDivision of Pediatric Gastroenterology, Hepatology and Nutrition, Cincinnati Children's Hospital Medical Center, MLC 2010, 3333 Burnet Avenue, Cincinnati, OH, 45229, USA.
Phillip MinarDivision of Pediatric Gastroenterology, Hepatology and Nutrition, Cincinnati Children's Hospital Medical Center, MLC 2010, 3333 Burnet Avenue, Cincinnati, OH, 45229, USA. phillip.minar@cchmc.org.ORCID http://orcid.org/0000-0003-4223-4211

Funding

Stem Cell/Organoid and Genome Editing CoreP30DK078392 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI Alexander Miethke · 2007 to 2026
$24.4M
PEDIATRIC GASTROENTEROLOGY AND NUTRITION TRAINING GRANTT32DK007727 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI Phillip P Minar · 1995 to 2026
$11.3M
Precise Infliximab Exposure and Pharmacodynamic Control to Achieve Deep Remission in Pediatric Crohn's DiseaseR01DK132408 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI Phillip P Minar · 2022 to 2026
$3.5M
Short Term Medical Student Training GrantT35DK060444 · NIDDK · UNIVERSITY OF CINCINNATI · PI JASON T BLACKARD · 2002 to 2026
$2.3M
Division of Diabetes, Endocrinology, and Metabolic Diseases P30DK078392Division of Diabetes, Endocrinology, and Metabolic Diseases R01DK132408Division of Diabetes, Endocrinology, and Metabolic Diseases T32DK007727Division of Diabetes, Endocrinology, and Metabolic Diseases T35DK060444NIDDK NIH HHS P30 DK078392NIDDK NIH HHS R01 DK132408NIDDK NIH HHS T32 DK007727NIDDK NIH HHS T35 DK060444
6 · The paper itself

Abstract

BACKGROUND AND

objectivePersonalizing anti-tumor necrosis factor (TNF) therapy in pediatric Crohn's disease (CD) remains challenging due to variable drug clearance and response. Identifying pharmacokinetic (PK) and pharmacodynamic (PD) predictors of deep remission could enable precision dosing strategies. The primary aim was to define PK metrics and PD biomarkers associated with deep remission.

methodsPatients initiating infliximab or adalimumab were prospectively enrolled from four pediatric centers with longitudinal blood and stool biospecimens collected for one year. Deep remission was defined as a combination of weighted pediatric CD activity index (wPCDAI) < 12.5 and Simple Endoscopic Score-CD < 3. Trough concentrations (cTrough) were measured throughout the study. Drug exposure (area under the curve, AUC) and clearance were estimated using drug-specific population PK models and Bayesian estimation using nonlinear mixed-effects modeling (NONMEM).

resultsDeep remission was achieved in 34/70 (48.6%) with no difference in outcomes between biologics. Infliximab cTrough thresholds associated with deep remission were 33 µg/mL (Week 2), 15 µg/mL (Week 6), and 4.7 µg/mL (Month 3) with Week 6 cTrough targets ranging 15-26 µg/mL depending on the outcome of interest. Higher AUC during induction for both infliximab and adalimumab was associated with deep remission, whereas rapid infliximab clearance at various timepoints was inversely associated with deep remission. Baseline predictors of rapid infliximab clearance included older age, low albumin, and elevations in body mass index, C-reactive protein, soluble CD64, and wPCDAI.

conclusionsWe identified PK/PD cut-points associated with deep remission and rapid infliximab clearance, providing actionable metrics to individualize induction dosing and optimize maintenance therapy for children starting anti-TNF therapy.

Indexed as

AdalimumabCrohn DiseaseInfliximabTumor Necrosis Factor-alphaAdolescentArea Under CurveBayes TheoremBiomarkersChildFemaleHumansMaleProspective StudiesRemission InductionAdalimumabBiomarkersInfliximabTumor Necrosis Factor-alpha

Identifiers

PMID42503050
PMCPMC13545114

What OpenQuestion holds

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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.