Literature DB >> 33505729

The Novelty of Icosapent Ethyl in the Management of Hypertriglyceridemia and Alleviating Cardiovascular Risk.

Muhammad Shoaib Khan1, Muhammad Ishaq1, Muhammad Talha Ayub2, Ateeq U Rehman1, John J Hayes3, Mohammad Mortada4, Robert W W Biederman5.   

Abstract

Hypertriglyceridemia is believed to be independently associated with an elevated risk of cardiovascular disease (CVD) events. Lifestyle changes and dietary modifications are recommended for individuals with high serum triglyceride (TG) levels (150-499 mg/dl), and pharmacological therapy in addition to lifestyle modification is recommended when serum TG levels ≥ 500 mg/dl. A residual cardiovascular risk remains even in statin appropriate treated patients with CVD risk factors, and in this patient population, hypertriglyceridemia poses an independent and increased risk of ischemic events. In December 2019, the US FDA approved icosapent ethyl (IPE) as an adjunct to a maximally tolerated statin to reduce the risk of CVD events in adults with serum triglycerides > 150 mg/dl and have either established cardiovascular disease or diabetes and two or more additional CVD risk factors. Since IPE significantly decreases total ischemic events in the aforementioned patient population, it would be intriguing to know whether IPE alone added an advantage to lifestyle modification in the low-risk population, who has serum triglyceride between 150 mg/dl and 499 mg/dl.
Copyright © 2021 Muhammad Shoaib Khan et al.

Entities:  

Year:  2021        PMID: 33505729      PMCID: PMC7815393          DOI: 10.1155/2021/6696915

Source DB:  PubMed          Journal:  J Lipids        ISSN: 2090-3049


  39 in total

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Journal:  Circulation       Date:  1980-02       Impact factor: 29.690

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Journal:  JAMA       Date:  2019-01-29       Impact factor: 56.272

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Journal:  Am J Cardiol       Date:  1998-02-26       Impact factor: 2.778

6.  Effect of High-Dose Omega-3 Fatty Acids vs Corn Oil on Major Adverse Cardiovascular Events in Patients at High Cardiovascular Risk: The STRENGTH Randomized Clinical Trial.

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Journal:  JAMA       Date:  2020-12-08       Impact factor: 56.272

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Journal:  J Clin Endocrinol Metab       Date:  2012-09       Impact factor: 5.958

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Journal:  N Engl J Med       Date:  2016-03-02       Impact factor: 91.245

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Authors:  Eliot A Brinton; Christie M Ballantyne; Harold E Bays; John J Kastelein; Rene A Braeckman; Paresh N Soni
Journal:  Cardiovasc Diabetol       Date:  2013-07-09       Impact factor: 9.951

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