Consumption of a diet low in advanced glycation end products for 4 weeks improves insulin sensitivity in overweight women.
Study Goal
The researchers aimed to determine whether high-AGE diets and fructose intake affect insulin sensitivity in overweight individuals.
Results Summary
The low-AGE diet reduced urinary AGEs, fasting insulin, and HOMA-IR compared to the high-AGE diet, suggesting AGEs may contribute to insulin resistance. Fructose intake did not influence outcomes.
Population
Overweight women (n=74)
Effective Dosage
Not specified
Duration
4 weeks
Interactions
None mentioned
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
low-AGE diet | decrease | urinary AGEs | overweight women | - | decreased | #1 |
low-AGE diet | decrease | fasting insulin concentrations | overweight women | - | decreased | #2 |
low-AGE diet | decrease | HOMA-IR | overweight women | - | decreased | #3 |
addition of fructose | no change | any outcomes | overweight women | - | did not affect | #4 |
high AGE content diets | increase | the development of insulin resistance | - | - | may increase | #5 |
modulation of cooking methods | decrease | AGEs | - | - | can be reduced | #6 |
moderate fructose intake | no change | AGEs | - | - | unaffected | #7 |
OBJECTIVE High-heat cooking of food induces the formation of advanced glycation end products (AGEs), which are thought to impair glucose metabolism in type 2 diabetic patients. High intake of fructose might additionally affect endogenous formation of AGEs. This parallel intervention study investigated whether the addition of fructose or cooking methods influencing the AGE content of food affect insulin sensitivity in overweight individuals. RESEARCH DESIGN AND METHODS Seventy-four overweight women were randomized to follow either a high- or low-AGE diet for 4 weeks, together with consumption of either fructose or glucose drinks. Glucose and insulin concentrations-after fasting and 2 h after an oral glucose tolerance test-were measured before and after the intervention. Homeostasis model assessment of insulin resistance (HOMA-IR) and insulin sensitivity index were calculated. Dietary and urinary AGE concentrations were measured (liquid chromatography tandem mass spectrometry) to estimate AGE intake and excretion. RESULTS When adjusted for changes in anthropometric measures during the intervention, the low-AGE diet decreased urinary AGEs, fasting insulin concentrations, and HOMA-IR, compared with the high-AGE diet. Addition of fructose did not affect any outcomes. CONCLUSIONS Diets with high AGE content may increase the development of insulin resistance. AGEs can be reduced by modulation of cooking methods but is unaffected by moderate fructose intake.