Published online Dec 15, 2021. doi: 10.4239/wjd.v12.i12.2087
Peer-review started: February 3, 2021
First decision: August 19, 2021
Revised: September 1, 2021
Accepted: December 8, 2021
Article in press: December 8, 2021
Published online: December 15, 2021
Processing time: 316 Days and 1.3 Hours
Dipeptidyl peptidase-4 inhibitors (DPP-4is) have become standard medications for glycemic control in patients with type 2 diabetes (T2D). Despite the high frequency of switching from various daily DPP-4is to once-weekly DPP-4is in actual clinical practice, data regarding its efficacy in patients with T2D after switching are limited.
Compound-specific effects can be present and influence the efficacy of daily DPP-4is in patients with T2D.
The authors analyzed the efficacy of omarigliptin, one of several once-weekly DPP-4is, in Japanese patients with T2D who had previously received treatment with other glucose-lowering agents.
The 49 patients in this study were divided into four groups defined as either add-on or switched from daily DPP-4is (linagliptin, sitagliptin, and vildagliptin), and the clinical parameters among these groups were assessed and compared during a 3-mo follow-up. Additionally, glycemic variability measured by continuous glucose monitoring was also assessed in the switched groups.
The glycemic control saw significant improvement in the add-on group, while the switched from vildagliptin to omarigliptin group experienced significant worsening. Multivariate logistic regression analysis revealed that switching from vildagliptin to omarigliptin was independently associated with worsening glycemic control (P = 0.0013). However, the mean of daily difference significantly improved when the patient was switched from either linagliptin or sitagliptin to omarigliptin but significantly worsened when patients were switched from vildagliptin.
Administering omarigliptin as add-on therapy or switching from sitagliptin and linagliptin, but not vildagliptin, provides more effective glycemic control. These results should help in decision-making regarding the selection and use of DPP-4is in patients with T2D.
To investigate the efficacy and safety of all types of daily DPP-4is, a prospective study using a larger cohort and inclusive of a control group should be conducted in the future.
