Evidence map›Paper›PMID 21272753›Full record

ArticleJournal of the American College of Cardiology2011

Genetic warfarin dosing: tables versus algorithms.

Brian S Finkelman, Brian F Gage, Julie A Johnson, Colleen M Brensinger, Stephen E Kimmel

2 registry-linked trialsAbstract readComparative StudyMulticenter Study
In one paragraph

Article in Journal of the American College of Cardiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 55 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 4 pooled it
–field-weighted citation impact
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.

NCT01006733 phase3completednot on this map

Genetics Informatics Trial (GIFT) of Warfarin to Prevent Deep Venous Thrombosis (DVT)

TypeinterventionalSponsorWashington University School of MedicineRan2011 to 2016Enrolled1,598ConditionsThromboembolismArmsPharmacogenetic, Target INR 1.8
NCT01520402 nacompletednot on this map

Quantitative Pharmacogenomics of the Anticoagulant Response to Warfarin in Healthy Subjects

TypeinterventionalSponsorIcahn School of Medicine at Mount SinaiRan2009 to 2011Enrolled35ConditionsHealthyArmsWarfarin
3 · Its place in the literature

Who cites it

55 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Warfarin dosing algorithms: A systematic review.British journal of clinical pharmacology · 2021
    Pooled it
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  15. Drug metabolism and disposition: the biological fate of chemicals · 2022
    Article
  16. Ethnic Diversity and Warfarin Pharmacogenomics.Frontiers in pharmacology · 2022
    Review
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  20. 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

5 authors.

Brian S FinkelmanCenter for Clinical Epidemiology and Biostatistics, Department of Biostatistics and Epidemiology, University of Pennsylvania School of Medicine, Philadelphia, USA.
Brian F Gage
Julie A Johnson
Colleen M Brensinger
Stephen E Kimmel

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007170 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI BRASS, LAWRENCE F · 1985 to 2022
$54.0M
Pharmacogenomic Evaluation of Antihypertensive ResponsesU01GM074492 · NIGMS · UNIVERSITY OF FLORIDA · PI COOPER-DEHOFF, RHONDA M, JOHNSON, JULIE A. · 2005 to 2014
$20.7M
PREDICTORS OF ANTICOAGULATION CONTROL ON WARFARINR01HL066176 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI KIMMEL, STEPHEN E. · 2001 to 2012
$7.3M
GENETICS-InFORMATICS TRIAL (GIFT) OF WARFARIN TO PREVENT DVTR01HL097036 · NHLBI · WASHINGTON UNIVERSITY · PI GAGE, BRIAN F · 2009 to 2015
$5.0M
NHLBI NIH HHS R01 HL066176NHLBI NIH HHS R01HL066176NHLBI NIH HHS R01 HL097036NHLBI NIH HHS R01HL097036NIGMS NIH HHS T32 GM007170NIGMS NIH HHS T32-GM07170NIGMS NIH HHS U01 GM074492
6 · The paper itself

Abstract

objectivesThe aim of this study was to compare the accuracy of genetic tables and formal pharmacogenetic algorithms for warfarin dosing.

backgroundPharmacogenetic algorithms based on regression equations can predict warfarin dose, but they require detailed mathematical calculations. A simpler alternative, recently added to the warfarin label by the U.S. Food and Drug Administration, is to use genotype-stratified tables to estimate warfarin dose. This table may potentially increase the use of pharmacogenetic warfarin dosing in clinical practice; however, its accuracy has not been quantified.

methodsA retrospective cohort study of 1,378 patients from 3 anticoagulation centers was conducted. Inclusion criteria were stable therapeutic warfarin dose and complete genetic and clinical data. Five dose prediction methods were compared: 2 methods using only clinical information (empiric 5 mg/day dosing and a formal clinical algorithm), 2 genetic tables (the new warfarin label table and a table based on mean dose stratified by genotype), and 1 formal pharmacogenetic algorithm, using both clinical and genetic information. For each method, the proportion of patients whose predicted doses were within 20% of their actual therapeutic doses was determined. Dosing methods were compared using McNemar's chi-square test.

resultsWarfarin dose prediction was significantly more accurate (all p < 0.001) with the pharmacogenetic algorithm (52%) than with all other methods: empiric dosing (37%; odds ratio [OR]: 2.2), clinical algorithm (39%; OR: 2.2), warfarin label (43%; OR: 1.8), and genotype mean dose table (44%; OR: 1.9).

conclusionsAlthough genetic tables predicted warfarin dose better than empiric dosing, formal pharmacogenetic algorithms were the most accurate.

Indexed as

AlgorithmsCohort StudiesDose-Response Relationship, DrugGenetic VariationHumansInternational Normalized RatioMiddle AgedPharmacogeneticsProspective StudiesRetrospective StudiesWarfarinWarfarin

Identifiers

PMID21272753
PMCPMC3107000

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Registered trials

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.