Evidence map›Paper›PMID 23623526›Full record

Trial reportThe Journal of pediatrics2013

Association of CYP2C19 polymorphisms and lansoprazole-associated respiratory adverse effects in children.

John J Lima, Jason E Lang, Edward B Mougey, Kathryn B Blake, Yan Gong, Janet T Holbrook, Robert A Wise, W G Teague

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of pediatrics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 16% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

  1. Guideline
  2. Utility of theClinical and translational science · 2022
    Trial
  3. Trial
  4. Trial
  5. Association betweenFrontiers in pharmacology · 2025
    Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Pharmacogenomics in Children.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  13. Frontiers in medicine · 2022
    Article
  14. Review
  15. Gene-Based Dose Optimization in Children.Annual review of pharmacology and toxicology · 2020
    Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Does Obesity Increase Respiratory Tract Infections in Patients with Asthma?The journal of allergy and clinical immunology. In practice · 2019
    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

8 authors at 5 institutions in 1 country.

John J LimaCenter for Pharmacogenomics and Translational Research, Nemours Children's Clinic, Jacksonville, FL, USA. jlima@nemours.org
Jason E Lang
Edward B Mougey
Kathryn B Blake
Yan Gong
Janet T Holbrook
Robert A Wise
W G Teague
Nemours Children’s Clinic · USUniversity of Virginia · USJohns Hopkins University · USNemours Children's Clinic · USUniversity of Florida · US

Funding

Clinical Trial of Acid Reflux Therapy in AsthmaU01HL072968 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI WISE, ROBERT A. · 2003 to 2007
$3.7M
Study of Asthma and Nasal Steroids Trial-An ancillary mechanistic studyF32AI091274 · NIAID · JOHNS HOPKINS UNIVERSITY · PI BIME, CHRISTIAN · 2010 to 2011
$119k
NHLBI NIH HHS U01 HL072968NIAID NIH HHS F32 AI091274
6 · The paper itself

Abstract

objectiveTo determine whether cytochrome P450 (CYP)2C19 haplotype associates with lansoprazole-associated adverse event frequency. STUDY

designRespiratory adverse events from a clinical trial of lansoprazole in children with asthma were analyzed for associations with extensive or poor metabolizer (PM) phenotype based on CYP2C19 haplotypes. Carriers of CYP2C19*2, *3, *8, or *9 alleles were PMs; carriers of 2 wild-type alleles were extensive metabolizers (EMs). Plasma concentrations of lansoprazole were determined in PM and EM phenotypes.

resultsThe frequency of upper respiratory infection among PMs (n = 45) was higher than that among EMs (n = 91), which in turn was higher than that in placebo subjects (n = 135; P = .0039). The frequency of sore throat (ST) was similarly distributed among EMs and PMs (P = .0015). The OR (95% CI) for upper respiratory infections in PMs was 2.46 (1.02-5.96) (P = .046); for EMs, the OR (95% CI) was 1.55 (0.86-2.79). The OR (95% CI) for ST in EMs and PMs was 2.94 (1.23-7.05, P = .016) vs 1.97 (1.09-3.55, P = .024), respectively. Mean ± SD plasma concentrations of lansoprazole were higher in PMs than in EMs: 207 ± 179 ng/mL vs 132 ± 141 ng/mL (P = .04).

conclusionsLansoprazole-associated upper respiratory infections and ST in children are related in part to CYP2C19 haplotype. Our data suggest that lansoprazole-associated adverse events in children may be mitigated by adjusting the conventional dose in PMs. Additional studies are required to replicate our findings.

Indexed as

Polymorphism, Single Nucleotide2-PyridinylmethylsulfinylbenzimidazolesAdolescentAryl Hydrocarbon HydroxylasesAsthmaBronchitisChildCytochrome P-450 CYP2C19FemaleGenetic MarkersGenotyping TechniquesHaplotypesHumansLansoprazoleLogistic ModelsMale2-PyridinylmethylsulfinylbenzimidazolesAryl Hydrocarbon HydroxylasesCYP2C19 protein, humanCytochrome P-450 CYP2C19Genetic MarkersLansoprazoleProton Pump InhibitorsCYPCytochrome P450EMExtensive metabolizerPMPoor metabolizerPPIProton pump inhibitorSingle nucleotide polymorphismSNPSore throatSTUpper respiratory tract infectionURIWild typeWT

Identifiers

PMID23623526
PMCPMC7274090
OpenAlexW1967834922

What OpenQuestion holds

Textmetadata
LicenceTDM
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.