Delgado-Noguera Mario F, Calvache Jose Andres, Bonfill Cosp Xavier, Kotanidou Eleni P, Galli-Tsinopoulou Assimina
Departamento de Pediatria, Facultad Ciencias de la Salud, Universidad del Cauca, Colombia, Hospital Universitario San Jose, Departamento de Pediatría, Popayan, Cauca, Colombia, NA.
Cochrane Database Syst Rev. 2015 Jul 14;2015(7):CD007901. doi: 10.1002/14651858.CD007901.pub3.
Long chain polyunsaturated fatty acids (LCPUFA), especially docosahexaenoic acid (DHA), are the most abundant fatty acids in the brain and are necessary for growth and maturation of an infant's brain and retina. LCPUFAs are named "essential" because they cannot be synthesised efficiently by the human body and come from maternal diet. It remains controversial whether LCPUFA supplementation to breastfeeding mothers is beneficial for the development of their infants.
To assess the effectiveness and safety of supplementation with LCPUFA in breastfeeding mothers in the cognitive and physical development of their infants as well as safety for the mother and infant.
We searched the Cochrane Pregnancy and Childbirth Group's Trials Register (6 August 2014), CENTRAL (Cochrane Library 2014, Issue 8), PubMed (1966 to August 2014), EMBASE (1974 to August 2014), LILACS (1982 to August 2014), Google Scholar (August 2014) and reference lists of published narrative and systematic reviews.
Randomised controlled trials or cluster-randomised controlled trials evaluating the effects of LCPUFA supplementation on breastfeeding mothers (including the pregnancy period) and their infants.
Two review authors independently assessed eligibility and trial quality, performed data extraction and evaluated data accuracy.
We included eight randomised controlled trials involving 1567 women. All the studies were performed in high-income countries. The longest follow-up was seven years.We report the results from the longest follow-up time point from included studies. Overall, there was moderate quality evidence as assessed using the GRADE approach from these studies for the following outcomes measured beyond 24 months age of children: language development and child weight. There was low-quality evidence for the outcomes: Intelligence or solving problems ability, psychomotor development, child attention, and child visual acuity.We found no significant difference in children's neurodevelopment at long-term follow-up beyond 24 months: language development (standardised mean difference (SMD) -0.27, 95% confidence interval (CI) -0.56 to 0.02; two trials, 187 participants); intelligence or problem-solving ability (three trials, 238 participants; SMD 0.00, 95% CI -0.36 to 0.36); psychomotor development (SMD -0.11, 95% CI -0.48 to 0.26; one trial, 113 participants); motor development (SMD -0.23, 95% CI -0.60 to 0.14; one trial, 115 participants), or in general movements (risk ratio, RR, 1.12, 95% CI 0.58 to 2.14; one trial, 77 participants; at 12 weeks of life). However, child attention scores were better at five years of age in the group of children whose mothers had received supplementation with fatty acids (mean difference (MD) 4.70, 95% CI 1.30 to 8.10; one study, 110 participants)). In working memory and inhibitory control, we found no significant difference (MD -0.02 95% CI -0.07 to 0.03 one trial, 63 participants); the neurological optimality score did not present any difference (P value: 0.55).For child visual acuity, there was no significant difference (SMD 0.33, 95% CI -0.04 to 0.71; one trial, 111 participants).For growth, there were no significant differences in length (MD -0.39 cm, 95% CI -1.37 to 0.60; four trials, 441 participants), weight (MD 0.13 kg, 95% CI -0.49 to 0.74; four trials, 441 participants), and head circumference (MD 0.15 cm, 95% CI -0.27 to 0.58; three trials, 298 participants). Child fat mass and fat mass distribution did not differ between the intervention and control group (MD 2.10, 95% CI -0.48 to 4.68; one trial, 115 participants, MD -0.50, 95% CI -1.69 to 0.69; one trial, 165 participants, respectively).One study (117 infants) reported a significant difference in infant allergy at short-term follow-up (risk ratio (RR) 0.13, 95% CI 0.02 to 0.95), but not at medium-term follow-up (RR 0.52, 95% CI 0.17 to 1.59).We found no significant difference in two trials evaluating postpartum depression. Data were not possible to be pooled due to differences in the describing of the outcome. One study (89 women) did not find any significant difference between the LCPUFA supplementation and the control group at four weeks postpartum (MD 1.00, 95%CI -1.72 to 3.72).No adverse effects were reported.
