Cardiovascular Diabetology (Jul 2004)

Ciprofibrate therapy in patients with hypertriglyceridemia and low high density lipoprotein (HDL)-cholesterol: greater reduction of non-HDL cholesterol in subjects with excess body weight (The CIPROAMLAT study)

  • Medel Octavio,
  • Hernández Ismael,
  • Salinas Saul,
  • Vazquez Cuauhtémoc,
  • Ramírez Erika,
  • Jiménez Sergio,
  • Hernández Ma,
  • Florenzano Fernando,
  • Saavedra Victor,
  • Reyes Eliana,
  • Machado Carlos,
  • Oliveira José,
  • Torres Kerginaldo,
  • Rabelo Lísia,
  • Neto Abrahão,
  • Filho José,
  • Rengifo Hector,
  • Stockins Benjamín,
  • Aguilar-Salinas Carlos A,
  • Assis-Luores-Vale Andréia,
  • Moreno Ricardo,
  • Lugo Paula,
  • Alvarado Ricardo,
  • Mehta Roopa,
  • Gutierrez Victor,
  • Gómez Pérez Francisco J

DOI
https://doi.org/10.1186/1475-2840-3-8
Journal volume & issue
Vol. 3, no. 1
p. 8

Abstract

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Abstract Background Hypertriglyceridemia in combination with low HDL cholesterol levels is a risk factor for cardiovascular disease. Our objective was to evaluate the efficacy of ciprofibrate for the treatment of this form of dyslipidemia and to identify factors associated with better treatment response. Methods Multicenter, international, open-label study. Four hundred and thirty seven patients were included. The plasma lipid levels at inclusion were fasting triglyceride concentrations between 1.6–3.9 mM/l and HDL cholesterol ≤ 1.05 mM/l for women and ≤ 0.9 mM/l for men. The LDL cholesterol was below 4.2 mM/l. All patients received ciprofibrate 100 mg/d. Efficacy and safety parameters were assessed at baseline and at the end of the treatment. The primary efficacy parameter of the study was percentage change in triglycerides from baseline. Results After 4 months, plasma triglyceride concentrations were decreased by 44% (p 2) compared to the rest of the population (8.2 vs 19.7%, p Conclusions Ciprofibrate is efficacious for the correction of hypertriglyceridemia / low HDL cholesterol. A greater decrease in non-HDL cholesterol was found among cases with excess body weight. The mechanism of action of ciprofibrate may be influenced by the pathophysiology of the disorder being treated.

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