Place of sodium-glucose cotransporter-2 inhibitors in East Asian subjects with type 2 diabetes mellitus: Insights into the management of Asian phenotype

被引:23
作者
Lim, Lee Ling [1 ]
Tan, Alexander Tong Boon [1 ]
Moses, Kevin [2 ]
Rajadhyaksha, Viraj [2 ]
Chan, Siew Pheng [1 ]
机构
[1] Univ Malaya, Dept Internal Med, Div Endocrinol, Kuala Lumpur, Malaysia
[2] AstraZeneca, Med Dept, Petaling Jaya, Malaysia
关键词
Type; 2; diabetes; East Asians; Visceral adiposity; SGLT2; inhibitors; Cardiovascular outcome; Renoprotection; LONG-TERM EFFICACY; INADEQUATE GLYCEMIC CONTROL; DOUBLE-BLIND; JAPANESE PATIENTS; ADD-ON; EMPAGLIFLOZIN MONOTHERAPY; INSULIN SENSITIVITY; ETHNIC-DIFFERENCES; VASCULAR-DISEASE; RENAL-DISEASE;
D O I
10.1016/j.jdiacomp.2016.10.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The burden of type 2 diabetes (T2DM) in East Asia is alarming. Rapid modernization and urbanization have led to major lifestyle changes and a tremendous increase in the prevalence of obesity, metabolic syndrome, and diabetes mellitus. The development of T2DM at a younger age, with lower body mass index, higher visceral adiposity, and more significant pancreatic beta-cell dysfunction compared to Caucasians are factors responsible for the increased prevalence of T2DM in East Asians. Sodium-glucose Cotransporter-2 (SGLT2) inhibitors (canagliflozin, dapaglifozin, empagliflozin, etc.) reduce renal.glucose reabsorption, leading to favorable effects on glycemic, blood pressure, and weight control. The insulin-independent mechanism enables their use as monotherapy or combination therapy with insulin and other oral antidiabetic agents. The role of SGLT2 inhibitors in the management of T2DM among East Asians is an interesting area of research, given that East Asians have been proven to be uniquely different from Caucasians. This review provides comprehensive coverage of the available literature not only on the efficacy and safety, but also on the recent cardiovascular and renal outcomes of SGLT2 inhibitors, focusing among East Asians. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:494 / 503
页数:10
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