Low incidence of paradoxical reductions in HDL-C levels in dyslipidemic patients treated with fenofibrate alone or in combination with ezetimibe or ezetimibe/simvastatin

Lipids Health Dis. 2011 Nov 16:10:212. doi: 10.1186/1476-511X-10-212.

Abstract

Background: Fibrates have been reported to cause paradoxical decreases in HDL-C in certain patients.

Design and methods: This post-hoc analysis explored the frequency/magnitude of HDL-C reductions in a pooled database of mixed dyslipidemic patients (LDL-C:3.4-5.7 mmol/L;TG:1.7-5.7 mmol/L) receiving placebo (PBO), fenofibrate (FENO), ezetimibe plus FENO (EZE+FENO), or EZE/simvastatin plus FENO (EZE/SIMVA+FENO) for 12 weeks.

Results: PBO-treated patients had the highest incidence of HDL-C reductions from baseline (45%) compared with patients taking FENO (14%), EZE+FENO (9%), or EZE/SIMVA+FENO (9%). Reductions <30% reflected natural variability since the largest reduction in HDL-C approached 30% in the PBO group. Only 3 patients exhibited HDL-C reductions ≥30% (i.e., 2 patients in the FENO group and 1 in the EZE+FENO group). There were no differences in demographic/biochemical characteristics between patients with and without HDL-C reductions.

Conclusions: The incidence of paradoxical HDL-C reductions was low in mixed dyslipidemic patients receiving FENO alone or combined with EZE or EZE/SIMVA.

Trial registration: ClinicalTrials.gov NCT00092560 NCT00092573.

Publication types

  • Multicenter Study
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Anticholesteremic Agents / therapeutic use*
  • Azetidines / therapeutic use*
  • Cholesterol, HDL / blood*
  • Double-Blind Method
  • Drug Therapy, Combination
  • Dyslipidemias / blood
  • Dyslipidemias / drug therapy*
  • Ezetimibe
  • Female
  • Fenofibrate / therapeutic use*
  • Humans
  • Male
  • Middle Aged
  • Simvastatin / therapeutic use*
  • Treatment Outcome

Substances

  • Anticholesteremic Agents
  • Azetidines
  • Cholesterol, HDL
  • Simvastatin
  • Ezetimibe
  • Fenofibrate

Associated data

  • ClinicalTrials.gov/NCT00092560
  • ClinicalTrials.gov/NCT00092573