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dc.contributor.authorPirillo, A.
dc.contributor.authorNorata, Giuseppe
dc.contributor.authorCatapano, A.
dc.date.accessioned2017-12-10T12:39:14Z
dc.date.available2017-12-10T12:39:14Z
dc.date.created2017-12-10T12:20:21Z
dc.date.issued2017
dc.identifier.citationPirillo, A. and Norata, G. and Catapano, A. 2017. Strategies for the use of nonstatin therapies. Current Opinion in Lipidology. 28 (6): pp. 458-464.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/59226
dc.identifier.doi10.1097/MOL.0000000000000459
dc.description.abstract

Purpose of review: Dyslipidaemias are a major risk factor for cardiovascular disease (CVD); in particular, high levels of low-density lipoprotein cholesterol (LDL-C) have been associated to a higher cardiovascular risk. Reducing LDL-C levels decreases the risk of coronary heart disease (CHD), and the greater the LDL-C reduction, the greater the decrease in cardiovascular risk. Although statins represent the first line lipid-lowering therapy, many patients do not reach the recommended goals or exhibit adverse side effects leading to therapy discontinuation; in addition, a significant percentage of statin-treated patients continue to experience cardiovascular events even in the presence of well controlled LDL-C levels, because of alterations in other lipid/lipoprotein classes, including triglycerides and high-density lipoprotein cholesterol. Recent findings: These conditions require further therapeutic interventions to achieve the recommended lipid goals. Several drugs have been developed to address these needs. Recent studies have shown that the association of ezetimibe with rosuvastatin or atorvastatin results in a better hypolipidaemic effect; in addition to this, PCSK9 inhibitors significantly reduce LDL-C levels and cardiovascular events. Summary: For patients who are intolerant to statins or not able to reach the recommended LDL-C levels, despite maximal tolerated dose of statin, or exhibiting additional lipid alterations, several drugs are available that can be used either in monotherapy or on top of the maximally tolerated dose of statins.

dc.publisherLippincott Williams & Wilkins
dc.titleStrategies for the use of nonstatin therapies
dc.typeJournal Article
dcterms.source.volume28
dcterms.source.number6
dcterms.source.startPage458
dcterms.source.endPage464
dcterms.source.issn0957-9672
dcterms.source.titleCurrent Opinion in Lipidology
curtin.departmentSchool of Biomedical Sciences
curtin.accessStatusOpen access


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