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Efficacy of dapagliflozin as an adjunct therapy in patients with inadequately controlled type 1 diabetes mellitus.

AbstractINTRODUCTION:
There is a clear unmet clinical need in people with Type 1 diabetes (T1DM) considering present day insulin therapy. New insulin analogues and novel technologies allowing more tailored insulin administration have improved the quality of life of people with T1DM, but issues like hypoglycemia, weight gain and variability in glucose profiles remain problematic. Areas covered: In this review, the clinical efficacy, safety and tolerability of dapagliflozin, a sodium-glucose cotransporter type 2 inhibitor, in type 1 diabetes (T1DM) is described based on a review of phase 2 and 3 studies to date. Expert opinion: Dapagliflozin has shown promising results as an adjunct therapy in T1DM, resulting in better glucose control, weight loss and lower blood pressure. No increase in hypoglycemia risk, in particular severe hypoglycemia, was observed, but, in comparison with reports in Type 2 diabetes (T2DM), genital infections were more prevalent. Dapagliflozin use was accompanied with decreases in insulin doses, but, to date, only a low risk of diabetic ketoacidosis (DKA) was reported. However, caution is needed when interpreting this data, arising from well controlled clinical trials, with intensive education programs around ketone measurements and DKA prevention. Further studies will need to establish how high the DKA risk is and how to mitigate this in a real-world setting.
AuthorsLaura Van den Mooter, Simon Caerels, Chantal Mathieu
JournalExpert opinion on pharmacotherapy (Expert Opin Pharmacother) Vol. 19 Issue 6 Pg. 617-622 (Apr 2018) ISSN: 1744-7666 [Electronic] England
PMID29537892 (Publication Type: Journal Article)
Chemical References
  • Benzhydryl Compounds
  • Glucosides
  • Hypoglycemic Agents
  • Sodium-Glucose Transport Proteins
  • dapagliflozin
Topics
  • Benzhydryl Compounds (pharmacology, therapeutic use)
  • Diabetes Mellitus, Type 1 (drug therapy)
  • Glucosides (pharmacology, therapeutic use)
  • Humans
  • Hypoglycemic Agents (therapeutic use)
  • Sodium-Glucose Transport Proteins (pharmacology, therapeutic use)

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