Low-density lipoprotein cholesterol levels exceed the recommended European threshold for PCSK9i initiation: lessons from the HEYMANS study

Author:

Ray Kausik K12ORCID,Dhalwani Nafeesa3,Sibartie Mahendra4,Bridges Ian5,Ebenbichler Christoph6,Perrone-Filardi Pasquale78,Villa Guillermo4,Vogt Anja9,Bruckert Eric10

Affiliation:

1. Imperial Centre for Cardiovascular Disease Prevention and Imperial Clinical Trials Unit, Imperial , Stadium House, 68 Wood Lane, London W12 7RH, UK

2. College London , Stadium House, 68 Wood Lane, London W12 7RH, UK

3. Center for Observational Research, Amgen Ltd, Uxbridge UB8 1DH, UK

4. Amgen (Europe) GmbH , Rotkreuz CH-6343, Switzerland

5. International Biostatistics, Amgen Ltd, Uxbridge UB8 1DH, UK

6. Metabolic Diseases, Medizinische Universität Innsbruck , Innsbruck 6020, Austria

7. Department of Advanced Biomedical Sciences, University of Naples Federico II, Naples 80138, Italy

8. Mediterranean CardioCentro , Naples, Italy

9. Medizinische Klinik und Poliklinik IV, Klinikum der Universität München , Munich 80366, Germany

10. Department of Medicine, University of Paris , Paris 75006, France

Abstract

Abstract Aims To describe the characteristics of patients receiving evolocumab in clinical practice across 12 European countries and simulate the association between low-density lipoprotein cholesterol (LDL-C) reduction and cardiovascular (CV) risk reduction. Methods and results The characteristics of hyperlipidaemic patients at initiation of evolocumab and treatment patterns study—HEYMANS (n = 1952) is a prospective registry of patients ≥18 years old who initiated evolocumab from 1 August 2015 onwards. Mean (standard deviation) age was 60 (10.8), 85% had a prior CV event, 45% were diagnosed with familial hypercholesterolaemia (FH), and 60% had statin intolerance. At evolocumab initiation, 43% were receiving any statin, 16% were receiving ezetimibe without statin, and 41% received no background lipid-lowering therapy (LLT), with LDL-C levels reflecting local proprotein convertase subtilisin/kexin type 9 inhibitor (PCSK9i) reimbursement criteria. Median LDL-C decreased from 3.98 to 1.63 mmol/L within 3 months of evolocumab initiation and was maintained over 24 months. Overall, 58% achieved risk-based 2019 European Society of Cardiology/European Atherosclerosis Society LDL-C goals but that proportion was higher (68%) in patients receiving background LLT compared with those not receiving background LLT (44%). In patients with atherosclerotic cardiovascular disease without FH, the simulated relative CV risk reduction associated with evolocumab treatment was 34% (25–44%). Conclusion Across Europe, LDL-C levels at evolocumab initiation were three times higher than recommended thresholds for PCSK9i initiation, reflecting disparities between implementation and guidelines. More patients attained risk-based LDL-C goals when receiving evolocumab in combination with LLT vs. those not receiving combination therapy. Population health could be improved and LDL-C goals better attained if LDL-C thresholds for PCSK9i reimbursement were lowered, enabling more patients to receive combination therapy when needed.

Funder

Amgen

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Health Policy

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