Evidence map›Paper›PMID 21851379›Full record

ArticleBritish journal of clinical pharmacology2012

The effects of a single nucleotide polymorphism in SLCO1B1 on the pharmacodynamics of pravastatin.

Nicholas G Martin, Ka Wah Li, Heather Murray, Wendy Putt, Chris J Packard, Steve E Humphries

Open access · bronzeAbstract read
In one paragraph

Article in British journal of clinical pharmacology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
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

9 citing papers in PubMed, 21 citations in OpenAlex.

  1. PharmVar GeneFocus: SLCO1B1.Clinical pharmacology and therapeutics · 2023
    Review
  2. Functional Consequences of Pravastatin Isomerization on OATP1B1-Mediated Transport.Drug metabolism and disposition: the biological fate of chemicals · 2020
    Article
  3. Observational
  4. Observational
  5. Review
  6. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 5 institutions in 1 country.

Nicholas G MartinCentre for Cardiovascular Genetics, British Heart Foundation Laboratories, The Royal Free and University College London Medical School, London, UK.
Ka Wah Li
Heather Murray
Wendy Putt
Chris J Packard
Steve E Humphries
British Heart Foundation · GBGlasgow Royal Infirmary · GBThe Royal Free Hospital · GBUniversity College London · GBUniversity of Glasgow · GB

Funding

British Heart Foundation RG/08/008/25291British Heart Foundation RG2008/008Department of Health
6 · The paper itself

Abstract

aimTo determine whether the SNP rs4149056 in SLCO1B1 alters the pharmacodynamics of pravastatin.

methodsrs4149056 was genotyped in 626 pravastatin-treated participants in the WOSCOPS trial and the response after 1 year of treatment was compared between the different genotypes.

resultsPravastatin reduced serum LDL cholesterol by 22.2% in TT homozygotes, by 22.2% in TC heterozygotes and by 17.7% in CC homozygotes (TT + TC vs. CC P value 0.33). There were no significant differences in the response of total cholesterol, LDL, HDL, triglycerides or CRP to pravastatin between the genotypes.

conclusionThe rs4149056 SNP did not significantly affect the pharmacodynamics of pravastatin.

Indexed as

Polymorphism, Single NucleotideAnalysis of VarianceAnticholesteremic AgentsCholesterolHumansLiver-Specific Organic Anion Transporter 1MaleMiddle AgedOrganic Anion TransportersPolymerase Chain ReactionPravastatinScotlandTime FactorsAnticholesteremic AgentsCholesterolLiver-Specific Organic Anion Transporter 1Organic Anion TransportersPravastatinSLCO1B1 protein, human

Identifiers

PMID21851379
PMCPMC3269589
OpenAlexW1657886501

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.