Acarbose (Precose)

Antidiabeticprescriptionoral · inferred

Competitive alpha-glucosidase inhibitor that slows intestinal carbohydrate digestion, blunting postprandial glucose excursions. Acts locally in the gut lumen with negligible systemic absorption (<2% of parent compound). Standard T2DM dosing 25-100 mg TID with first bite of meals. Notable as the most robustly life-extending pharmacological intervention in the NIA Interventions Testing Program (male mice), driving longevity-community interest despite modest HbA1c effect vs. metformin.

Projected serum levels — 50 mg, custom (shown daily)

Acarbose (Precose)
Acarbose (Precose) modeled serum levels, 50 mg custom (shown daily) over 15 days Population-based pharmacokinetic estimate. Steady state reached after approximately 7 days. 0 0.25 0.50 0.75 1 Day 0 Day 4 Day 8 Day 11 Day 15 Time on a regular schedule ≈ steady state · day 7

Maintenance schedule: 50 mg custom (shown daily) (oral).

Modeled steady state after ~7 days: peak ≈ 0 mg, trough ≈ 0 mg body load. Population-based estimate over 15 days for a 50 mg dose at a 70 kg reference body mass — the interactive app scales curves to your doses, timing, and body mass.

Key facts

Category
Antidiabetic
Route modeled
Oral
Model confidence
inferred
Common dose
50 mg
Suggested maximum
300 mg/day
Reference dose range
25–300 mg (single dose)
Suggested cadence
custom (shown daily)

Research behind this entry

  1. Longer lifespan in male mice treated with a weakly estrogenic agonist, an antioxidant, an alpha-glucosidase inhibitor or a Nrf2-inducer Strong R et al. · Aging Cell, 2016 DOI

    NIA Interventions Testing Program study showing acarbose extended median lifespan in male mice by 22% and by 5% in females, making it one of the most reproducible pharmacologic lifespan extenders.

  2. Effect of intensive blood-glucose control with metformin on complications in overweight patients with type 2 diabetes (UKPDS 34) UK Prospective Diabetes Study Group · Lancet, 1998 DOI

    UKPDS context for alpha-glucosidase inhibitor positioning alongside metformin in T2DM glycemic management, establishing clinical framework for postprandial glucose control.

  3. Acarbose reduces the risk for myocardial infarction in type 2 diabetic patients: meta-analysis of seven long-term studies Hanefeld M et al. · European Heart Journal, 2004 DOI

    Meta-analysis of 7 long-term trials (2,180 patients) found acarbose significantly reduced risk of myocardial infarction and any cardiovascular event in T2DM, linking postprandial glucose control to CV outcomes.

3 published studies referenced in the app, each with a plain-language summary.