Abstract
Beta blockers are even more powerful in reducing cardiac events in the patient with diabetes, than they are in others. This is because that in addition to lowering blood pressure, lowering heart rate, and acting as an anti-inflammatory, beta blockers, in the patient with diabetes, shift the metabolism of the myocardium away from fatty acid utilization and toward glucose utilization, which decreases the cardiac workload and reduces ischemia. Furthermore, hyperglycemia is a stimulus to myocardial remodeling, which is not only prevented but is reversed by beta blockade, and the incidence of heart failure that would otherwise be increased in the patient with diabetes, is reduced. The first and second generation beta blockers induce peripheral vasoconstriction and increase insulin resistance, causing an increase in serum glucose and triglycerides, and a decrease in HDL levels. These problems can be circumvented by using a third generation beta blocker, which are vasodilatory and reduce serum glucose and triglycerides, and increase HDL cholesterol. Therefore, the traditional and long-standing reluctance of endocrinologists to utilize beta blockade in the diabetic patient is unfounded and outdated due to the availability of later-generation beta blockers.

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