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dc.contributor.authorNorata, Giuseppe
dc.contributor.authorBallantyne, C.
dc.contributor.authorCatapano, A.
dc.date.accessioned2017-08-24T02:18:22Z
dc.date.available2017-08-24T02:18:22Z
dc.date.created2017-08-23T07:21:47Z
dc.date.issued2013
dc.identifier.citationNorata, G. and Ballantyne, C. and Catapano, A. 2013. New therapeutic principles in dyslipidaemia: Focus on LDL and Lp(a) lowering drugs. European Heart Journal. 34 (24).
dc.identifier.urihttp://hdl.handle.net/20.500.11937/55365
dc.identifier.doi10.1093/eurheartj/eht088
dc.description.abstract

Dyslipidaemias play a key role in determining cardiovascular risk; the discovery of statins has contributed a very effective approach. However, many patients do not achieve, at the maximal tolerated dose, the recommended goals for low-density lipoprotein-cholesterol (LDL-C), non-high-density lipoprotein-cholesterol, and apolipoprotein B (apoB). Available agents combined with statins can provide additional LDL-C reduction, and agents in development will increase therapeutic options impacting also other atherogenic lipoprotein classes. In fact, genetic insights into mechanisms underlying regulation of LDL-C levels has expanded potential targets of drug therapy and led to the development of novel agents. Among them are modulators of apoB containing lipoproteins production and proprotein convertase subtilisin/kexin type-9 inhibitors. Alternative targets such as lipoprotein(a) also require attention; however, until we have a better understanding of these issues, further LDL-C lowering in high and very high-risk patients will represent the most sound clinical approach. © 2013 Author(s).

dc.publisherOxford University Press
dc.titleNew therapeutic principles in dyslipidaemia: Focus on LDL and Lp(a) lowering drugs
dc.typeJournal Article
dcterms.source.volume34
dcterms.source.number24
dcterms.source.issn0195-668X
dcterms.source.titleEuropean Heart Journal
curtin.departmentSchool of Biomedical Sciences
curtin.accessStatusOpen access via publisher


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