Predictors of the Therapeutic Efficacy and Consideration of the Best Combination Therapy of Sodium-Glucose Co-transporter 2 Inhibitors.

Ji Yeon Lee, Yongin Cho, Minyoung Lee, You Jin Kim, Yong Ho Lee, Byung Wan Lee, Bong Soo Cha, Eun Seok Kang

Journal: Diabetes & metabolism journal 2020;43(2):158-173

PMID: 30688052

Abstract

BACKGROUND

We investigated the predictive markers for the therapeutic efficacy and the best combination of sodium-glucose co-transporter 2 (SGLT2) inhibitors (empagliflozin, dapagliflozin, and ipragliflozin) therapy in patients with type 2 diabetes mellitus (T2DM).

METHODS

A total of 804 patients with T2DM who had taken SGLT2 inhibitor as monotherapy or an add-on therapy were analyzed. Multivariate regression analyses were performed to identify the predictors of SGLT2 inhibitor response including the classes of baseline anti-diabetic medications.

RESULTS

After adjusting for age, sex, baseline body mass index (BMI), diabetes duration, duration of SGLT2 inhibitor use, initial glycosylated hemoglobin (HbA1c) level, estimated glomerular filtration rate (eGFR), and other anti-diabetic agent usage, multivariate analysis revealed that shorter diabetes duration, higher initial HbA1c and eGFR were associated with better glycemic response. However, baseline BMI was inversely correlated with glycemic status; lean subjects with well-controlled diabetes and obese subjects with inadequately controlled diabetes received more benefit from SGLT2 inhibitor treatment. In addition, dipeptidyl peptidase 4 (DPP4) inhibitor use was related to a greater reduction in HbA1c in patients with higher baseline HbA1c ≥7%. Sulfonylurea users experienced a larger change from baseline HbA1c but the significance was lost after adjustment for covariates and metformin and thiazolidinedione use did not affect the glycemic outcome.

CONCLUSION

A better response to SGLT2 inhibitors is expected in Korean T2DM patients who have higher baseline HbA1c and eGFR with a shorter diabetes duration. Moreover, the add-on of an SGLT2 inhibitor to a DPP4 inhibitor is likely to show the greatest glycemic response.

Copyright © 2019 Korean Diabetes Association.

Address: Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.; Brain Korea 21 Plus Project for Medical Science, Yonsei University College of Medicine, Seoul, Korea.; Institute of Endocrine Research, Yonsei University College of Medicine, Seoul, Korea.; Institute of Endocrine Research, Yonsei University College of Medicine, Seoul, Korea. [email protected].
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