TY - JOUR
T1 - Efficacy and safety of dapagliflozin, a sodium glucose cotransporter 2 (SGLT2) inhibitor, in diabetes mellitus.
AU - Fioretto, Paola
AU - Giaccari, Andrea
AU - Sesti, Giorgio
PY - 2015
Y1 - 2015
N2 - 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 β-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.
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 β-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.
KW - Antidiabetic drugs
KW - Dapagliflozin
KW - Glycemic control
KW - Glycosylated hemoglobin
KW - Sodium-glucose cotransporter 2 inhibitors
KW - Type 1 diabetes mellitus
KW - Type 2 diabetes mellitus
KW - Weight reduction
KW - Antidiabetic drugs
KW - Dapagliflozin
KW - Glycemic control
KW - Glycosylated hemoglobin
KW - Sodium-glucose cotransporter 2 inhibitors
KW - Type 1 diabetes mellitus
KW - Type 2 diabetes mellitus
KW - Weight reduction
UR - http://hdl.handle.net/10807/71748
U2 - 10.1186/s12933-015-0297-x
DO - 10.1186/s12933-015-0297-x
M3 - Article
SN - 1475-2840
VL - 14
SP - 1
EP - 13
JO - Cardiovascular Diabetology
JF - Cardiovascular Diabetology
ER -