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Metaanálisis2017Financiado por la industriaVínculos de autores con la industriaAcceso abierto

Financiado en parte por Amgen

Systematic Review and Network Meta-Analysis on the Efficacy of Evolocumab and Other Therapies for the Management of Lipid Levels in Hyperlipidemia

Toth PP, Worthy G, Gandra SR, Sattar N, Bray S, Cheng LI, Bridges I, Worth GM, Dent R, Forbes CA, Deshpande S, Ross J, Kleijnen J, Stroes ESG

Journal of the American Heart Association · 62 citas

Etiquetas de revisión

Vínculos de autores con la industriaFinanciado por la industria

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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
Financiado por la industria
Empresa
Amgen
Autores
Al menos un autor declara un vínculo económico con la industria

Según 1 financiador declarado y la declaración de financiación del texto completo.

Publicación

Publicado
2017-10-03 · J Am Heart Assoc · vol. 6 · número 10
Editorial
Wiley
Citado
92 citas · más que el 91% de estudios similares · 2.4× el promedio de su campo
Impacto
Entre el 10 % más citado de su campo
Referencias
48 trabajos
Acceso
Acceso abierto (revista) · CC-BY-NC-ND
Áreas de investigación
Lipoproteins and Cardiovascular Health · Lipid metabolism and disorders · Cholesterol and Lipid Metabolism
Palabras clave
evolocumab, alirocumab, PCSK9 inhibitors, hyperlipidemia, LDL cholesterol lowering, ezetimibe, statin therapy, lipid-lowering therapy, adverse events
MeSH
humans, cardiovascular diseases, lipids, antibodies, monoclonal, anticholesteremic agents, hydroxymethylglutaryl-coa reductase inhibitors, serine proteinase inhibitors, treatment outcome, drug therapy, combination, risk factors, down-regulation, adult, aged, aged, 80 and over, middle aged, female, male, hyperlipidemias, randomized controlled trials as topic, antibodies, monoclonal, humanized, biomarkers, proprotein convertase 9, pcsk9 inhibitors

14 autores

  • Peter Paul Toth🇺🇸Johns Hopkins University; CGH Medical Center
  • Gillian Worthy🇺🇸🇬🇧Amgen (United States); Kleijnen Systematic Reviews (United Kingdom)
  • Shravanthi R. Gandra🇺🇸Amgen (United States)
  • Naveed A. Sattar🇬🇧University of Glasgow
  • Sarah L Bray🇺🇸Amgen (United States)
  • Lung‐I Cheng🇺🇸Amgen (United States)
  • Ian M. Bridges🇺🇸Amgen (United States)
  • Gavin M. Worth🇺🇸Amgen (United States)
  • Ricardo E. Dent🇺🇸Amgen (United States)
  • Carol A. Forbes🇬🇧Kleijnen Systematic Reviews (United Kingdom)
  • Sohan Deshpande🇬🇧Kleijnen Systematic Reviews (United Kingdom)
  • Janine Ross🇬🇧Kleijnen Systematic Reviews (United Kingdom)
  • Jos Kleijnen🇳🇱🇬🇧Maastricht University; Kleijnen Systematic Reviews (United Kingdom)
  • Erik S.G. Stroes🇳🇱University of Amsterdam

Resumen

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

Background

The proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors evolocumab and alirocumab substantially reduce low-density lipoprotein cholesterol (LDL-C) when added to statin therapy in patients who need additional LDL-C reduction.

Methods and results

We conducted a systematic review and network meta-analysis of randomized trials of lipid-lowering therapies from database inception through August 2016 (45 058 records retrieved). We found 69 trials of lipid-lowering therapies that enrolled patients requiring further LDL-C reduction while on maximally tolerated medium- or high-intensity statin, of which 15 could be relevant for inclusion in LDL-C reduction networks with evolocumab, alirocumab, ezetimibe, and placebo as treatment arms. PCSK9 inhibitors significantly reduced LDL-C by 54% to 74% versus placebo and 26% to 46% versus ezetimibe. There were significant treatment differences for evolocumab 140 mg every 2 weeks at the mean of weeks 10 and 12 versus placebo (-74.1%; 95% credible interval -79.81% to -68.58%), alirocumab 75 mg (-20.03%; 95% credible interval -27.32% to -12.96%), and alirocumab 150 mg (-13.63%; 95% credible interval -22.43% to -5.33%) at ≥12 weeks. Treatment differences were similar in direction and magnitude for PCSK9 inhibitor monthly dosing. Adverse events were similar between PCSK9 inhibitors and control. Rates of adverse events were similar between PCSK9 inhibitors versus placebo or ezetimibe.

Conclusions

PCSK9 inhibitors added to medium- to high-intensity statin therapy significantly reduce LDL-C in patients requiring further LDL-C reduction. The network meta-analysis showed a significant treatment difference in LDL-C reduction for evolocumab versus alirocumab.

Resumen vía Europe PMC. Los derechos de autor siguen siendo de los autores o la editorial (CC BY-NC-ND).

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