Maternal obesity and offspring neurodevelopment: Mechanisms, risks, and prevention opportunities.

IF 1.5 3区 生物学 Q2 ANATOMY & MORPHOLOGY
Iroda Djamalutdinova, Khusan Turdibekov, Azam Kholikov, Diyorjon Abdullaev, Gulsara Ruziyeva
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Abstract

The prevalence of maternal obesity is continuously increasing worldwide, making maternal overweight and obesity one of the most important early life risk factors that can affect the neurodevelopment of offspring. Data from large epidemiological studies indicate that higher prepregnancy BMI, as well as excessive weight gain during pregnancy, are associated with an increased risk of autism spectrum disorder, attention deficit/hyperactivity disorder, internalizing symptoms, cognitive impairment, cerebral palsy, and other neurodevelopmental outcomes. Preclinical studies have also provided a clearer understanding of the biological mechanisms, suggesting that maternal obesity can induce oxidative stress, metabolic inflammation, and placental dysfunction, which impair nutrient and oxygen delivery during critical periods of brain development. Other proposed pathways include activation of microglia and astroglia, dysbiosis of the gut microbiota with alterations in microbial metabolites, epigenetic rearrangements of DNA and histones, and disruption of serotonergic and dopaminergic signaling. Collectively, these biological alterations affect processes such as synaptogenesis, neuroimmune maturation, and neuroplasticity, and sex-specific and even multigenerational effects have been reported in animal studies. Although the presence of familial factors and socioeconomic conditions makes it difficult to draw causal conclusions in human studies, the body of evidence supports the existence of a real biological vulnerability. Various interventions, including improved maternal nutrition, n-3 fatty acid intake, antioxidant strategies, and prenatal physical activity, have shown promising potential to improve metabolic and inflammatory status during pregnancy. Understanding these intertwined mechanisms highlights the importance of early prevention and implementation of targeted maternal health strategies to achieve the best neurodevelopmental outcomes in offspring.

母亲肥胖与后代神经发育:机制、风险和预防机会。
在世界范围内,孕产妇肥胖患病率不断上升,使孕产妇超重和肥胖成为影响后代神经发育的最重要的早期生命危险因素之一。来自大型流行病学研究的数据表明,较高的孕前BMI以及孕期体重过度增加与自闭症谱系障碍、注意力缺陷/多动障碍、内化症状、认知障碍、脑瘫和其他神经发育后果的风险增加有关。临床前研究也为其生物学机制提供了更清晰的认识,表明母体肥胖可诱导氧化应激、代谢性炎症和胎盘功能障碍,从而损害大脑发育关键时期的营养和氧气输送。其他提出的途径包括小胶质细胞和星形胶质细胞的激活,肠道微生物群的生态失调,微生物代谢物的改变,DNA和组蛋白的表观遗传重排,血清素能和多巴胺能信号的破坏。总的来说,这些生物学改变影响突触发生、神经免疫成熟和神经可塑性等过程,性别特异性甚至多代效应已在动物研究中得到报道。虽然家族因素和社会经济条件的存在使得在人体研究中难以得出因果结论,但大量证据支持存在真正的生物脆弱性。各种干预措施,包括改善孕产妇营养、n-3脂肪酸摄入、抗氧化策略和产前体育活动,已经显示出改善妊娠期间代谢和炎症状态的良好潜力。了解这些相互交织的机制突出了早期预防和实施有针对性的孕产妇保健战略的重要性,以实现后代的最佳神经发育结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Developmental Dynamics
Developmental Dynamics 生物-发育生物学
CiteScore
5.10
自引率
8.00%
发文量
116
审稿时长
3-8 weeks
期刊介绍: Developmental Dynamics, is an official publication of the American Association for Anatomy. This peer reviewed journal provides an international forum for publishing novel discoveries, using any model system, that advances our understanding of development, morphology, form and function, evolution, disease, stem cells, repair and regeneration.
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