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[Effect of therapy with atorvastatin on parameters of postprandial lipemia and factors of inflammation in patients with ischemic heart disease].

Abstract
Reaction of parameters of lipid transport system to standard fat load (J.Patsch method), C-reactive protein (CRP) and fibrinogen levels were studied in 30 patients with ischemic heart disease before and after 3 months of therapy with atorvastatin (10 mg/day). Atorvastatin therapy resulted in 25, 34, 17 and 16% lowering of concentrations of total cholesterol (CH), low density lipoprotein CH, triglycerides (TG), and apolipoprotein (apo) B, respectively, 6 and 9% elevation of high density lipoprotein CH and apo A-1 levels, respectively. Moreover atorvastatin improved although not completely normalized parameters of postprandial lipemia: significant lowering of baseline (-17%), 3 (-19%) and 6 hour (-14%) post load TG levels was noted. However relative TG elevation from baseline level to 3 and 6 hours after fat load did not change (+100 and 148% before, +95 and 156% after treatment, respectively). Changes of CRP (-22%) and fibrinogen (-8%) were not significant (p>0.05).
AuthorsE Iu Samoĭlenko, V G Naumov, M G Tvorogova, M V Ezhov, I V Sergienko, V V Kukharchuk
JournalKardiologiia (Kardiologiia) Vol. 47 Issue 2 Pg. 4-8 ( 2007) ISSN: 0022-9040 [Print] Russia (Federation)
PMID17495815 (Publication Type: Clinical Trial, Journal Article)
Chemical References
  • Anticholesteremic Agents
  • Heptanoic Acids
  • Lipids
  • Pyrroles
  • Fibrinogen
  • C-Reactive Protein
  • Atorvastatin
Topics
  • Adult
  • Anticholesteremic Agents (pharmacology, therapeutic use)
  • Atorvastatin
  • C-Reactive Protein (analysis)
  • Female
  • Fibrinogen (analysis)
  • Heptanoic Acids (pharmacology, therapeutic use)
  • Humans
  • Hyperlipidemias (complications, drug therapy)
  • Inflammation (complications, drug therapy)
  • Lipids (blood)
  • Male
  • Myocardial Ischemia (complications)
  • Postprandial Period (drug effects)
  • Pyrroles (pharmacology, therapeutic use)
  • Treatment Outcome

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