Evolocumab in paediatric heterozygous familial hypercholesterolaemia: cognitive function during 80 weeks of open-label extension treatment.

atherosclerotic cardiovascular disease central nervous system children low-density lipoprotein cholesterol proprotein convertase subtilisin kexin 9 (PCSK9) safety

Journal

European journal of preventive cardiology
ISSN: 2047-4881
Titre abrégé: Eur J Prev Cardiol
Pays: England
ID NLM: 101564430

Informations de publication

Date de publication:
19 Oct 2023
Historique:
received: 10 08 2023
revised: 20 09 2023
accepted: 17 10 2023
medline: 19 10 2023
pubmed: 19 10 2023
entrez: 19 10 2023
Statut: aheadofprint

Résumé

PCSK9 inhibition intensively lowers low-density lipoprotein cholesterol and is well tolerated in adults and paediatric patients with familial hypercholesterolaemia (FH). HAUSER-RCT showed that 24 weeks of treatment with evolocumab in paediatric patients did not affect cognitive function. This study determined the effects of 80 additional weeks of evolocumab treatment on cognitive function in paediatric patients with heterozygous FH. HAUSER-OLE was an 80-week open-label extension of HAUSER-RCT, a randomized, double-blind, 24-week trial evaluating the efficacy and safety of evolocumab in paediatric patients (ages 10-17 years) with FH. During the OLE, all patients received monthly 420 mg subcutaneous evolocumab injections. Tests of psychomotor function, attention, visual learning, and executive function were administered at baseline and weeks 24 and 80 of the OLE. Changes over time were analysed descriptively and using analysis of covariance (ANCOVA). Cohen's d statistic was used to evaluate the magnitude of treatment effects. ANCOVA results indicated no decrease in performance across visits during 80 weeks of evolocumab treatment for Groton Maze Learning, One Card Learning accuracy, Identification speed, or Detection speed (all P > 0.05). Performance on all tasks was similar for those who received placebo or evolocumab in the RCT (all P > 0.05). For all tests, the least square mean differences between patients who received placebo vs evolocumab in the parent study were trivial (all Cohen's d magnitude < 0.2). In paediatric patients with FH, 80 weeks of open-label evolocumab treatment had no negative impact on cognitive function. Some children are born with a genetic disorder that causes high cholesterol, which leads to heart disease. Children with high cholesterol can be treated with evolocumab, a medication that lowers blood cholesterol. Because cholesterol is important for development and adequate function of the brain, there is a concern that lowering cholesterol in children may affect mental ability. In this study, we tested whether treating children with evolocumab for 80 weeks affected mental ability in performing several tasks. A battery of tests that measure executive function (Groton Maze Learning Test), visual learning (One Card Learning Test), visual attention (Identification Test), and psychomotor function (Detection Test) showed no decrease in performance across visits during 80 weeks of evolocumab treatment. Performance on all tasks was similar for the children who received placebo for the first 24 weeks then received evolocumab for an additional 80 weeks (placebo/evolocumab) and those who received evolocumab for 24 weeks then received evolocumab for an additional 80 weeks (evolocumab/evolocumab).

Autres résumés

Type: plain-language-summary (eng)
Some children are born with a genetic disorder that causes high cholesterol, which leads to heart disease. Children with high cholesterol can be treated with evolocumab, a medication that lowers blood cholesterol. Because cholesterol is important for development and adequate function of the brain, there is a concern that lowering cholesterol in children may affect mental ability. In this study, we tested whether treating children with evolocumab for 80 weeks affected mental ability in performing several tasks. A battery of tests that measure executive function (Groton Maze Learning Test), visual learning (One Card Learning Test), visual attention (Identification Test), and psychomotor function (Detection Test) showed no decrease in performance across visits during 80 weeks of evolocumab treatment. Performance on all tasks was similar for the children who received placebo for the first 24 weeks then received evolocumab for an additional 80 weeks (placebo/evolocumab) and those who received evolocumab for 24 weeks then received evolocumab for an additional 80 weeks (evolocumab/evolocumab).

Identifiants

pubmed: 37855448
pii: 7321877
doi: 10.1093/eurjpc/zwad332
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of the European Society of Cardiology.

Auteurs

Raul D Santos (RD)

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

Andrea Ruzza (A)

Global Development, Amgen, Thousand Oaks, CA, United States.

Bei Wang (B)

Biostatistics Department, Amgen, Thousand Oaks, CA, United States.

Paul Maruff (P)

Cogstate Ltd., Melbourne, VIC, Australia.

Adrian Schembri (A)

Cogstate Ltd., Melbourne, VIC, Australia.

Ajay K Bhatia (AK)

Global Development, Amgen, Thousand Oaks, CA, United States.

François Mach (F)

Cardiology Department, Geneva University Hospital, Geneva, Switzerland.

Jean Bergeron (J)

Lipid Clinic, Department of Medicine, Centre Hospitalier Universitaire de Québec-Université Laval, QC, Canada.

Isabelle Gaudet (I)

Department of Health Sciences, Université du Quebec à Chicoutimi, and ECOGENE-21, Chicoutimi, QC, Canada.

Julie St Pierre (J)

Department of Pediatrics, Faculty of Medicine, McGill University, Montréal, QC, Canada.

John J P Kastelein (JJP)

Department of Vascular Medicine, Amsterdam UMC, Amsterdam, Netherlands.

G Kees Hovingh (G)

Department of Vascular Medicine, Amsterdam UMC, Amsterdam, Netherlands.

Albert Wiegman (A)

Department of Pediatrics, Amsterdam UMC, Amsterdam, Netherlands.

Daniel Gaudet (D)

The Clinical Lipidology and Rare Lipid Disorders Unit, Community Genomic Medicine Centre and ECOGENE-21, Department of Medicine, Université de Montréal, Chicoutimi, QC, Canada.

Frederick J Raal (FJ)

Division of Endocrinology and Metabolism, Department of Medicine Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Classifications MeSH