Skip to main content
Top
Published in: Clinical Research in Cardiology Supplements 1/2015

Open Access 01-04-2015

Clinical benefit of long-term lipoprotein apheresis in patients with severe hypercholesterolemia or Lp(a)-hyperlipoproteinemia with progressive cardiovascular disease

Authors: Franz Heigl, Reinhard Hettich, Norbert Lotz, Harduin Reeg, Tobias Pflederer, Dirk Osterkorn, Klaus Osterkorn, Reinhard Klingel

Published in: Clinical Research in Cardiology Supplements | Special Issue 1/2015

Login to get access

Abstract

Low-density lipoprotein cholesterol (LDL-C) and lipoprotein(a) (Lp(a)) are established causal risk factors for cardiovascular disease (CVD). Efficacy, safety, and tolerability of lipoprotein apheresis (LA) were investigated in 118 patients with CVD covering a period with 36,745 LA treatments in a retrospective, monocentric study. Indications for LA were severe hypercholesterolemia (n = 83) or isolated Lp(a) hyperlipoproteinemia (Lp(a)-HLP) (n = 35). In patients with hypercholesterolemia, initial pre-LA LDL-C was 176.4 ± 67.0 mg/dL. In patients with isolated Lp(a)-HLP, initial pre-LA Lp(a) was 127.2 ± 67.3 mg/dL. Mean reduction rates of LA were 67 % for both LDL-C and Lp(a). During chronic LA, the average annual rate of major adverse cardiac events of all patients declined by 79.7 % (p < 0.0001). Subgroup analysis showed decline by 73.7 % (p < 0.0001) in patients with severe hypercholesterolemia, and by 90.4 % (p < 0.0001) in patients with isolated Lp(a)-HLP. Adverse events occurred in 1.1 % of treatments. LA treatment of patients with a high risk for CVD due to hypercholesterolemia and/or Lp(a)-HLP demonstrated clinical benefit and was safe and well tolerated.
Literature
1.
go back to reference Castelli WP (1984) Epidemiology of coronary heart disease: the Framingham study. Am J Med 76:4–12CrossRefPubMed Castelli WP (1984) Epidemiology of coronary heart disease: the Framingham study. Am J Med 76:4–12CrossRefPubMed
2.
go back to reference Pedersen TR, for the Scandinavian Simvastatin Survival Study (4S) Group (1994) Randomised trial of cholesterol lowering in 4444 patients with coronary heart disease. Lancet 344:1383–1389 Pedersen TR, for the Scandinavian Simvastatin Survival Study (4S) Group (1994) Randomised trial of cholesterol lowering in 4444 patients with coronary heart disease. Lancet 344:1383–1389
3.
go back to reference O’Keefe JH Jr, Cordain L, Harris WH et al (2004) Optimal low-density lipoprotein is 50–70 mg/dL: lower is better and physiologically normal. J Am Coll Cardiol 43:2142–2146CrossRefPubMed O’Keefe JH Jr, Cordain L, Harris WH et al (2004) Optimal low-density lipoprotein is 50–70 mg/dL: lower is better and physiologically normal. J Am Coll Cardiol 43:2142–2146CrossRefPubMed
4.
go back to reference Berg K (1963) A new serum type system in man: the Lp system. Acta Pathol Microbiol Scand 59:369–382CrossRefPubMed Berg K (1963) A new serum type system in man: the Lp system. Acta Pathol Microbiol Scand 59:369–382CrossRefPubMed
5.
go back to reference Cremer P, Nagel D, Labrot B et al (1994) Lipoprotein Lp(a) as predictor of myocardial infarction in comparison to fibrinogen, LDL cholesterol and other risk factors: results from the prospective Goettingen Risk Incidence and Prevalence Study (GRIPS). Eur J Clin Invest 24:444–453CrossRefPubMed Cremer P, Nagel D, Labrot B et al (1994) Lipoprotein Lp(a) as predictor of myocardial infarction in comparison to fibrinogen, LDL cholesterol and other risk factors: results from the prospective Goettingen Risk Incidence and Prevalence Study (GRIPS). Eur J Clin Invest 24:444–453CrossRefPubMed
6.
go back to reference Emerging Risk Factors Collaboration (2009) Lipoprotein(a) concentration and the risk of coronary heart disease, stroke, and nonvascular mortality. JAMA 302:412–423CrossRef Emerging Risk Factors Collaboration (2009) Lipoprotein(a) concentration and the risk of coronary heart disease, stroke, and nonvascular mortality. JAMA 302:412–423CrossRef
7.
go back to reference Kamstrup PR (2010) Lipoprotein(a) and ischemic heart disease -a causal association? A review. Atherosclerosis 211:15–23CrossRefPubMed Kamstrup PR (2010) Lipoprotein(a) and ischemic heart disease -a causal association? A review. Atherosclerosis 211:15–23CrossRefPubMed
8.
go back to reference Nordestgaard BG, Chapman MJ, Ray K, European Atherosclerosis Society Consensus Panel et al (2010) Lipoprotein(a) as a cardiovascular risk factor: current status. Eur Heart J 31:2844–2853CrossRefPubMedCentralPubMed Nordestgaard BG, Chapman MJ, Ray K, European Atherosclerosis Society Consensus Panel et al (2010) Lipoprotein(a) as a cardiovascular risk factor: current status. Eur Heart J 31:2844–2853CrossRefPubMedCentralPubMed
9.
go back to reference Ariyo AA, Thach C, Tracy R, Cardiovascular Health Study Investigators (2003) Lp(a) lipoprotein, vascular disease, and mortality in the elderly. N Engl J Med 349:2108–2115CrossRefPubMed Ariyo AA, Thach C, Tracy R, Cardiovascular Health Study Investigators (2003) Lp(a) lipoprotein, vascular disease, and mortality in the elderly. N Engl J Med 349:2108–2115CrossRefPubMed
10.
go back to reference Jaeger BR, Richter Y, Nagel D et al (2009) Longitudinal cohort study on the effectiveness of lipid apheresis treatment to reduce high lipoprotein(a) levels and prevent major adverse coronary events. Nat Clin Pract Cardiovasc Med 6:229–239CrossRefPubMed Jaeger BR, Richter Y, Nagel D et al (2009) Longitudinal cohort study on the effectiveness of lipid apheresis treatment to reduce high lipoprotein(a) levels and prevent major adverse coronary events. Nat Clin Pract Cardiovasc Med 6:229–239CrossRefPubMed
11.
go back to reference Leebmann J, Roeseler E, Julius U et al, Pro(a)LiFe Study Group et al (2013) Lipoprotein apheresis in patients with maximally tolerated lipid-lowering therapy, lipoprotein(a)-hyperlipoproteinemia, and progressive cardiovascular disease: prospective observational multicenter study. Circulation 128:2567–2576 Leebmann J, Roeseler E, Julius U et al, Pro(a)LiFe Study Group et al (2013) Lipoprotein apheresis in patients with maximally tolerated lipid-lowering therapy, lipoprotein(a)-hyperlipoproteinemia, and progressive cardiovascular disease: prospective observational multicenter study. Circulation 128:2567–2576
12.
go back to reference German Federal Ministry of Health (2008) Publication of a decision of Federal Joint Committee on apheresis for isolated Lp(a) elevation with progressive cardiovascular disease. Transactions of the German Federal Ministries (BAnz) 138: 3321, and most recent modification in January 2013 at Transactions of the German Federal Ministries (BAnz) AT 08.04.2013 (Articles in German) German Federal Ministry of Health (2008) Publication of a decision of Federal Joint Committee on apheresis for isolated Lp(a) elevation with progressive cardiovascular disease. Transactions of the German Federal Ministries (BAnz) 138: 3321, and most recent modification in January 2013 at Transactions of the German Federal Ministries (BAnz) AT 08.04.2013 (Articles in German)
13.
go back to reference Heigl F, Hettich R, Lotz N et al (2015) Efficacy, safety, and tolerability of long-term lipoprotein apheresis in patients with LDL- or Lp(a) hyperlipoproteinemia: findings gathered from more than 36,000 treatments at one center in Germany. Atheroscler Suppl (in press) Heigl F, Hettich R, Lotz N et al (2015) Efficacy, safety, and tolerability of long-term lipoprotein apheresis in patients with LDL- or Lp(a) hyperlipoproteinemia: findings gathered from more than 36,000 treatments at one center in Germany. Atheroscler Suppl (in press)
14.
go back to reference Kroon AA, van’t Hof MA, Demacker PN et al (2000) The rebound of lipoproteins after LDL-apheresis. Kinetics and estimation of mean lipoprotein levels. Atherosclerosis 152:519–526CrossRefPubMed Kroon AA, van’t Hof MA, Demacker PN et al (2000) The rebound of lipoproteins after LDL-apheresis. Kinetics and estimation of mean lipoprotein levels. Atherosclerosis 152:519–526CrossRefPubMed
15.
go back to reference National Association of Statutory Health Insurance Physicians (KBV Qualitätsbericht) (2013) Quality report 2013:47–48 (Article in German) National Association of Statutory Health Insurance Physicians (KBV Qualitätsbericht) (2013) Quality report 2013:47–48 (Article in German)
16.
go back to reference Wang Y, Blessing F, Walli AK et al (2004) Effects of heparin-mediated extracorporeal low-density lipoprotein precipitation beyond lowering proatherogenic lipoproteins-reduction of circulating proinflammatory and procoagulatory markers. Atherosclerosis 175:145–150CrossRefPubMed Wang Y, Blessing F, Walli AK et al (2004) Effects of heparin-mediated extracorporeal low-density lipoprotein precipitation beyond lowering proatherogenic lipoproteins-reduction of circulating proinflammatory and procoagulatory markers. Atherosclerosis 175:145–150CrossRefPubMed
17.
go back to reference Briel M, Ferreira-Gonzalez I, You JJ et al (2009) Association between change in high density lipoprotein cholesterol and cardiovascular disease morbidity and mortality: systematic review and meta-regression analysis. BMJ 338:38b92CrossRef Briel M, Ferreira-Gonzalez I, You JJ et al (2009) Association between change in high density lipoprotein cholesterol and cardiovascular disease morbidity and mortality: systematic review and meta-regression analysis. BMJ 338:38b92CrossRef
Metadata
Title
Clinical benefit of long-term lipoprotein apheresis in patients with severe hypercholesterolemia or Lp(a)-hyperlipoproteinemia with progressive cardiovascular disease
Authors
Franz Heigl
Reinhard Hettich
Norbert Lotz
Harduin Reeg
Tobias Pflederer
Dirk Osterkorn
Klaus Osterkorn
Reinhard Klingel
Publication date
01-04-2015
Publisher
Springer Berlin Heidelberg
Published in
Clinical Research in Cardiology Supplements / Issue Special Issue 1/2015
Print ISSN: 1861-0706
Electronic ISSN: 1861-0714
DOI
https://doi.org/10.1007/s11789-015-0071-3

Other articles of this Special Issue 1/2015

Clinical Research in Cardiology Supplements 1/2015 Go to the issue

EditorialNotes

Editorial