[Effects of different statins, ezetimibe/simvastatin combination on hsCRP levels in unstable angina pectoris and non-ST elevation myocardial infarction patients: a randomized trial]

Anadolu Kardiyol Derg. 2011 Dec;11(8):703-10. doi: 10.5152/akd.2011.192. Epub 2011 Nov 16.
[Article in Turkish]

Abstract

Objective: The aim of our study was to evaluate the effects of two different statins and a statin/ezetimibe combination on high sensitive C-reactive protein (hsCRP) values, which were given at high doses in the early period of acute coronary syndromes.

Methods: A total of 150 patients with non-ST elevation myocardial infarction and unstable angina pectoris were enrolled to our prospective, randomized, single-blind study. Patients were divided into three groups by block randomization method. One group received 20 mg/day atorvastatin, one group received 10 mg/day rosuvastatin and the other group received 10 mg/day ezetimibe/simvastatin combination therapy, which was initiated within the first 24 hours of admission. Follow-up duration was 2 months . Biochemical investigations and hsCRP levels (by nephelometric method) were performed with 138 patients evaluated at baseline, 10th and 60th days of therapy. Decreases of hsCRP levels were analyzed with one-way MANOVA and repeated measures of ANOVA methods. Post-hoc Tukey HSD test was performed for finding the different group, when the difference was detected between the groups.

Results: Tenth day hsCRP levels in ezetimibe/simvastatin group was significantly lower than the other groups (p<0.001). Further, after 60 days of follow-up a significant reduction was seen in hsCRP levels in ezetimib/simvastatin group (in ezetimibe/simvastatin group the mean hsCRP was reduced from 38.4±15.0 mg/L to 2.4±1.3 mg/L, in atorvastatin group the mean hsCRP was reduced from 27.3±11.7 mg/L to 4.1±2.4 mg/L and in rosuvastatin group the mean hsCRP was reduced from 22.0±6.9 mg/L to 3.6±1.7 mg/L (F (1.1, 148.2) = 746.9, p<0.01 and the difference between drugs; F (2.2, 148.2) = 32.1, p<0.01). No side effects related to drugs were seen during follow-up in all three treatment groups.

Conclusion: This study showed that ezetimibe/simvastatin 10 mg/day combination treatment was superior to atorvastatin 20 mg/day and rosuvastatin 10 mg/day treatment in reducing the inflammatory markers when high dose statins was started in the early period of unstable angina and non ST elevation myocardial infarction.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Angina, Unstable / blood
  • Angina, Unstable / drug therapy*
  • Atorvastatin
  • Azetidines / administration & dosage
  • Azetidines / therapeutic use*
  • C-Reactive Protein / metabolism*
  • Drug Combinations
  • Ezetimibe, Simvastatin Drug Combination
  • Female
  • Fluorobenzenes / administration & dosage
  • Fluorobenzenes / therapeutic use
  • Heptanoic Acids / administration & dosage
  • Heptanoic Acids / therapeutic use
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / administration & dosage
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / therapeutic use*
  • Male
  • Middle Aged
  • Myocardial Infarction / blood
  • Myocardial Infarction / drug therapy*
  • Prospective Studies
  • Pyrimidines / administration & dosage
  • Pyrimidines / therapeutic use
  • Pyrroles / administration & dosage
  • Pyrroles / therapeutic use
  • Rosuvastatin Calcium
  • Simvastatin / administration & dosage
  • Simvastatin / therapeutic use*
  • Single-Blind Method
  • Sulfonamides / administration & dosage
  • Sulfonamides / therapeutic use
  • Treatment Outcome

Substances

  • Azetidines
  • Drug Combinations
  • Ezetimibe, Simvastatin Drug Combination
  • Fluorobenzenes
  • Heptanoic Acids
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Pyrimidines
  • Pyrroles
  • Sulfonamides
  • Rosuvastatin Calcium
  • C-Reactive Protein
  • Atorvastatin
  • Simvastatin