PMID- 33106149 OWN - NLM STAT- MEDLINE DCOM- 20211025 LR - 20211025 IS - 2212-3911 (Electronic) IS - 1574-8863 (Linking) VI - 16 IP - 2 DP - 2021 TI - Efficacy and Cardiovascular Safety of Meglitinides. PG - 207-216 LID - 10.2174/1574886315666201026125848 [doi] AB - Meglitinides are a group of oral hypoglycemic medications currently approved for the treatment of type 2 diabetes mellitus (T2DM). Two meglitinide molecules, Repaglinide and Nateglinide, are presently in use. Repaglinide is preferred because of its superior glycemic efficacy. They have modest efficacy with a mean decrement of glycosylated haemoglobin (HbA1c) ranging between -0.2 to -1.50% with individual therapy. Additional HbA1c reduction can occur with combination therapy with other oral hypoglycemics. This class of drugs is effective in controlling postprandial hyperglycemia with minimal risk of hypoglycemia. It is also useful in patients with variable meal timings, especially in the elderly, and in patients with renal failure. There are a dearth of long-term studies on meglitinides to assess cardiovascular outcomes or mortality in T2DM, although the Nateglinide and Valsartan in Impaired Glucose ToleranceOutcomes Research (NAVIGATOR) study showed no difference between Nateglinide and placebo with regard to the core composite cardiovascular outcomes. Based on a PubMed literature search using key words: 'meglitinides', 'repaglinide', 'nateglinide', 'HbA1c', 'glycated haemoglobin', 'cardiovascular safety', 'cardiovascular events', 'cardiovascular outcome trials', 'type 2 diabetes mellitus' and heart failure, and combining the search terms using Boolean operators 'AND', 'OR' and 'NOT' as needed we compiled current evidence for use of these oral hypoglycemic agents in clinical use. This article is an attempt to review the efficacy and cardiovascular (CV) safety of Meglitinides to help clinicians to use this class of oral hypoglycaemic agents prudently. CI - Copyright(c) Bentham Science Publishers; For any queries, please email at epub@benthamscience.net. FAU - Philip, Jim AU - Philip J AD - Department of Endocrinology & Metabolism, NMC Speciality Hospital, Al Ain, United Arab Emirates. FAU - Fernandez, Cornelius James AU - Fernandez CJ AD - Department of Endocrinology & Metabolism, Pilgrim Hospital, PE21 9QS, Boston, United Kingdom. LA - eng PT - Journal Article PL - United Arab Emirates TA - Curr Drug Saf JT - Current drug safety JID - 101270895 RN - 0 (Benzamides) RN - 0 (Blood Glucose) RN - 0 (Hypoglycemic Agents) RN - 41X3PWK4O2 (Nateglinide) RN - 8V6OK1I088 (meglitinide) SB - IM MH - Aged MH - Benzamides MH - Blood Glucose MH - *Diabetes Mellitus, Type 2/diagnosis/drug therapy MH - Humans MH - Hypoglycemic Agents/adverse effects MH - Nateglinide OTO - NOTNLM OT - Meglitinides OT - cardiovascular outcome trial (CVOT) OT - heart failure OT - nateglinide OT - repaglinide OT - type 2 diabetes mellitus (T2DM) EDAT- 2020/10/28 06:00 MHDA- 2021/10/26 06:00 CRDT- 2020/10/27 05:35 PHST- 2020/05/13 00:00 [received] PHST- 2020/07/01 00:00 [revised] PHST- 2020/08/08 00:00 [accepted] PHST- 2020/10/28 06:00 [pubmed] PHST- 2021/10/26 06:00 [medline] PHST- 2020/10/27 05:35 [entrez] AID - CDS-EPUB-110903 [pii] AID - 10.2174/1574886315666201026125848 [doi] PST - ppublish SO - Curr Drug Saf. 2021;16(2):207-216. doi: 10.2174/1574886315666201026125848.