Journal
ACTA DIABETOLOGICA
Volume 46, Issue 3, Pages 173-181Publisher
SPRINGER-VERLAG ITALIA SRL
DOI: 10.1007/s00592-009-0134-3
Keywords
Antidiabetic drugs; Diabetes mellitus, type 2; Disease management; Beta-cell function; Cardiovascular disease
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Funding
- Bioscript Stirling Ltd, UK
- ESOCAP
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The prevalence of diabetes is expected to rise together with an increase in morbidity and a reduction in life expectancy. A leading cause of death is cardiovascular disease, and hypertension and diabetes are additive risk factors for this complication. Selected treatment options should neither increase cardiovascular risk in patients with diabetes, nor increase risk of hyperglycaemia in patients with hypertension. The efficacy of present antihyperglycaemic agents is limited and new therapies, such as incretin-targeted agents, are under development. Even though most patients do not achieve glycated haemoglobin targets, trial data show that such interventions reduce the incidence of macrovascular events; however, intensive lowering may be detrimental in patients with existing cardiovascular disease. Currently available oral drugs do not address the key driver of type 2 diabetes-loss of functional beta-cell mass. In the future, new oral treatments must improve this, whilst providing durable blood glucose control and long-term tolerability.
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