Literature DB >> 34037950

Bempedoic Acid: The New Kid on the Block for the Treatment of Dyslipidemia and LDL Cholesterol: A Narrative Review.

Uazman Alam1,2, Dalal Y Al-Bazz3, Handrean Soran4.   

Abstract

Diabetes is a major risk factor for atherosclerotic cardiovascular disease (ASCVD) in which dyslipidaemia plays a crucial role. Statins are first line therapy for primary and secondary prevention of ASCVD; however, adverse events include reversible musculoskeletal and liver side effects in addition to a diabetogenic association. In this short review, we provide a succinct narrative of the future role and current trial data of a novel first-in-class molecule, bempedoic acid. The authors provide their expert insight with a focus on Phase III randomised controlled trials (RCT) of bempedoic acid. Bempedoic acid was approved by the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA) in February and March 2020, respectively, and is a novel molecule which inhibits cholesterol biosynthesis in the same mechanistic pathway as statins. It is a first-in-class small molecule, delivered as a prodrug and administered as an oral, once-daily dose that decreases low-density lipoprotein cholesterol (LDL-C) levels. Phase II and III RCTs have demonstrated efficacy with adequate safety data as mono- or combination therapy with statins and ezetimibe. Bempedoic acid is hepatically converted to the active drug with a lack of activation in skeletal muscle. Due to this novel mechanism, musculoskeletal-related adverse events exhibit a lower prevalence providing an alternative pharmacotherapy in statin-intolerant patients. Bempedoic acid may be used as an adjunct to diet and maximally tolerated statin therapy or in statin-intolerant patients for the treatment of dyslipidaemia. The recent National Institute of Health and Care Excellence (NICE) (UK) technology appraisal guidance [TA694] published in April 2021 recommended bempedoic acid with ezetimibe as a treatment option for primary hypercholesterolaemia or mixed dyslipidaemia if statins are not tolerated or contraindicated and if there is inadequate control of LDL-C with ezetimibe alone. Additionally, outcomes trials evaluating 'hard' endpoints in statin-intolerant patients or those with ASCVD are currently underway.

Entities:  

Keywords:  Atherosclerotic cardiovascular disease; Bempedoic acid; Diabetes; Dyslipidaemia; Statins

Year:  2021        PMID: 34037950     DOI: 10.1007/s13300-021-01070-6

Source DB:  PubMed          Journal:  Diabetes Ther        ISSN: 1869-6961            Impact factor:   2.945


  38 in total

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Review 2.  Quantitative evaluation of statin effectiveness versus intolerance and strategies for management of intolerance.

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Journal:  JAMA       Date:  1986-11-28       Impact factor: 56.272

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Journal:  Diabetes Care       Date:  1997-04       Impact factor: 19.112

9.  Cholesterol, not just cardiovascular risk, is important in deciding who should receive statin treatment.

Authors:  Handrean Soran; Jonathan D Schofield; Paul N Durrington
Journal:  Eur Heart J       Date:  2015-08-04       Impact factor: 29.983

10.  Efficacy and safety of more intensive lowering of LDL cholesterol: a meta-analysis of data from 170,000 participants in 26 randomised trials.

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Journal:  Lancet       Date:  2010-11-08       Impact factor: 79.321

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  1 in total

Review 1.  Bempedoic acid: a novel oral LDL-cholesterol lowering agent.

Authors:  Ishwarlal Jialal; Neeraj Ramakrishnan
Journal:  Int J Physiol Pathophysiol Pharmacol       Date:  2022-04-15
  1 in total

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