KidZ Health Castle, UZ Brussel, Vrije Universiteit Brussel, 1090 Jette, Belgium.
Centre Hospitalier Universitaire of Liège (CHU), Centre Hospitalier Régional of Liège (CHR), 4000 Liège, Belgium.
Nutrients. 2020 Nov 20;12(11):3560. doi: 10.3390/nu12113560.
This study investigated growth, safety, and tolerance in healthy infants consuming a partly fermented infant formula (IF) with postbiotics, 2'-linked fucosyllactose (2'-FL), a specific prebiotic mixture of short-chain galacto-oligosaccharides (scGOS) and long-chain fructo-oligosaccharides (lcFOS), and milk fat. This double-blind, controlled trial randomised 215 fully IF-fed infants ≤ 14 days of age to either: Test Group (IF) containing 26% fermented formula with postbiotics derived from Lactofidus fermentation process (including 3'-Galactosyllactose; 3'-GL), 0.8 g/100 mL scGOS/lcFOS (9:1), 0.1 g/100 mL 2'-FL, and milk fat), or Control group (IF with 0.8 g/100 mL scGOS/lcFOS (9:1)) until 17 weeks of age. Fully breastfed infants were included as a reference. Anthropometric measures, gastrointestinal symptoms, and safety were assessed monthly. Equivalence in weight gain (primary outcome) between the Test and Control groups was confirmed (difference in means -0.08 g/day; 90% CI (-1.47;1.31)) with estimated mean weight gain (SE) of 31.00 (0.59) g/day and 31.08 (0.60) g/day, respectively, (PP population, = 196). Equivalence in length and head circumference gain between the randomised groups was also confirmed. No statistically significant differences were observed in adverse events or gastrointestinal tolerance between randomised IF groups. A partly fermented IF with postbiotics, specific oligosaccharides, 2'-FL, and milk fat supports adequate infant growth and is safe and well-tolerated in healthy term infants.
本研究旨在调查食用添加后生元、2'-岩藻糖基乳糖(2'-FL)、特定短链半乳糖寡糖(scGOS)和长链果糖寡糖(lcFOS)混合物的部分发酵婴儿配方(IF)和乳脂的健康婴儿的生长、安全性和耐受性。这项双盲、对照试验将 215 名≤14 天的完全 IF 喂养婴儿随机分为试验组(IF)和对照组(IF)。试验组(IF)含 26%发酵配方,含有源自 Lactofidus 发酵过程的后生元(包括 3'-半乳糖基乳糖;3'-GL)、0.8 g/100 mL scGOS/lcFOS(9:1)、0.1 g/100 mL 2'-FL 和乳脂),对照组(IF 含 0.8 g/100 mL scGOS/lcFOS(9:1)),直至 17 周龄。完全母乳喂养的婴儿也被纳入参考组。每月评估体格测量、胃肠道症状和安全性。试验组和对照组之间体重增加(主要结局)的等效性得到确认(平均差值-0.08 g/天;90%置信区间(-1.47;1.31)),估计平均体重增加(SE)分别为 31.00(0.59)g/天和 31.08(0.60)g/天,(PP 人群,=196)。随机分组之间的长度和头围增加也得到了等效性确认。在随机 IF 组之间,不良事件或胃肠道耐受性没有观察到统计学上的显著差异。含有后生元、特定寡糖、2'-FL 和乳脂的部分发酵 IF 支持婴儿的充分生长,并且在健康足月婴儿中是安全且耐受良好的。