Drug metabolism may be perturbed by genetically determined differences in the metabolic activity of cytochrome P450 enzymes. The authors encountered extensive bleeding in a patient receiving warfarin for anticoagulation after the introduction of celecoxib, an anti-inflammatory drug. As the CYP2C9 enzyme metabolises these drugs, it was determined whether variant alleles were responsible for altering warfarin handling. Genetic analysis established that the patient was a compound heterozygote with CYP2C9*2 and *3 variant alleles, which exhibit lower drug metabolising capacity and enhance susceptibility to drug toxicity.
- bp, base pair
- COX, cyclo-oxygenase
- INR, international normalised ratio
- PCR, polymerase chain reaction
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Genetic differences in the activity of cytochrome P450 (CYP) genes often account for variable drug metabolism. Many common drugs, including warfarin and non-steroidal anti-inflammatory drugs, are metabolised by the CYP2C9 enzyme. Three variants of CYP2C9 gene, designated CYP2C9*1, *2 and *3, are encountered in white people.1–3 The enzymatic activity of *2 and *3 variant genes is decreased significantly, and carriers of the *3 variant are at risk for complications, such as bleeding after use of warfarin in small amounts.2,3 Recently, inflammatory drugs that work by inhibiting cyclo-oxygenase (COX)-2 activity attracted interest.4 For instance, COX-2 inhibitors were thought to have less potential for causing gastrointestinal bleeding. The COX-2 inhibitor, celecoxib, is primarily metabolised by the CYP2C9 enzyme,5 and is being increasingly popular. In a limited sample of patients, celecoxib was not found to alter the pharmacokinetics of warfarin.6 However, whether this group of subjects included any with variant CYP2C9 alleles, which might have resulted in altered pharmacokinetics of warfarin, was unknown. Our experience suggests that celecoxib may perturb warfarin metabolism, leading to greater anticoagulation in the presence of variant CYP2C9 genes.
An elderly woman developed ecchymoses with a decline in haemoglobin concentration from 160 to 85 g/l over one week. She was receiving 2.5 mg warfarin daily after a pacemaker one year previously. The international normalised ratio (INR) of prothrombin time on this dose of warfarin ranged from 2.2 to 2.6. She was given celecoxib four weeks previously for pain in multiple joints. This resulted in prolongation of prothrombin time within two weeks with the INR increasing to 3.5 and the dose of warfarin was decreased to 1 mg daily. The other routine medications included digoxin, ranitidine, and atorvastatin. Her diet was unchanged; her bowel habits were also unchanged.
Physical examination showed that vital signs were stable. Extensive ecchymotic areas involved both flanks, left upper limb, under breasts, perineal area, and posterior thorax. There was no oedema, arthritis, stigmata of chronic liver disease, or evidence for vasculitis. Cardiac sounds were normal without significant murmurs, chest was clear, the abdomen was soft and non-tender, without liver or spleen enlargement. No focal neurological deficits were found. The INR was >10. Blood urea nitrogen, serum creatinine, and liver tests were normal. Computed tomography of the abdomen excluded internal haemorrhage.
The coagulation abnormality resolved completely one month after celecoxib and warfarin were discontinued. The patient made a full recovery.
ANALYSIS OF CYP2C9 POLYMORPHISM
These studies followed the guidelines established by the institutional review board and informed consent was obtained from the patient. Genomic DNA was extracted from whole blood and an established human liver cell line, HepG2 (DNA Extractor WB Kit, Wako Chemicals USA, Inc, Richmond, VA). Reference CYP2C9 variant DNAs were available (collection of Dr A K Daly). CYP2C9 primers were according to Sullivan-Klose et al.7 A 50 μl polymerase chain reaction (PCR) used 2.5 mM magnesium chloride, 1.2 μM primers, 1 μg genomic DNA, and 0.5 U DNA polymerase (AmpliTaq, PE Biosystems, Foster City, CA) with 35 cycles (94°C, 5 min; 94°C, 60 s; 55°C, 90 s; 72°C, 30 s; and 72°C, 7 min). PCR products were digested with Ava II or Kpn I (Promega Corp, Madison, WI) and resolved in 1% agarose containing ethidium bromide. The CYP2C9*2 allele loses an Ava II site and the *3 allele gains a Kpn I site.7
*2 Variant analysis
All samples showed the expected 691 base pair (bp) band. Reference DNAs (*1/*1 and *1/*3) produced 527 and 164 bp Ava II fragments (fig 1A). Ava II digestion of *1/*2 product produced 691, 527, and 164 bp bands. Our patient showed 691, 527 and 164 bp Ava II fragments, indicating an *2 allele (lane 9, fig 1A).
*3 Variant analysis
All samples showed the expected 141 bp product (fig 1B). Kpn I did not digest *1/*1, *1/*2, and HepG2 DNAs, whereas *1/*3 reference and test DNAs were partially digested with 141, 111 and 30 bp fragments (lanes 7 and 9, fig 1B).
Sequence analysis verified *2 and *3 CYP2C9 alleles in the patient.
This patient was a compound *2/*3 CYP2C9 heterozygote. Despite the lower warfarin dose of 1 mg daily, competition between celecoxib and warfarin led to severe anticoagulation and bleeding. These findings are quite compatible with warfarin and celecoxib interaction. Such an interaction has been suspected relatively rarely.8,9 We focused on CYP2C9 because this pathway inactivates both warfarin and celecoxib, accounting for ∼80% of drug clearances, whereas *2 and *3 variants possess only ∼12% and 5% enzyme activity, which should increase drug retention.10–12
Aithal et al2 and Taube et al3 established that markedly lower warfarin doses were sufficient for anticoagulation in *2 and *3 CYP2C9 carriers (average <1.5 mg v 5 mg warfarin daily).3 Moreover, warfarin maintenance in compound CYP2C9*2/*3 heterozygotes was 82% of the dose required by *1/*1 CYP2C9 carriers. Although overanticoagulation rates during warfarin maintenance with variant CYP2C9 alleles were (not surprisingly) similar,3 our patient indicates that drug interactions can obviously alter this situation. Celecoxib metabolism decreases up to 90% with *2 and *3 variant alleles and celecoxib exhibits high CYP2C9 affinity.10,12 These perturbations could delay or prevent warfarin metabolism, leading to gradual warfarin accumulation and delayed bleeding, as seen in our patient.
Patients receiving drugs metabolised by the same cytochrome P450 system could be at risk for drug interactions.
Presence of variant cytochrome P450 genes with lower enzymatic activity increases susceptibility for drug interactions.
This case demonstrates the following specific points:
– Metabolism of warfarin was perturbed and led to bleeding in the presence of variant CYP2C9 genes by coadministration of celecoxib, which is a COX-2 inhibitor.
– Analysis of potential interactions between warfarin and other drugs sharing metabolic pathways should include the context of CYP2C9 polymorphisms.
The CYP2C9 *1/*1 allele was encountered most frequently (∼80%) in European populations.1,3 However, *2 and *3 alleles were prevalent in 11% and 5%–7%, respectively, of these populations, which is not insignificant. Therefore, many patients will be at risk for drug interactions mediated by CYP2C9 variants. Use of warfarin for anticoagulation, as well as celecoxib and related drugs, for arthritis and/or other conditions will rise further in the older age groups and thus it will be appropriate to consider the type of drug interaction seen in our patient. This suggests that suitable ways to define the risk for such complications in large patient populations should be examined. For example, the value of prospective CYP2C9 genotyping needs to be addressed in people requiring long term anticoagulation, since single nucleotide polymorphisms are amenable to high throughput testing, which should make such an approach practical.
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