Recent Progress and Perspectives in Sodium-Glucose Co-transporter 1/2 Inhibitors.

Mini Rev Med Chem

Department of Medical Pharmacology, Faculty of Medicine, Gaziantep University, 27310, Gaziantep, Turkiye.

Published: August 2024

AI Article Synopsis

  • SGLT1/2 inhibitors, known as glifozins, lower blood sugar levels in adults with Type 2 Diabetes (T2D) by reducing sodium and glucose reabsorption in the kidneys.
  • Recent studies indicate that SGLT2 inhibitors are also effective in treating conditions beyond diabetes, such as chronic renal disease and heart failure, making them essential for both glycemic control and cardiovascular protection.
  • Currently, there are 11 approved SGLT1/2 inhibitors, and ongoing research suggests they may offer benefits for metabolic and various other disorders, highlighting their potential in broader therapeutic applications.

Article Abstract

Sodium-Glucose Co-transporter-1/2 (SGLT1/2) inhibitors (also called glifozins) are a class of glucose-decreasing drugs in adults with Type 2 Diabetes (T2D). SGLT2 inhibitors diminish sodium and glucose reabsorption in the renal proximal convoluted tubule. Recent clinical trials have revealed that SGLT2 inhibitors might be beneficial for treating diseases other than diabetes, including chronic renal disease and Heart Failure (HF). Currently, SGLT2 inhibitors are recommended not only for the glycemic management of T2D but also for cardiovascular protection. SGLT2 inhibitors have become one of the foundational drugs for HF with reduced Ejection Fraction (HFrEF) treatment and the first medications with proven prognostic benefit in HF with preserved Ejection Fraction (HFpEF). At present, 11 SGLT1/2 inhibitors have been approved for clinical use in different countries. Beyond their anti-hyperglycemic effect, these inhibitors have shown clear cardio- and nephroprotective properties. A growing body of research studies suggests that SGLT1/2 inhibitors may provide potential clinical benefits in metabolic as well as oncological, hematological, and neurological disorders.

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Source
http://dx.doi.org/10.2174/0113895575325210240805092741DOI Listing

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