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Abstract
Among 29,269 patients, 1,591 (5.4%) received combined therapy of SGLT2 inhibitors and GLP-1 receptor agonists.
- The combined therapy group had significantly lower risks of all-cause mortality compared to SGLT2 inhibitor monotherapy (adjusted hazard ratio = 0.53) and GLP-1 receptor agonist monotherapy (adjusted hazard ratio = 0.43) after a mean follow-up of 2.4 years.
- Lower risks of major adverse kidney events were observed in the combined therapy group compared to SGLT2 inhibitor monotherapy (adjusted hazard ratio = 0.70) and GLP-1 receptor agonist monotherapy (adjusted hazard ratio = 0.45) after a mean follow-up of 2.7 years.
- The risk of major adverse cardiovascular events was similar across all treatment groups.
- The combined therapy group had a higher risk of hypoglycemia (adjusted hazard ratio = 1.51) and diabetic retinopathy (adjusted hazard ratio = 1.59) compared to the SGLT2 inhibitor monotherapy group.
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