Background: Troglitazone is a CYP3A4 isoenzyme inducer known to decrease th
e plasma concentration of drugs metabolized by CYP3A4. Atorvastatin, a know
n substrate of the CYP3A4 pathway, is often used in combination with trogli
tazone for diabetic patients with dyslipidemia.
Aims: The purpose of this study was to investigate the clinical effects of
troglitazone on the fasting lipid profiles of patients receiving atorvastat
in.
Method: We retrospectively reviewed the medical records of patients who rec
eived concomitant troglitazone and atorvastatin therapy during a 24-month p
eriod. Patients were included in the analysis if during the study period, c
omplete laboratory data were available (fasting lipid profile and glycosyla
ted haemoglobin), the dose of atorvastatin remained unchanged, there were n
o changes in the diabetic drug regimen, patients received at least 3 months
of combination therapy and patients were adherent with their medication.
Results: Four out of 31 (13%) patients satisfied the inclusion criteria. Al
l of these patients were male, with a mean age of 63. All patients were rec
eiving insulin only for diabetes control when the troglitazone was added. T
here was an increase in LDL-cholesterol and triglycerides of 23.3% and 21.3
%, respectively.
Conclusions: The increase in LDL-cholesterol and triglycerides on atorvasta
tin and troglitazone combination therapy compared with atorvastatin mono-th
erapy is suggestive of a drug interaction. Further studies involving trogli
tazone and atorvastatin may be warranted to substantiate this interaction.