Division of Neonatology, Department of Pediatrics, University of Rochester, Rochester, NY, USA.
Division of Developmental and Behavioral Pediatrics, University of Rochester, Rochester, NY, USA.
Pediatr Res. 2019 Jan;85(2):191-197. doi: 10.1038/s41390-018-0216-4. Epub 2018 Oct 23.
Bilirubin-induced brain injury in the neonatal period has detrimental effects on neurodevelopment that persist into childhood and adulthood, contributing to childhood developmental disorders. Unconjugated bilirubin is a potent antioxidant that may be useful for protecting against oxidative injuries, but it becomes a potent neurotoxin once it crosses the blood brain barrier. Because bilirubin toxicity involves a myriad of pathological mechanisms, can damage most types of brain cells, and affects brain circuits or loops that influence cognition, learning, behavior, sensory, and language, the clinical effects of bilirubin-induced neurotoxicity are likely to be manifold. One possible effect that several experts have identified is bilirubin-induced neurological dysfunction (subtle kernicterus). However, the underlying biological mechanisms or pathways by which subtle kernicterus could lead to developmental disorders has not been elucidated previously. Our aim in this review is to describe a spectrum of developmental disorders that may reflect subtle kernicterus and outline plausible biological mechanisms for this possible association. We review existing evidence that support or refute the association between unconjugated hyperbilirubinemia and developmental disorders, and limitations associated with these studies.
胆红素引起的新生儿期脑损伤对神经发育有不良影响,并持续到儿童期和成年期,导致儿童发育障碍。未结合胆红素是一种有效的抗氧化剂,可用于预防氧化损伤,但一旦它穿过血脑屏障,就会变成一种有效的神经毒素。由于胆红素毒性涉及多种病理机制,可损害大多数类型的脑细胞,并影响影响认知、学习、行为、感觉和语言的脑回路或环路,胆红素诱导的神经毒性的临床影响可能是多方面的。一些专家已经确定的一个可能的影响是胆红素诱导的神经功能障碍(轻微核黄疸)。然而,以前尚未阐明轻微核黄疸如何导致发育障碍的潜在生物学机制或途径。我们在这篇综述中的目的是描述可能反映轻微核黄疸的一系列发育障碍,并概述这种可能关联的合理生物学机制。我们回顾了现有的证据,这些证据支持或反驳未结合高胆红素血症与发育障碍之间的关联,以及这些研究的局限性。