Literature DB >> 19262375

Statin and ezetimibe combination therapy in cardiovascular disease.

Ewa Dembowski1, Michael H Davidson.   

Abstract

PURPOSE OF REVIEW: To summarize the available data regarding the benefits of combination therapy with statins and ezetimibe in patients with cardiovascular disease. RECENT
FINDINGS: Extensive evidence, mostly in statin outcome trials, has shown that the magnitude of cardiovascular benefit is directly proportional to the degree of LDL cholesterol (LDL-C) reduction. As such, aggressive target goals for LDL-C levels have been established by guideline committees. Although statins are considered first-line agents in lipid therapy, LDL-C targets are difficult to achieve with statin therapy alone. Ezetimibe, a cholesterol absorption inhibitor, has been shown to be well tolerated and effective in lowering LDL-C. Adding ezetimibe to ongoing statin therapy leads to a substantial additional reduction in LDL-C, facilitating the achievement of target goals.
SUMMARY: The combination of ezetimibe, a cholesterol absorption inhibitor, and statins has been shown to be well tolerated and effective in lowering LDL-C and high-sensitivity C-reactive protein to target goals. Whether this greater LDL-C reduction translates into reduced cardiovascular events is the subject of ongoing clinical trials. Until such data is available, ezetimibe seems to be a reasonable choice for a second-line, lipid-lowering agent in patients on a potent statin who are not at their LDL-C goal.

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Year:  2009        PMID: 19262375     DOI: 10.1097/MED.0b013e3283295297

Source DB:  PubMed          Journal:  Curr Opin Endocrinol Diabetes Obes        ISSN: 1752-296X            Impact factor:   3.243


  5 in total

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Authors:  Antonio M Gotto; Jennifer E Moon
Journal:  Nat Rev Cardiol       Date:  2013-08-20       Impact factor: 32.419

2.  Economic evaluation of ezetimibe combined with simvastatin for the treatment of primary hypercholesterolaemia.

Authors:  F van Nooten; G M Davies; J W Jukema; A H Liem; E Yap; X H Hu
Journal:  Neth Heart J       Date:  2011-02       Impact factor: 2.380

3.  LDLR-Gene therapy for familial hypercholesterolaemia: problems, progress, and perspectives.

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Journal:  Int Arch Med       Date:  2010-12-13

4.  Molecular Dynamics Simulation Reveals Exposed Residues in the Ligand-Binding Domain of the Low-Density Lipoprotein Receptor that Interacts with Vesicular Stomatitis Virus-G Envelope.

Authors:  Faisal A Al-Allaf; Zainularifeen Abduljaleel; Mohiuddin M Taher; Ahmed A H Abdellatif; Mohammad Athar; Neda M Bogari; Mohammed N Al-Ahdal; Futwan Al-Mohanna; Zuhair N Al-Hassnan; Kamal H Y Alzabeedi; Talib M Banssir; Abdellatif Bouazzaoui
Journal:  Viruses       Date:  2019-11-15       Impact factor: 5.048

5.  LJ-1888, a selective antagonist for the A3 adenosine receptor, ameliorates the development of atherosclerosis and hypercholesterolemia in apolipoprotein E knock-out mice.

Authors:  Jong-Gil Park; Se-Jin Jeong; Jinha Yu; Gyudong Kim; Lak Shin Jeong; Goo Taeg Oh
Journal:  BMB Rep       Date:  2018-10       Impact factor: 4.778

  5 in total

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