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Comparative Clinical Analysis of DPP-4 inhibitors and SGLT2 Inhibitors: A Real-World Switch Study
Hun Jee Choe1, Mi Kyung Kwak1, Ji Woo Lee1
1Department of Internal Medicine, Hallym University Dongtan Sacred Heart Hospital, Hwaseong, Korea.
Switching to DPP-4 inhibitors more effectively lowers HbA1c in type 2 diabetes patients. Conversely, SGLT2 inhibitors better improve fasting plasma glucose and liver enzymes, particularly in specific patient subgroups.
Area of Science:
- Endocrinology
- Pharmacology
- Metabolic Diseases
Background:
- Dipeptidyl peptidase-4 (DPP-4) inhibitors and sodium-glucose co-transporter 2 (SGLT2) inhibitors are key oral antidiabetic agents.
- Real-world comparative effectiveness data is vital for optimizing type 2 diabetes mellitus (T2DM) treatment.
Purpose of the Study:
- To compare the real-world effectiveness of switching between DPP-4 and SGLT2 inhibitors in adults with T2DM.
- To evaluate changes in glycemic control, metabolic parameters, and organ function post-switch.
Main Methods:
- Retrospective analysis of adults with T2DM switching between DPP-4 and SGLT2 inhibitors (2014-2023).
- Inclusion criteria: baseline HbA1c 6.5-10.0%, metformin use, eGFR ≥45 mL/min/1.73 m².
- 1:1 propensity-score matching for baseline HbA1c and FPG; 84 patients per group (n=168 total).
Main Results:
- Switching to DPP-4 inhibitors showed a significantly greater reduction in HbA1c (β, -0.26; P<0.001).
- Switching to SGLT2 inhibitors led to significant improvements in fasting plasma glucose (FPG) (β, 10.50; P<0.001) and liver enzymes.
- DPP-4 inhibitor benefits were more pronounced in older patients, those with lower BMI, higher baseline HbA1c, or chronic kidney disease.
Conclusions:
- DPP-4 inhibitors significantly reduce HbA1c levels.
- SGLT2 inhibitors effectively improve FPG and liver-related metabolic parameters.
- Treatment choice may be guided by patient characteristics and specific therapeutic goals.
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