» Articles » PMID: 39165612

A UK Multicentre Audit of the Management of Patients with Primary Hypercholesterolaemia or Mixed Dyslipidaemia with Bempedoic Acid Against Published Lipid-lowering Treatment Targets

Overview
Journal Drugs Context
Specialty Pharmacology
Date 2024 Aug 21
PMID 39165612
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Bempedoic acid, an adenosine triphosphate citrate lyase inhibitor, was introduced to UK practice via a pre-reimbursement access scheme for adults with primary hypercholesterolaemia or mixed dyslipidaemia who are at high risk of cardiovascular disease, in whom statins are either not tolerated or contraindicated, who have not achieved target cholesterol, despite being on ezetimibe therapy, and do not qualify for PCSK9 inhibitor treatment. This retrospective multicentre audit aimed to evaluate the achievement of lipid-lowering targets with bempedoic acid in UK patients based on recommendations in the Joint British Societies (JBS) guidelines for the prevention of cardiovascular disease.

Methods: Pseudo-anonymized medical record data for 221 adults treated with bempedoic acid as part of the UK scheme were entered into a bespoke data collection tool at four UK hospitals. Patient demographics, clinical characteristics, treatment pathways and lipid assessment results (against JBS lipid-lowering targets) were collected against pre-specified criteria.

Results: Overall, 54% (99/184) of patients achieved the JBS2 audit standard (total cholesterol (TC) <5 mmol/L and low-density lipoprotein cholesterol (LDL-C) <3 mmol/L or ≥25% reduction in TC and ≥30% reduction in LDL-C) at 12 weeks post-initiation. At week 12, the mean absolute change in LDL-C was -1.0 mmol/L; the mean percentage reduction from baseline was 22.0%. Additionally, 52% (96/185) of patients had an LDL-C of <3 mmol/L and 10% (18/185) an LDL-C of <1.8 mmol/L at 12 weeks (as per JBS3).

Conclusion: This audit highlights the role of bempedoic acid as part of combination therapy for a population with previously limited treatment options.

References
1.
Pinkosky S, Newton R, Day E, Ford R, Lhotak S, Austin R . Liver-specific ATP-citrate lyase inhibition by bempedoic acid decreases LDL-C and attenuates atherosclerosis. Nat Commun. 2016; 7:13457. PMC: 5133702. DOI: 10.1038/ncomms13457. View

2.
Tramacere I, Boncoraglio G, Banzi R, Del Giovane C, Kwag K, Squizzato A . Comparison of statins for secondary prevention in patients with ischemic stroke or transient ischemic attack: a systematic review and network meta-analysis. BMC Med. 2019; 17(1):67. PMC: 6436237. DOI: 10.1186/s12916-019-1298-5. View

3.
Bilitou A, Were J, Farrer A, Rabe A, Ming S, Haq I . Prevalence and Patient Outcomes of Adult Primary Hypercholesterolemia and Dyslipidemia in the UK: Longitudinal Retrospective Study Using a Primary Care Dataset from 2009 to 2019. Clinicoecon Outcomes Res. 2022; 14:189-203. PMC: 8994561. DOI: 10.2147/CEOR.S347085. View

4.
Banach M, Duell P, Gotto Jr A, Laufs U, Leiter L, Mancini G . Association of Bempedoic Acid Administration With Atherogenic Lipid Levels in Phase 3 Randomized Clinical Trials of Patients With Hypercholesterolemia. JAMA Cardiol. 2020; 5(10):1124-1135. PMC: 7330832. DOI: 10.1001/jamacardio.2020.2314. View

5.
Ray K, Bays H, Catapano A, Lalwani N, Bloedon L, Sterling L . Safety and Efficacy of Bempedoic Acid to Reduce LDL Cholesterol. N Engl J Med. 2019; 380(11):1022-1032. DOI: 10.1056/NEJMoa1803917. View