Evidence map›Paper›PMID 19319511›Full record

ArticleEuropean journal of clinical pharmacology2009

Pharmacogenetic characteristics of patients with complicated phenprocoumon dosing.

D Werner, U Werner, A Wuerfel, A Grosch, H G Lestin, T Eschenhagen, T Rau

Open access · greenAbstract readComparative Study
PubMed Publisher
In one paragraph

Article in European journal of clinical pharmacology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

2 citing papers in PubMed, 10 citations in OpenAlex.

  1. Trial
  2. 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

7 authors at 4 institutions in 3 countries.

D WernerDepartment of Cardiology/Angiology, Protestant Community Hospital, Ludwigslust, Germany.
U Werner
A Wuerfel
A Grosch
H G Lestin
T Eschenhagen
T Rau
Universität Hamburg · DECommunity Hospital · USHelios Hospital Schwerin · DEHelios (Slovenia) · SI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAnticoagulation therapy with coumarins necessitates a strict individualization of dosing. Whereas the impacts of the cytochrome P450 2C9 (CYP2C9) and vitamin K epoxide reductase (VKORC1) polymorphisms on warfarin dosing are clearly established, the role of these genetic variants on dosing and the safe use of phenprocoumon are less well investigated and, to a certain degree, controversial.

methodsWe studied the most frequent functional polymorphisms of VKORC1, CYP2C9, and CYP3A5 in 60 consecutive patients demonstrating complicated phenprocoumon-mediated anticoagulation and in 120 controls.

resultsThe frequencies of the less active VKORC1 haplotype A-group alleles (p < 0.0001) and of CYP2C9 genotypes with two variant alleles (p = 0.035) were higher in the patient cohort than in the control group, while the frequency of patients carrying only one variant CYP2C9 allele was unchanged relative to the control subjects (RR 1.2; p = 0.49).

conclusionThe data suggest a fundamental role of VKORC1 haplotypes and a minor role of CYP2C9 variants in the anticoagulation property of phenprocoumon.

Indexed as

Polymorphism, GeneticAdministration, OralAgedAged, 80 and overAnticoagulantsAryl Hydrocarbon HydroxylasesCytochrome P-450 CYP2C9Cytochrome P-450 CYP3ADose-Response Relationship, DrugDrug Administration ScheduleFemaleGene FrequencyGenotypeGermanyHaplotypesHumansAnticoagulantsAryl Hydrocarbon HydroxylasesCYP2C9 protein, humanCYP3A5 protein, humanCytochrome P-450 CYP2C9Cytochrome P-450 CYP3AMixed Function OxygenasesPhenprocoumonVitamin K Epoxide ReductasesVKORC1 protein, human

Identifiers

PMID19319511
OpenAlexW2144805022

What OpenQuestion holds

Textmetadata
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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.