DeLong G R, Glick T H
Pediatrics. 1982 Jan;69(1):53-63.
The pathogenesis of Reye's syndrome encephalopathy was analyzed in terms of uniform criteria designed to clarify and assist evaluation of the leading hypotheses. Three of these hypotheses derive from known metabolic sequelae of hepatic mitochondrial dysfunction and the severe systemic catabolism of protein, fats, and carbohydrates that characterize the syndrome biochemically: hyperammonemia, hyperfattyacidemia, and hyperlactatemia. In addition, there is a fourth hypothesis of generalized mitochondrial insult affecting brain, muscle, and other organs as well as liver. The weight of evidence favors hyperammononemia as a sufficient factor while recognizing important interrelationships with the other observed biochemical derangements. How the catabolism and hepatic mitochondrial dysfunction are produced by the triggering viral infection remains unknown. Therapeutic efforts have thus far not succeeded in definitive metabolic intervention. Such reversal of the clinical syndrome would lead to confirmation of the necessary pathogenetic factors; this type of intervention remains the chief goal of metabolic research in Reye's syndrome.
根据旨在阐明和辅助评估主要假说的统一标准,对瑞氏综合征脑病的发病机制进行了分析。其中三个假说源于肝线粒体功能障碍已知的代谢后遗症以及该综合征生化特征所具有的蛋白质、脂肪和碳水化合物的严重全身分解代谢:高氨血症、高脂肪酸血症和高乳酸血症。此外,还有第四个假说,即全身性线粒体损伤会影响大脑、肌肉以及肝脏和其他器官。现有证据倾向于认为高氨血症是一个充分因素,同时也认识到它与其他观察到的生化紊乱之间存在重要的相互关系。引发病毒感染如何导致分解代谢和肝线粒体功能障碍仍不清楚。迄今为止,治疗措施尚未成功实现确定性的代谢干预。这种临床综合征的逆转将证实必要的致病因素;这种干预类型仍然是瑞氏综合征代谢研究的主要目标。