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Published on: November 10, 2017
Combination therapy for combined dyslipidemia
Antonios M Xydakis1, Christie M Ballantyne
1Division of Endocrinology and Metabolism, Baylor College of Medicine, Houston, Texas 77030, USA.
Insights
Patients with combined dyslipidemia need combination drug therapy for coronary artery disease risk. Optimal treatment requires further clinical trials to balance benefits and risks.
Area of Science:
- Cardiology
- Pharmacology
- Metabolic Disorders
Background:
- Combined dyslipidemia presents a high risk for coronary artery disease.
- The National Cholesterol Education Program's Adult Treatment Panel III (ATP III) provides lipid level guidelines.
- Metabolic syndrome is common in combined dyslipidemia, increasing cardiovascular risk.
Purpose of the Study:
- To review current treatment strategies for combined dyslipidemia.
- To evaluate the role of combination drug therapy in managing lipid levels.
- To identify emerging agents and future research needs.
Main Methods:
- Literature review of clinical trials and treatment guidelines.
- Analysis of statin monotherapy versus combination therapy benefits.
- Evaluation of risks associated with combination therapies (e.g., myopathy).
Main Results:
- Combination therapy may offer greater reductions in LDL cholesterol and triglycerides and increases in HDL cholesterol.
- Combining statins with niacin or fibrates may increase myopathy risk.
- New agents like ezetimibe and fixed-dose niacin-lovastatin show promise.
Conclusions:
- Combination therapy can be beneficial but requires careful risk-benefit assessment.
- Further clinical trials are necessary to establish optimal treatment regimens.
- Balancing efficacy, safety, cost, and compliance is crucial for managing combined dyslipidemia.
Abstract:
Patients with combined dyslipidemia are at high risk for coronary artery disease and often require combination drug therapy to achieve lipid levels recommended by the US National Cholesterol Education Program's third Adult Treatment Panel (ATP III). In addition to recommendations for low-density lipoprotein (LDL) cholesterol and triglyceride levels, ATP III established non-high-density lipoprotein (HDL) cholesterol goals for individuals with triglycerides >or=2.26 mmol/L (>or=200 mg/dL). It also introduced certain criteria for the diagnosis of the metabolic syndrome, a clustering of risk factors (abdominal obesity, elevated triglycerides, low HDL cholesterol, elevated blood pressure, impaired fasting glucose) that increases cardiovascular risk and is common in patients with combined dyslipidemia. Statin monotherapy has been shown to benefit these patients, and additional benefit may be obtained by combination therapy that provides greater reductions in both LDL cholesterol and triglycerides as well as greater increases in HDL cholesterol. However, combining a statin with either niacin or a fibrate may increase the risk for myopathy and therefore requires careful monitoring and evaluation of the risk-benefit ratio for each patient. Moreover, combination therapy may be associated with increased drug costs and decreased patient compliance. Recently developed agents that may improve the effectiveness of combination therapy include ezetimibe-a cholesterol absorption inhibitor-and a formulation that combines extended-release niacin and lovastatin in a single pill. Clinical trials are needed to determine the optimal treatment in patients with combined dyslipidemia.
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