Review Article
SGLT2 Inhibitors, GLP-1 Agonists, and DPP-4 Inhibitors in Diabetes and Microvascular Complications: A Review
Table 2
Overview of the neurological protective studies.
| Authors | Treatment | Size | Duration | Population | Outcome | Clinical | Animal |
| Takakura et al. [19] | Ipragliflozin | 44 | 12 weeks | | SDT fatty and SD rats | Reduced prolonged peak latency Improved MNCV | Tsuboi et al. [25] | Vildagliptin | 30 | 18 weeks | | Goto-Kakizaki (GK) DM rats | Improved nerve conduction velocity and atrophy | Davidson et al. [26] | Alogliptin | 32 | 12 weeks | | STZ-induced DM rats | Improved nerve conduction velocity | Kolaczynski et al. [27] | Vildagliptin | 16321 | — | DM II | | Lower incidence of neuropathy | Da Silva et al. [28] | Sitagliptin | 30 | 1 year | DM II | | No benefit on nerve conduction | Jaiswal et al. [29] | Exenatide | 42 | 1.5 years | DM II Mild-to-moderate DPN | | No effect on neuropathy |
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DM II: diabetes mellitus type 2; MNCV: motor neuron conduction velocity; DPN: diabetic peripheral neuropathy; DM: diabetes mellitus; SD: Sprague Dawley; SDT: spontaneously diabetic Torii; STZ: streptozotocin.
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