Blood Biomarkers in the Fetally Growth Restricted and Small for Gestational Age Neonate: Associations with Brain Injury.

IF 2.3 4区 医学 Q2 DEVELOPMENTAL BIOLOGY Developmental Neuroscience Pub Date : 2024-01-01 Epub Date: 2023-05-10 DOI:10.1159/000530492
Hannah Musco, Kate Beecher, Kirat K Chand, Paul B Colditz, Julie A Wixey
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Abstract

Fetal growth restriction (FGR) and small for gestational age (SGA) infants have increased risk of mortality and morbidity. Although both FGR and SGA infants have low birthweights for gestational age, a diagnosis of FGR also requires assessments of umbilical artery Doppler, physiological determinants, neonatal features of malnutrition, and in utero growth retardation. Both FGR and SGA are associated with adverse neurodevelopmental outcomes ranging from learning and behavioral difficulties to cerebral palsy. Up to 50% of FGR, newborns are not diagnosed until around the time of birth, yet this diagnosis lacks further indication of the risk of brain injury or adverse neurodevelopmental outcomes. Blood biomarkers may be a promising tool. Defining blood biomarkers indicating an infant's risk of brain injury would provide the opportunity for early detection and therefore earlier support. The aim of this review was to summarize the current literature to assist in guiding the future direction for the early detection of adverse brain outcomes in FGR and SGA neonates. The studies investigated potential diagnostic blood biomarkers from cord and neonatal blood or serum from FGR and SGA human neonates. Results were often conflicting with heterogeneity common in the biomarkers examined, timepoints, gestational age, and definitions of FGR and SGA used. Due to these variations, it was difficult to draw strong conclusions from the results. The search for blood biomarkers of brain injury in FGR and SGA neonates should continue as early detection and intervention is critical to improve outcomes for these neonates.

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胎儿生长受限和胎龄小新生儿的血液生物标志物:与脑损伤的关系
胎儿生长受限(FGR)和胎龄小(SGA)婴儿的死亡和发病风险都会增加。虽然 FGR 和 SGA 婴儿的出生体重都低于胎龄,但诊断 FGR 还需要评估脐动脉多普勒、生理决定因素、新生儿营养不良特征和子宫内生长迟缓。FGR 和 SGA 都与不良的神经发育结果有关,从学习和行为障碍到脑瘫不等。多达 50% 的 FGR 新生儿直到出生时才被确诊,但这一诊断并不能进一步说明脑损伤或不良神经发育结果的风险。血液生物标志物可能是一种很有前途的工具。确定表明婴儿脑损伤风险的血液生物标志物将为早期检测提供机会,从而尽早提供支持。本综述旨在总结目前的文献,以帮助指导未来早期检测FGR和SGA新生儿不良脑损伤的方向。这些研究调查了来自FGR和SGA新生儿的脐带血、新生儿血或血清中的潜在诊断性血液生物标志物。研究结果往往相互矛盾,在所研究的生物标志物、时间点、胎龄以及所使用的 FGR 和 SGA 定义方面普遍存在异质性。由于这些差异,很难从结果中得出有力的结论。应继续寻找FGR和SGA新生儿脑损伤的血液生物标志物,因为早期检测和干预对改善这些新生儿的预后至关重要。
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来源期刊
Developmental Neuroscience
Developmental Neuroscience 医学-发育生物学
CiteScore
4.00
自引率
3.40%
发文量
49
审稿时长
>12 weeks
期刊介绍: ''Developmental Neuroscience'' is a multidisciplinary journal publishing papers covering all stages of invertebrate, vertebrate and human brain development. Emphasis is placed on publishing fundamental as well as translational studies that contribute to our understanding of mechanisms of normal development as well as genetic and environmental causes of abnormal brain development. The journal thus provides valuable information for both physicians and biologists. To meet the rapidly expanding information needs of its readers, the journal combines original papers that report on progress and advances in developmental neuroscience with concise mini-reviews that provide a timely overview of key topics, new insights and ongoing controversies. The editorial standards of ''Developmental Neuroscience'' are high. We are committed to publishing only high quality, complete papers that make significant contributions to the field.
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