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ESC-Leitlinien 2016 – Dyslipidämien

ECS guidelines 2016 – dyslipidaemias

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Zusammenfassung

Von der European Society of Cardiology (ESC) und der European Atherosclerosis Society (EAS) wurden im August 2016 gemeinsame neue Leitlinien zur Behandlung der Dyslipidämien vorgestellt und veröffentlicht. Die europäischen Leitlinien empfehlen, bei der Behandlung der Dyslipidämien risikoadaptierte LDL („low-density-lipoprotein“)-Cholesterin-Zielwerte anzustreben. Das LDL-Cholesterin wird als primäres Behandlungsziel hervorgehoben (was u. a. auch auf die fehlende Wirksamkeit HDL [„high-density lipoprotein“]-Cholesterin-anhebender Therapieansätze zurückzuführen ist). Für Patienten mit einem sehr hohen Risiko für kardiovaskuläre Ereignisse besteht ein LDL-Cholesterin-Zielwert von unter 70 mg/dl. Zusätzlich wird nun bei Patienten mit LDL-Cholesterin-Ausgangswert zwischen 70 und 135 mg/dl bei sehr hohem kardiovaskulären Risiko bzw. zwischen 100 und 200 mg/dl bei hohem kardiovaskulären Risiko eine Reduktion des LDL-Cholesterins um mehr als 50 % empfohlen. Bei der medikamentösen Therapie sind Statine das Mittel der ersten Wahl. Weiterhin wurde der Empfehlungsgrad für die zusätzliche Therapie mit Ezetimib bei Patienten, welche trotz maximal tolerierter Statintherapie weiterhin deutlich erhöhte LDL-Cholesterin-Werte haben, angehoben (aktuell IIa-Empfehlung). Neu wird die PCSK9 (Proproteinkonvertase Subtilisin/Kexin Typ 9)-Hemmer-Therapie erwähnt. Ein weiteres gerade veröffentlichtes ESC/EAS-Konsensusdokument gibt genauere Informationen darüber, bei welchen Patienten heute eine solche Therapie erwogen werden kann. Insbesondere sind dies Patienten mit familiärer Hypercholesterinämie oder Patienten mit sehr hohem kardiovaskulären Risiko, welche trotz maximal tolerierter Statin- und Ezetimibtherapie anhaltend deutlich erhöhte LDL-Cholesterin-Werte aufweisen.

Abstract

Dyslipidaemia is a major cause of atherosclerotic cardiovascular disease and its progression towards clinical complications, such as acute coronary syndromes and stroke. In August 2016 the European Society of Cardiology (ESC) and the European Atherosclerosis Society (EAS) issued new joint guidelines for the management of dyslipidaemias. In these new guidelines, the concept of treating patients to a risk-based low-density lipoprotein (LDL) cholesterol target is reinforced. The task force considers LDL cholesterol as the primary target for dyslipidaemia treatment, whereas high-density lipoprotein (HDL) cholesterol is not recommended as a treatment target (based on the failure of HDL cholesterol elevation treatment strategies to reduce cardiovascular risk in recent studies). In patients with a very high risk for cardiovascular events it is recommended to treat to an LDL cholesterol target of less than 70 mg/dl. Moreover, the new guidelines now additionally recommend a > 50% reduction of LDL cholesterol in patients with very high cardiovascular risk patients and baseline levels between 70 and 135 mg/dl as well as in patients with high cardiovascular risk and baseline LDL cholesterol levels between 100 and 200 mg/dl. Statins are recommended as first-line medicinal treatment and the LDL cholesterol goals given imply the more frequent use of maximum tolerated statin therapy, in particular for patients with very high cardiovascular risk. Treatment with ezetimibe in patients with substantially elevated LDL cholesterol levels despite maximum tolerated statin therapy has now received a stronger recommendation (currently IIa recommendation). The guidelines also now include the potential use of the novel proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors and a recent ESC/EAS consensus document provides more detailed information on which patients can be considered for treatment with PCSK9 inhibitors, i. e. in particular patients with familial hypercholesterolemia and patients at very high cardiovascular risk who have markedly elevated LDL cholesterol levels despite maximum tolerated statin and ezetimibe therapy.

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Literatur

  1. Ford ES, Ajani UA, Croft JB et al (2007) Explaining the decrease in U.S. deaths from coronary disease, 1980–2000. N Engl J Med 356(23):2388–2398. doi:10.1056/NEJMsa053935

    Article  CAS  PubMed  Google Scholar 

  2. Townsend N, Nichols M, Scarborough P, Rayner M (2015) Cardiovascular disease in Europe–epidemiological update 2015. Eur Heart J 36(40):2696–2705. doi:10.1093/eurheartj/ehv428

    Article  PubMed  Google Scholar 

  3. Catapano AL, Graham I, De Backer G et al (2016) 2016 ESC/EAS guidelines for the management of dyslipidaemias: the task force for the management of dyslipidaemias of the European Society of Cardiology (ESC) and European Atherosclerosis Society (EAS) developed with the special contribution of the European Assocciation for Cardiovascular Prevention & Rehabilitation (EACPR). Eur Heart J. doi:10.1093/eurheartj/ehw272