AUTHORS' CONCLUSIONS: Based on the available evidence, LCPUFA supplementation did not appear to improve children's neurodevelopment, visual acuity or growth. In child attention at five years of age, weak evidence was found (one study) favouring the supplementation. Currently, there is inconclusive evidence to support or refute the practice of giving LCPUFA supplementation to breastfeeding mothers in order to improve neurodevelopment or visual acuity.
长链多不饱和脂肪酸(LCPUFA),尤其是二十二碳六烯酸(DHA),是大脑中含量最丰富的脂肪酸,对婴儿大脑和视网膜的生长及成熟至关重要。LCPUFA被称为“必需”脂肪酸,因为人体无法有效合成,需从母体饮食中获取。哺乳期母亲补充LCPUFA是否对婴儿发育有益仍存在争议。
评估哺乳期母亲补充LCPUFA对其婴儿认知和身体发育的有效性及安全性,以及对母婴的安全性。
我们检索了Cochrane妊娠与分娩组试验注册库(2014年8月6日)、CENTRAL(Cochrane图书馆2014年第8期)、PubMed(1966年至2014年8月)、EMBASE(1974年至2014年8月)、LILACS(1982年至2014年8月)、谷歌学术(2014年8月)以及已发表的叙述性综述和系统评价的参考文献列表。
评估补充LCPUFA对哺乳期母亲(包括孕期)及其婴儿影响的随机对照试验或整群随机对照试验。
两位综述作者独立评估纳入标准和试验质量,进行数据提取并评估数据准确性。
我们纳入了八项随机对照试验,涉及1567名女性。所有研究均在高收入国家进行。最长随访时间为七年。我们报告纳入研究中最长随访时间点的结果。总体而言,使用GRADE方法评估,这些研究在儿童24个月龄之后测量的以下结局方面有中等质量证据:语言发育和儿童体重。在以下结局方面有低质量证据:智力或解决问题能力、心理运动发育、儿童注意力和儿童视力。我们发现,在24个月之后的长期随访中,儿童神经发育无显著差异:语言发育(标准化均数差(SMD)-0.27,95%置信区间(CI)-0.56至0.02;两项试验,187名参与者);智力或解决问题能力(三项试验,238名参与者;SMD 0.00,95%CI -0.36至0.36);心理运动发育(SMD -0.11,95%CI -0.48至0.26;一项试验,113名参与者);运动发育(SMD -0.23,95%CI -0.60至0.14;一项试验,115名参与者),或一般运动(风险比,RR,1.12,95%CI 0.58至2.14;一项试验,77名参与者;在12周龄时)。然而,母亲接受脂肪酸补充的儿童组在五岁时的注意力得分更好(均数差(MD)4.70,95%CI 1.30至8.10;一项研究,110名参与者)。在工作记忆和抑制控制方面,我们未发现显著差异(MD -0.02,95%CI -0.07至0.03;一项试验,63名参与者);神经最优性得分无差异(P值:0.55)。对于儿童视力,无显著差异(SMD 0.33,95%CI -0.04至0.71;一项试验,111名参与者)。对于生长,在身长(MD -0.39厘米,95%CI -1.37至0.60;四项试验,441名参与者)、体重(MD 0.13千克,95%CI -0.49至0.74;四项试验,441名参与者)和头围(MD 0.15厘米,95%CI -0.27至0.58;三项试验,298名参与者)方面均无显著差异。干预组和对照组之间儿童脂肪量和脂肪量分布无差异(MD 2.10,95%CI -0.48至4.68;一项试验,115名参与者,MD -0.50,95%CI -1.69至0.69;一项试验,165名参与者,分别)。一项研究(117名婴儿)报告,在短期随访中婴儿过敏有显著差异(风险比(RR)0.13,95%CI 0.02至0.95),但在中期随访中无差异(RR 0.52,95%CI 0.17至1.59)。我们在两项评估产后抑郁症的试验中未发现显著差异。由于结局描述不同,数据无法合并。一项研究(89名女性)在产后四周未发现补充LCPUFA组与对照组之间有任何显著差异(MD 1.00,95%CI -1.72至3.72)。未报告不良反应。
基于现有证据,补充LCPUFA似乎并未改善儿童的神经发育、视力或生长。在五岁儿童的注意力方面,有微弱证据(一项研究)支持补充LCPUFA。目前,尚无确凿证据支持或反驳哺乳期母亲补充LCPUFA以改善神经发育或视力的做法。