Literature DB >> 15383192

Effects of ezetimibe added to on-going statin therapy on the lipid profile of hypercholesterolemic patients with diabetes mellitus or metabolic syndrome.

Leon Simons1, Melvin Tonkon, Luis Masana, Darbie Maccubbin, Arvind Shah, Michael Lee, Barry Gumbiner.   

Abstract

OBJECTIVE: To conduct a post-hoc assessment of the lipid-modifying effects of adding the cholesterol absorption inhibitor, ezetimibe, to on-going statin therapy in patients with diabetes mellitus (DM) or metabolic syndrome (MetS). RESEARCH DESIGN AND METHODS: This was a post-hoc analysis of data from a randomized, double-blind, placebo-controlled trial designed to evaluate the low-density lipoprotein cholesterol (LDL-C)-lowering efficacy and safety of adding ezetimibe 10 mg/day versus placebo to ongoing, open-label statin treatment for 8 weeks in hypercholesterolemic patients. Qualifying LDL-C levels and target LDL-C goals were based on National Cholesterol Education Program risk categories. The DM subgroup were patients who entered the study with a prior diagnosis of DM. Patients were classified as having MetS if they met 3 or more of the following criteria at baseline: triglycerides (TG) > or = 150 mg/dL (1.69 mmol/L); high-density lipoprotein cholesterol (HDL-C) < 40 mg/dL (1.04 mmol/L) for men or < 50 mg/dL (1.29 mmol/L) for women; fasting serum glucose (FSG) > or = 110 mg/dL (> or = 6.1 mmol/L); a diagnosis of hypertension or taking hypertension medication or blood pressure > or = 130/> or = 85 mmHg; waist circumference > 88 cm (women) or > 102 cm (men). DM patients were excluded from the MetS subgroup analysis. MAIN OUTCOME MEASURES: The objectives were to assess the effects of treatment on plasma concentrations of LDL-C and other lipid variables, and on the percentage of patients achieving LDL-C target levels at the end of the study.
RESULTS: Of 769 patients enrolled in the original study, there were 191 (24.8%) with DM and 195 (25.4%) with MetS. Regardless of subgroup, ezetimibe + statin was significantly more effective than statin alone at lowering plasma levels of LDL-C, non-HDL-C, total cholesterol, apolipoprotein B, and triglycerides (between-group p < 0.001 for all). For all lipid parameters, the relative treatment effects were generally consistent regardless of DM or MetS status. Significantly more ezetimibe than placebo patients in all subgroups achieved prespecified LDL-C goals (p < 0.001 for all), and although more patients in the DM and MetS groups, respectively, achieved the goal compared with their non-DM and non-MetS counterparts [83.6% (DM) versus 67.2 (non-DM) and 71.8% (MetS) versus 65.6% (non-MetS)], these differences were not significant after adjusting for differences in baseline LDL-C levels. Ezetimibe was well-tolerated and had a favorable safety profile in all subgroups.
CONCLUSIONS: The co-administration of ezetimibe with statins, a therapeutic regimen that inhibits both the absorption and synthesis of cholesterol, offers a well-tolerated and efficacious treatment to lower LDL-C in patients with DM and MetS.

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Year:  2004        PMID: 15383192     DOI: 10.1185/030079904x2321

Source DB:  PubMed          Journal:  Curr Med Res Opin        ISSN: 0300-7995            Impact factor:   2.580


  14 in total

Review 1.  The metabolic syndrome.

Authors:  Marc-Andre Cornier; Dana Dabelea; Teri L Hernandez; Rachel C Lindstrom; Amy J Steig; Nicole R Stob; Rachael E Van Pelt; Hong Wang; Robert H Eckel
Journal:  Endocr Rev       Date:  2008-10-29       Impact factor: 19.871

2.  Efficacy and tolerability of ezetimibe 10 mg/day coadministered with statins in patients with primary hypercholesterolemia who do not achieve target LDL-C while on statin monotherapy: A Canadian, multicentre, prospective study--the Ezetrol Add-On Study.

Authors:  Stéphane Bissonnette; Rafik Habib; Fotini Sampalis; Stella Boukas; John S Sampalis
Journal:  Can J Cardiol       Date:  2006-10       Impact factor: 5.223

Review 3.  Combination of statin and ezetimibe for the treatment of dyslipidemias and the prevention of coronary artery disease.

Authors:  Jacques Genest
Journal:  Can J Cardiol       Date:  2006-08       Impact factor: 5.223

4.  Current Treatment Options for the Metabolic Syndrome.

Authors:  Prakash C Deedwania; Natalia Volkova
Journal:  Curr Treat Options Cardiovasc Med       Date:  2005-05

Review 5.  The effect of statin therapy in combination with ezetimibe on circulating C-reactive protein levels: a systematic review and meta-analysis of randomized controlled trials.

Authors:  Seyyed Mostafa Arabi; Mahla Chambari; Mahsa Malek-Ahmadi; Leila Sadat Bahrami; Vahid Hadi; Manfredi Rizzo; Amirhossein Sahebkar
Journal:  Inflammopharmacology       Date:  2022-08-21       Impact factor: 5.093

6.  Comparison of Efficacy and Safety of Statin-Ezetimibe Combination Therapy with Statin Monotherapy in Patients with Diabetes: A Meta-Analysis of Randomized Controlled Studies.

Authors:  Kwang-Hee Shin; Hye Duck Choi
Journal:  Am J Cardiovasc Drugs       Date:  2021-12-20       Impact factor: 3.283

7.  Ezetimibe + simvastatin versus doubling the dose of simvastatin in high cardiovascular risk diabetics: a multicenter, randomized trial (the LEAD study).

Authors:  Gianluca Bardini; Carlo B Giorda; Antonio E Pontiroli; Cristina Le Grazie; Carlo M Rotella
Journal:  Cardiovasc Diabetol       Date:  2010-05-21       Impact factor: 9.951

8.  Ezetimibe/simvastatin vs simvastatin in coronary heart disease patients with or without diabetes.

Authors:  Carlo M Rotella; Augusto Zaninelli; Cristina Le Grazie; Mary E Hanson; Gian Franco Gensini
Journal:  Lipids Health Dis       Date:  2010-07-27       Impact factor: 3.876

Review 9.  Diabetes: managing dyslipidaemia.

Authors:  Jigisha Patel
Journal:  BMJ Clin Evid       Date:  2008-06-09

10.  Treatment of dyslipidemia in the elderly.

Authors:  Hong Shao; Li-Quan Chen; Jun Xu
Journal:  J Geriatr Cardiol       Date:  2011-03       Impact factor: 3.327

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