Evidence map›Paper›PMID 19026029›Full record

ArticleDrug safety2008

Role of cytochrome P450 polymorphisms in the development of pulmonary drug toxicity: a case-control study in the Netherlands.

Petal A H M Wijnen, Marjolein Drent, Patty J Nelemans, Petra M J C Kuijpers, Ger H Koek, Cees Neef, Guido R M M Haenen, Otto Bekers

Abstract read
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Article in Drug safety, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

12 citing papers in PubMed.

  1. Observational
  2. Observational
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Drug induced interstitial lung disease.The open respiratory medicine journal · 2012
    Article
  10. Article
  11. Article
  12. Simultaneous interstitial pneumonitis and cardiomyopathy induced by venlafaxine.Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia
    Article
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.

Petal A H M WijnenDepartment of Clinical Chemistry, Maastricht University Medical Centre, Maastricht, The Netherlands.
Marjolein Drent
Patty J Nelemans
Petra M J C Kuijpers
Ger H Koek
Cees Neef
Guido R M M Haenen
Otto Bekers

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDrug-induced pulmonary toxicity is a serious and expanding problem with often unknown aetiology. Many drugs are metabolized by cytochrome P450 (CYP) enzymes.

objectiveTo establish whether allelic variation in CYP polymorphic genes contributes to variability in drug response and unexpected toxicity.

methodsA case-control study was conducted. The cases consisted of patients with drug-induced interstitial lung disease (DI-ILD; n = 59). Two control groups were used: one group of healthy volunteers (n = 173) and one group of patients with idiopathic pulmonary fibrosis (IPF; n = 110).

resultsOf the patients with DI-ILD 91.5% (54/59) had at least one of the studied variant genes compared with 70.5% (122/173, p < 0.001) of the healthy volunteers and 69.1% (76/110, p < 0.001) of the IPF patients. The percentage of individuals with one or more variant CYP genes was higher in the DI-ILD group. Odds ratios were significantly increased and ranged from 3.25 to 40.8, indicating a significant association between the development of DI-ILD and the presence of one or more variant CYP genes.

conclusionDI-ILD appeared to be associated with the presence of at least one variant CYP allele. This study supports the potential usefulness of personalized medicine by genotyping aiming to improve efficacy, tolerability and drug safety.

Indexed as

AdultAgedAged, 80 and overCase-Control StudiesCytochrome P-450 Enzyme SystemFemaleGenotypeHumansLung Diseases, InterstitialMaleMiddle AgedNetherlandsPolymorphism, GeneticPrescription DrugsCytochrome P-450 Enzyme SystemPrescription Drugs

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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.