Evidence map›Paper›PMID 16094537›Full record

Trial reportEuropean journal of clinical pharmacology2005

CYP2C9*3 allelic variant is associated with metabolism of irbesartan in Chinese population.

Xiumei Hong, Shanchun Zhang, Guangyun Mao, Shanqun Jiang, Yan Zhang, Yunxian Yu, Genfu Tang, Houxun Xing, Xiping Xu

Abstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in European journal of clinical pharmacology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.3field-weighted citation impact, top 30% 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

13 citing papers in PubMed, 38 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Genetic polymorphisms of pharmacogenomic VIP variants in the lhoba population of southwest China.International journal of clinical and experimental pathology · 2015
    Article
  7. Drug-gene interactions: inherent variability in drug maintenance dose requirements.P & T : a peer-reviewed journal for formulary management · 2014
    Article
  8. Article
  9. Article
  10. Applications of CYP450 testing in the clinical setting.Molecular diagnosis & therapy · 2013
    Review
  11. Article
  12. Article
  13. Review
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

9 authors at 2 institutions in 2 countries.

Xiumei HongLife Science School, University of Science and Technology of China, Huangshan Road, Hefei City, Anhui Province, China.
Shanchun Zhang
Guangyun Mao
Shanqun Jiang
Yan Zhang
Yunxian Yu
Genfu Tang
Houxun Xing
Xiping Xu
Anhui Medical University · CNUniversity of Science and Technology of China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThere is considerable variability in the individual pharmaceutical dosages required to achieve optimal therapeutic effects, which may be due to environmental or genetic factors. The objective of this study was to test the presence of the CYP2C9*3 allelic variant in the Chinese population and to investigate the association of this variant with both metabolism and therapeutic efficacy of irbesartan on essential hypertension.

methodsIn this study, we enrolled 711 subjects from Taihu County and 376 subjects from Dongzhi County in Anhui Province, China. All subjects received a single oral dose of 150 mg irbesartan daily for 28 days. The plasma concentration of irbesartan at 24 h after dosing on the 27th day and at 6 h after dosing on the 28th day was detected using fluorescence-high-performance liquid chromatography. CYP2C9 genotypes were determined using polymerase chain reaction-restriction fragment length polymorphism.

resultsNo CYP2C9*2 allele was found in 235 Chinese samples and was removed from further study. The mean frequency of the CYP2C9*3 allele was 3.65%, while no CYP2C9*3/*3 genotype was detected. Multiple linear regression analyses revealed that the CYP2C9*3 allele carriers had significantly higher irbesartan concentrations in plasma at 6 h (Taihu: P < 0.0001; Dongzhi: P = 0.03) and 24 h (Taihu: P < 0.0001; Dongzhi: P = 0.00013) after dosing. No significant association was found between the CYP2C9*3 allelic variant and the therapeutic effect of irbesartan on essential hypertension.

conclusionOur study suggests that the CYP2C9*3 plays an important role in the metabolism of irbesartan and/or is in linkage disequilibrium with another potential CYP2C9 allele, both of which possibly modify the pharmacokinetics of irbesartan.

Indexed as

Administration, OralAdultAllelesAngiotensin II Type 1 Receptor BlockersAryl Hydrocarbon HydroxylasesAsian PeopleBiphenyl CompoundsCytochrome P-450 CYP2C9FemaleGene FrequencyGenotypeHumansHypertensionIrbesartanLinear ModelsLinkage DisequilibriumAngiotensin II Type 1 Receptor BlockersAryl Hydrocarbon HydroxylasesBiphenyl CompoundsCYP2C9 protein, humanCytochrome P-450 CYP2C9IrbesartanTetrazoles

Identifiers

PMID16094537
OpenAlexW2001110690

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.