Romantsik Olga, Bruschettini Matteo, Ley David
Department of Clinical Sciences Lund, Pediatrics, Lund University, Skane University Hospital, Lund, Sweden.
Neoreviews. 2019 Nov;20(11):e636-e652. doi: 10.1542/neo.20-11-e636.
Germinal matrix-intraventricular hemorrhage (IVH) occurs in nearly half of infants born at less than 26 weeks' gestation. Up to 50% of survivors with IVH develop cerebral palsy, cognitive deficits, behavioral disorders, posthemorrhagic ventricular dilatation, or a combination of these sequelae. After the initial bleeding and the primary brain injury, inflammation and secondary brain injury might lead to periventricular leukomalacia or diffuse white matter injury. Potential factors that are involved include microglia and astrocyte activation, degradation of blood components with release of "toxic" products, infiltration of the brain by systemic immune cells, death of neuronal and glial cells, and arrest of preoligodendrocyte maturation. In addition, impairment of the blood-brain barrier may play a major role in the pathophysiology. A wide range of animal models has been used to explore causes and mechanisms leading to IVH-induced brain injury. Preclinical studies have identified potential targets for enhancing brain repair. However, little has been elucidated about the effectiveness of potential interventions in clinical studies. A systematic review of available preclinical and clinical studies might help identify research gaps and which types of interventions may be prioritized. Future trials should report clinically robust and long-term outcomes after IVH.
生发基质-脑室内出血(IVH)发生在近一半孕周小于26周出生的婴儿中。IVH幸存者中高达50%会出现脑瘫、认知缺陷、行为障碍、出血后脑室扩张或这些后遗症的组合。在初始出血和原发性脑损伤后,炎症和继发性脑损伤可能导致脑室周围白质软化或弥漫性白质损伤。涉及的潜在因素包括小胶质细胞和星形胶质细胞活化、血液成分降解并释放“有毒”产物、全身免疫细胞浸润大脑、神经元和神经胶质细胞死亡以及少突胶质前体细胞成熟停滞。此外,血脑屏障受损可能在病理生理学中起主要作用。已使用多种动物模型来探索导致IVH诱导脑损伤的原因和机制。临床前研究已经确定了增强脑修复的潜在靶点。然而,关于临床研究中潜在干预措施的有效性,目前了解甚少。对现有临床前和临床研究进行系统综述可能有助于确定研究空白以及哪些类型的干预措施可能需要优先考虑。未来的试验应报告IVH后临床稳健且长期的结果。