    Google Scholar 

  4. Emerging Risk Factors Collaboration, Di Angelantonio E, Sarwar N, Perry P et al (2009) Major lipids, apolipoproteins, and risk of vascular disease. JAMA 302(18):1993–2000. doi:10.1001/jama.2009.1619

    Article  Google Scholar 

  5. European Association for Cardiovascular Prevention & Rehabilitation, Reiner Z, Catapano AL, De Backer G et al (2011) ESC/EAS Guidelines for the management of dyslipidaemias: the task force for the management of dyslipidaemias of the European Society of Cardiology (ESC) and the European Atherosclerosis Society (EAS). Eur Heart J 32(14):1769–1818. doi:10.1093/eurheartj/ehr158

    Article  Google Scholar 

  6. Catapano AL, Graham I, De Backer G et al (2016) 2016 ESC/EAS guidelines for the management of dyslipidaemias: the task force for the management of dyslipidaemias of the European Society of Cardiology (ESC) and European Atherosclerosis Society (EAS) developed with the special contribution of the European Assocciation for Cardiovascular Prevention & Rehabilitation (EACPR). Atherosclerosis 253:281–344. doi:10.1016/j.atherosclerosis.2016.08.018

    Google Scholar 

  7. Piepoli MF, Hoes AW, Agewall S et al (2016) 2016 European guidelines on cardiovascular disease prevention in clinical practice: The sixth joint task force of the European Society of Cardiology and other societies on cardiovascular disease prevention in clinical practice (constituted by representatives of 10 societies and by invited experts) developed with the special contribution of the European Association for Cardiovascular Prevention & Rehabilitation (EACPR). Eur Heart J 37(29):2315–2381. doi:10.1093/eurheartj/ehw106

    Article  PubMed  Google Scholar 

  8. Jorgensen AB, Frikke-Schmidt R, West AS et al (2013) Genetically elevated non-fasting triglycerides and calculated remnant cholesterol as causal risk factors for myocardial infarction. Eur Heart J 34(24):1826–1833. doi:10.1093/eurheartj/ehs431

    Article  CAS  PubMed  Google Scholar 

  9. Kolovou GD, Mikhailidis DP, Kovar J et al (2011) Assessment and clinical relevance of non-fasting and postprandial triglycerides: an expert panel statement. Curr Vasc Pharmacol 9(3):258–270

    Article  CAS  PubMed  Google Scholar 

  10. Mihas C, Kolovou GD, Mikhailidis DP et al (2011) Diagnostic value of postprandial triglyceride testing in healthy subjects: a meta-analysis. Curr Vasc Pharmacol 9(3):271–280

    Article  CAS  PubMed  Google Scholar 

  11. Nordestgaard BG, Varbo A (2014) Triglycerides and cardiovascular disease. Lancet 384(9943):626–635. doi:10.1016/S0140-6736(14)61177-6

    Article  CAS  PubMed  Google Scholar 

  12. Kamstrup PR, Tybjaerg-Hansen A, Nordestgaard BG (2014) Elevated lipoprotein(a) and risk of aortic valve stenosis in the general population. J Am Coll Cardiol 63(5):470–477. doi:10.1016/j.jacc.2013.09.038

    Article  CAS  PubMed  Google Scholar 

  13. Kronenberg F, Utermann G (2013) Lipoprotein(a): resurrected by genetics. J Intern Med 273(1):6–30. doi:10.1111/j.1365-2796.2012.02592.x

    Article  CAS  PubMed  Google Scholar 

  14. Nordestgaard BG, Chapman MJ, Ray K et al (2010) Lipoprotein(a) as a cardiovascular risk factor: current status. Eur Heart J 31(23):2844–2853. doi:10.1093/eurheartj/ehq386

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Nordestgaard BG, Chapman MJ, Humphries SE et al (2013) Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: consensus statement of the European Atherosclerosis Society. Eur Heart J 34(45):3478–3490a. doi:10.1093/eurheartj/eht273

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Conroy RM, Pyorala K, Fitzgerald AP et al (2003) Estimation of ten-year risk of fatal cardiovascular disease in Europe: the SCORE project. Eur Heart J 24(11):987–1003

    Article  CAS  PubMed  Google Scholar 

  17. Stone NJ, Robinson JG, Lichtenstein AH et al (2014) 2013 ACC/AHA guideline on the treatment of blood cholesterol to reduce atherosclerotic cardiovascular risk in adults: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. Circulation 129(25 Suppl 2):1–45. doi:10.1161/01.cir.0000437738.63853.7a

    Article  Google Scholar 

  18. Cholesterol Treatment Trialists (CTT) Collaboration, Fulcher J, O’Connell R, Voysey M et al (2015) Efficacy and safety of LDL-lowering therapy among men and women: meta-analysis of individual data from 174,000 participants in 27 randomised trials. Lancet 385(9976):1397–1405. doi:10.1016/S0140-6736(14)61368-4

