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pubmed-article:20145583pubmed:abstractTextUCP2 -866G>A (rs659366) has been implicated in cardiometabolic disease and represents a novel candidate gene for beta-blocker response, particularly among patients with diabetes. We assessed the function of -866G>A and its role as a modifier of beta-blocker treatment outcomes by diabetes status in an acute coronary syndrome (ACS) cohort.lld:pubmed
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pubmed-article:20145583pubmed:articleTitleInteraction between the UCP2 -866 G>A polymorphism, diabetes, and beta-blocker use among patients with acute coronary syndromes.lld:pubmed
pubmed-article:20145583pubmed:affiliationEndocrinology, Diabetes and Nutrition Division, University of Maryland School of Medicine, 660 W. Redwood Street, Baltimore, MD 21201, USA. abeitels@medicine.umaryland.edulld:pubmed
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