Low-density lipoprotein cholesterol goal achievement in patients with familial hypercholesterolemia in countries outside Western Europe: The International ChoLesterol management Practice Study.


Journal

Journal of clinical lipidology
ISSN: 1933-2874
Titre abrégé: J Clin Lipidol
Pays: United States
ID NLM: 101300157

Informations de publication

Date de publication:
Historique:
received: 07 02 2019
revised: 16 04 2019
accepted: 07 05 2019
pubmed: 19 6 2019
medline: 23 6 2020
entrez: 19 6 2019
Statut: ppublish

Résumé

The cross-sectional observational International ChoLesterol management Practice Study study assessed achievement of European Society of Cardiology/European Atherosclerosis Society low-density lipoprotein cholesterol (LDL-C) targets in patients outside Western Europe. The aim of the study was to assess LDL-C goal achievement in International ChoLesterol management Practice Study participants with familial hypercholesterolemia (FH). A total of 334 patients (aged ≥18 years) with definite or probable FH (Dutch Lipid Clinic Network score ≥6; 43.1% genetically confirmed) who had been receiving stable lipid-modifying therapy (LMT) for ≥3 months were enrolled. The mean ± standard deviation age of the patients was 58.5 ± 13.1 years, 49.1% were male, and 48.2% had coronary artery disease. Most were receiving statin (∼99%). Of these, 57.6% were on high-intensity statin therapy, 49.1% on the highest dose available, and 13.0% used a statin together with a cholesterol absorption inhibitor (CAI). Mean ± standard deviation LDL-C level was 5.6 ± 3.0 mmol/L before LMT and 3.3 ± 2.0 mmol/L at enrollment. Overall, 32.0% of patients achieved their LDL-C target. Target achievement rates were 36.6% for patients with coronary artery disease, and 27.5% for those without, and 27.9%, 28.0%, and 37.5% for patients treated with a statin plus CAI, highest-dose statin (no CAI), and lower-dose statin (no CAI), respectively. LDL-C target achievement rates were low in patients with FH, even in those receiving intensive LMT. Factors that are likely to have contributed to the low LDL-C target achievement rates include high baseline LDL-C, inadequate statin dosages, and low use of CAI. Many patients would have been eligible for proprotein convertase subtilisin/kexin type 9 inhibitor therapy.

Sections du résumé

BACKGROUND
The cross-sectional observational International ChoLesterol management Practice Study study assessed achievement of European Society of Cardiology/European Atherosclerosis Society low-density lipoprotein cholesterol (LDL-C) targets in patients outside Western Europe.
OBJECTIVE
The aim of the study was to assess LDL-C goal achievement in International ChoLesterol management Practice Study participants with familial hypercholesterolemia (FH).
METHODS
A total of 334 patients (aged ≥18 years) with definite or probable FH (Dutch Lipid Clinic Network score ≥6; 43.1% genetically confirmed) who had been receiving stable lipid-modifying therapy (LMT) for ≥3 months were enrolled.
RESULTS
The mean ± standard deviation age of the patients was 58.5 ± 13.1 years, 49.1% were male, and 48.2% had coronary artery disease. Most were receiving statin (∼99%). Of these, 57.6% were on high-intensity statin therapy, 49.1% on the highest dose available, and 13.0% used a statin together with a cholesterol absorption inhibitor (CAI). Mean ± standard deviation LDL-C level was 5.6 ± 3.0 mmol/L before LMT and 3.3 ± 2.0 mmol/L at enrollment. Overall, 32.0% of patients achieved their LDL-C target. Target achievement rates were 36.6% for patients with coronary artery disease, and 27.5% for those without, and 27.9%, 28.0%, and 37.5% for patients treated with a statin plus CAI, highest-dose statin (no CAI), and lower-dose statin (no CAI), respectively.
CONCLUSIONS
LDL-C target achievement rates were low in patients with FH, even in those receiving intensive LMT. Factors that are likely to have contributed to the low LDL-C target achievement rates include high baseline LDL-C, inadequate statin dosages, and low use of CAI. Many patients would have been eligible for proprotein convertase subtilisin/kexin type 9 inhibitor therapy.

Identifiants

pubmed: 31208705
pii: S1933-2874(19)30179-5
doi: 10.1016/j.jacl.2019.05.004
pii:
doi:

Substances chimiques

Anticholesteremic Agents 0
Cholesterol, LDL 0
Fibric Acids 0
Hydroxymethylglutaryl-CoA Reductase Inhibitors 0
Ezetimibe EOR26LQQ24

Types de publication

Clinical Trial Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

594-600

Informations de copyright

Copyright © 2019 National Lipid Association. Published by Elsevier Inc. All rights reserved.

Auteurs

Dirk J Blom (DJ)

Division of Lipidology and Hatter Institute for Cardiovascular Research in Africa, Department of Medicine, University of Cape Town, Cape Town, South Africa. Electronic address: dirk.blom@uct.ac.za.

Wael Almahmeed (W)

Heart and Vascular Institute, Cleveland Clinic, Abu Dhabi, United Arab Emirates.

Khalid Al-Rasadi (K)

Sultan Qaboos University, Muscat, Oman.

Joseph Azuri (J)

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Veronique Daclin (V)

Sanofi-Aventis, Paris, France.

Meral Kayikcioglu (M)

Ege University, Medical School Cardiology Department, Izmir, Turkey.

Florence Mercier (F)

Stat Process, Paris, France.

Alvaro J Ruiz (AJ)

Department of Clinical Epidemiology and Biostatistics, Department of Internal Medicine, School of Medicine, Pontificia Universidad Javeriana, Bogota, Colombia.

Raul D Santos (RD)

Lipid Clinic, Heart Institute (InCor), University of Sao Paulo Medical School Hospital and Hospital Israelita Albert Einstein, Sao Paulo, Brazil.

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Classifications MeSH