肠道高剂量多可萨酸与极度早产婴儿的神经发育:系统性审查和元分析
Emily Shepherd1,2, Naho Ikeda1,3, Thomas R Sullivan1,4
1Women and Kids Theme, South Australian Health and Medical Research Institute, Adelaide, South Australia, Australia.
Current developments in nutrition
|September 2, 2025
概括
在极度早产的婴儿中,高剂量的多可萨赫萨诺酸 (DHA) 补充剂并没有显著改善整体认知评分. 然而,直接乳液形式显示出潜在的益处,支持目前对神经发育支持的建议.
科学领域:
- 新生儿医学
- 神经科学
- 营养科学
背景情况:
- 极度早产的婴儿可能需要高剂量的DHA来实现最佳的神经发育和认知.
- 在这种人群中,高剂量DHA对神经发育的疗效的证据有限.
研究的目的:
- 在新生儿期内输入高剂量的DHA与在怀孕29周或之前出生的婴儿的神经发育结果之间的关联.
- 综合DHA补充和婴儿神经发育随机对照试验 (RCT) 的证据.
主要方法:
- 在多个数据库 (CINAHL,Cochrane Library,Embase,Medline,Scopus,Web of Science) 进行了系统的文献搜索,截至2024年4月11日.
- 符合条件的RCT涉及妊娠29周以下的婴儿,评估直接肠道DHA (≥40 mg/kg/d) 或强化母乳/配方 (≥0.60%的总脂肪酸).
- 使用元分析汇总数据,以全球认知分数为主要结果.
主要成果:
- 其中包括3项高质量的RCT,涉及2028名婴儿. 在经过校正的18-36个月或5-7岁的年龄段,元分析显示全球认知得分没有显著差异.
- 然而,使用直接肠道乳液的最大RCT在5年后显示认知得分有所改善 (MD3. 45;95%CI:0. 38,6. 52).
- 高剂量的DHA与轻度运动和认知障碍的减少有关,没有观察到不良反应.
结论:
- 在超早产的婴儿中,高剂量的DHA补充并没有通过元分析对整体认知得分产生显著影响.
- 一种直接的肠道乳液形式的DHA显示出改善认知结果的潜力.
- 这些发现支持目前对这种脆弱人群的DHA补充剂的建议.
更多相关视频
07:36Modeling Encephalopathy of Prematurity Using Prenatal Hypoxia-ischemia with Intra-amniotic Lipopolysaccharide in Rats
Published on: November 20, 2015
11.4K
03:19Author Spotlight: Studying the Impact of Maternal Dietary Deficiencies on Long-Term Offspring Health Outcomes
Published on: June 28, 2024
495
相关概念视频
Teratogenicity
2.7K
The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...
2.7K
Drugs Affecting Neurotransmitter Synthesis
1.6K
Drugs affecting neurotransmitter synthesis can impact the adrenergic neuron and the synthesis of neurotransmitters. For example, α-methyltyrosine and carbidopa target specific enzymes involved in catecholamine synthesis. α-methyltyrosine inhibits the enzyme tyrosine hydroxylase, which converts tyrosine into dopamine. By blocking this enzyme, α-methyltyrosine reduces dopamine production and other catecholamines. Carbidopa, on the other hand, inhibits the enzyme dopa decarboxylase,...
1.6K
