Saccone Gabriele, Saccone Irene, Berghella Vincenzo
a Department of Neuroscience , Reproductive Sciences and Dentistry, School of Medicine, University of Naples Federico II , Naples , Italy .
b Department of Pharmacy , University of Naples Federico II , Naples , Italy , and.
J Matern Fetal Neonatal Med. 2016;29(15):2389-97. doi: 10.3109/14767058.2015.1086742. Epub 2015 Sep 18.
The aim of this study was to provide evidence-based recommendations for omega-3 supplementation during pregnancy through a systematic review of level-1 data published on this topic.
We reviewed all randomized-controlled trials (RCTs) including women who were randomized to treatment with either omega-3 supplementation or control (placebo or no treatment) during pregnancy and analyzed all the outcomes reported in the trials, separately. We planned to evaluate the effect of omega-3 on: preterm birth (PTB); pre-eclampsia (PE) and intrauterine growth restriction (IUGR); gestational diabetes; perinatal mortality; small for gestational age (SGA) and birth weight; infant eye and brain development; and postpartum depression.
We identified 34 RCTs including 14 106 singletons and 2578 twins. These level-1 data showed that omega-3 was not associated with prevention of PTB, PE, IUGR, gestational diabetes, SGA, post-partum depression or better children development. Data about birth weight, perinatal mortality and childhood cognitive outcome were limited. Women with gestational diabetes who received omega-3 had significantly lower serum C-reactive protein concentrations, low incidence of hyperbilirubinemia in newborns and decreased newborns' hospitalization rate.
There was not enough evidence to support the routine use of omega-3 supplementation during pregnancy. Given the 73% significant decrease in perinatal death in the singleton gestations who started omega-3 supplementation ≤ 20 weeks, further research is needed. Large RCTs in multiple gestations and longer follow-up are also required.
本研究旨在通过对该主题发表的一级数据进行系统评价,为孕期补充ω-3提供循证建议。
我们检索了所有随机对照试验(RCT),这些试验纳入了孕期被随机分配接受ω-3补充剂治疗或对照(安慰剂或不治疗)的女性,并分别分析了试验中报告的所有结局。我们计划评估ω-3对以下方面的影响:早产(PTB);子痫前期(PE)和胎儿生长受限(IUGR);妊娠期糖尿病;围产期死亡率;小于胎龄儿(SGA)和出生体重;婴儿眼睛和大脑发育;以及产后抑郁。
我们确定了34项RCT,包括14106名单胎和2578对双胞胎。这些一级数据表明,ω-3与预防PTB、PE、IUGR、妊娠期糖尿病、SGA、产后抑郁或改善儿童发育无关。关于出生体重、围产期死亡率和儿童认知结局的数据有限。接受ω-3的妊娠期糖尿病女性血清C反应蛋白浓度显著降低,新生儿高胆红素血症发生率低,新生儿住院率降低。
没有足够的证据支持孕期常规使用ω-3补充剂。鉴于在妊娠≤20周开始补充ω-3的单胎妊娠中围产期死亡显著降低73%,需要进一步研究。还需要在多胎妊娠中进行大型RCT并进行更长时间的随访。