Lee Brendan, Singh Rani H, Rhead William J, Sniderman King Lisa, Smith Wendy, Summar Marshall L
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Crit Care Clin. 2005 Oct;21(4 Suppl):S19-25. doi: 10.1016/j.ccc.2005.05.001.
Today, patients with urea cycle disorder (UCD) may survive well beyond infancy. The goal of keeping them in consistent nitrogen balance can be undermined by changing metabolic needs throughout various stages of life, resulting in hyperammonemia in the short term, and poor growth and development in the long term. The specific UCD genotype can affect the risk of metabolic destabilization and management difficulties, as can variable protein tolerance secondary to changing growth demands, biochemical complications, and environmental influences. Preventing catabolic stress is as important as controlling dietary protein intake for avoiding metabolic decompensation. Optimal treatment, specifically pharmacologic therapy, possible branched chain amino acid (BCAA) supplementation, accurate laboratory monitoring, and psychosocial support, requires thorough understanding and careful application of each component.
如今,尿素循环障碍(UCD)患者可能存活至婴儿期之后。在生命的各个阶段,代谢需求不断变化,这可能会破坏维持他们氮平衡稳定的目标,短期内导致高氨血症,长期则导致生长发育不良。特定的UCD基因型会影响代谢不稳定和管理困难的风险,生长需求变化、生化并发症及环境影响所导致的蛋白质耐受性差异也会产生同样的影响。预防分解代谢应激与控制饮食蛋白质摄入量对于避免代谢失代偿同样重要。最佳治疗,特别是药物治疗、可能的支链氨基酸(BCAA)补充、精确的实验室监测以及心理社会支持,需要对每个组成部分有透彻的理解并谨慎应用。