Bempedoic Acid: A New Avenue for the Treatment of Dyslipidemia

被引:2
|
作者
Smith, William [1 ]
Cheng-Lai, Angela [2 ]
Nawarskas, James [3 ]
机构
[1] Good Samaritan Hosp, Dept Pharm, Suffern, NY USA
[2] Montefiore Med Ctr, Dept Pharm, 111 E 210th St, Bronx, NY 10467 USA
[3] Univ New Mexico, Coll Pharm, Dept Pharm Practice & Adm Sci, Albuquerque, NM 87131 USA
关键词
bempedoic acid; lipid-lowering therapy; cholesterol; statin; DENSITY-LIPOPROTEIN-CHOLESTEROL; STATIN THERAPY; ETC-1002; RISK; EFFICACY; DISEASE; SAFETY; HYPERCHOLESTEROLEMIA;
D O I
10.1097/CRD.0000000000000401
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Uncontrolled dyslipidemia, specifically elevation of low-density lipoprotein cholesterol, is a major risk factor for developing cardiovascular disease. Currently, statin therapy remains as first-line treatment for reducing both serum cholesterol levels and cardiovascular risk. However, certain patients are unable to achieve desired serum cholesterol levels despite maximally tolerated statin therapy. As a result, several nonstatin therapy avenues have been evaluated for their potential benefits in reducing cholesterol and cardiovascular risk. Bempedoic acid is one such nonstatin therapy option, which has been explored over the past few years to potentially assist patients in further reducing serum cholesterol. Bempedoic acid is a novel prodrug that inhibits cholesterol synthesis upstream of statins by inhibiting adenosine triphosphate-citrate lyase. Bempedoic acid has been studied as a single, once daily 180 mg dose. Administered as monotherapy or in combination with statin or ezetimibe, bempedoic acid significantly reduces low-density lipoprotein cholesterol. Furthermore, bempedoic acid was generally well tolerated by patients and rates of adverse events were similar to placebo with few exceptions. Despite proven reductions in cholesterol and favorable safety profile, bempedoic acid will likely remain a third- or fourth-line agent for the treatment of dyslipidemia behind other nonstatin therapies until the improvement of cardiovascular outcomes is demonstrated in future clinical trials.
引用
收藏
页码:274 / 280
页数:7
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