Continual evolution of type 2 diabetes: an update on pathophysiology and emerging treatment options

被引:33
作者
Cornell, Susan [1 ]
机构
[1] Midwestern Univ, Chicago Coll Pharm, Downers Grove, IL 60515 USA
关键词
diabetes; hyperglycemia; oral antidiabetic therapies; pharmacotherapy; sodium-glucose cotransporter 2; INADEQUATE GLYCEMIC CONTROL; BROWN ADIPOSE-TISSUE; FREE FATTY-ACIDS; ADD-ON THERAPY; METFORMIN PLUS SULFONYLUREA; SELECTIVE SGLT2 INHIBITOR; CHRONIC KIDNEY-DISEASE; LOWERS BODY-WEIGHT; BETA-CELL FUNCTION; DOUBLE-BLIND;
D O I
10.2147/TCRM.S67387
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Diabetes is a complex and progressive disease that has a major societal and economic impact. The most common form of diabetes, type 2 diabetes mellitus (T2DM), is a multifactorial disease, the pathophysiology of which involves not only the pancreas but also the liver, skeletal muscle, adipose tissue, gastrointestinal tract, brain, and kidney. Novel therapies with mechanisms of action that are different from most existing drugs are emerging. One such class consists of compounds that inhibit renal sodium-glucose cotransporter 2, which is responsible for the bulk of glucose reabsorption by the kidneys. This new class of compounds improves glycemic control independently of insulin and promotes weight reduction, providing an additional tool to treat patients with T2DM. This review discusses the underlying pathophysiology of T2DM, clinical guidelines, and available and emerging treatment options, with particular emphasis on sodium-glucose cotransporter 2 inhibitors.
引用
收藏
页码:621 / 632
页数:12
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