- The gut cannot absorb disaccharides such as sucrose
- Alpha-glucosidase in the intestinal brush border normally cleaves disaccharides into absorbable monosaccharides
- Acarbose is a competitive inhibitor of this enzyme, and also inhibits pancreatic alpha-amylase (which hydrolyses complex carbohydrates)
- This delays carbohydrate absorption, limiting the rate of rise of plasma glucose and reducing total carbohydrate absorbed
- HbA1c reduction is modest, ~8mmol/mol (0.75%)
- Can be used with sulphonylureas, metformin or insulin
Acarbose
Acarbose
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- Acarbose is an intestinal alpha-glucosidase inhibitor that reduces post-prandial hyperglycaemia
- Its efficacy depends on carbohydrate intake, so the risk of hypoglycaemia is very low
- It is no longer recommended in UK guidelines and is not widely used
Absorption
- Minimal systemic absorption; acts locally in the gut
Metabolism
- Degraded within the GI tract by intestinal bacteria and digestive enzymes
Excretion
- The small absorbed fraction is renally excreted
Gastrointestinal
- Colonic bacteria ferment the increased carbohydrate load, causing flatulence, bloating, abdominal pain and diarrhoea
- The dose must therefore be built up gradually
- May raise hepatic transaminases
Nutritional and metabolic
- Few systemic effects
- Hypoglycaemia only occurs in combination with other agents
- This should be treated with glucose rather than sucrose, whose digestion is inhibited
Contraindications
- Inflammatory bowel disease or colonic ulceration
- Intestinal obstruction, or predisposition to it
- Previous abdominal surgery
- Severe hepatic impairment
- Renal impairment with eGFR <25ml/min/1.73m2
Perioperative management
- Morning surgery: omit the morning dose if not eating
- Afternoon surgery: take the morning dose if eating breakfast
- Discontinue when a liver reduction diet starts before bariatric surgery
- Low risk of hypoglycaemia when used alone; target capillary blood glucose 4-10mmol/L
- Restart once normal enteral intake resumes
- Its GI side-effects (flatulence, diarrhoea) may be relevant postoperatively
- Normally discontinued in critical illness given its mode of action and its contraindications in GI, hepatic and renal disease