Update on the clinical applications of SGLTis: Insight to benefits beyond hypoglycemic and cardiorenal protection.
Shibing TaoShanlan GuoNanwei TongPublished in: Pharmacotherapy (2024)
Sodium glucose cotransporter inhibitor (SGLTi) drugs have been widely used in clinical practice. In addition to their benefits in hyperglycemia, heart failure (HF), and kidney disease, their effects on obesity, metabolic dysfunction-associated steatotic liver disease (MASLD, formerly named nonalcoholic fatty liver disease [NAFLD]), polycystic ovarian syndrome (PCOS), abnormal lipid metabolism, hyperuricemia, obstructive sleep apnea syndrome (OSAS), anemia, and syndrome of inappropriate antidiuresis (SIAD, formerly named syndrome of inappropriate antidiuretic hormone [SIADH]) have been explored. In this review, we searched the data of clinical randomized controlled trials (RCTs) and meta-analyses of SGLTis in patients with diabetes from the PubMed library between January 1, 2020, and February 1, 2024. According to our review, certain SGLTis exhibit relatively superior clinical safety and effectiveness for treating the abovementioned diseases. Proper utilization of SGLTis in these patients can provide additional medication options for patients with different disease scenarios. However, studies of SGLTis in these diseases are relatively rare, with shortcomings such as small sample sizes and short intervention periods. Therefore, further large-scale, long-term, well-designed studies are needed to clarify the findings.
Keyphrases
- randomized controlled trial
- heart failure
- obstructive sleep apnea
- meta analyses
- systematic review
- clinical practice
- case report
- end stage renal disease
- type diabetes
- healthcare
- chronic kidney disease
- ejection fraction
- metabolic syndrome
- insulin resistance
- left ventricular
- climate change
- prognostic factors
- oxidative stress
- fatty acid
- skeletal muscle
- machine learning
- clinical trial
- study protocol
- physical activity
- case control
- artificial intelligence
- peritoneal dialysis
- liver fibrosis
- cardiac resynchronization therapy
- diabetic rats
- adverse drug