Statin combination therapy and cardiovascular risk reduction
- PMID: 27079178
- DOI: 10.2217/fca-2015-0011
Statin combination therapy and cardiovascular risk reduction
Abstract
In numerous clinical trials, lowering LDL-C with statin therapy has been demonstrated to reduce the risk of cardiovascular disease (CVD) in primary and secondary prevention settings. Guidelines recommend statins for first-line therapy in cholesterol-lowering management of patients with CVD risk. Despite increased statin monotherapy use over the last decade, a number of patients with high CVD risk do not achieve optimal LDL-C lowering. Guidelines recommend consideration of statin combination therapy with nonstatin agents for these patients. However, combination therapy approaches have been hampered by neutral findings. Recently, ezetimibe added to simvastatin therapy reduced cardiovascular events in acute coronary syndrome patients, more than simvastatin alone. This article provides an overview of various agents in combination with statin therapy on cardiovascular outcomes. Other lipid-lowering agents in development, including PCSK9 and CETP inhibitors in development, are also described.
Keywords: CETP; PCSK9; bile acid sequestrants; combination therapy; ezetimibe; fibrates; niacin; omega 3-polyunsaturated long-chain fatty acids; statin.
Similar articles
-
Nonstatin therapies for management of dyslipidemia: a review.Clin Ther. 2015 Oct 1;37(10):2153-79. doi: 10.1016/j.clinthera.2015.09.001. Epub 2015 Sep 26. Clin Ther. 2015. PMID: 26412799 Review.
-
[ACUTE CORONARY SYNDROME AND LIPID-LOWERING THERAPY. DOES THE IMPROVE-IT STUDY MAKE ANY DIFFERENCE?].Rev Med Liege. 2015 Sep;70(9):450-5. Rev Med Liege. 2015. PMID: 26638446 Clinical Trial. French.
-
Ezetimibe Added to Statin Therapy after Acute Coronary Syndromes.N Engl J Med. 2015 Jun 18;372(25):2387-97. doi: 10.1056/NEJMoa1410489. Epub 2015 Jun 3. N Engl J Med. 2015. PMID: 26039521 Clinical Trial.
-
Clinical implications of the IMPROVE-IT trial in the light of current and future lipid-lowering treatment options.Expert Opin Pharmacother. 2016;17(3):369-80. doi: 10.1517/14656566.2016.1118055. Epub 2015 Nov 30. Expert Opin Pharmacother. 2016. PMID: 26559810 Review.
-
2017 Taiwan lipid guidelines for high risk patients.J Formos Med Assoc. 2017 Apr;116(4):217-248. doi: 10.1016/j.jfma.2016.11.013. Epub 2017 Feb 24. J Formos Med Assoc. 2017. PMID: 28242176 Review.
Cited by
-
Vitamin D was Superior to Omega-3 as a Simvastatin Adjuvant in Improving Blood Lipids and Atherogenic Index in Type-I Dyslipidemic Rats.Turk J Pharm Sci. 2024 Jan 19;20(6):390-396. doi: 10.4274/tjps.galenos.2023.56958. Turk J Pharm Sci. 2024. PMID: 38256280 Free PMC article.
-
Di'ao Xinxuekang Capsule Improves the Anti-Atherosclerotic Effect of Atorvastatin by Downregulating the SREBP2/PCSK9 Signalling Pathway.Front Pharmacol. 2022 Apr 28;13:857092. doi: 10.3389/fphar.2022.857092. eCollection 2022. Front Pharmacol. 2022. PMID: 35571088 Free PMC article.
-
Statin-Induced Myopathy: Translational Studies from Preclinical to Clinical Evidence.Int J Mol Sci. 2021 Feb 19;22(4):2070. doi: 10.3390/ijms22042070. Int J Mol Sci. 2021. PMID: 33669797 Free PMC article. Review.
-
Prodigiosin Modulates the Immune Response and Could Promote a Stable Atherosclerotic Lession in C57bl/6 Ldlr-/- Mice.Int J Mol Sci. 2020 Sep 3;21(17):6417. doi: 10.3390/ijms21176417. Int J Mol Sci. 2020. PMID: 32899258 Free PMC article.
-
A Population-Based Study of Simvastatin Drug-Drug Interactions in Cardiovascular Disease Patients.AMIA Jt Summits Transl Sci Proc. 2020 May 30;2020:664-673. eCollection 2020. AMIA Jt Summits Transl Sci Proc. 2020. PMID: 32477689 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous