Official journal of the Slovak Society of Cardiology,
Slovak Society of Hypertension and Slovak Association for Cardiac Arrhythmias

Cardiology Letters 2020, 29(4):240-242

Is it important to reduce serum levels of Lp(a) in secondary prevention of cardiovascular morbidity and mortality?

Murín J1, Bulas J1, Wavruch M2
1 I. interná klinika LFUK a UN Bratislava
2 Ústav farmakológie a klinickej farmakológie LFUK, Bratislava, Slovenská republika

Reduction of serum lipids, mainly of LDL-Ch level, with lipid lowering treatments (statins, event with ezetimibe and PCSK9 inhibitors in special patients) reduces cardiovascular (CV) morbidity and mortality. These days we want, in secondary CV prevention, to lower serum LDL-Ch levels even more and we also want to start with this treatment very much earlier. There are also other new serum lipids, and Lp(a) is one of them, and an association of its serum levels with CV atherosclerotic diseases was found. It is not a (bio)marker, but a risk factor. Up to now we have not had the possibility to reduce serum levels of Lp(a), but treatment with PCSK9 inhibitors recently documented not only a great reduction of serum levels of LDL-Ch but also serum levels of Lp(a): patients after acute coronary syndrome were treated with alirocumab (ODYSSEY OUTCOMES Study), there was great reduction of CV events and the reduction of serum levels of Lp(a) in patients in the highest quartile of these levels contributed to this benefit. In the near future we expect that examination of serum levels of Lp(a) will be important, mostly in patients with CV disease.

Keywords: Lp(a); cardiovascular atherosclerotic disease; PCSK9 inhibitors; reduction of CV morbidity

Published: April 1, 2020  Show citation

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Murín J, Bulas J, Wavruch M. Is it important to reduce serum levels of Lp(a) in secondary prevention of cardiovascular morbidity and mortality? Cardiology Letters. 2020;29(4):240-242.
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References

  1. Tsimikas S. A test in context: lipoprotein(a): diagnosis, prognosis, controversies, and emerging therapies. J Am Coll Cardiol 2017;69:692-711. Go to original source...
  2. Loscalzo J, Weinfeld M, Fless GM, et al. Lipoprotein(a) fibrin binding, and plasminogen activation. Arteriosclerosis 1990;10:240-245. Go to original source...
  3. Zioncheck TF, Powell LM, Rice GC, et al. Interaction of recombinant apolipoprotein(a) and lipoprotein(a) with macrophages. J Clin Invest 1991;87:767-771. Go to original source...
  4. Zheng kH, Tsimikas S, Pawade T, et al. Lipoprotein(a) and oxidized phospholipids promote valve calcification in patients with aortic stenosis. J Am Coll Cardiol 2019;73:2150-2162. Go to original source...
  5. Emerging Risk Factors Collaboratin, Erqou S, Kaptoge S, et al. Lipoprotein(a) concentration and the risk of coronary heart disease, stroke, and nonvascular mortality. JAMA 2009;302:412423. Go to original source...
  6. Willeit P, Ridker PM Nestel PJ, et al. Baseline and on-statin treatment lipoprotein(a) levels for prediction of cardiovascular events: individual patient-data meta-analysis of statin outcome trials. Lancet 2018;392:1311-1320. Go to original source...
  7. Boerwinkle E, Leffert CC, Lin J, et al. Apolipoprotein(a) gene accounts for greater than 90% of the variation in plasma lipoprotein(a) concentrations. J Clin Invest 1992;90:52-60. Go to original source...
  8. Kamstrup PR, Tybjaerg-Hansen A, Steffensen R, et al. Genetically elevated lipoprotein(a) and increased risk of myocardial infarction. JAMA 2009;301:2331-2339. Go to original source...
  9. Clarke R, Peden JF, Hopewell JC, et al. PROCARDIS Consortium. Genetic variants associated with Lp(a) lipoprotein level and coronary disease. N Engl J Med 2009;361:2518-2528. Go to original source...
  10. Kamstrup PR, Tybjaerg-Hansen A, Nordestgaard BG. Extreme lipoprotein(a) levels and improved cardiovascular risk prediction. J Am Coll Cardiol 2013;61:1146-1156. Go to original source...
  11. Afshar M, Pilote L, Dufresne L, et al. Lipoprotein(a) interactions with low-density lipoprotein cholesterol and other cardiovacular risk factors in premature acute coronary syndrome (ACS). J Am Heart Assoc 2016;5: 35-45. Go to original source...
  12. Chasman DI, Shiffman D, Zee RY, et al. Polymorphism in the apolipoprotein(a) gene, plasma lipoprotein(a), cardiovascular disease, and low-dose aspirin therapy. Atherosclerosis 2009;203:371-376. Go to original source...
  13. Yeang C, Hung MY, Byun YS, et al. Effect of therapeutic interventions on oxidized phospholipids on apolipoprotein B100 and lipoprotein(a). J Clin Lipidol 2016;10:594-603. Go to original source...
  14. Maggi FM, Biasi GM, Catapano AL. Reduction of Lp(a) plasma levels by bezafibrate. Atherosclerosis 1993;100:127-128. Go to original source...
  15. Kim CJ, Min YK, Ryu WS, et al. Effect of hormone replacement therapy on lipoprotein(a) and lipid levels in postmenopausal women. Influence of various progestogens and duration of theapy. Arch Intern Med 1996;156:1693-1700. Go to original source...
  16. Rossouw JE, Anderson GL, Prentice RL, et al. Writing Group for the Women's Health Initiative Investigators. Risks and benefits of estrogen plus progestin in healthy postmenopausal women: principal results from the Women's Health Initiative randomized controlled trial. JAMA 2002;288:321-333. Go to original source...
  17. Navarese EP, Kolodziejczak M, Schulze V, et al. Effects of proprotein convertase subtilisin/kexin type 9 antibodies in adults with hypercholesterolemia: a systematic review and meta-analysis. Ann Intern Med 2015;163:40-51. Go to original source...
  18. O'Donoghue ML, Fazio S, Gliugliano RP, et al. Lipoprotein(a), PCSK9 inhibition, and cardiovascular risk. Circulation 2019;139:1483-1492 Go to original source...
  19. Murín J. ODYSSEY OUTCOMES štúdia: ďalšie klinicky užitočné analýzy. Athero Rev 2019;4:101-104.