Allulose
A rare sugar that tastes close to sucrose but is barely metabolised, so it contributes almost no calories. It reliably blunts the glucose and insulin rise after a meal; what it has not been shown to do is reduce body weight or long-term HbA1c.
Evidence last reviewed: August 2026
What the science says
- Lowers postprandial glucose and insulin Moderate evidence
A 2026 systematic review and meta-analysis of 20 controlled human trials (1,033 participants) found allulose significantly reduced postprandial glucose and insulin area under the curve, both rated moderate certainty. Twelve of the trials tested allulose specifically.
- No effect on fasting glucose, HbA1c or body composition Moderate evidence
The same meta-analysis found no significant effects on HbA1c, fasting glucose or insulin, blood lipids, uric acid or measures of adiposity, with very low to moderate certainty. Its value is as a sugar substitute, not as a weight-loss or metabolic agent in its own right.
- Blunts the response to a sugar load Moderate evidence
A randomized cross-over trial found that adding allulose to a standard oral sucrose load improved glucose tolerance and reduced the insulin response in healthy adults. A separate randomized study confirmed acute metabolic effects and acceptable tolerability at typical serving sizes.
Dosage & safety
Scientific references
- Glycemic and cardiometabolic effects of rare sugars allulose and tagatose: a systematic review and meta-analysis of controlled human intervention trials
- Effects of D-allulose on glucose tolerance and insulin response to a standard oral sucrose load: results of a prospective, randomized, crossover study
- Metabolic Effects and Safety Aspects of Acute D-allulose and Erythritol Administration in Healthy Subjects
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