Efficacy and safety of GLP-1 receptor agonists as add-on to SGLT2 inhibitors in type 2 diabetes mellitus: A meta-analysis.
Marco CastellanaAngelo CignarelliFrancesco BresciaFrancesco GiorginoAnnalisa NatalicchioLuigi LaviolaFrancesco GiorginoPublished in: Scientific reports (2019)
GLP-1 receptor agonists (GLP-1RA) and SGLT2 inhibitors (SGLT2i) have been associated with improved glycemic control, body weight loss and favorable changes in cardiovascular risk factors and outcomes. We conducted a systematic review and meta-analysis to evaluate the effects of the addition of GLP-1RA to SGLT2i in patients with type 2 diabetes mellitus and inadequate glycemic control. Six databases were searched until March 2019. Randomized controlled trials (RCT) with a follow-up of at least 24 weeks reporting on HbA1c, body weight, systolic blood pressure, lipids, achievement of HbA1c < 7%, requirement of rescue therapy due to hyperglycemia and hypoglycemic events were selected. Four RCTs were included. Compared to SGLT2i, the GLP-1RA/SGLT2i combination was associated with greater reduction in HbA1c (-0.74%), body weight (-1.61 kg), and systolic blood pressure (-3.32 mmHg). A higher number of patients achieved HbA1c < 7% (RR = 2.15), with a lower requirement of rescue therapy (RR = 0.37) and similar incidence of hypoglycemia. Reductions in total and LDL cholesterol were found. The present review supports treatment intensification with GLP-1RA in uncontrolled type 2 diabetes on SGLT2i. This drug regimen could provide improved HbA1c control, together with enhanced weight loss and blood pressure and lipids control.
Keyphrases
- glycemic control
- blood pressure
- type diabetes
- weight loss
- body weight
- blood glucose
- bariatric surgery
- rheumatoid arthritis
- cardiovascular risk factors
- roux en y gastric bypass
- insulin resistance
- hypertensive patients
- heart rate
- gastric bypass
- end stage renal disease
- randomized controlled trial
- ejection fraction
- left ventricular
- heart failure
- disease activity
- cardiovascular disease
- risk factors
- systematic review
- fatty acid
- peritoneal dialysis
- metabolic syndrome
- obese patients
- interstitial lung disease
- clinical trial
- chronic kidney disease
- bone marrow
- stem cells
- emergency department
- systemic lupus erythematosus
- skeletal muscle
- systemic sclerosis
- big data
- artificial intelligence
- low density lipoprotein
- adipose tissue
- combination therapy
- cell therapy
- oxidative stress
- mesenchymal stem cells