Department of Pediatrics, Division of Neonatology, VU University Medical Center Amsterdam, De Boelelaan 1117, 1081 HV, Amsterdam, The Netherlands.
Eur J Pediatr. 2013 Mar;172(3):317-23. doi: 10.1007/s00431-012-1886-2. Epub 2012 Nov 7.
Short-term supplementation of non-human neutral and acidic oligosaccharides during the first postnatal weeks may enhance the maturation of the immune response in preterm infants and may lead to less allergic and infectious diseases during the first year of life. In a randomized controlled trial, 113 preterm infants (gestational age <32 weeks and/or birth weight <1500 g) were allocated to receive enteral neutral and acidic oligosaccharide supplementation or placebo between days 3 and 30 of life. The median age at follow-up was not different in both groups: 12 months corrected age (interquartile range [IQR], 11-15) in the prebiotic mixture group and 12 months corrected age in the placebo group (IQR, 10-19), respectively. In addition, baseline patient, maternal, and environmental characteristics were not different between the prebiotic mixture (n = 48) and placebo (n = 46) group. Incidence of allergic and infectious diseases was assessed by validated questionnaires. In total, 94/98 (96 %) of the eligible, surviving infants participated in this follow-up study. The incidence of atopic dermatitis (odds ratio [OR], 0.80; 95 % confidence interval [CI], 0.24-2.67), bronchial hyper-reactivity (OR, 1.04; 95 % CI, 0.38-2.87) and infections of the upper respiratory (OR, 0.95; 95 % CI, 0.37-2.44), lower respiratory (OR, 1.03; 95 % CI, 0.37-2.88), and gastrointestinal (OR, 1.77; 95 % CI, 0.55-5.73) tract was not different between the groups. Adjustment for potential confounding factors did not change the results of the primary analysis.
Short-term enteral supplementation of non-human neutral and acidic oligosaccharides during the neonatal period in preterm infants does not decrease the incidence of allergic and infectious diseases during the first year of life.
在新生儿期短期补充非人类中性和酸性低聚糖可能会增强早产儿的免疫成熟度,并可能导致生命的第一年中较少发生过敏和感染性疾病。在一项随机对照试验中,113 名早产儿(胎龄<32 周和/或出生体重<1500g)被分配在生命的第 3 天至第 30 天之间接受肠内中性和酸性低聚糖补充或安慰剂。两组的中位随访年龄无差异:分别为接受益生元混合物组的校正后 12 个月龄(四分位距[IQR],11-15)和安慰剂组的校正后 12 个月龄(IQR,10-19)。此外,两组之间的患者、产妇和环境基线特征无差异(益生元混合物组 n=48,安慰剂组 n=46)。通过验证的问卷评估过敏和感染性疾病的发生率。共有 98 名符合条件的存活婴儿中有 94 名(96%)参加了这项随访研究。特应性皮炎的发生率(比值比[OR],0.80;95%置信区间[CI],0.24-2.67)、支气管高反应性(OR,1.04;95%CI,0.38-2.87)和上呼吸道感染(OR,0.95;95%CI,0.37-2.44)、下呼吸道(OR,1.03;95%CI,0.37-2.88)和胃肠道(OR,1.77;95%CI,0.55-5.73)感染在两组之间无差异。调整潜在混杂因素并未改变主要分析的结果。
在早产儿新生儿期短期肠内补充非人类中性和酸性低聚糖不会降低生命第一年过敏和感染性疾病的发生率。