Evidence map›Paper›PMID 25594941›Full record

Trial reportPloS one2015

Warfarin dosage response related pharmacogenetics in Chinese population.

Siyue Li, Yuangao Zou, Xia Wang, Xunbei Huang, Yong Sun, Yuqing Wang, Li Dong, Hong Jiang

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in PloS one, 2015. 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
6.0field-weighted citation impact, top 4% 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

12 citing papers in PubMed, 38 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
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  6. Article
  7. Article
  8. Mitral valve replacement in a dialysis-dependent patient.Annals of translational medicine · 2016
    Article
  9. Impact of theBiomedical reports · 2016
    Article
  10. Article
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  12. 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

8 authors at 2 institutions in 1 country.

Siyue LiDepartment of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu, P. R. China.
Yuangao ZouDepartment of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu, P. R. China.
Xia WangDepartment of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu, P. R. China.
Xunbei HuangDepartment of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu, P. R. China.
Yong SunDepartment of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu, P. R. China.
Yuqing WangDepartment of Cardiac Surgery, West China Hospital, Sichuan University, Chengdu, P. R. China.
Li DongDepartment of Cardiac Surgery, West China Hospital, Sichuan University, Chengdu, P. R. China.
Hong JiangDepartment of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu, P. R. China.
Sichuan University · CNWest China Hospital of Sichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesAs the most frequently prescribed anticoagulant, warfarin has large inter-individual variability in dosage. Genetic polymorphisms could largely explain the differences in dosage requirement. rs9923231 (VKORC1), rs7294 (VKORC1), rs1057910 (CYP2C9), rs2108622 (CYP4F2), and rs699664 (GGCX) involved in the warfarin action mechanism and the circulatory vitamin K were selected to investigate their polymorphism characteristics and their effects on the pharmacodynamics and pharmacokinetics of warfarin in Chinese population.

methods220 patients with cardiac valve replacement were recruited. International normalized ratio and plasma warfarin concentrations were determined. The five genetic polymorphisms were genotyping by pyro-sequencing. The relationships of maintenance dose, plasma warfarin concentration and INR were assessed among groups categorized by genotypes.

resultsrs9923231 and rs7294 in VKORC1 had the analogous genotype frequencies (D': 0.969). 158 of 220 recruited individuals had the target INR (1.5-2.5). Patients with AA of rs9923231 and CC of rs7294 required a significantly lower maintenance dose and plasma concentration than those with AG and TC, respectively. The mean weekly maintenance dose was also significantly lower in CYP2C9 rs1057910 mutated heterozygote than in patients with the wild homozygote. Eliminating the influence from environment factors (age, body weight and gender), rs9923231 and rs1057910 could explain about 32.0% of the variability in warfarin maintenance dose; rs7294 could explain 26.7% of the variability in plasma concentration. For patients with allele G of rs9923231 and allele T of rs7294, higher plasma concentration was needed to achieve the similar goal INR.

conclusionsA better understanding of the genetic variants in individuals can be the foundation of warfarin dosing algorithm and facilitate the reasonable and effective use of warfarin in Chinese.

Indexed as

AdultAlgorithmsChinaDose-Response Relationship, DrugFemaleGenetic VariationGenotypeHumansMaleMiddle AgedPharmacogeneticsPolymorphism, GeneticVitamin K Epoxide ReductasesWarfarinVitamin K Epoxide ReductasesVKORC1 protein, humanWarfarin

Identifiers

PMID25594941
PMCPMC4296935
OpenAlexW2005176718

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.