Factors Associated With Enhanced Low-Density Lipoprotein Cholesterol Lowering With Bempedoic Acid

Christie M Ballantyne, Harold E Bays, Michael J Louie, Jeremy Smart, Yang Zhang, Kausik K Ray, Christie M Ballantyne, Harold E Bays, Michael J Louie, Jeremy Smart, Yang Zhang, Kausik K Ray

Abstract

Background Bempedoic acid (BA) inhibits ATP-citrate lyase in the cholesterol synthesis pathway and lowers low-density lipoprotein cholesterol (LDL-C). As with other lipid-lowering therapies, interindividual variation in response to BA was observed in clinical trials. We characterized LDL-C response to BA using guideline-defined statin intensity categories and identified clinical factors associated with enhanced LDL-C lowering with BA. Methods and Results This post hoc analysis used pooled data from 4 phase 3 studies. Patients were randomized 2:1 to once-daily BA 180 mg (n=2321) or placebo (n=1167) for 12 to 52 weeks and grouped based on percent change in LDL-C from baseline to week 12 according to guideline-established statin intensity categories. Factors associated with ≥30% reduction in LDL-C were identified using logistic regression analyses. From baseline to week 12, BA lowered LDL-C levels comparable to a moderate- or high-intensity statin (≥30%) in 28.9% of patients; this degree of LDL-C lowering was observed in 50.9% of patients not receiving background statin therapy. In a multivariable analysis, the absence of statins, female sex, a history of diabetes, ezetimibe use, and higher high-sensitivity C-reactive protein level were associated with increased rates of achieving ≥30% LDL-C reduction with BA (P<0.01 for each). Conclusions A large percentage of patients receiving BA achieved LDL-C reductions comparable to a moderate- or high-intensity statin. Factors including statin absence, female sex, diabetes history, ezetimibe use, and a higher high-sensitivity C-reactive protein level may be useful to identify patients who may have a greater LDL-C reduction with BA. Registration URL: https://www.clinicaltrials.gov; Unique identifiers: NCT02666664, NCT02991118, NCT02988115, NCT03001076.

Keywords: atherosclerotic cardiovascular disease; statin intolerance.

Figures

Figure 1. Proportion of patients achieving at…
Figure 1. Proportion of patients achieving at least a 30% or at least a 50% reduction in LDL‐C with bempedoic acid or placebo.
LDL‐C indicates low‐density lipoprotein cholesterol.
Figure 2. Multivariable analysis of baseline variables…
Figure 2. Multivariable analysis of baseline variables on achieving at least a 30% reduction in low‐density lipoprotein cholesterol among patients treated with bempedoic acid.
CI indicates confidence interval; hsCRP, high‐sensitivity C‐reactive protein; and OR, odds ratio.

