BackgroundApolipoprotein (Apo) B-48 is an intestinally derived lipoprotein that is expected to be a marker for cardiovascular disease (CVD). Lipoprotein-associated phospholipase A2 (Lp-PLA2) is a vascular-specific inflammatory marker and important risk predictor of CVD. The aim of this study was to explore the effect of pitavastatin treatment and life style modification (LSM) on ApoB-48 and Lp-PLA2 levels in metabolic syndrome (MS) patients at relatively low risk for CVD, as a sub-analysis of a previous multi-center prospective study.MethodsWe enrolled 75 patients with MS from the PROPIT study and randomized them into two treatment groups: 2 mg pitavastatin daily+intensive LSM or intensive LSM only. We measured the change of lipid profiles,...
BACKGROUND: Pitavastatin is a 3-hydroxy-3-methyl-glutaryl coenzyme A (HMG-CoA) reductase inhibitor u...
ObjectivesThis study sought to examine the relationship between baseline and on-study apolipoprotein...
Background - Statins lower cholesterol by inhibiting HMG-CoA reductase, the rate-limiting enzyme of ...
Purpose: Although the role of high-intensity lipid-lowering therapy in cardiovascular protection has...
Aims Microalbuminuria frequently clusters with the metabolic syndrome and may identify subjects at i...
Pitavastatin is the newest member of the HMG-CoA reductase inhibitor family and is approved as adjun...
Aims Microalbuminuria frequently clusters with the metabolic syndrome and may identify subjects at i...
Intensive as compared to mild statin therapy has been proven to be superior in improving cardiovascu...
OBJECTIVE: Intensive as compared to mild statin therapy has been proven to be superior in improving ...
Aims Microalbuminuria frequently clusters with the metabolic syndrome and may identify subjects at i...
Abstract Background The diabetogenic action of statins remains a concern, particularly in patients a...
AbstractBackgroundMany large-scale clinical trials have confirmed that statins are effective in redu...
Background and Objectives:Pitavastatin, a recently approved synthetic 3-hydroxy-3-methylglutaryl coe...
AIM: The metabolic syndrome (MS) increases the risk of coronary heart disease, yet few data are ava...
Currently, different statins are available for the treatment of dyslipidemia: Atorvastatin, Simvasta...
BACKGROUND: Pitavastatin is a 3-hydroxy-3-methyl-glutaryl coenzyme A (HMG-CoA) reductase inhibitor u...
ObjectivesThis study sought to examine the relationship between baseline and on-study apolipoprotein...
Background - Statins lower cholesterol by inhibiting HMG-CoA reductase, the rate-limiting enzyme of ...
Purpose: Although the role of high-intensity lipid-lowering therapy in cardiovascular protection has...
Aims Microalbuminuria frequently clusters with the metabolic syndrome and may identify subjects at i...
Pitavastatin is the newest member of the HMG-CoA reductase inhibitor family and is approved as adjun...
Aims Microalbuminuria frequently clusters with the metabolic syndrome and may identify subjects at i...
Intensive as compared to mild statin therapy has been proven to be superior in improving cardiovascu...
OBJECTIVE: Intensive as compared to mild statin therapy has been proven to be superior in improving ...
Aims Microalbuminuria frequently clusters with the metabolic syndrome and may identify subjects at i...
Abstract Background The diabetogenic action of statins remains a concern, particularly in patients a...
AbstractBackgroundMany large-scale clinical trials have confirmed that statins are effective in redu...
Background and Objectives:Pitavastatin, a recently approved synthetic 3-hydroxy-3-methylglutaryl coe...
AIM: The metabolic syndrome (MS) increases the risk of coronary heart disease, yet few data are ava...
Currently, different statins are available for the treatment of dyslipidemia: Atorvastatin, Simvasta...
BACKGROUND: Pitavastatin is a 3-hydroxy-3-methyl-glutaryl coenzyme A (HMG-CoA) reductase inhibitor u...
ObjectivesThis study sought to examine the relationship between baseline and on-study apolipoprotein...
Background - Statins lower cholesterol by inhibiting HMG-CoA reductase, the rate-limiting enzyme of ...