健康志愿者口服乳果糖后的血糖反应:一项随机、对照、交叉研究

Jasmin Steudle, Christiane Schön, Manfred Wargenau, Lioba Pauly, Susann Schwejda-Güttes, Barbara Gaigg, Angelika Kuchinka-Koch, John F Stover
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引用次数: 7

摘要

目的:探讨健康受试者口服乳果糖后血糖水平可能发生的变化。方法:本研究采用前瞻性、随机、两部分、4位交叉设计,每个研究组n = 12人。在摄入单剂量10g或20g乳果糖晶体或液体制剂后180分钟内测定毛细血管血糖水平。在乳果糖的生产过程中,会产生含糖杂质(如乳糖、果糖、半乳糖)。以水和20 g葡萄糖作为对照和参比。因为乳果糖被用作功能性食品成分,它也可能被糖耐量受损的人食用,包括糖尿病患者。因此,确定所描述的碳水化合物杂质在摄入后是否会增加血糖水平是有意义的。结果:摄入10 g乳果糖、20 g乳果糖和水后血糖浓度-时间曲线基本相同。三种应用都没有显示血糖水平有任何变化。摄入20 g葡萄糖后,血糖浓度升高约3 mmol/L(平均Cmax = 8.3 mmol/L),约30 min后达到最高水平,约90 min后恢复到基线水平,与相应的20 g乳果糖制剂差异显著(P < 0.0001)。晶体乳果糖和液体乳果糖在添加量为10 g和20 g时,尽管碳水化合物杂质含量不同(晶体为1.5%,液体为26.45%),但血糖谱和计算的药代动力学参数没有差异。无论如何,在20 g剂量下,单糖的绝对含量很低,晶体为0.3 g,液体为5.29 g。大多数志愿者对乳果糖耐受性良好,只有一些人报告了轻微到中度的主要胃肠道副作用。结论:健康受试者摄入乳果糖后血糖水平不变,提示其用于糖耐量受损的受试者是安全的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Blood glucose response after oral intake of lactulose in healthy volunteers: A randomized, controlled, cross-over study.

Blood glucose response after oral intake of lactulose in healthy volunteers: A randomized, controlled, cross-over study.

Blood glucose response after oral intake of lactulose in healthy volunteers: A randomized, controlled, cross-over study.

Blood glucose response after oral intake of lactulose in healthy volunteers: A randomized, controlled, cross-over study.

Aim: To investigate possible changes of blood glucose levels after oral intake of lactulose in healthy subjects.

Methods: The study was performed as prospective, randomized, two-part study with 4-way cross-over design with n = 12 in each study arm. Capillary blood glucose levels were determined over a time period of 180 min after intake of a single dose of 10 g or 20 g lactulose provided as crystal or liquid formulation. During the manufacturing process of lactulose, impurities with sugars (e.g., lactose, fructose, galactose) occur. Water and 20 g glucose were used as control and reference. Because lactulose is used as a functional food ingredient, it may also be consumed by people with impaired glucose tolerance, including diabetics. Therefore, it is of interest to determine whether the described carbohydrate impurities may increase blood glucose levels after ingestion.

Results: The blood glucose concentration-time curves after intake of 10 g lactulose, 20 g lactulose, and water were almost identical. None of the three applications showed any changes in blood glucose levels. After intake of 20 g glucose, blood glucose concentration increased by approximately 3 mmol/L (mean Cmax = 8.3 mmol/L), reaching maximum levels after approximately 30 min and returning to baseline within approximately 90 min, which was significantly different to the corresponding 20 g lactulose formulations (P < 0.0001). Comparing the two lactulose formulations, crystals and liquid, in the dosage of 10 g and 20 g, there was no difference in the blood glucose profile and calculated pharmacokinetic parameters despite the different amounts of carbohydrate impurities (1.5% for crystals and 26.45% for liquid). Anyhow, the absolute amount of single sugars was low with 0.3 g in crystals and 5.29 g in liquid formulation in the 20 g dosages. Lactulose was well tolerated by most volunteers, and only some reported mild to moderate mainly gastrointestinal side effects.

Conclusion: The unchanged blood glucose levels after lactulose intake in healthy subjects suggest its safe use in subjects with impaired glucose tolerance.

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