379. SGLT Inhibitors: The Biology of SGLT Inhibition with Dr. Katherine Tuttle

Published: July 9, 2024, 1:33 a.m.

CardioNerds (Drs. Gurleen Kaur and Richard Ferraro) and episode FIT Lead Dr. Saahil Jumkhawala (Cardiology Fellow at the University of Miami) discuss SGLT inhibitors, focusing on the biology of SGLT and its inhibition, with Dr. Katherine Tuttle (Executive Director for Research at Providence Healthcare, Co-Principal Investigator of the Institute of Translational Health Sciences, and Professor of Medicine at the University of Washington).\xa0\xa0Show notes were drafted by Dr. Saahil Jumkhawala. The episode audio was engineered by CardioNerds intern Christiana Dangas.\n\n\n\nThis episode was produced in collaboration with the American Society of Preventive Cardiology (ASPC) with independent medical education grant support from Lexicon Pharmaceuticals. \n\n\n\n\n\n\n\n\n\n\n\nCardioNerds Prevention PageCardioNerds Episode PageCardioNerds AcademyCardionerds Healy Honor Roll\n\n\n\n\n\nCardioNerds Journal ClubSubscribe to The Heartbeat Newsletter!Check out CardioNerds SWAG!Become a CardioNerds Patron!\n\n\n\n\n\n\n\n\n\nPearls - The Biology of SGLT Inhibition with Dr. Katherine Tuttle\n\n\n\n\nSGLT inhibitors, while initially developed as antidiabetic medications, have been shown to be beneficial for cardiovascular and renal outcomes. These benefits result from their on-target glucosuric effects and additional off-target effects.\n\n\n\nThe side effect profiles of SGLTis are primarily mediated by glucose reabsorption in their target tissues. The side effect profile of SGLTis must be considered when prescribing these medications and is generally favorable for SGLT2is versus SGLT1is.\n\n\n\nOnce SGLTis are prescribed, patients should be given specific attention to their eGFR, serum potassium, and clinical evaluations of volume status and blood pressure.\n\n\n\nStrategies to increase implementation of and reduce clinical inertia for these important class of medication remain an area of active investigation\n\n\n\n\nShow notes - The Biology of SGLT Inhibition with Dr. Katherine Tuttle\n\n\n\nWhat should prompt consideration of starting an SGLT inhibitor?\n\n\n\n\nConsiderations for SGLT inhibitor initiation are based on a history of heart failure, kidney disease, and diabetes status.\n\nIn the EMPA-KIDNEY trial, empagliflozin improved cardiovascular and kidney outcomes in those with low GFR (regardless of level of albuminuria).\n\n\n\n\n\n\nWhat is the mechanism of action of SGLT2 inhibitors?\n\n\n\n\nSGLT2 inhibitors improve glycemic control by blocking SGLT2 receptor-mediated reabsorption of glucose in the proximal convoluted tubule, where 80-90% of this reuptake occurs, and increased downstream excretion of glucose and sodium chloride. SGLT2 inhibitors provide only a modest glucose-lowering effect, particularly for patients with GFR <45.\n\n\n\n\nHow do SGLT2 inhibitors improve cardiac function?\n\n\n\n\nThrough corrected glomerular hyperfiltration, there is a reduction in blood pressure, a reduction in sympathetic neural activity, and increased glucosuria, improving diuresis. Systemically, there is an increase in erythropoietin, which raises red blood cell mass and oxygen-carrying capacity.Beyond inhibition of the SGLT2 receptor, which is isolated to the proximal convoluted tubule, there are additional off-target effects. Through non-receptor-mediated mechanisms, glucose transport is blocked into cells by blocking GLUT1 and GLUT4 receptors. They also reduce the mTORC signal transduction pathway, thereby reducing inflammation and glycolysis, leading to a cardioprotective effect in myocytes.In the DAPA-CKD and CREDENCE trials, GFR decreases of up to 30% were correlated with improved renal and cardiovascular outcomes.\n\nThe cardiovascular benefit of SGLT2 inhibitors is not dose-dependent.\n\n\n\n\n\n\nWhere are SGLT1 receptors located?\n\n\n\n\nSGLT1 receptors are found primarily in small and large bowel enterocytes, as well as the kidney proximal tubule, beyond the convoluted segment.\n\nAround 10% of glucose re-uptake is mediated by SGLT1 receptors in the proximal tubule.\n\n\n\n\n\n\nWhat are some common side effects of SGLT inhibitors?