Effect of Lipoprotein Apheresis on Progression of Carotid Intima-Media Thickness in Patients with Severe Hypercholesterolemia.


Journal

The American journal of cardiology
ISSN: 1879-1913
Titre abrégé: Am J Cardiol
Pays: United States
ID NLM: 0207277

Informations de publication

Date de publication:
15 08 2022
Historique:
received: 27 02 2022
revised: 11 04 2022
accepted: 16 05 2022
pubmed: 20 6 2022
medline: 20 7 2022
entrez: 19 6 2022
Statut: ppublish

Résumé

The extent of intervention effects on carotid intima-media thickness (CIMT) can predict the degree of atherosclerotic cardiovascular risk-reduction. We hypothesized that regular lipoprotein apheresis over the course of 10 years might slow down progression of CIMT in patients with severe hypercholesterolemia. This case series describes 10 Caucasian patients (mean age 60 ± 9 years, 70% female, 80% statin intolerant) with a severe hypercholesterolemia phenotype treated with lipoprotein apheresis between 2005 and 2020 (mean duration, 10 ± 4 years). The median pretreatment low-density lipoprotein cholesterol (LDL-C) level was 214 mg/100 ml (95% confidence interval, 145 to 248), lipoprotein(a) (Lp[a]), 26 mg/100 ml (15 to 109; 40% with Lp(a)>60 mg/100 ml). Three patients were diagnosed with a monogenic cause. The baseline mean CIMT was 850 ± 170 µm, and maximum CIMT was 1,040 ± 220 µm across the age range of 46 to 70 years. Acute effects of lipoprotein apheresis determined as a difference before and immediately after the procedure were estimated as a median of 72 ± 8% and 75 ± 7% reduction in the LDL-C and Lp(a) levels, respectively. Using the imputed trajectories, period-specific on-treatment time-weighted averages for LDL-C and Lp(a) were 141 mg/100 ml (interquartile range, 89 to 152; 38% reduction from the baseline) and 24 mg/100 ml (interquartile range, 12 to 119; 19% reduction from baseline), respectively. The number of patients with CIMT above their "vascular age" decreased from 80% to 30% over the treatment course. In conclusion, an increase in CIMT seen with advanced age and severe hypercholesterolemia was halted with lipoprotein apheresis with an estimated annual rate of change in mean common CIMT of -4 µm/y and maximum CIMT of -3 µm/y.

Identifiants

pubmed: 35718549
pii: S0002-9149(22)00520-3
doi: 10.1016/j.amjcard.2022.05.002
pii:
doi:

Substances chimiques

Cholesterol, LDL 0
Hydroxymethylglutaryl-CoA Reductase Inhibitors 0
Lipoprotein(a) 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

22-27

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Disclosures PMM reports modest honoraria from Kaneka Medical America LLC. The other authors have no conflicts of interest to declare.

Auteurs

Maya S Safarova (MS)

Department of Cardiovascular Medicine, University of Kansas Medical Center, Kansas City, Kansas.

Anne K Nugent (AK)

Division of Clinical Pharmacology, Department of Internal Medicine, Atherosclerosis and Lipoprotein Apheresis Center, University of Kansas Medical Center, Kansas City, Kansas.

Lauryn Gorby (L)

Division of Clinical Pharmacology, Department of Internal Medicine, Atherosclerosis and Lipoprotein Apheresis Center, University of Kansas Medical Center, Kansas City, Kansas.

Julie-Ann Dutton (JA)

Division of Clinical Pharmacology, Department of Internal Medicine, Atherosclerosis and Lipoprotein Apheresis Center, University of Kansas Medical Center, Kansas City, Kansas.

W Jake Thompson (WJ)

Accessible Teaching, Learning, and Assessment Systems, University of Kansas, Lawrence, Kansas.

Patrick M Moriarty (PM)

Division of Clinical Pharmacology, Department of Internal Medicine, Atherosclerosis and Lipoprotein Apheresis Center, University of Kansas Medical Center, Kansas City, Kansas. Electronic address: pmoriart@kumc.edu.

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Classifications MeSH