    Article  Google Scholar 

  19. Cholesterol Treatment Trialists (CTT) Collaborators, Mihaylova B, Emberson J, Blackwell L et al (2012) The effects of lowering LDL cholesterol with statin therapy in people at low risk of vascular disease: meta-analysis of individual data from 27 randomised trials. Lancet 380(9841):581–590. doi:10.1016/S0140-6736(12)60367-5

    Article  Google Scholar 

  20. Cannon CP, Blazing MA, Giugliano RP et al (2015) Ezetimibe added to statin therapy after acute coronary syndromes. N Engl J Med 372(25):2387–2397. doi:10.1056/NEJMoa1410489

    Article  CAS  PubMed  Google Scholar 

  21. Boekholdt SM, Hovingh GK, Mora S et al (2014) Very low levels of atherogenic lipoproteins and the risk for cardiovascular events: a meta-analysis of statin trials. J Am Coll Cardiol 64(5):485–494. doi:10.1016/j.jacc.2014.02.615

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Weng TC, Yang YH, Lin SJ, Tai SH (2010) A systematic review and meta-analysis on the therapeutic equivalence of statins. J Clin Pharm Ther 35(2):139–151. doi:10.1111/j.1365-2710.2009.01085.x

    Article  CAS  PubMed  Google Scholar 

  23. Law MR, Wald NJ, Rudnicka AR (2003) Quantifying effect of statins on low density lipoprotein cholesterol, ischaemic heart disease, and stroke: systematic review and meta-analysis. BMJ 326(7404):1423. doi:10.1136/bmj.326.7404.1423

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. Parker BA, Capizzi JA, Grimaldi AS et al (2013) Effect of statins on skeletal muscle function. Circulation 127(1):96–103. doi:10.1161/CIRCULATIONAHA.112.136101

    Article  CAS  PubMed  Google Scholar 

  25. Landmesser U, Chapman MJ, Farnier M et al (2016) European Society of Cardiology/European Atherosclerosis Society Task Force consensus statement on proprotein convertase subtilisin/kexin type 9 inhibitors: practical guidance for use in patients at very high cardiovascular risk. Eur Heart J. doi:10.1093/eurheartj/ehw480

    Google Scholar 

  26. Lyseng-Williamson KA (2012) Ezetimibe/simvastatin: a guide to its clinical use in hypercholesterolemia. Am J Cardiovasc Drugs 12(1):49–56. doi:10.2165/11209150-000000000-00000

    Article  CAS  PubMed  Google Scholar 

  27. Sudhop T, Lutjohann D, Kodal A et al (2002) Inhibition of intestinal cholesterol absorption by ezetimibe in humans. Circulation 106(15):1943–1948

    Article  CAS  PubMed  Google Scholar 

  28. Norata GD, Tibolla G, Catapano AL (2014) Targeting PCSK9 for hypercholesterolemia. Annu Rev Pharmacol Toxicol 54:273–293. doi:10.1146/annurev-pharmtox-011613-140025

    Article  CAS  PubMed  Google Scholar 

  29. Koren MJ, Lundqvist P, Bolognese M et al (2014) Anti-PCSK9 monotherapy for hypercholesterolemia: the MENDEL-2 randomized, controlled phase III clinical trial of evolocumab. J Am Coll Cardiol 63(23):2531–2540. doi:10.1016/j.jacc.2014.03.018

    Article  CAS  PubMed  Google Scholar 

  30. Roth EM, McKenney JM (2015) ODYSSEY MONO: effect of alirocumab 75 mg subcutaneously every 2 weeks as monotherapy versus ezetimibe over 24 weeks. Future Cardiol 11(1):27–37. doi:10.2217/fca_.14.82

    Article  CAS  PubMed  Google Scholar 

  31. Robinson JG, Farnier M, Krempf M et al (2015) Efficacy and safety of alirocumab in reducing lipids and cardiovascular events. N Engl J Med 372(16):1489–1499. doi:10.1056/NEJMoa1501031

    Article  CAS  PubMed  Google Scholar 

  32. Sabatine MS, Giugliano RP, Wiviott SD et al (2015) Efficacy and safety of evolocumab in reducing lipids and cardiovascular events. N Engl J Med 372(16):1500–1509. doi:10.1056/NEJMoa1500858

    Article  CAS  PubMed  Google Scholar 

  33. Navarese EP, Kolodziejczak M, Kereiakes DJ et al (2016) Proprotein convertase subtilisin/kexin type 9 monoclonal antibodies for acute coronary syndrome: a narrative review. Ann Intern Med 164(9):600–607. doi:10.7326/M15-2994

    Article  PubMed  Google Scholar 

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Correspondence to U. Landmesser.

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D. Sinning hat Advisory-Honorare von Amgen erhalten. U. Landmesser hat Vortrags- bzw. Advisory-Honorare von MSD, Amgen, Sanofi, Pfizer und Berlin-Chemie erhalten.

Dieser Beitrag beinhaltet keine von den Autoren durchgeführten Studien an Menschen oder Tieren.

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Sinning, D., Landmesser, U. ESC-Leitlinien 2016 – Dyslipidämien. Herz 41, 671–676 (2016). https://doi.org/10.1007/s00059-016-4505-6

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