Hypolipidaemic and anti-inflammatory effects of fixed dose combination of atorvastatin plus ezetimibe in Indian patients with dyslipidaemia.
- Author:
Biswa Mohan PADHY
1
;
Rakesh YADAV
;
Yogendra Kumar GUPTA
Author Information
- Publication Type:Journal Article
- MeSH: Anti-Inflammatory Agents; therapeutic use; Anticholesteremic Agents; administration & dosage; Atorvastatin Calcium; Azetidines; administration & dosage; C-Reactive Protein; metabolism; Double-Blind Method; Drug Therapy, Combination; methods; Dyslipidemias; drug therapy; Ezetimibe; Female; Heptanoic Acids; administration & dosage; Humans; Hypolipidemic Agents; therapeutic use; India; Intercellular Adhesion Molecule-1; metabolism; Lipoproteins, LDL; metabolism; Male; Middle Aged; Pyrroles; administration & dosage; Treatment Outcome
- From:Singapore medical journal 2013;54(2):90-95
- CountrySingapore
- Language:English
-
Abstract:
INTRODUCTIONWe aimed to assess the efficacy of fixed dose combination of atorvastatin plus ezetimibe in Indian patients with dyslipidaemia.
METHODSA double-blind study was conducted to assess the effect of fixed dose combination of ezetimibe 10 mg plus atorvastatin 10 mg on lipid profile, oxidised low-density lipoprotein (ox-LDL), high-sensitivity C-reactive protein (hsCRP) and soluble intercellular cell adhesion molecule (sICAM) in dyslipidaemic patients with or at high risk of coronary artery disease, and compare it with atorvastatin 10 mg monotherapy. 30 patients were randomised to receive ezetimibe plus atorvastatin or atorvastatin once daily for four weeks.
RESULTSOf the 30 patients, 10 men and 5 women (mean age 54.3 ± 1.6 years) received ezetimibe plus atorvastatin, while 13 men and 2 women (mean age 53.7 ± 2.8 years) received only atorvastatin. The combination treatment significantly reduced total cholesterol (percentage treatment difference -14.4 ± 6.5, 95% confidence interval [CI] -1.0 to -27.7; p = 0.041) and LDL cholesterol (LDL-C; percentage treatment difference -19.9 ± 6.1, 95% CI -7.4 to -32.4; p = 0.003) compared to atorvastatin monotherapy. 13 patients on combination treament achieved the National Cholesterol Education Program target for LDL-C as compared to 9 patients on atorvastatin monotherapy (p = 0.032). Significant reductions in very low-density lipoprotein cholesterol, triglyceride, ox-LDL and sICAM were observed with combination treatment compared to atorvastatin monotherapy. However, no significant change was seen in high-density lipoprotein cholesterol or hsCRP levels between the two groups.
CONCLUSIONCombination treatment with atorvastatin and ezetimibe had relatively better lipid-lowering and anti-inflammatory efficacy than atorvastatin monotherapy.
