HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Effects of rosuvastatin on myeloperoxidase levels in patients with chronic heart failure: a randomized placebo-controlled study.

AbstractBACKGROUND:
Studies indicate that myeloperoxidase (MPO) is associated with disease progression and severity in heart failure (HF), while it may provide a mechanistic link between inflammation and adverse cardiac remodeling. The mechanisms that regulate MPO are unclear, while it is unknown whether specific treatments such as HMG-CoA reductase inhibitors and xanthine oxidase inhibitors may modify MPO. Therefore in the present study we examined the effects of rosuvastatin and allopurinol on MPO levels in patients HF.
METHODS:
Sixty clinically stable patients with systolic HF were randomized to receive rosuvastatin 10mg/day, allopurinol 300mg/day or placebo and followed up for 1 month. Plasma levels of MPO and serum levels of soluble CD40 ligand, interleukin-6, and oxidized LDL were determined using ELISA. All measurements were made before and after 1-month treatment.
RESULTS:
Rosuvastatin significantly reduced plasma levels of MPO (p=0.003), which remained unchanged in the other groups. Furthermore, the change of MPO levels in the rosuvastatin-treated group was significantly different compared with the other groups (p<0.05). Rosuvastatin administration also led to a significant decrease in oxidized LDL (p=0.009), while the other inflammatory markers remained unchanged in all groups. In the total population, a significant correlation was observed between the baseline levels of MPO and hsCRP (r=0.275, p=0.027), fibrinogen (r=0.278, p=0.025), and sCD40L (r=0.288, p=0.021).
CONCLUSIONS:
Short-term treatment with rosuvastatin regulates inflammatory process in patients with heart failure by significantly reducing plasma levels of MPO. This finding reveals a novel pleiotropic effect of statins in patients with heart failure, and provides further insights into the pathophysiological mechanisms of MPO in heart failure.
AuthorsIoannis Andreou, Dimitris Tousoulis, Antigoni Miliou, Costas Tentolouris, Kostas Zisimos, Panagiota Gounari, Gerasimos Siasos, Nikos Papageorgiou, Christos A Papadimitriou, Meletios-Athanasios Dimopoulos, Christodoulos Stefanadis
JournalAtherosclerosis (Atherosclerosis) Vol. 210 Issue 1 Pg. 194-8 (May 2010) ISSN: 1879-1484 [Electronic] Ireland
PMID19962701 (Publication Type: Journal Article, Randomized Controlled Trial)
CopyrightCopyright 2009 Elsevier Ireland Ltd. All rights reserved.
Chemical References
  • Biomarkers
  • Cholesterol, LDL
  • Fluorobenzenes
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Pyrimidines
  • Sulfonamides
  • Triglycerides
  • Allopurinol
  • Rosuvastatin Calcium
  • Cholesterol
  • Peroxidase
Topics
  • Aged
  • Allopurinol (pharmacology, therapeutic use)
  • Biomarkers (blood)
  • Cholesterol (blood)
  • Cholesterol, LDL (blood)
  • Chronic Disease
  • Female
  • Fluorobenzenes (pharmacology, therapeutic use)
  • Heart Failure (blood, drug therapy)
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors (pharmacology, therapeutic use)
  • Inflammation (drug therapy)
  • Male
  • Peroxidase (blood)
  • Pyrimidines (pharmacology, therapeutic use)
  • Rosuvastatin Calcium
  • Sulfonamides (pharmacology, therapeutic use)
  • Triglycerides (blood)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: