Lipoprotein Apheresis for Lipoprotein(a)-Associated Cardiovascular Disease

E. Roeseler(PHV Dialysezentrum), Ulrich Julius(PHV Dialysezentrum), Franz Heigl(PHV Dialysezentrum), Ralf Spitthoever(PHV Dialysezentrum), Dennis Heutling(PHV Dialysezentrum), Paul Breitenberger(PHV Dialysezentrum), Josef Leebmann(PHV Dialysezentrum), Walter Lehmacher(PHV Dialysezentrum), Pia R. Kamstrup(PHV Dialysezentrum), Børge G. Nordestgaard(PHV Dialysezentrum), Winfried Maerz(PHV Dialysezentrum), Asma Noureen(PHV Dialysezentrum), Konrad Schmidt(PHV Dialysezentrum), Florian Kronenberg(PHV Dialysezentrum), Andreas Heibges(PHV Dialysezentrum), Reinhard Klingel(PHV Dialysezentrum), Volker Schettler(Nephrologisches Zentrum Goettingen), Thomas Benzing(CBS International Business School), Hildegard Christ(CBS International Business School), S. Wehner, Ines Schulz-Merkel(Kempten University of Applied Sciences), Ralf Kuehn, Albrecht Wagner, W Dschietzig(Carl-Thiem-Klinikum Cottbus), Claudia Ernst(Carl-Thiem-Klinikum Cottbus), Michael Koziolek(Nephrologisches Zentrum Goettingen), Johannes Bunia, Peter Kulzer(Schneider Electric (Germany)), Klaus-Dieter Kraenzle(Kernkraftwerk Gundremmingen), M. Toelle, Gerhard Riechers, Christine Kuehnel, Tobias A. Marsen(CBS International Business School), Christina Saehn, J Ringel, Harald Messner(University of Wuppertal), Andreas Oehring, Carsten Schuerfeld, Michael Wintergalen, Volker Schettler(Nephrologisches Zentrum Goettingen), Falko Neumann(Technische Universität Dresden), Harald Kaul(Deggendorf Institute of Technology), Martin Haesner, J. Paßfall, Andrea Benschneider, Stefan Heidenreich(FH Aachen), Winfried März, Ruediger Klaes, Priska Binner, Hans Dieplinger, Gertraud Erhart, Cordula Fassbender(CBS International Business School), Hildegard Christ(CBS International Business School)
Arteriosclerosis Thrombosis and Vascular Biology
July 15, 2016
Cited by 212Open Access
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Abstract

OBJECTIVE: Lipoprotein(a)-hyperlipoproteinemia (Lp(a)-HLP) along with progressive cardiovascular disease has been approved as indication for regular lipoprotein apheresis (LA) in Germany since 2008. We aimed to study the long-term preventive effect of LA and to assess hypothetical clinical correlations of apolipoprotein(a) (apo(a)) by analyzing genotypes and phenotypes. APPROACH AND RESULTS: This prospective observational multicenter study included 170 patients with Lp(a)-HLP and progressive cardiovascular disease (48.9 years median age at diagnosis) despite other cardiovascular risk factors, including low-density lipoprotein cholesterol had maximally been treated (mean baseline low-density lipoprotein cholesterol: measured, 2.56 mmol/L [98.9 mg/dL] and corrected, 1.72 mmol/L [66.3 mg/dL]). Patients were prospectively investigated during a 5-year period about annual incidence rates of cardiovascular events. In addition, apo(a) isoforms and polymorphisms at the apo(a) gene (LPA) were characterized. One hundred fifty-four patients (90.6%) completed 5 years of follow-up. Mean Lp(a) concentration before commencing regular LA was 108.1 mg/dL. This was reduced by a single LA treatment by 68.1% on average. Significant decline of the mean annual cardiovascular event rate was observed from 0.58±0.53 2 years before regular LA to 0.11±0.15 thereafter (P<0.0001); 95.3% of patients expressed at least 1 small apo(a) isoform. Small apo(a) isoform (35.2%) carrying phenotypes were not tagged by single-nucleotide polymorphisms rs10455872 or rs3798220. CONCLUSIONS: Results of 5 years of prospective follow-up confirm that LA has a lasting effect on prevention of cardiovascular events in patients with Lp(a)-HLP. Patients clinically selected by progressive cardiovascular disease were characterized by a highly frequent expression of small apo(a) isoforms. Only Lp(a) concentration seemed to comprehensively reflect Lp(a)-associated cardiovascular risk, however.


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