The effect of small doses of fructose and allulose on postprandial glucose metabolism in type 2 diabetes: A double-blind, randomized, controlled, acute feeding, equivalence trial

被引:37
作者
Noronha, Jarvis C. [1 ,2 ]
Braunstein, Catherine R. [1 ,2 ]
Glenn, Andrea J. [1 ,2 ]
Khan, Tauseef A. [1 ,2 ]
Viguiliouk, Effie [1 ,2 ]
Noseworthy, Rebecca [1 ,2 ]
Mejia, Sonia Blanco [1 ,2 ]
Kendall, Cyril W. C. [1 ,2 ,3 ]
Wolever, Thomas M. S. [1 ,2 ,4 ,5 ]
Leiter, Lawrence A. [1 ,2 ,4 ,5 ]
Sievenpiper, John L. [1 ,2 ,4 ,5 ]
机构
[1] St Michaels Hosp, Clin Nutr & Risk Factor Modificat Ctr, Toronto Diet Digest Tract & Dis Knowledge Synth &, 6138-61 Queen St East, Toronto, ON M5C 2T2, Canada
[2] Univ Toronto, Dept Nutr Sci, Fac Med, Toronto, ON, Canada
[3] Univ Saskatchewan, Coll Pharm & Nutr, Saskatoon, SK, Canada
[4] St Michaels Hosp, Li Ka Shing Knowledge Inst, Toronto, ON, Canada
[5] St Michaels Hosp, Div Endocrinol, Toronto, ON, Canada
基金
加拿大健康研究院;
关键词
clinical trial; dietary intervention; dose-response relationship; glucose; metabolism; type; 2; diabetes; randomized trial; TOLERANCE-TEST; D-PSICOSE; ADMINISTRATION DECREASES; REGULATORY PROTEIN; INSULIN-RESISTANCE; GLYCEMIC RESPONSE; LIVER GLUCOKINASE; METAANALYSIS; HYPERGLYCEMIA; IMPROVES;
D O I
10.1111/dom.13374
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim: To assess and compare the effect of small doses of fructose and allulose on postprandial blood glucose regulation in type 2 diabetes. Methods: A double-blind, multiple-crossover, randomized, controlled, acute feeding, equivalence trial in 24 participants with type 2 diabetes was conducted. Each participant was randomly assigned six treatments separated by >= 1-week washouts. Treatments consisted of fructose or allulose at 0 g (control), 5 g or 10 g added to a 75-g glucose solution. A standard 75-g oral glucose tolerance test protocol was followed with blood samples at -30, 0, 30, 60, 90 and 120 minutes. The primary outcome measure was plasma glucose incremental area under the curve (iAUC). Results: Allulose significantly reduced plasma glucose iAUC by 8% at 10 g compared with 0 g (717.4 +/- 38.3 vs. 777.5 +/- 39.9 mmol x min/L, P = 0.015) with a linear dose response gradient between the reduction in plasma glucose iAUC and dose (P = 0.016). Allulose also significantly reduced several related secondary and exploratory outcome measures at 5 g (plasma glucose absolute mean and total AUC) and 10 g (plasma glucose absolute mean, absolute and incremental maximum concentration [C-max], and total AUC) (P < .0125). There was no effect of fructose at any dose. Although allulose showed statistically significant reductions in plasma glucose iAUC compared with fructose at 5 g, 10 g and pooled doses, these reductions were within the prespecified equivalence margins of +/- 20%. Conclusion: Allulose, but not fructose, led to modest reductions in the postprandial blood glucose response to oral glucose in individuals with type 2 diabetes. There is a need for long-term randomized trials to confirm the sustainability of these improvements.
引用
收藏
页码:2361 / 2370
页数:10
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