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Renal sodium glucose cotransporter 2 inhibitors as a novel therapeutic approach to treatment of type 2 diabetes: Clinical data and mechanism of action

期刊

JOURNAL OF DIABETES INVESTIGATION
卷 5, 期 3, 页码 265-275

出版社

WILEY
DOI: 10.1111/jdi.12214

关键词

Novel antidiabetic agents; Renal glucose reabsorption; Sodium glucose cotransporter 2 inhibitors

资金

  1. Astellas Pharma Inc.
  2. Taisho Pharmaceutical Co., Ltd.
  3. Mitsubishi Tanabe Pharma Corporation
  4. Takeda Pharmaceutical Company Limited.
  5. GlaxoSmithKline plc
  6. Daiichi Sankyo Company, Limited.
  7. MSD
  8. Sanofi
  9. Novartis Pharma
  10. Dainippon Sumitomo Pharma Co., Ltd.
  11. Kyowa Hakko Kirin Co., Ltd.
  12. Eli Lilly Japan K.K.
  13. Shiratori Pharmaceutical Co., Ltd.
  14. Roche Diagnostics
  15. JT
  16. Nippon Boehringer Ingelheim Co., Ltd.
  17. Ono Pharmaceutical Co. Ltd.
  18. AstraZeneca PLC
  19. Kowa Company, Ltd.
  20. Japan Diabetes Foundation

向作者/读者索取更多资源

Type 2 diabetes is characterized by impaired insulin secretion from pancreatic -cells and/or reduced response of target tissues to insulin. Good glycemic control delays the development and slows the progression of micro- and macrovascular complications. Although there are numerous glucose-lowering agents in clinical use, only approximately half of type 2 diabetic patients achieve glycemic control, and undesirable side-effects often hamper treatment in those treated with the medications. There is a need for novel treatment options that can help overcome these difficulties. Sodium glucose cotransporter 2 (SGLT2) inhibitors have recently been developed as a novel potential therapeutic option for the treatment of type 2 diabetes. These drugs lower the plasma glucose concentration through inhibition of glucose reuptake in the kidney, independent of insulin secretion and insulin action, with a consequent lower risk of hypoglycemia. The data of clinical trials with monotherapy as well as combination therapy show that SGLT2 inhibitors have a blood glucose-lowering effect and also reduce bodyweight. A follow-up study shows long-term efficacy and the durability of these effects. SGLT2 inhibitors have the potential to reverse glucose toxicity, and to improve insulin resistance, blood pressure and lipid profile. The available data suggest a good tolerability profile. However, clinicians should carefully prescribe these drugs in light of already reported and/or unexpected side-effects. Further studies in larger numbers and longer-term clinical use data are required to place these agents in standard treatment of type 2 diabetes.

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