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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.
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页码:2361 / 2370
页数:10
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