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Combination therapy with SGLT-2 inhibitors and GLP-1 receptor agonists as complementary agents that address
1Diabetes360 Health Center, Plano, TX, USA.
Abstract:
Type 2 diabetes (T2D) has a complex pathophysiology composed of multiple underlying defects that lead to impaired glucose homeostasis and the development of macrovascular and microvascular complications. Of the currently available glucose-lowering therapies, sodium-glucose cotransporter-2 inhibitors (SGLT-2is) and glucagon-like peptide-1 receptor agonists (GLP-1RAs) both provide effective glycemic control and have been shown to reduce cardiovascular (CV) events in patients with T2D and a high CV risk or established CV disease. Because these agents have complementary mechanisms of action, they are able to act on multiple defects of T2D when used in combination. This review discusses the rationale for and potential benefits of SGLT-2i plus GLP-1RA combination therapy in patients with T2D. A search of the PubMed database was conducted for studies and reviews describing the combined use of SGLT-2is and GLP-1RAs, with a specific focus on identifying clinical studies of combination therapy in patients with T2D. In clinical studies, glycated hemoglobin (A1c) was significantly reduced over 28-52 weeks with SGLT-2i plus GLP-1RA therapy versus the individual agents or baseline. Several CV risk factors, including body weight, blood pressure, and lipid parameters, were also improved. SGLT-2i plus GLP-1RA therapy was generally well tolerated, with a low risk of hypoglycemia and no unexpected findings. Taken together with results from large CV outcomes trials of SGLT-2is and GLP-1RAs, combination therapy with these agents potentially provides effective durable glycemic control and CV benefits due to their complementary actions on the defects of T2D.
Insights
Combining sodium-glucose cotransporter-2 inhibitors (SGLT-2is) and glucagon-like peptide-1 receptor agonists (GLP-1RAs) offers effective glycemic control for type 2 diabetes. This combination therapy also improves cardiovascular risk factors and is well-tolerated.
Area of Science:
- Endocrinology
- Metabolic Diseases
- Cardiovascular Medicine
Background:
- Type 2 diabetes (T2D) involves complex defects impairing glucose homeostasis and leading to complications.
- Sodium-glucose cotransporter-2 inhibitors (SGLT-2is) and glucagon-like peptide-1 receptor agonists (GLP-1RAs) are effective glucose-lowering therapies with cardiovascular benefits.
Purpose of the Study:
- To review the rationale and potential benefits of combining SGLT-2is and GLP-1RAs for T2D management.
- To evaluate clinical studies on SGLT-2i plus GLP-1RA combination therapy in T2D patients.
Main Methods:
- PubMed database search for studies on combined SGLT-2i and GLP-1RA use.
- Focus on clinical studies assessing combination therapy efficacy and safety in T2D.
Main Results:
- Combination therapy significantly reduced glycated hemoglobin (A1c) over 28-52 weeks compared to individual agents.
- Improvements observed in cardiovascular risk factors including body weight, blood pressure, and lipid profiles.
- Therapy was well-tolerated with a low risk of hypoglycemia and no unexpected adverse events.
Conclusions:
- SGLT-2i plus GLP-1RA combination therapy provides durable glycemic control and cardiovascular benefits.
- Complementary mechanisms of action address multiple T2D defects, enhancing therapeutic outcomes.
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