Pasman W, Wils D, Saniez M-H, Kardinaal A
TNO Quality of Life, Zeist, The Netherlands. pasman@
Eur J Clin Nutr. 2006 Aug;60(8):1024-34. doi: 10.1038/sj.ejcn.1602418. Epub 2006 Feb 15.
To determine the gastrointestinal (GI) tolerance of NUTRIOSE FB in men.
A randomized, placebo-controlled, parallel, double-blind study.
The metabolic ward of TNO Quality of Life.
Forty-eight subjects started the study: 16 men participated in one of the three treatments. SUBJECTS consumed either 22.5 g of pure maltodextrin (Glucidex 6), or 30 or 45 g of the dextrin NUTRIOSE FB daily for 4-5 weeks. Forty-three subjects completed the study (age: 34.7 +/- 8.2 years; BMI 24.9 +/- 3.3 kg m2).
Tolerance of NUTRIOSE FB was examined with a GI complaints questionnaire; effectiveness on colonic flora was examined by faecal analysis; fermentation by breath hydrogen excretion measurement. Furthermore, the effect on body weight (BW), energy intake and blood parameters were examined in the study.
Both doses of NUTRIOSE FB were very well tolerated and GI complaints hardly differed from the placebo treatment. No diarrhoea was reported due to NUTRIOSE FB supplementation. In the course of the study, some habituation and adaptation of GI symptoms were found. Fermentation and faecal characteristics (pH and enzyme activity) were significantly positively affected with NUTRIOSE FB treatment. Body weight in both NUTRIOSE FB groups remained stable over time, although the placebo-treated group showed a small increase in BW (Deltaday35-1 0.8 +/- 1.0 kg) (P = 0.07). However, total food intake and macronutrient composition of the diet remained the same throughout the study. No significant differences were found between the three treatment groups in hunger and satiety scores and food preferences.
Long-term supplementation of 30 or 45 g of the dextrin NUTRIOSE FB per day was well tolerated, and may act as a pre-biotic supplement.
TNO Quality of Life was assigned by Roquette Frères to perform the study.
确定NUTRIOSE FB在男性中的胃肠道耐受性。
一项随机、安慰剂对照、平行、双盲研究。
荷兰应用科学研究院生活质量代谢病房。
48名受试者开始本研究,其中16名男性参与三种治疗中的一种。受试者每天分别摄入22.5克纯麦芽糊精(Glucidex 6),或30克或45克糊精NUTRIOSE FB,持续4 - 5周。43名受试者完成了研究(年龄:34.7±8.2岁;体重指数24.9±3.3千克/平方米)。
通过胃肠道不适问卷检查NUTRIOSE FB的耐受性;通过粪便分析检查对结肠菌群的有效性;通过呼气氢排泄测量检查发酵情况。此外,在研究中还检查了对体重、能量摄入和血液参数的影响。
两种剂量的NUTRIOSE FB耐受性都非常好,胃肠道不适与安慰剂治疗几乎没有差异。未报告因补充NUTRIOSE FB导致腹泻。在研究过程中,发现胃肠道症状有一些适应性变化。NUTRIOSE FB治疗对发酵和粪便特征(pH值和酶活性)有显著的积极影响。NUTRIOSE FB两个组的体重随时间保持稳定,尽管安慰剂治疗组的体重有小幅增加(第35天至第1天增加0.8±1.0千克)(P = 0.07)。然而,在整个研究过程中,食物总摄入量和饮食中的宏量营养素组成保持不变。三个治疗组在饥饿和饱腹感评分以及食物偏好方面没有发现显著差异。
每天长期补充30克或45克糊精NUTRIOSE FB耐受性良好,可能作为益生元补充剂。
罗盖特兄弟公司委托荷兰应用科学研究院生活质量部进行本研究。