[The effect of early fluvastatin therapy on inflammatory factors in acute coronary syndrome]

Zhonghua Nei Ke Za Zhi. 2005 Mar;44(3):184-7.
[Article in Chinese]

Abstract

Objective: To investigate the effects of different doses of fluvastatin on serum levels of high-sensitive C-reactive protein (hs-CRP) and tumour necrosis factor-alpha (TNFalpha) in the early phase of acute coronary syndrome (ACS).

Methods: Fifty eight patients with ACS were randomly separated into three groups. 20 patients in group A were given routine therapy, 20 patients in group B were given routine therapy with oral fluvastatin 40 mg once daily for 1 week and 18 patients in group C received routine therapy with oral fluvastatin 80 mg once daily for 1 week. 20 patients with stable coronary heart disease served controls. The serum levels of hs-CRP and TNFalpha before and after therapy were measured with immunoturbidimetric assay and ELISA method.

Results: (1) The serum levels of hs-CRP and TNFalpha in the patients with ACS were significantly higher than those in the control group (P < 0.05). (2) The serum levels of hs-CRP and TNFalpha significantly lowered after one week of therapy in the two fluvastatin treated groups (P < 0.01 in all), especially in the 80 mg fluvastatin group, while no significant difference was observed before and after treatment in the routine therapy group. (3) The serum levels of hs-CRP and TNFalpha had a significant positive correlation in the patients with ACS (r = 0.70, P < 0.01), but no relationship were observed between TC, TG, LDL-C, or HDL-C and hs-CRP or TNFalpha by Pearson correlation analysis.

Conclusions: The serum levels of inflammatory factors including CRP and TNFalpha are increased in patients with ACS and early fluvastatin intervention may decease dose-dependently the serum levels of hs-CRP and TNFalpha. The anti-inflammatory effect of fluvastatin may be beyond that of lipid lowering. Early intensive fluvastatin treatment may yield more significant benefits in the patients with ACS.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Anticholesteremic Agents / administration & dosage*
  • C-Reactive Protein / metabolism
  • Coronary Disease / blood
  • Coronary Disease / drug therapy*
  • Dose-Response Relationship, Drug
  • Drug Administration Schedule
  • Fatty Acids, Monounsaturated / administration & dosage*
  • Female
  • Fluvastatin
  • Humans
  • Indoles / administration & dosage*
  • Inflammation / blood
  • Lipids / blood
  • Male
  • Middle Aged
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Anticholesteremic Agents
  • Fatty Acids, Monounsaturated
  • Indoles
  • Lipids
  • Tumor Necrosis Factor-alpha
  • Fluvastatin
  • C-Reactive Protein