The Journal of Experimental Medicine · 2013 · 10 citations · 2 references
MedicinePharmacologyPharmacotherapyClinical PharmacologyDiabetologyMolecular PharmacologyDiabetes ManagementDiabetes MellitusDiabetes PharmacotherapyGlycemic ControlInsulin ResistanceSodium-glucose Cotransporter 2 InhibitorsAdd-on TherapyAntidiabetic ActivityAntidiabetic Drug TherapyRenal Glucose ReabsorptionSodium-glucose Cotransporter 2 InhibitionType 2 Diabetes Mellitus TreatmentType 2 Diabetes PharmacotherapyType 2 Diabetes Treatment
BACKGROUND: Because of the progressive nature of the disease, most patients with type 2 diabetes mellitus eventually require multiple treatments to achieve glycaemic targets. The majority of available therapies are insulin dependent, aiming to decrease insulin resistance and increase insulin secretion. Sodium glucose co-transporter 2 (SGLT2) inhibitors, a new class of antidiabetic agents, limit renal glucose reabsorption promoting urinary excretion of glucose, thereby reducing plasma glucose. OBJECTIVE: This article explores the mechanism of action and clinical data surrounding SGLT2 inhibitors, with a particular focus on dapagli-flozin. CONCLUSION: Clinical trials have shown dapagliflozin to be effective in reducing glycosylated haemoglobin, weight and fasting plasma glucose, either as monotherapy or as add-on therapy to metformin, sulphonylurea and insulin. Other SGLT2 inhibitors are currently under investigation.
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A novel T-cell line derived from adult T-cell leukemia.
Isao Miyoshi, Ichiro Kubonishi, Mitsuo Sumida et al. · PubMed · 1980 · 224 citations
Medicine, Hematology, Oncology +8