Circulation · 2013 · 316 citations · 7 references
MedicineCardiologyPharmacotherapyClinical CardiologyClinical PharmacologyLipid BiochemistryCardiovascular DiseaseCardiovascular Disease PreventionDyslipidemia ManagementLipid DisordersLipid-lowering TherapyLipoprotein AnalysisCardiovascular Disease IncidenceHyperlipidemia TreatmentLipid ApheresisLipid-lowering Drug EfficacyLipoprotein(a) ElevationLipoprotein(a) GeneticsLipoprotein(a) Lowering TherapyTherapeutic Apheresis
Lipoprotein(a) hyperlipoproteinemia is a major cardiovascular risk factor that is not mitigated by conventional lipid‑lowering therapies. The study aimed to evaluate the impact of chronic lipoprotein apheresis on cardiovascular event incidence in patients with progressive disease despite maximally tolerated lipid‑lowering treatment. In a prospective multicenter observational study of 170 patients, researchers compared plasma lipid profiles, LPA gene variants, and cardiovascular event rates two years before and during lipoprotein apheresis. Lipoprotein apheresis lowered major adverse coronary event rates from 0.41 to 0.09 per year and all‑vascular event rates from 0.61 to 0.16 per year over two years, with significant reductions observed during treatment. The trial is registered as DRKS00003119 (https://drks-neu.uniklinik-freiburg.de).
Lipoprotein(a) (Lp(a)) hyperlipoproteinemia is a major risk factor for cardiovascular disease, which is not affected by treatment of other cardiovascular risk factors. This study sought to assess the effect of chronic lipoprotein apheresis (LA) on the incidence of cardiovascular events in patients with progressive cardiovascular disease receiving maximally tolerated lipid-lowering treatment.In a prospective observational multicenter study, 170 patients were investigated who commenced LA because of Lp(a)-hyperlipoproteinemia and progressive cardiovascular disease. Patients were characterized regarding plasma lipid status, lipid-lowering drug treatment, and variants at the LPA gene locus. The incidence rates of cardiovascular events 2 years before (y-2 and y-1) and prospectively 2 years during LA treatment (y+1, y+2) were compared. The mean age of patients was 51 years at the first cardiovascular event and 57 years at the first LA. Before LA, mean low-density lipoprotein cholesterol and Lp(a) were 2.56±1.04 mmol·L(-1) (99.0±40.1 mg·dL(-1)) and Lp(a) 3.74±1.63 µmol·L(-1) (104.9±45.7 mg·dL(-1)), respectively. Mean annual rates for major adverse coronary events declined from 0.41 for 2 years before LA to 0.09 for 2 years during LA (P<0.0001). Event rates including all vascular beds declined from 0.61 to 0.16 (P<0.0001). Analysis of single years revealed increasing major adverse coronary event rates from 0.30 to 0.54 (P=0.001) for y-2 to y-1 before LA, decline to 0.14 from y-1 to y+1 (P<0.0001) and to 0.05 from y+1 to y+2 (P=0.014).In patients with Lp(a)-hyperlipoproteinemia, progressive cardiovascular disease, and maximally tolerated lipid-lowering medication, LA effectively lowered the incidence rate of cardiovascular events.https://drks-neu.uniklinik-freiburg.de. Unique identifier: DRKS00003119.
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cDNA sequence of human apolipoprotein(a) is homologous to plasminogen
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