Correlates of LDL-cholesterol goal attainment in patients under lipid lowering therapy

Atherosclerosis. 2008 Aug;199(2):368-77. doi: 10.1016/j.atherosclerosis.2007.11.033. Epub 2008 Jan 11.

Abstract

Background: LDL-cholesterol therapeutic objectives attainment under lipid lowering therapy remains inadequate. The correlates of LDL-cholesterol therapeutic objective attainment have not been thoroughly explored in an observational setting.

Methods: Patients under lipid lowering therapy and managed by general practitioners were included. LDL-cholesterol therapeutic objective was defined according to the number of cardiovascular risk factors associated with dyslipidemia (AFSSAPS-2005 guidelines).

Results: Most of the 2727 patients (mean age: 64.7+/-11.0) received a statin (70.0%) or a fibrate (24.3%) in monotherapy. 58.5% of patients at high cardiovascular risk did not reach therapeutic objective. Compared to simvastatin, patients receiving fibrates were less likely to be at therapeutic objective (OR=0.38, 95% CI=[0.26-0.54]). So were patients receiving fluvastatin (OR=0.41, IC95%=[0.26-0.64]) or pravastatin (OR=0.49, IC95%=[0.35-0.70]) at the dosages used by GPs. No significant difference appeared with atorvastatin (OR=0.99, 95% CI=[0.71-1.39]) or rosuvastatin (OR=1.25, CI95%=[0.77-2.02]). Patients with LDL-cholesterol levels<0.7 g/L tended to be prescribed high doses of lipid lowering therapy.

Conclusions: In real conditions of lipid lowering therapy use, LDL-cholesterol therapeutic objective attainment was inadequate in high-risk patients, and TO differences were observed between drugs at prescribed doses.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Anticholesteremic Agents / pharmacology
  • Cardiovascular System / metabolism
  • Cholesterol, LDL / metabolism*
  • Fatty Acids, Monounsaturated / pharmacology
  • Female
  • Fluorobenzenes / pharmacology
  • Fluvastatin
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / pharmacology
  • Indoles / pharmacology
  • Lipids / chemistry*
  • Male
  • Middle Aged
  • Pravastatin / pharmacology
  • Pyrimidines / pharmacology
  • Risk Factors
  • Rosuvastatin Calcium
  • Sulfonamides / pharmacology
  • Treatment Outcome

Substances

  • Anticholesteremic Agents
  • Cholesterol, LDL
  • Fatty Acids, Monounsaturated
  • Fluorobenzenes
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Indoles
  • Lipids
  • Pyrimidines
  • Sulfonamides
  • Fluvastatin
  • Rosuvastatin Calcium
  • Pravastatin