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©The Author(s) 2022.
World J Diabetes. Dec 15, 2022; 13(12): 1168-1183
Published online Dec 15, 2022. doi: 10.4239/wjd.v13.i12.1168
Published online Dec 15, 2022. doi: 10.4239/wjd.v13.i12.1168
Ref. | Primary study objective | Study design | Study population | CVD excluded | Number of participants | Study duration | Endpoint (hypoglycemia) | Hypoglycemia definition | Hypoglycemia results | Endpoint (MACE) | MACE definition | MACE results |
Gliclazide vs DPP4 inhibitor (vildagliptin) | ||||||||||||
Foley et al[34], 2009 | Compare the efficacy and safety of vildagliptin vs gliclazide | Randomized, multicenter, double-blind, active-controlled study | Drug-naïve patients with T2D, HbA1c of 7.5%-11.0% | CHF NYHA class III or IV, ECG abnormalities | 1092 | 104 wk | AEs were safety endpoints | Grade 1 hypoglycemic events per week: symptoms suggestive of low blood glucose confirmed by SMBG measurement of < 3.1 mmol/L plasma glucose equivalent not requiring the assistance of another party; Grade 2 hypoglycemic event (requiring the assistance of another party) or if there were 3 or more asymptomatic glucose values < 3.1 mmol/L per week | Grade 1 hypoglycemia: 4 patients (0.7%) in the vildagliptin group and 14 (1.7%) in the gliclazide group. ≥ 2 HEs: 2 patients in the gliclazide group and none in vildagliptin group No grade 2 HEs in either group | - | - | - |
Gliclazide + metformin vs DPP4 inhibitor (vildagliptin) + metformin | ||||||||||||
Vianna et al[35], 2018 (Part of BoneGlic Trial) | Compare the effects on glycemic variability and bone metabolism | Single center, randomized, controlled, open-label (blinded to the observer) | Postmenopausal Brazilian women with T2D and treated with a stable metformin dose for ≤ 3 mo | CV complications | 56 (42 randomized) | 2-wk pre-randomization period followed by 24 wk | As AE | Major hypoglycemia: glucagon, carbohydrates administration by another person or other resuscitative measures; minor hypoglycemia: BG ≤ 3.9 mmol/L with or without typical symptoms or hypoglycemia symptoms without BG test | No differences from baseline in time to hypoglycemia (% of time ≤ 3.9 mmol/L) | As SAE | Vildagliptin: 1 hemorrhagic stroke gliclazide MR group: 1 death due to AMI, the investigator did not consider the SAEs to be related to the study medications | |
No major hypoglycemia | ||||||||||||
Minor hypoglycemia events: 7 in the gliclazide; 2 in the vildagliptin group (P = 0.062) | ||||||||||||
Hassanein et al[36], 2014 (STEADFAST study) | HE during Ramadan | Multiregional, randomized double-blind | Patients fasting during Ramadan | CHF (NYHA class III or IV); other significant CV history within 6 mo | 557 | 4-wk Ramadan period | Primary | Hypoglycemia: Low BG symptoms with or without confirmatory, SMBG measurement < 3.9 mmol/L; PGE or asymptomatic SMBG < 3.9 mmol/L PGE; confirmed hypoglycemia: symptomatic/asymptomatic SMBG measurement < 3.9 mmol/L; PGE and severe HE requiring assistance from another party irrespective of whether SMBG value was available or not | Confirmed and/or severe HE during Ramadan: vildagliptin vs glicalzide was 3.0% vs 7.0% (P = 0.039; one-sided test); HEs: vildagliptin vs gliclazide was 6.0% and 8.7% (P = 0.173) | - | - | - |
Filozof and Gautier[37], 2010 | Demonstrate non-inferiority of vildagliptin compared with gliclazide, as an add-on therapy | Randomized, double-blind, active-controlled | T2D uncontrolled with metformin | Serious cardiac conditions (torsades de pointes, sustained and clinically relevant VT or VF, PCI ≤ 3 mo, MI, CABG, unstable angina, or stroke ≤ 6 mo and CHF requiring pharmacological treatment, 2nd- or 3rd-degree AV block or prolonged QTc) | 1007 | 52 wk | AE | Symptoms suggestive of hypoglycemia and confirmed by SMBG < 3.1 mmol/L | HE vildagliptin vs gliclazide (6 vs 11 events) | - | - | - |
- Citation: Mohan V, Wangnoo S, Das S, Dhediya R, Gaurav K. Comparison of gliclazide vs linagliptin on hypoglycemia and cardiovascular events in type 2 diabetes mellitus: A systematic review. World J Diabetes 2022; 13(12): 1168-1183
- URL: https://www.wjgnet.com/1948-9358/full/v13/i12/1168.htm
- DOI: https://dx.doi.org/10.4239/wjd.v13.i12.1168