Increased FH-Risk-Score and Diabetes Are Cardiovascular Risk Equivalents in Heterozygous Familial Hypercholesterolemia.

atherosclerosis cardiovascular diseases cholesterol, LDL hyperlipoproteinemia type II risk factors

Journal

Arteriosclerosis, thrombosis, and vascular biology
ISSN: 1524-4636
Titre abrégé: Arterioscler Thromb Vasc Biol
Pays: United States
ID NLM: 9505803

Informations de publication

Date de publication:
30 Nov 2023
Historique:
medline: 30 11 2023
pubmed: 30 11 2023
entrez: 30 11 2023
Statut: aheadofprint

Résumé

Familial hypercholesterolemia (FH) is a genetic condition causing premature atherosclerotic cardiovascular disease (ASCVD). It is well established that patients with FH should be treated with statin therapy. However, there exists discordance concerning low-density lipoprotein cholesterol-lowering goals in the management of these patients between different guidelines worldwide. The objective was to compare the 10-year ASCVD risk of different subgroups of patients with and without FH including those with diabetes or a history of ASCVD and patients with FH within different FH-Risk-Score categories. This multinational observational study used data from 3 different prospective cohorts. A total of 3383 FH and 6917 non-FH controls matched for age and sex were included (104 363 person-years of follow-up). The 10-year incident ASCVD risk was assessed using Kaplan-Meier estimates, whereas the relative risk was estimated using Cox proportional hazards regression models. FH patients with a high (score >20%) FH-Risk-Score (hazard ratio, 8.45 [95% CI, 6.69-10.67]; This study strongly suggests that the observed risk of FH patients with diabetes, history of ASCVD, and FH-Risk-Score >20% is as high or higher than non-FH individuals with a history of ASCVD. More aggressive management should be recommended for these patients.

Sections du résumé

BACKGROUND UNASSIGNED
Familial hypercholesterolemia (FH) is a genetic condition causing premature atherosclerotic cardiovascular disease (ASCVD). It is well established that patients with FH should be treated with statin therapy. However, there exists discordance concerning low-density lipoprotein cholesterol-lowering goals in the management of these patients between different guidelines worldwide. The objective was to compare the 10-year ASCVD risk of different subgroups of patients with and without FH including those with diabetes or a history of ASCVD and patients with FH within different FH-Risk-Score categories.
METHODS UNASSIGNED
This multinational observational study used data from 3 different prospective cohorts. A total of 3383 FH and 6917 non-FH controls matched for age and sex were included (104 363 person-years of follow-up). The 10-year incident ASCVD risk was assessed using Kaplan-Meier estimates, whereas the relative risk was estimated using Cox proportional hazards regression models.
RESULTS UNASSIGNED
FH patients with a high (score >20%) FH-Risk-Score (hazard ratio, 8.45 [95% CI, 6.69-10.67];
CONCLUSIONS UNASSIGNED
This study strongly suggests that the observed risk of FH patients with diabetes, history of ASCVD, and FH-Risk-Score >20% is as high or higher than non-FH individuals with a history of ASCVD. More aggressive management should be recommended for these patients.

Identifiants

pubmed: 38031840
doi: 10.1161/ATVBAHA.123.319957
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Martine Paquette (M)

Lipids, Nutrition, and Cardiovascular Prevention Clinic of the Montreal Clinical Research Institute, Québec, Canada (M.P., S. Bernard, A.B.).

Bertrand Cariou (B)

Nantes Université, CHU Nantes, CNRS, INSERM, L'institut Du Thorax, France (B.C.).

Sophie Bernard (S)

Lipids, Nutrition, and Cardiovascular Prevention Clinic of the Montreal Clinical Research Institute, Québec, Canada (M.P., S. Bernard, A.B.).
Department of Medicine, Division of Endocrinology, Université de Montreal, Québec, Canada (S. Bernard).
Research Centre of the Centre Hospitalier Universitaire de Montréal, Québec, Canada (S. Bernard).

Robert A Hegele (RA)

Department of Medicine, Schulich School of Medicine & Dentistry, Western University, London, Ontario, Canada. (R.A.H.).
Department of Biochemistry, Schulich School of Medicine & Dentistry, Western University, London, Ontario, Canada. (R.A.H.).
Robarts Research Institute, Schulich School of Medicine & Dentistry, Western University, London, Ontario, Canada. (R.A.H.).

Antonio Gallo (A)

Sorbonne Université, INSERM UMR1166, Lipidology and Cardiovascular Prevention Unit, Department of Nutrition, APHP, Hôpital Pitié-Salpètriêre, Paris, France (A.G.).

Jacques Genest (J)

Research Institute of the McGill University Health Centre, Montreal, Québec, Canada (J.G.).

Mark Trinder (M)

Faculty of Medicine, Centre for Heart and Lung Innovation, University of British Columbia, Vancouver, Canada. (M.T., L.R.B.).
Department of Medicine, University of British Columbia, Vancouver, Canada. (M.T., L.R.B.).

Liam R Brunham (LR)

Faculty of Medicine, Centre for Heart and Lung Innovation, University of British Columbia, Vancouver, Canada. (M.T., L.R.B.).
Department of Medicine, University of British Columbia, Vancouver, Canada. (M.T., L.R.B.).

Sophie Béliard (S)

Aix Marseille University, INSERM, INRAE, C2VN, Department of Nutrition, Metabolic Diseases, Endocrinology, La Conception Hospital, France (S. Béliard).

Alexis Baass (A)

Lipids, Nutrition, and Cardiovascular Prevention Clinic of the Montreal Clinical Research Institute, Québec, Canada (M.P., S. Bernard, A.B.).
Department of Medicine, Divisions of Experimental Medicine and Medical Biochemistry, McGill University, Montreal, Québec, Canada (A.B.).

Classifications MeSH