Literature DB >> 21261182

Exposure to non-therapeutic INR in a high risk cardiovascular patient: potential hazard reduction with genotype-guided warfarin (Coumadin) dosing.

Rosángela Rodríguez-Vélez1, Oscar J Ortiz-Rivera, Bruce Bower, Krystyna Gorowski, Andreas Windemuth, David Villagra, Mohan Kocherla, Richard L Seip, Darrin D'Agostino, Cunegundo Vergara, Gualberto Ruaño, Jorge Duconge.   

Abstract

A case to illustrate the utility of genetic screening in warfarin (Coumadin) management is reported. A 45 year-old woman of Puerto Rican ancestry was admitted to the emergency room twice within one month with chest pain. She was diagnosed with congestive heart failure, which was stabilized both times. At her second release, warfarin therapy was initiated at 5 mg/ day to prevent thrombus formation and was lowered to 3.75 mg/day at day 7 by her primary physician. International Normalized Ratio (INR) test results in the follow-up period at days 1, 7, and 10 of warfarin therapy were 4.5, 6.5, and 7.3, respectively-far in excess of the therapeutic range, despite the lower dosage in effect from day 7 onward. The patient achieved target INR over the next 43 days after downward adjustment of the dose to a dose of 1.5 mg/day by trial and error. DNA-typing specific for the CYP2C9*2,*3,*4,*5,*6 alleles and seven variants in the VKORC1 gene, including the VKORC1-1639 G > A polymorphism, revealed the presence of combinatorial CYP2C9*2/*3 and VKORC1-1639 G/A genotypes in this patient. Entering the patient's demographic and genotype status data into independent algorithms available in the public domain to predict effective warfarin dose yielded predicted doses which ranged from 1.5 to 1.8 mg/day. Notably, the prediction of 1.5 mg/day, which was generated by the online resource www.warfarindosing.org, coincided with the patient's actual effective warfarin dose. We conclude that the rapid rise in INR observed upon the initiation of warfarin therapy and the final effective warfarin dose of 1.5 mg/day, are attributable in some part to the presence of two minor alleles in CYP2C9, which together significantly reduce warfarin metabolism. Warfarin genotyping can therefore inform the clinician of the predicted effective warfarin dose. The results highlight the potential for warfarin genetic testing to improve patient care.

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Year:  2010        PMID: 21261182      PMCID: PMC3679530     

Source DB:  PubMed          Journal:  P R Health Sci J        ISSN: 0738-0658            Impact factor:   0.705


  31 in total

1.  Association between CYP2C9 genetic variants and anticoagulation-related outcomes during warfarin therapy.

Authors:  Mitchell K Higashi; David L Veenstra; L Midori Kondo; Ann K Wittkowsky; Sengkeo L Srinouanprachanh; Fred M Farin; Allan E Rettie
Journal:  JAMA       Date:  2002-04-03       Impact factor: 56.272

2.  Influence of cytochrome P-450 CYP2C9 polymorphisms on warfarin sensitivity and risk of over-anticoagulation in patients on long-term treatment.

Authors:  J Taube; D Halsall; T Baglin
Journal:  Blood       Date:  2000-09-01       Impact factor: 22.113

3.  Genetic modulation of oral anticoagulation with warfarin.

Authors:  M Margaglione; D Colaizzo; G D'Andrea; V Brancaccio; A Ciampa; E Grandone; G Di Minno
Journal:  Thromb Haemost       Date:  2000-11       Impact factor: 5.249

4.  Bleeding complications in oral anticoagulant therapy. An analysis of risk factors.

Authors:  F J van der Meer; F R Rosendaal; J P Vandenbroucke; E Briët
Journal:  Arch Intern Med       Date:  1993-07-12

5.  Warfarin dose adjustments based on CYP2C9 genetic polymorphisms.

Authors:  Mark W Linder; Stephen Looney; Jesse E Adams; Nancy Johnson; Deborah Antonino-Green; Nichole Lacefield; Bonny L Bukaveckas; Roland Valdes
Journal:  J Thromb Thrombolysis       Date:  2002-12       Impact factor: 2.300

6.  Warfarin dosing and cytochrome P450 2C9 polymorphisms.

Authors:  Hylton V Joffe; Ruliang Xu; F Bradley Johnson; Janina Longtine; Nils Kucher; Samuel Z Goldhaber
Journal:  Thromb Haemost       Date:  2004-06       Impact factor: 5.249

7.  Influence of CYP2C9 and CYP2C19 genetic polymorphisms on warfarin maintenance dose and metabolic clearance.

Authors:  Maria Gabriella Scordo; Vittorio Pengo; Edoardo Spina; Marja Liisa Dahl; Milena Gusella; Roberto Padrini
Journal:  Clin Pharmacol Ther       Date:  2002-12       Impact factor: 6.875

8.  Relative impact of covariates in prescribing warfarin according to CYP2C9 genotype.

Authors:  Michael A Hillman; Russell A Wilke; Michael D Caldwell; Richard L Berg; Ingrid Glurich; James K Burmester
Journal:  Pharmacogenetics       Date:  2004-08

9.  Prevalence of combinatorial CYP2C9 and VKORC1 genotypes in Puerto Ricans: implications for warfarin management in Hispanics.

Authors:  Jorge Duconge; Carmen L Cadilla; Andreas Windemuth; Mohan Kocherla; Krystyna Gorowski; Richard L Seip; Kali Bogaard; Jessica Y Renta; Paola Piovanetti; Darrin D'Agostino; Pedro J Santiago-Borrero; Gualberto Ruaño
Journal:  Ethn Dis       Date:  2009       Impact factor: 1.847

10.  Clinical impact of bleeding in patients taking oral anticoagulant therapy for venous thromboembolism: a meta-analysis.

Authors:  Lori-Ann Linkins; Peter T Choi; James D Douketis
Journal:  Ann Intern Med       Date:  2003-12-02       Impact factor: 25.391

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