Kardiologie up2date, Table of Contents Kardiologie up2date 2012; 08(04): 335-343DOI: 10.1055/s-0032-1325923 Koronare Herzerkrankung und Atherosklerose © Georg Thieme Verlag KG Stuttgart · New YorkNeue Entwicklungen in der Lipidologie Authors Klaus G. Parhofer Recommend Article Abstract Buy Article(opens in new window) All articles of this category(opens in new window) Abstract Statins are the cornerstone of lipid therapy because they have been proven beneficial in numerous outcome studies. Combinations of statins with omega-3-fatty acids or fibrates have shown no additional risk reduction, although subgroups may benefit from such combinations. Combinations of statins with either ezetimibe or niacin are currently investigated in large outcome trials. New compounds such as mipomersen (apoB antisense oligonucleotide), MTP inhibitors, and PCSK9 antibodies primarily decrease LDL-cholesterol but also reduce lipoprotein(a) to a varying degree. CETP inhibitors and apoA1 directed approaches primarily enhance reverse cholesterol transport but may also affect LDL-cholesterol concentration (CETP inhibitors). Although the lipid effects of these new compounds are promising only clinical studies will show which drugs will ultimately be beneficial to the patients. Full Text References Literatur 1 Baigent C, Blackwell L, Emberson J et al. Efficacy and safety of more intensive lowering of LDL cholesterol: a meta-analysis of data from 170,000 participants in 26 randomised trials. Lancet 2010; 376: 1670-1681 2 Baigent C, Landray MJ, Reith C et al. The effects of lowering LDL cholesterol with simvastatin plus ezetimibe in patients with chronic kidney disease (Study of Heart and Renal Protection): a randomised placebo-controlled trial. Lancet 2011; 377: 2181-2192 3 Lipid Research Clinics Program. The Lipid Research Clinics Coronary Primary Prevention Trial results. I. Reduction in incidence of coronary heart disease. JAMA 1984; 251: 351-364 4 Jun M, Foote C, Lv J et al. Effects of fibrates on cardiovascular outcomes: a systematic review and meta-analysis. Lancet 2010; 375: 1875-1884 5 Ginsberg HN, Elam MB, Lovato LC et al. Effects of combination lipid therapy in type 2 diabetes mellitus. N Engl J Med 2010; 362: 1563-1574 6 Bruckert E, Labreuche J, Amarenco P. Meta-analysis of the effect of nicotinic acid alone or in combination on cardiovascular events and atherosclerosis. Atherosclerosis 2010; 210: 353-361 7 Boden WE, Probstfield JL, Anderson T et al. Niacin in patients with low HDL cholesterol levels receiving intensive statin therapy. N Engl J Med 2011; 365: 2255-2267 8 Parhofer KG. Review of extended-release niacin/laropiprant fixed combination in the treatment of mixed dyslipidemia and primary hypercholesterolemia. Vasc Health Risk Manag 2009; 5: 901-908 9 Bosch J, Gerstein HC, Dagenais GR et al. n-3 fatty acids and cardiovascular outcomes in patients with dysglycemia. N Engl J Med 2012; 367: 309-318 10 Parhofer KG. Mipomersen: evidence-based review of its potential in the treatment of homozygous and severe heterozygous familial hypercholesterolemia. Core Evid 2012; 7: 29-38 11 Cuchel M, Bloedon LT, Szapary PO et al. Inhibition of microsomal triglyceride transfer protein in familial hypercholesterolemia. N Engl J Med 2007; 356: 148-156 12 Stein EA, Mellis S, Yancopoulos GD et al. Effect of a monoclonal antibody to PCSK9 on LDL cholesterol. N Engl J Med 2012; 366: 1108-1118 13 Konrad RJ, Troutt JS, Cao G. Effects of currently prescribed LDL-C-lowering drugs on PCSK9 and implications for the next generation of LDL-C-lowering agents. Lipids Health Dis 2011; 10: 38 14 Barter PJ, Caulfield M, Eriksson M et al. Effects of torcetrapib in patients at high risk for coronary events. N Engl J Med 2007; 357: 2109-2122 15 Cannon CP, Shah S, Dansky HM et al. Safety of anacetrapib in patients with or at high risk for coronary heart disease. N Engl J Med 2010; 363: 2406-2415 16 Voight BF, Peloso GM, Orho-Melander M et al. Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study. Lancet 2012; 380: 572-580