Comparing and Contrasting Statins and Fibrates

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Statins and fibrates are two classes of lipid-regulating drugs. The statins competitively inhibit 3-hydroxy-3-methylglutaryl coenzyme A, HMG-CoA, reductase, an enzyme involved in cholesterol synthesis, especially in the liver. While fibrates, fibric acid derivatives, are a class of amphipathic carboxylic acids. Clinical trials reveal that statins reduce cardiovascular event rate and all-cause mortality in a broad range of demographic and risk populations. Furthermore, six statins are available in the United States; cerivastatin, a type of statin, was withdrawn from the market due to excess rates of morbidity. Moreover, statins include various drugs that differ in low-density lipoprotein, LDL, lowering efficacy and metabolic rates, thus they differ in their potential for drug and disease interactions. These drugs include atorvastatin, fluvastatin, pravastatin sodium, rosuvastatin, and simvastatin. On the other hand, fibrates, such as benzafibrate, ciprofibrate, fenofibrate, and gemfibrozil, are used for patients who cannot tolerate statin (Joint Formulary Committee, 2012). Additionally, a study indicates that patients with one of two single-nucleotide polymorphisms, SNPs, a small genetic variation, in the HMG-CoA reductase gene were less responsive to statins (mayo clinic staff, 2013). Statins and fibrates can be further compared and contrasted according to their clinical uses, precautions, side effects, contraindications, and interactions. The clinical uses of both statins and fibrates are mostly similar. Both classes lower the LDL concentration; however, Statins lower it more than the fibrates. Also, they increase the HDL, high-density lipoprotein, and decrease the triglyceride concentration, which is more in fibrates than in statins. On the other hand, statins reduce coronary events and mortality in patients with ischemic heart disease (Venes, 2009).

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