SGLT2 inhibitors: a narrative review of efficacy and safety

Donald S Nelinson1, Jose M Sosa2, Robert J Chilton3

  • 1American College of Osteopathic Internists , Rockville , MD 20852 , USA.

Insights

Sodium-glucose co-transporter-2 (SGLT2) inhibitors offer significant cardiovascular and renal benefits for type 2 diabetes mellitus (T2DM) patients. This review clarifies their efficacy and addresses concerns regarding adverse events.

Area of Science:

  • Cardiology
  • Nephrology
  • Endocrinology

Background:

  • Type 2 diabetes mellitus (T2DM) is a complex cardio-renal-metabolic condition often accompanied by atherosclerotic cardiovascular disease (ASCVD), heart failure (HF), and chronic kidney disease (CKD).
  • Sodium-glucose co-transporter-2 (SGLT2) inhibitors represent a significant advancement in T2DM management, offering benefits beyond glycemic control.

Purpose of the Study:

  • To review the efficacy of SGLT2 inhibitors in reducing cardiovascular and renal outcomes in T2DM patients with comorbidities.
  • To clarify the mechanism of action and address adverse event concerns associated with SGLT2 inhibitors.

Main Methods:

  • Narrative review of existing clinical trial data and scientific literature.
  • Analysis of SGLT2 inhibitor effects on glycemic control, body weight, blood pressure, and cardiovascular/renal outcomes.
  • Examination of safety profiles and adverse events associated with SGLT2 inhibitors.

Main Results:

  • SGLT2 inhibitors effectively lower glycated hemoglobin, body weight, and blood pressure.
  • These agents demonstrate significant risk reduction for cardiovascular and renal outcomes in T2DM patients, including those with ASCVD, HF, and CKD.
  • SGLT2 inhibitors are compatible with most glucose-lowering agents and suitable for patients with reduced estimated glomerular filtration rates (eGFR ≥ 30 mL/min/1.73 m²).

Conclusions:

  • SGLT2 inhibitors have transformed T2DM management by providing substantial cardio-renal protection.
  • Understanding their mechanism and safety profile is crucial for optimizing clinical use and mitigating potential adverse events.

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