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Comprehensive review of statin-intolerance and the practical application of Bempedoic Acid.
Yarrarapu, Siva Naga S; Goyal, Amandeep; Venkata, Vikramaditya Samala; Panchal, Viraj; Sivasubramanian, Barath Prashanth; Du, Doantrang T; Jakulla, Roopesh Sai; Pamulapati, Hema; Afaq, Mazhar A; Owens, Steven; Dalia, Tarun.
Afiliação
  • Yarrarapu SNS; Department of Internal Medicine, Rutgers/Monmouth Medical Center, Long Branch, NJ, USA.
  • Goyal A; Department of Cardiology, University of Kansas Medical Center, Kansas City, KS, USA.
  • Venkata VS; Department of Hospital Medicine, Cheshire Medical Center/Dartmouth Health Hitchcock, Keene, NH, USA.
  • Panchal V; Department of Medicine, Smt. NHL Municipal Medical College, Ahmedabad, Gujarat, India.
  • Sivasubramanian BP; Department of Infectious Diseases, University of Texas Health Science Centre, San Antonio, TX, USA.
  • Du DT; Department of Internal Medicine, Rutgers/Monmouth Medical Center, Long Branch, NJ, USA.
  • Jakulla RS; Department of Internal Medicine, University of Missouri, Kansas City, MO, USA.
  • Pamulapati H; Department of Cardiology, Hays Medical Center, Hays, KS, USA.
  • Afaq MA; Department of Cardiology, University of Kansas Medical Center, Kansas City, KS, USA.
  • Owens S; Department of Cardiology, University of Kansas Medical Center, Kansas City, KS, USA.
  • Dalia T; Department of Cardiology, University of Kansas Medical Center, Kansas City, KS, USA. Electronic address: tdalia2@kumc.edu.
J Cardiol ; 84(1): 22-29, 2024 Jul.
Article em En | MEDLINE | ID: mdl-38521120
ABSTRACT
Statin-intolerance (SI) has prevalence between 8.0 % and 10 %, and muscular complaints are the most common reason for discontinuation. Bempedoic acid (BA), an ATP citrate lyase inhibitor, decreases hepatic generation of cholesterol, upregulates low-density lipoprotein (LDL) receptor expression in the liver, and eventually clears circulating LDL-cholesterol from the blood. Multiple randomized clinical trials studying BA demonstrate a reduction in LDL levels by 17-28 % in SI. The CLEAR OUTCOME trial established significant cardiovascular benefits with BA. A dose of 180 mg/day of BA showed promising results. BA alone or in combination with ezetimibe is US Food and Drug Administration-approved for use in adults with heterozygous familial hypercholesterolemia and/or established atherosclerotic cardiovascular disease. BA reduced HbA1c by 0.12 % (p < 0.0001) in patients with diabetes. Adverse events of BA include myalgia (4.7 %), anemia (3.4 %), and increased aminotransferases (0.3 %). BA can cause up to four times higher risk of gout in those with a previous gout diagnosis or high serum uric acid levels. Reports of increased blood urea nitrogen and serum creatinine were noted. Current evidence does not demonstrate a reduction in deaths from cardiovascular causes. More studies that include a diverse population and patients with both high and low LDL levels should be conducted. We recommend that providers consider BA as an adjunct to statin therapy in patients with a maximally tolerated dosage to specifically target LDL levels.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Inibidores de Hidroximetilglutaril-CoA Redutases / Ácidos Dicarboxílicos / Ácidos Graxos Limite: Humans Idioma: En Revista: J Cardiol Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Inibidores de Hidroximetilglutaril-CoA Redutases / Ácidos Dicarboxílicos / Ácidos Graxos Limite: Humans Idioma: En Revista: J Cardiol Ano de publicação: 2024 Tipo de documento: Article