人脑神经复杂性产前发育的性别差异

Joel Frohlich, Julia Moser, Katrin Sippel, Pedro A. M. Mediano, Hubert Preissl, Alireza Gharabaghi
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摘要

神经活动的复杂性是大脑皮层回路健康功能的常用读数。以前的研究发现,神经复杂性与早产儿的母体护理水平有关,而早产儿有患精神疾病的风险,但神经复杂性在人类早期发育过程中的演变在很大程度上是未知的。我们假设,随着出生日期的临近,大脑皮层的动态进化将优化信息处理,从而增加大脑皮层活动的复杂性。为了验证这一假设,我们进行了一项有关出生前神经复杂性与成熟的队列研究。我们从胎儿和新生儿样本中获得了脑磁图(MEG)记录,包括出生前后的纵向数据。利用大脑皮层对听觉不规则现象的反应,我们计算了几种反映脑磁图信号复杂性的熵指标。尽管我们提出了假设,但随着胎儿和新生儿的成熟,神经复杂性显著下降。此外,我们还发现,就大多数熵指标而言,男性胎儿的神经复杂性下降得更快。我们令人惊讶的结果描绘了围产期人类发育过程中神经复杂性的演变,并为未来将胎儿神经复杂性与发育表型相关联的工作奠定了基础,尤其是在围产期风险领域,因为该领域非常需要生物标记物。一项脑磁图研究提供了证据,证明神经信号的复杂性随着人类胎儿和新生儿大脑的成熟而下降,男性胎儿下降得更快。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Sex differences in prenatal development of neural complexity in the human brain

Sex differences in prenatal development of neural complexity in the human brain
The complexity of neural activity is a commonly used readout of healthy functioning in cortical circuits. Previous work has linked neural complexity to the level of maternal care in preterm infants at risk for developing mental disorders, yet the evolution of neural complexity in early human development is largely unknown. We hypothesized that cortical dynamics would evolve to optimize information processing as birth approaches, thereby increasing the complexity of cortical activity. To test this hypothesis, we conducted a cohort study relating prenatal neural complexity to maturation. Magnetoencephalography (MEG) recordings were obtained from a sample of fetuses and newborns, including longitudinal data before and after birth. Using cortical responses to auditory irregularities, we computed several entropy measures that reflect the complexity of the MEG signal. Despite our hypothesis, neural complexity decreased significantly with maturation in both fetuses and newborns. Furthermore, we found that complexity decreased significantly faster in male fetuses for most entropy measures. Our surprising results chart the evolution of neural complexity in perinatal human development and may lay a foundation for future work that would relate fetal neural complexity to developmental phenotypes, especially in the area of perinatal risk where biomarkers are greatly needed. A magnetoencephalography study provides evidence that neural signal complexity declines with brain maturation in human fetuses and newborns and the decline occurs faster in male fetuses.
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