References

    1. Boekholdt SM, Hovingh GK, Mora S, Arsenault BJ, Amarenco P, Pedersen TR, LaRosa JC, Waters DD, DeMicco DA, Simes RJ, et al. Very low levels of atherogenic lipoproteins and the risk for cardiovascular events: a meta‐analysis of statin trials. J Am Coll Cardiol. 2014;64:485–494. doi: 10.1016/j.jacc.2014.02.615
    1. Karlson BW, Wiklund O, Palmer MK, Nicholls SJ, Lundman P, Barter PJ. Variability of low‐density lipoprotein cholesterol response with different doses of atorvastatin, rosuvastatin, and simvastatin: results from VOYAGER. Eur Heart J Cardiovasc Pharmacother. 2016;2:212–217. doi: 10.1093/ehjcvp/pvw006
    1. Banach M, Duell PB, Gotto AM Jr, Laufs U, Leiter LA, Mancini GBJ, Ray KK, Flaim J, Ye Z, Catapano AL. Association of bempedoic acid administration with atherogenic lipid levels in phase 3 randomized clinical trials of patients with hypercholesterolemia. JAMA Cardiol. 2020;5:1124–1135. doi: 10.1001/jamacardio.2020.2314
    1. Grundy SM, Stone NJ, Bailey AL, Beam C, Birtcher KK, Blumenthal RS, Braun LT, de Ferranti S, Faiella‐Tommasino J, Forman DE, et al. 2018 AHA/ACC/AACVPR/AAPA/ABC/ACPM/ADA/AGS/APhA/ASPC/NLA/PCNA guideline on the management of blood cholesterol: a report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. Circulation. 2019;139:e1082–e1143. doi: 10.1161/CIR.0000000000000625
    1. Vupputuri S, Joski PJ, Kilpatrick R, Woolley JM, Robinson BE, Farkouh ME, Yun H, Safford MM, Muntner P. LDL cholesterol response and statin adherence among high‐risk patients initiating treatment. Am J Manag Care. 2016;22:e106–e115.
    1. Handelsman Y, Jellinger PS, Guerin CK, Bloomgarden ZT, Brinton EA, Budoff MJ, Davidson MH, Einhorn D, Fazio S, Fonseca VA, et al. Consensus statement by the American Association of Clinical Endocrinologists and American College of Endocrinology on the management of dyslipidemia and prevention of cardiovascular disease algorithm—2020 executive summary. Endocr Pract. 2020;26:1196–1224. doi: 10.4158/CS-2020-0490
    1. Descamps O, Tomassini JE, Lin J, Polis AB, Shah A, Brudi P, Hanson ME, Tershakovec AM. Variability of the LDL‐C lowering response to ezetimibe and ezetimibe + statin therapy in hypercholesterolemic patients. Atherosclerosis. 2015;240:482–489. doi: 10.1016/j.atherosclerosis.2015.03.004
    1. Robinson JG, Ballantyne CM, Hsueh WA, Rosen JB, Lin J, Shah AK, Tomassini JE, Lowe RS, Tershakovec AM. Age, abdominal obesity, and baseline high‐sensitivity C‐reactive protein are associated with low‐density lipoprotein cholesterol, non‐high‐density lipoprotein cholesterol, and apolipoprotein B responses to ezetimibe/simvastatin and atorvastatin in patients with metabolic syndrome. J Clin Lipidol. 2013;7:292–303. doi: 10.1016/j.jacl.2013.03.007
    1. Swiger KJ, Martin SS, Blaha MJ, Toth PP, Nasir K, Michos ED, Gerstenblith G, Blumenthal RS, Jones SR. Narrowing sex differences in lipoprotein cholesterol subclasses following mid‐life: the very large database of lipids (VLDL‐10B). J Am Heart Assoc. 2014;3:e000851. doi: 10.1161/JAHA.114.000851
    1. Nanna MG, Wang TY, Xiang Q, Goldberg AC, Robinson JG, Roger VL, Virani SS, Wilson PWF, Louie MJ, Koren A, et al. Sex differences in the use of statins in community practice. Circ Cardiovasc Qual Outcomes. 2019;12:e005562. doi: 10.1161/CIRCOUTCOMES.118.005562
    1. Jacobs MJ, Kleisli T, Pio JR, Malik S, L'Italien GJ, Chen RS, Wong ND. Prevalence and control of dyslipidemia among persons with diabetes in the United States. Diabetes Res Clin Pract. 2005;70:263–269. doi: 10.1016/j.diabres.2005.03.032
    1. Glovaci D, Fan W, Wong ND. Epidemiology of diabetes mellitus and cardiovascular disease. Curr Cardiol Rep. 2019;21:21. doi: 10.1007/s11886-019-1107-y
    1. Buckley DI, Fu R, Freeman M, Rogers K, Helfand M. C‐reactive protein as a risk factor for coronary heart disease: a systematic review and meta‐analyses for the U.S. Preventive Services Task Force. Ann Intern Med. 2009;151:483–495. doi: 10.7326/0003-4819-151-7-200910060-00009
    1. Bays HE, Rosenson RS, Baccara‐Dinet MT, Louie MJ, Thompson D, Hovingh GK. Assessment of the 1% of patients with consistent < 15% reduction in low‐density lipoprotein cholesterol: pooled analysis of 10 phase 3 ODYSSEY alirocumab trials. Cardiovasc Drugs Ther. 2018;32:175–180. doi: 10.1007/s10557-018-6784-z
    1. Trompet S, Postmus I, Slagboom PE, Heijmans BT, Smit RA, Maier AB, Buckley BM, Sattar N, Stott DJ, Ford I, et al. Non‐response to (statin) therapy: the importance of distinguishing non‐responders from non‐adherers in pharmacogenetic studies. Eur J Clin Pharmacol. 2016;72:431–437. doi: 10.1007/s00228-015-1994-9

Source: PubMed

3
Sottoscrivi