PMID- 26474563 OWN - NLM STAT- MEDLINE DCOM- 20160707 LR - 20231111 IS - 1475-2840 (Electronic) IS - 1475-2840 (Linking) VI - 14 DP - 2015 Oct 17 TI - Efficacy and safety of dapagliflozin, a sodium glucose cotransporter 2 (SGLT2) inhibitor, in diabetes mellitus. PG - 142 LID - 10.1186/s12933-015-0297-x [doi] LID - 142 AB - Although antidiabetic agents have been developed to target one or more of the core defects of type 2 diabetes mellitus (T2DM), many patients do not achieve glycemic goals. Inhibition of the sodium-glucose cotransporter 2 (SGLT2) induces glycosuria, reduces glucose toxicity and improves insulin sensitivity and beta-cell function. As the mechanism of action of SGLT2 inhibitors is different from other agents and completely insulin-independent, the use of these drugs might potentially be efficacious alone or in combination with any other antidiabetic drug, including insulin. Dapagliflozin is a highly selective and reversible SGLT2 inhibitor approved for use in adult patients with T2DM as monotherapy in patients intolerant of metformin or as adjunctive therapy in patients inadequately controlled on existing antidiabetic medications, including insulin. A literature search conducted using PubMed identified key publications related to the use of dapagliflozin in the treatment of patients with diabetes mellitus. No date limits were applied. This review focuses on the safety and efficacy of this SGLT2 inhibitor. Dapagliflozin produces dose-related reductions in glycosylated hemoglobin (HbA1c) as monotherapy and as add-on to other antidiabetic agents, with significant reductions in body weight. Hypoglycemia is uncommon. Preliminary data from a phase 2 pharmacokinetic/pharmacodynamic study suggest that dapagliflozin may also improve glycemic control in patients with type 1 diabetes mellitus. Clinical trials published to date show that dapagliflozin is safe and effective as monotherapy or as an add-on to insulin or oral antidiabetic agents in patients with T2DM. FAU - Fioretto, Paola AU - Fioretto P AD - Department of Medicine, University of Padua, Via Giustiniani 2, 35128, Padua, Italy. paola.fioretto@unipd.it. FAU - Giaccari, Andrea AU - Giaccari A AD - EndoMetabolic Diseases Unit, Policlinico Gemelli, Universita Cattolica del Sacro Cuore, Largo A. Gemelli 8, 00168, Rome, Italy. giaccari@rm.unicatt.it. FAU - Sesti, Giorgio AU - Sesti G AD - Department of Medical and Surgical Sciences, University Magna-Graecia of Catanzaro, Viale Europa, 88100, Catanzaro, Italy. sesti@unicz.it. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Review DEP - 20151017 PL - England TA - Cardiovasc Diabetol JT - Cardiovascular diabetology JID - 101147637 RN - 0 (Benzhydryl Compounds) RN - 0 (Glucosides) RN - 0 (Glycated Hemoglobin A) RN - 0 (Hypoglycemic Agents) RN - 0 (Insulin) RN - 0 (Sodium-Glucose Transporter 2 Inhibitors) RN - 0 (hemoglobin A1c protein, human) RN - 1ULL0QJ8UC (dapagliflozin) SB - IM MH - Benzhydryl Compounds/*therapeutic use MH - Diabetes Mellitus, Type 1/*drug therapy/metabolism MH - Diabetes Mellitus, Type 2/*drug therapy/metabolism MH - Drug Therapy, Combination MH - Glucosides/*therapeutic use MH - Glycated Hemoglobin/metabolism MH - Humans MH - Hypoglycemia/chemically induced MH - Hypoglycemic Agents/*therapeutic use MH - Insulin/*therapeutic use MH - Sodium-Glucose Transporter 2 Inhibitors MH - Treatment Outcome PMC - PMC4609166 EDAT- 2015/10/18 06:00 MHDA- 2016/07/09 06:00 PMCR- 2015/10/17 CRDT- 2015/10/18 06:00 PHST- 2015/07/28 00:00 [received] PHST- 2015/09/25 00:00 [accepted] PHST- 2015/10/18 06:00 [entrez] PHST- 2015/10/18 06:00 [pubmed] PHST- 2016/07/09 06:00 [medline] PHST- 2015/10/17 00:00 [pmc-release] AID - 10.1186/s12933-015-0297-x [pii] AID - 297 [pii] AID - 10.1186/s12933-015-0297-x [doi] PST - epublish SO - Cardiovasc Diabetol. 2015 Oct 17;14:142. doi: 10.1186/s12933-015-0297-x.