The new evidence on cardiorenal benefits of sodium-glucose cotransporter 2 inhibitors in type 1 diabetes: one step closer to their use in this setting?
Djordje S PopovicTheocharis KoufakisDimitrios PatouliasNikolaos PapanasPublished in: Expert review of clinical pharmacology (2023)
Chronic kidney disease (CKD) affects 30-40% of persons with type 1 diabetes mellitus (T1DM), markedly increasing the risk of kidney failure and cardiovascular events. The excessive mortality observed in T1DM compared to the general population can be attributed to the presence of CKD, with cardiovascular disease as the leading cause of premature death. A recently published, robust real-world study investigated the impact of sodium-glucose cotransporter 2 inhibitors (SGLT2i) and glucagon-like peptide-1 receptor agonists (GLP-1 RA) adjunctive therapy on blood glucose levels, adverse events and cardio-renal outcomes among individuals with T1DM. GLP-1 RA provided greater reduction in glycated hemoglobin in comparison to SGLT2i therapy, whereas the latter reduced the risk of CKD, heart failure and hospitalization for any cause. However, the SGLT2i treated cohort had a higher risk of diabetic ketoacidosis (DKA). The study provides promising evidence that the protective cardiorenal effects of SGLT2i, previously confirmed in people with and without type 2 diabetes mellitus, might be also present in T1DM. However, the benefits and risks, especially the risk of DKA, should be further examined in dedicated large-scale randomized controlled trials.
Keyphrases
- chronic kidney disease
- glycemic control
- cardiovascular events
- type diabetes
- blood glucose
- cardiovascular disease
- heart failure
- end stage renal disease
- rheumatoid arthritis
- coronary artery disease
- left ventricular
- insulin resistance
- skeletal muscle
- clinical trial
- weight loss
- adipose tissue
- disease activity
- body mass index
- risk assessment
- high resolution
- wound healing
- physical activity
- newly diagnosed
- red blood cell
- study protocol
- systemic lupus erythematosus
- atomic force microscopy
- cardiac resynchronization therapy