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Metaanálisis2007Financiación no declarada

Meta-analysis of the cholesterol-lowering effect of ezetimibe added to ongoing statin therapy

Mikhailidis DP, Sibbring GC, Ballantyne CM, Davies GM, Catapano AL

Current medical research and opinion · 116 citas

Etiquetas de revisión

Financiación no declarada

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Cómo se estudió

Diseño
Metaanálisis (indexado por PubMed)
Estudiado en
Personas
Resultado principal
Marcadores de salud y funcionamiento

Quién lo pagó

Financiación
Financiación no declarada

Publicación

Publicado
2007-07-19 · Curr Med Res Opin · vol. 23 · número 8 · págs. 2009–2026
Editorial
Taylor & Francis
Citado
146 citas · más que el 91% de estudios similares · 2.8× el promedio de su campo
Impacto
Entre el 10 % más citado de su campo
Referencias
46 trabajos
Acceso
De pago
Áreas de investigación
Lipoproteins and Cardiovascular Health · Cholesterol and Lipid Metabolism · Cancer, Lipids, and Metabolism
Palabras clave
ezetimibe, statin combination therapy, hypercholesterolemia, LDL cholesterol lowering, total cholesterol, HDL cholesterol, coronary artery disease, statin adverse effects, creatine kinase, liver enzymes, lipid-lowering therapy, statin intolerance, statin-induced myopathy, statin-induced rhabdomyolysis, statin-induced liver injury
MeSH
humans, hypercholesterolemia, azetidines, cholesterol, triglycerides, lipoproteins, placebos, anticholesteremic agents, hydroxymethylglutaryl-coa reductase inhibitors, randomized controlled trials as topic, ezetimibe

5 autores

  • Dimitri P. Mikhailidis🇬🇧 · autor de correspondenciaThe Royal Free Hospital; University College London
  • Gillian C. Sibbring
  • Christie Mitchell Ballantyne🇺🇸Baylor College of Medicine
  • G. M. Davies🇺🇸Merck & Co., Inc., Rahway, NJ, USA (United States)
  • Alberico Luigi Catapano🇮🇹University of Milan

Resumen

El texto original del estudio, en el idioma en que se publicó.

Objective

To review and analyse the evidence for the cholesterol-lowering effect of ezetimibe in adult patients with hypercholesterolaemia who are not at low-density lipoprotein cholesterol (LDL-C) goal on statin monotherapy.

Research design

Systematic review and meta-analysis.

Methods

MEDLINE and EMBASE were searched to identify ezetimibe randomised controlled trials (RCTs) published between January 1993 and December 2005. The meta-analysis combined data from RCTs, with a minimum treatment duration of 6 weeks, that compared treatment with ezetimibe 10 mg/day or placebo added to current statin therapy. The difference between treatments was analysed for four co-primary outcomes: mean percentage change from baseline in total cholesterol (TC), LDL-C, and high-density lipoprotein cholesterol (HDL-C), and number of patients achieving LDL-C treatment goal. Meta-analysis results are presented for a modified version of the inverse variance random effects model.

Results

Five RCTs involving a total of 5039 patients were included in the meta-analysis. The weighted mean difference (WMD) between treatments significantly favoured the ezetimibe/statin combination over placebo/statin for TC (-16.1% (-17.3, -14.8); p < 0.0001), LDL-C (-23.6% (-25.6, -21.7); p < 0.0001) and HDL-C (1.7% (0.9, 2.5); p < 0.0001). The relative risk of reaching the LDL-C treatment goal was significantly higher for patients on ezetimibe/statin relative to those on placebo/statin (3.4 (2.0, 5.6); p < 0.0001). In pre-defined sub-group analyses of studies in patients with coronary heart disease, the WMD between treatments remained significantly in favour of ezetimibe/statin (p < 0.0001) for TC and LDL-C but was no longer significant for HDL-C. Elevations in creatine kinase, alanine aminotransferase or aspartate aminotransferase that were considered as an adverse effect did not differ significantly between treatments.

Conclusions

The meta-analysis we performed included only five studies and was restricted to analysis of the changes in cholesterol levels relative to baseline. However, the results suggest that ezetimibe co-administered with ongoing statin therapy provides significant additional lipid-lowering in patients not at LDL-C goal on statin therapy alone, allowing more patients to reach their LDL-C goal.

Resumen vía Europe PMC. Los derechos de autor siguen siendo de los autores o la editorial.

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