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10.1093/eurheartj/eht088

http://scihub22266oqcxt.onion/10.1093/eurheartj/eht088
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C3857929!3857929!23509227
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suck abstract from ncbi


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pmid23509227      Eur+Heart+J 2013 ; 34 (24): 1783-1789a
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  • New therapeutic principles in dyslipidaemia: focus on LDL and Lp(a) lowering drugs #MMPMID23509227
  • Norata GD; Ballantyne CM; Catapano AL
  • Eur Heart J 2013[Jun]; 34 (24): 1783-1789a PMID23509227show ga
  • 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.
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