Review Article

Effectiveness and Safety of Newer Antidiabetic Medications for Ramadan Fasting Diabetic Patients

Table 1

Summary of the included studies.

Class studiedMedicationType of studyResearch conclusions

DPP-4 inhibitorsVildagliptin as monotherapySmall scale observational studyVildagliptin was significantly more effective than SU to reduce and body weight; vildagliptin is associated with fewer hypoglycemic episodes than SU [12]
large scale multiregional observational studyVildagliptin was significantly more effective to reduce and less inducing hypoglycemia than SU [13]

DPP-4 inhibitorsVildagliptin as add-on therapyRandomized small scale studyVildagliptin has similar effectiveness on and body weight to gliclazide; vildagliptin was significantly less inducing of hypoglycemia than gliclazide [14]
Small scale, observational prospective studyVildagliptin was not associated with hypoglycemic events while nearly half of the patients in the SU group suffered from hypoglycemic events. There was significantly greater reduction by vildagliptin than SU [15]
Small scale, randomized open-label studyVildagliptin was less significantly associated with hypoglycemia but with similar effectiveness on to SU [17]
Large, prospective observational studyVildagliptin was associated with fewer episodes of severe hypoglycemia but with similar glycemic control to SU/glinide [18]
Large, multicenter, prospective observational studyVildagliptin using patients suffered from hypoglycemia less frequently than those using SU. The reduction in was greater but not significantly different with vildagliptin than in SU [19]
Multiregional, large scale, randomized double blind studyVildagliptin had similar effectiveness to lower but with less hypoglycemic risk than gliclazide [20]

DPP-4 inhibitorsSitagliptin as add-on therapyPilot prospective observational studySitagliptin usage was not associated with hypoglycemic attacks [22]
Large, multinational randomized studySitagliptin was associated with significantly less risk of hypoglycemia than glibenclamide and glimepiride but similar risk to gliclazide [23]
Large, multicenter, randomized studySitagliptin was associated with significantly less risk of hypoglycemia than glibenclamide and glimepiride but higher hypoglycemic risk than gliclazide [24]

GLP-1 RAExenatide as add-on therapyPilot observational studyNo risk of hypoglycemia even if pre-Ramadan dose of exenatide is not adjusted during Ramadan [27]
Observational studyExenatide was associated with less risk of hypoglycemia than gliclazide [28]

GLP-1 RALiraglutide as add-on therapySmall scale randomized studyLiraglutide was associated with significant reduction in body weight and nonsignificant but greater reduction in than SU
Liraglutide was less significantly inducing hypoglycemia than SU [29]
Large, open-label, multinational randomized trialLiraglutide was less likely to produce confirmed hypoglycemic attacks compared with SU. Moreover, patients on liraglutide experienced significantly greater weight loss and had significantly greater improvements in than those on SU [30]

SGLT-2 inhibitorsDapagliflozin as add-on therapyRandomized open-label studyThere was a nonsignificant difference in the incidence of dehydration between patients in the dapagliflozin and SU group [34]

DPP-4: dipeptidyl peptidase-4 inhibitor; GLP-1 RA: glucagon-like peptide-1 receptor agonist; SGLT-2: sodium-glucose cotransporter-2; SU: sulfonylurea; : glycosylated hemoglobin.