Evidence map›Paper›PMID 23571513›Full record

ArticleThrombosis and haemostasis2013

VKORC1 Asp36Tyr geographic distribution and its impact on warfarin dose requirements in Egyptians.

Mohamed Hossam A Shahin, Larisa H Cavallari, Minoli A Perera, Sherief I Khalifa, Anne Misher, Taimour Langaee, Shitalben Patel, Kimberly Perry, David O Meltzer, Howard L McLeod and 1 more

Abstract read
In one paragraph

Article in Thrombosis and haemostasis, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
3.9field-weighted citation impact, top 7% 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, 2 syntheses or guidelines pooled it, 32 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Article
  4. Targeted Genotyping in Clinical Pharmacogenomics: What Is Missing?The Journal of molecular diagnostics : JMD · 2022
    Article
  5. Determination of Pleiotropic Effect of Warfarin inFrontiers in cardiovascular medicine · 2022
    Article
  6. Article
  7. Observational
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Pharmacogenetics in Jewish populations.Drug metabolism and drug interactions · 2014
    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

11 authors at 4 institutions in 2 countries.

Mohamed Hossam A ShahinCenter for Pharmacogenomics, University of Florida, Health Science Center, PO Box 100486, Gainesville, FL 32610, USA.
Larisa H Cavallari
Minoli A Perera
Sherief I Khalifa
Anne Misher
Taimour Langaee
Shitalben Patel
Kimberly Perry
David O Meltzer
Howard L McLeod
Julie A Johnson
University of Chicago · USUniversity of Florida · USUniversity of Illinois Chicago · USQatar University · QA

Funding

Pharmacogenomic Evaluation of Antihypertensive ResponsesU01GM074492 · NIGMS · UNIVERSITY OF FLORIDA · PI JOHNSON, JULIE A. · 2005 to 2014
$20.7M
The implementation of a pharmacogenomics-based algorithm for warfarin dosingK23HL089808 · NHLBI · UNIVERSITY OF CHICAGO · PI PERERA, MINOLI A · 2009 to 2013
$601k
NHLBI NIH HHS K23 HL089808NHLBI NIH HHS K23HL089808-01A2NIGMS NIH HHS U01 GM074492
6 · The paper itself

Abstract

The VKORC1 Asp36Tyr single nucleotide polymorphism (SNP) is one of the most promising predictors of high warfarin dose, but data on its population prevalence is incomplete. We determined the frequency of this SNP in participants from seven countries on four continents and investigated its effect on warfarin dose requirement. One thousand samples were analysed to define the population prevalence of this SNP. Those samples included individuals from Egypt, Ghana, Sudan, Kenya, Saudi Arabia, Peru and African Americans from the United States. A total of 206 Egyptian samples were then used to investigate the effect of this SNP on warfarin dose requirements. This SNP was most frequent among Kenyans and Sudanese, with a minor allele frequency (MAF) of 6% followed by Saudi Arabians and Egyptians with a MAF of 3% and 2.5%, respectively. It was not detected in West Africans, based on our data from Ghana, and a large cohort of African Americans. Egyptian carriers of the VKORC1 Tyr36 showed higher warfarin dose requirement (57.1 ± 29.4 mg/week) than those with the Asp36Asp genotype (35.8 ± 16.6 mg/week; p=0.03). In linear regression analysis, this SNP had the greatest effect size among the genetic factors (16.6 mg/week increase in dose per allele), and improved the warfarin dose variability explained in Egyptians (model R2 from 31% to 36.5%). The warfarin resistant VKORC1 Asp36Tyr appears to be confined to north-eastern Africa and nearby Middle-Eastern populations, but in those populations where it is present, it has a significant influence on warfarin dose requirement and the percent of warfarin dose variability that can be explained.

Indexed as

Genetic VariationPolymorphism, Single NucleotideAllelesCohort StudiesEgyptGene FrequencyGenotypeGeographyHumansPharmacogeneticsPolymorphism, GeneticThromboembolismVitamin K Epoxide ReductasesWarfarinVitamin K Epoxide ReductasesVKORC1 protein, humanWarfarin

Identifiers

PMID23571513
PMCPMC3712827
OpenAlexW2100821160

What OpenQuestion holds

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LicenceTDM
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.