Evidence map›Paper›PMID 37016150›Full record

ArticleThe pharmacogenomics journal2023

One year of experience with combined pharmacokinetic/pharmacogenetic monitoring of anti-TNF alpha agents: a retrospective study.

Stefania Cheli, Diego Savino, Annalisa De Silvestri, Lorenzo Norsa, Naire Sansotta, Francesca Penagini, Dario Dilillo, Roberto Panceri, Dario Cattaneo, Emilio Clementi and 1 more

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in The pharmacogenomics journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 2 pooled it
0.9field-weighted citation impact, top 21% 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

3 citing papers in PubMed, 2 syntheses or guidelines pooled it, 3 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 1 country.

Stefania CheliUnit of Clinical Pharmacology, ASST Fatebenefratelli Sacco, University Hospital, Milano, Italy.ORCID 0000-0002-2837-5248
Diego SavinoUnit of Clinical Pharmacology, ASST Fatebenefratelli Sacco, University Hospital, Milano, Italy.
Annalisa De SilvestriClinical Epidemiology and Biometry Unit, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.ORCID 0000-0003-3128-8441
Lorenzo NorsaPediatric Hepatology, Gastroenterology and Transplantation Unit, ASST Papa Giovanni XXIII, Bergamo, Italy.
Naire SansottaPediatric Hepatology, Gastroenterology and Transplantation Unit, ASST Papa Giovanni XXIII, Bergamo, Italy.
Francesca PenaginiPediatric Department, "Vittore Buzzi" Children's Hospital, University of Milan, Milano, Italy.
Dario DililloPediatric Department, "Vittore Buzzi" Children's Hospital, University of Milan, Milano, Italy.
Roberto PanceriPediatrics, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.
Dario CattaneoUnit of Clinical Pharmacology, ASST Fatebenefratelli Sacco, University Hospital, Milano, Italy.
Emilio ClementiScientific Institute IRCCS Eugenio Medea, Bosisio Parini, Italy. emilio.clementi@unimi.it.ORCID 0000-0001-7333-8270
Giovanna ZuinPediatrics, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.
ASST Fatebenefratelli Sacco · ITUniversity of Milan · ITAzienda Ospedaliera San Gerardo · ITOspedale Papa Giovanni XXIII · ITPoliclinico San Matteo Fondazione · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anti-tumor necrosis factor alpha (anti-TNFα) inhibitors are used extensively for the management of moderate to severe inflammatory bowel disease (IBD) in both adult and pediatric patients. Unfortunately, not all patients show an optimal response to induction therapy, while others lose their response over time for reasons yet poorly understood. We report on a pharmacokinetic/pharmacogenetic approach to monitor the therapy with anti-TNFα in a real-world cohort of seventy-nine pediatric patients affected by IBD that was analyzed retrospectively. We evaluated plasma concentrations of infliximab, adalimumab, and related anti-drug antibodies (ADAs), and single nucleotide polymorphisms (SNPs) in genes involved in immune processes and inflammation on the anti-TNFα response. We found a significant association between the SNP in TNFα promoter (-308G>A) and clinical remission without steroids in patients on infliximab therapy. Additionally, a potential connection between HLA-DQA1*05 genetic variant carriers and a higher risk of anti-TNFα immunogenicity emerged.

Indexed as

Crohn DiseaseInflammatory Bowel DiseasesAdalimumabAdultChildHumansInfliximabPharmacogeneticsRetrospective StudiesTumor Necrosis Factor-alphaTumor Necrosis Factor InhibitorsAdalimumabInfliximabTumor Necrosis Factor-alphaTumor Necrosis Factor Inhibitors

Identifiers

PMID37016150
OpenAlexW4362555560

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.