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Emerging Non-statin Treatment Options for Lowering Low-Density Lipoprotein Cholesterol.
Bardolia, Chandni; Amin, Nishita Shah; Turgeon, Jacques.
Afiliación
  • Bardolia C; Office of Translational Research and Residency Programs, Tabula Rasa HealthCare, Moorestown, NJ, United States.
  • Amin NS; Office of Translational Research and Residency Programs, Tabula Rasa HealthCare, Moorestown, NJ, United States.
  • Turgeon J; Precision Pharmacotherapy Research and Development Institute, Tabula Rasa HealthCare, Lake Nona, FL, United States.
Front Cardiovasc Med ; 8: 789931, 2021.
Article en En | MEDLINE | ID: mdl-34869702
ABSTRACT
Low-density lipoprotein cholesterol (LDL-C) is a modifiable risk factor for the development of atherosclerotic cardiovascular disease. Statins have been the gold standard for managing cholesterol levels and reducing the risks associated with atherosclerotic cardiovascular disease; however, many patients do not achieve their cholesterol goals or are unable to tolerate this drug class due to adverse drug events. Recent studies of non-statin cholesterol lowering drugs (i.e., ezetimibe, PCSK9 inhibitors) have demonstrated cardiovascular benefits; and new drugs [i.e., bempedoic acid (BDA), inclisiran] have produced promising results in pre-clinical and clinical outcome trials. This narrative review aims to discuss the place in therapy of ezetimibe, PCSK9 inhibitors, BDA, and inclisiran and describe their relative pharmacokinetic (PK) profiles, efficacy and safety as monotherapy and combination therapy, and cardiovascular benefit(s) when used for hypercholesterolemia.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Front Cardiovasc Med Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Front Cardiovasc Med Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos
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