Unbound MEDLINE

Sodium Glucose Cotransporter 2 Inhibitors as a New Treatment for Diabetes Mellitus. The Journal of clinical endocrinology and metabolism [J Clin Endocrinol Metab] Journal article

 
TitleSodium Glucose Cotransporter 2 Inhibitors as a New Treatment for Diabetes Mellitus.
Author(s)Nair S, Wilding JP 
InstitutionDiabetes and Endocrinology Research Unit, Clinical Sciences Centre, University Hospital Aintree, Liverpool L9 7AL, United Kingdom.
SourceJ Clin Endocrinol Metab 2009 Nov 5.
AbstractContext: Sodium-glucose cotransporter 2 (SGLT2) expressed in the proximal renal tubules accounts for about 90% of the reabsorption of glucose from tubular fluid. Genetic defects of SGLT2 result in a benign familial renal glucosuria. Pharmacological agents that block SGLT2 are being tested as potential treatment for type 2 diabetes mellitus. Evidence Acquisition: A Pubmed search was used to identify all relevant articles on the physiology of SGLTs as well as published preclinical and clinical experimental studies with SGLT2 inhibitors; a reference search of all retrieved articles was also undertaken. Evidence Synthesis: SGLT2 is almost exclusively expressed in the proximal renal tubules. Preclinical studies with selective SLGT2 inhibitors show dose-dependent glucosuria and lowering of blood glucose in models of type 2 diabetes. Preliminary clinical studies of up to 3-month duration show dose-dependent lowering of glycosylated hemoglobin up to 0.9% along with modest weight loss. Side effects include an increase in genital fungal infection compared to placebo, increased urine volume (300-400 ml/24 h), and evidence of volume depletion consistent with mild diuretic effect.
Conclusion: SGLT2 inhibitors are showing promise as a useful addition to the current therapeutic options in type 2 diabetes mellitus. Results of ongoing phase III clinical trials are awaited and will determine whether the risk-benefit ratio will allow approval of this new class of drug for the management of type 2 diabetes mellitus.
LanguageENG
Pub Type(s)JOURNAL ARTICLE
PubMed ID19892839
  
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