4.7 Review

The current role of sodium-glucose cotransporter 2 inhibitors in type 2 diabetes mellitus management

Journal

CARDIOVASCULAR DIABETOLOGY
Volume 21, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12933-022-01512-w

Keywords

Sodium-glucose cotransporter 2 inhibitor; Heart failure; Type 2 diabetes mellitus; Cardiovascular disease; Diabetic kidney disease

Funding

  1. NSFC [82003872]
  2. Natural Science Foundation of Hunan Province [2020JJ5513]
  3. Scientific research Fund of hunan provincial education department [19A418]
  4. Scientific Research Fund Project of Hunan Provincial Health Commission [20201973]
  5. Hunan Province Clinical Medical Technology Innovation Guidance Project [2020SK51823]
  6. Postgraduate Scientific Research Innovation Project of Hunan Province [CX20210974]
  7. Central government funds for guiding local scientific and Technological Development [2021QZY016]

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This article examines the clinical benefit, safety, and tolerability of the four SGLT2 inhibitors approved by the US FDA for the treatment of type 2 diabetes mellitus. SGLT2 inhibitors reduce hyperglycemia by increasing urinary glucose excretion and improving beta-cell function. Early clinical trials have shown their beneficial effects with acceptable safety and excellent tolerability.
Type 2 diabetes mellitus (T2DM) is a chronic, complex metabolic disease characterized by chronic hyperglycemia causing from insufficient insulin signaling because of insulin resistance or defective insulin secretion, and may induce severe complications and premature death. Sodium-glucose cotransporter-2 (SGLT2) inhibitors are oral drugs used to reduce hyperglycemia in patients with T2DM, including empagliflozin, ertugliflozin, dapagliflozin and canagliflozin. The primary objective of this article is to examine the clinical benefit, safety, and tolerability of the four SGLT2 inhibitors approved by the US FDA. SGLT2 inhibitors increase urinary glucose excretion via inhibiting SGLT2 to decrease renal reabsorption of filtered glucose and reduce the renal threshold for glucose. Rather than stimulating insulin release, SGLT2 inhibitors improve beta-cell function by improving glucotoxicity, as well as reduce insulin resistance and increase insulin sensitivity. Early clinical trials have confirmed the beneficial effects of SGLT2 in T2DM with acceptable safety and excellent tolerability. In recent years, SGLT2 inhibitors has been successively approved by the FDA to decrease cardiovascular death and decrease the risk of stroke and cardiac attack in T2DM adults who have been diagnosed with cardiovascular disease, treating heart failure (HF) with reduced ejection fraction and HF with preserved ejection fraction, and treat diabetic kidney disease (DKD), decrease the risk of hospitalization for HF in T2DM and DKD patients. SGLT2 inhibitors are expected to be an effective treatment for T2DM patients with non alcoholic fatty liver disease. SGLT2 inhibitors have a similar safety profile to placebo or other active control groups, with major adverse events such as Ketoacidosis or hypotension and genital or urinary tract infections.

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