Literature DB >> 24631482

Blood pressure effects of sodium-glucose co-transport 2 (SGLT2) inhibitors.

Raymond V Oliva1, George L Bakris2.   

Abstract

Management of hypertension in diabetes is critical for reduction of cardiovascular mortality and morbidity. While blood pressure (BP) control has improved over the past two decades, the control rate is still well below 50% in the general population of patients with type 2 diabetes mellitus (T2DM). A new class of oral glucose-lowering agents has recently been approved; the sodium-glucose co-transporter 2 (SGLT2) inhibitors, which act by eliminating large amounts of glucose in the urine. Two agents, dapagliflozin and canagliflozin, are currently approved in the United States and Europe, and empagliflozin and ipragliflozin have reported Phase 3 trials. In addition to glucose lowering, SGLT2 inhibitors are associated with weight loss and act as osmotic diuretics, resulting in a lowering of BP. While not approved for BP-lowering, they may potentially aid BP goal achievement in people within 7-10 mm Hg of goal. It should be noted that the currently approved agents have side effects that include an increased incidence of genital infections, predominantly in women. The approved SGLT2 inhibitors have limited use based on kidney function and should be used only in those with an estimated glomerular filtration rate (eGFR) > 60 mL/min/1.73 m2 for dapagliflozin and ≥45 mL/min/1.73 m2 for canagliflozin. Cardiovascular outcome trials are ongoing with these agents and will be completed within the next 4-5 years.
Copyright © 2014 American Society of Hypertension. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Diabetes; SGLT2; glucose; hypertension; transporters

Mesh:

Substances:

Year:  2014        PMID: 24631482     DOI: 10.1016/j.jash.2014.02.003

Source DB:  PubMed          Journal:  J Am Soc Hypertens        ISSN: 1878-7436


  75 in total

1.  Hypertension: SGLT2 inhibitors: not just another glucose-lowering agent.

Authors:  Hillel Sternlicht; George L Bakris
Journal:  Nat Rev Nephrol       Date:  2015-12-30       Impact factor: 28.314

Review 2.  Molecular Mechanisms Underlying the Cardiovascular Benefits of SGLT2i and GLP-1RA.

Authors:  Dorrin Zarrin Khat; Mansoor Husain
Journal:  Curr Diab Rep       Date:  2018-06-09       Impact factor: 4.810

Review 3.  Effect of SGLT2 Inhibitors on the Sympathetic Nervous System and Blood Pressure.

Authors:  André J Scheen
Journal:  Curr Cardiol Rep       Date:  2019-06-21       Impact factor: 2.931

Review 4.  What Are We Learning from the FDA-Mandated Cardiovascular Outcome Studies for New Pharmacological Antidiabetic Agents?

Authors:  Dragana Lovre; Wynn Htun; Carly Carrion; Vivian A Fonseca
Journal:  Curr Diab Rep       Date:  2016-10       Impact factor: 4.810

5.  Pendrin-A New Target for Diuretic Therapy?

Authors:  Carsten A Wagner
Journal:  J Am Soc Nephrol       Date:  2016-08-11       Impact factor: 10.121

Review 6.  Cardiovascular benefits of the newer medications for treating type 2 diabetes mellitus.

Authors:  Srikanth Yandrapalli; Wilbert S Aronow
Journal:  J Thorac Dis       Date:  2017-07       Impact factor: 2.895

7.  SGLT2 inhibition in a kidney with reduced nephron number: modeling and analysis of solute transport and metabolism.

Authors:  Anita T Layton; Volker Vallon
Journal:  Am J Physiol Renal Physiol       Date:  2018-01-17

Review 8.  Targeting renal glucose reabsorption to treat hyperglycaemia: the pleiotropic effects of SGLT2 inhibition.

Authors:  Volker Vallon; Scott C Thomson
Journal:  Diabetologia       Date:  2016-11-22       Impact factor: 10.122

Review 9.  Pharmacodynamics, efficacy and safety of sodium-glucose co-transporter type 2 (SGLT2) inhibitors for the treatment of type 2 diabetes mellitus.

Authors:  André J Scheen
Journal:  Drugs       Date:  2015-01       Impact factor: 9.546

Review 10.  Renal, metabolic and cardiovascular considerations of SGLT2 inhibition.

Authors:  Ralph A DeFronzo; Luke Norton; Muhammad Abdul-Ghani
Journal:  Nat Rev Nephrol       Date:  2016-12-12       Impact factor: 28.314

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