Florey Institute of Neuroscience and Mental Health, Parkville, VIC, Australia; University of Melbourne, Department of Florey Institute of Neuroscience and Mental Health, Parkville, VIC, Australia.
Florey Institute of Neuroscience and Mental Health, Parkville, VIC, Australia.
Brain Behav Immun. 2024 Nov;122:471-482. doi: 10.1016/j.bbi.2024.08.033. Epub 2024 Aug 18.
Increasing rates of child neurodevelopmental vulnerability are a significant public health challenge. The adverse effect of socioeconomic adversity on offspring cognition may be mediated through elevated prenatal maternal systemic inflammation, but the role of modifiable antecedents such as maternal nutrition has not yet been clarified. This study aimed to examine (1) whether prenatal factors, with an emphasis on maternal nutrition, were associated with prenatal maternal systemic inflammation at 28 weeks' gestation, including the metabolomic marker glycoprotein acetyls (GlycA); (2) the extent to which the association between prenatal maternal nutrition and child cognition and language at age two years was mediated by elevated maternal inflammation in pregnancy; (3) the extent to which the associations between prenatal socioeconomic adversity and child neurodevelopment were mediated through prenatal maternal nutrition and GlycA levels. We used a prospective population-derived pre-birth longitudinal cohort study, the Barwon Infant Study (Barwon region of Victoria, Australia), where 1074 mother-child pairs were recruited by 28 weeks' gestation using an unselected sampling frame. Exposures included prenatal factors such as maternal diet measured by a validated food frequency questionnaire at 28 weeks' gestation and dietary patterns determined by principal component analysis. The main outcome measures were maternal inflammatory biomarkers (GlycA and hsCRP levels) at 28 weeks' gestation, and offspring Bayley-III cognition and language scores at age two years. Results showed that the 'modern wholefoods' and 'processed' maternal dietary patterns were independently associated with reduced and elevated maternal inflammation respectively (GlycA or hsCRP p < 0.001), and also with higher and reduced offspring Bayley-III scores respectively (cognition p ≤ 0.004, language p ≤ 0.009). Associations between dietary patterns and offspring cognition and language were partially mediated by higher maternal GlycA (indirect effect: cognition p ≤ 0.036, language p ≤ 0.05), but were less evident for hsCRP. The maternal dietary patterns mediated 22 % of the association between socioeconomic adversity (lower maternal education and/or lower household income vs otherwise) and poorer offspring cognition (indirect effect p = 0.001). Variation in prenatal GlycA levels that were independent of these dietary measures appeared less important. In conclusion, modifiable prenatal maternal dietary patterns were associated with adverse child neurocognitive outcomes through their effect on maternal inflammation (GlycA). Maternal diet may partially explain the association between socioeconomic adversity and child neurocognitive vulnerability. Maternal diet-by-inflammation pathways are an attractive target for future intervention studies.
儿童神经发育脆弱性的发生率不断上升,是一个重大的公共卫生挑战。社会经济逆境对后代认知的不利影响可能通过升高的产前母体全身炎症来介导,但母体营养等可改变的前置因素的作用尚未阐明。本研究旨在检验:(1) 产前因素(重点是母体营养)是否与 28 孕周的母体全身炎症相关,包括代谢标志物糖蛋白乙酰基(GlycA);(2) 妊娠期间母体炎症在多大程度上介导了产前母体营养与儿童 2 岁时认知和语言的关联;(3) 产前社会经济逆境与儿童神经发育之间的关联在多大程度上通过产前母体营养和 GlycA 水平来介导。我们使用了一项前瞻性人群衍生的产前纵向队列研究,即 Barwon 婴儿研究(澳大利亚维多利亚州的 Barwon 地区),该研究在 28 孕周时通过无选择的抽样框架招募了 1074 对母婴。暴露因素包括 28 孕周时通过验证后的食物频率问卷测量的母体饮食以及通过主成分分析确定的饮食模式。主要结局测量指标为 28 孕周时的母体炎症生物标志物(GlycA 和 hsCRP 水平)以及儿童 2 岁时的贝利婴幼儿发展量表认知和语言评分。结果显示,“现代全食物”和“加工”两种母体饮食模式分别与母体炎症的降低和升高独立相关(GlycA 或 hsCRP,p<0.001),也与较高和较低的儿童贝利婴幼儿发展量表评分相关(认知,p≤0.004;语言,p≤0.009)。饮食模式与儿童认知和语言之间的关联部分通过较高的母体 GlycA 来介导(间接效应:认知,p≤0.036;语言,p≤0.05),但 hsCRP 的影响较小。社会经济逆境(母亲教育程度较低和/或家庭收入较低)与较差的儿童认知之间的关联有 22%是通过母体饮食模式来介导(间接效应 p=0.001)。与这些饮食措施无关的产前 GlycA 水平的变化似乎不太重要。总之,可改变的产前母体饮食模式通过对母体炎症(GlycA)的影响,与不良的儿童神经认知结局相关。母亲的饮食可能部分解释了社会经济逆境与儿童神经认知脆弱性之间的关联。母体饮食-炎症途径是未来干预研究的一个有吸引力的目标。