Fewtrell Mary S, Morley Ruth, Abbott Rebecca A, Singhal Atul, Isaacs Elizabeth B, Stephenson Terence, MacFadyen Una, Lucas Alan
MRC Childhood Nutrition Research Center, Institute of Child Health, London, United Kingdom.
Pediatrics. 2002 Jul;110(1 Pt 1):73-82. doi: 10.1542/peds.110.1.73.
We tested the hypothesis that balanced addition of long-chain polyunsaturated fatty acid (LCPUFA) to preterm formula during the first weeks of life would confer long-term neurodevelopmental advantage in a double-blind, randomized, controlled trial of preterm formula with and without preformed LCPUFA.
The participants were 195 formula-fed preterm infants (birth weight <1750 g, gestation <37 weeks) from 2 UK neonatal units and 88 breast milk-fed infants. Main outcome measures were Bayley Mental Developmental Index (MDI) and Psychomotor Developmental Index (PDI) at 18 months and Knobloch, Passamanick and Sherrard's Developmental Screening Inventory at 9 months' corrected age. Safety outcome measures were anthropometry at 9 and 18 months, tolerance, infection, necrotizing enterocolitis, and death.
There were no significant differences in developmental scores between randomized groups, although infants who were fed LCPUFA-supplemented formula showed a nonsignificant 2.6-point (0.25 standard deviation) advantage in MDI and PDI at 18 months, with a greater (nonsignificant) advantage (MDI: 4.5 points; PDI: 5.8 points) in infants below 30 weeks' gestation. LCPUFA-supplemented infants were shorter than control infants at 18 months (difference in length standard deviation score: 0.44; 95% confidence interval: 0.08-0.8). No other significant short- or long-term differences in safety outcomes were observed. Breastfed infants had significantly higher developmental scores at 9 and 18 months than both formula groups and were significantly heavier and longer at 18 months than LCPUFA-supplemented but not control infants.
With the dose, duration, and preparation of LCPUFA used, efficacy was not demonstrated, although an advantage in later neurodevelopment cannot be excluded by global tests of development up to 18 months, particularly in infants below 30 weeks' gestation. The surprising effect of LCPUFA-supplemented formula on growth 18 months beyond the intervention period needs to be confirmed in other studies using similar supplementation strategies. Additional follow-up of this cohort is critical at an age when more specific tests of cognitive function are possible.
在一项针对添加和未添加预制长链多不饱和脂肪酸(LCPUFA)的早产配方奶粉的双盲、随机对照试验中,我们检验了在生命最初几周向早产配方奶粉中均衡添加LCPUFA会带来长期神经发育优势这一假设。
参与者为来自英国2个新生儿病房的195名配方奶喂养的早产儿(出生体重<1750 g,孕周<37周)和88名母乳喂养的婴儿。主要结局指标为18个月时的贝利智力发育指数(MDI)和精神运动发育指数(PDI),以及矫正年龄9个月时的诺布罗克、帕萨马尼克和谢拉德发育筛查量表。安全性结局指标为9个月和18个月时的人体测量、耐受性、感染、坏死性小肠结肠炎和死亡情况。
随机分组的各组之间发育评分无显著差异,尽管喂养添加LCPUFA配方奶粉的婴儿在18个月时MDI和PDI有2.6分(0.25标准差)的非显著优势,孕周低于30周的婴儿优势更大(非显著)(MDI:4.5分;PDI:5.8分)。添加LCPUFA的婴儿在18个月时比对照婴儿更矮(身长标准差得分差异:0.44;95%置信区间:0.08 - 0.8)。未观察到其他安全性结局方面的显著短期或长期差异。母乳喂养的婴儿在9个月和18个月时的发育评分显著高于两个配方奶组,且在18个月时比添加LCPUFA的婴儿更重、更高,但比对照婴儿无显著差异。
就所使用的LCPUFA剂量、持续时间和制剂而言,未证明其有效性,尽管在18个月的整体发育测试中不能排除其对后期神经发育有优势,特别是对于孕周低于30周的婴儿。添加LCPUFA配方奶粉在干预期后18个月对生长的惊人影响需要在其他使用类似补充策略的研究中得到证实。在能够进行更具体认知功能测试的年龄对该队列进行额外随访至关重要。