Siri Barbara, Greco Benedetta, Martinelli Diego, Cairoli Sara, Guarnera Alessia, Longo Daniela, Napolitano Antonio, Parrillo Chiara, Ravà Lucilla, Simeoli Raffaele, Spagnoletti Gionata, Taurisano Roberta, Veraldi Silvio, Pietrobattista Andrea, Spada Marco, Dionisi-Vici Carlo
Division of Metabolic Diseases and Hepatology, Bambino Gesù Children's Hospital IRCCS, Rome, Italy.
Neuroradiology Unit, Imaging Department, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
J Inherit Metab Dis. 2025 Jan;48(1):e12843. doi: 10.1002/jimd.12843.
Liver transplantation (LTx) is increasingly used in Urea Cycle Defects (UCDs) to prevent recurrent hyperammonemia and related neurological irreversible injury. Among UCDs, argininosuccinate lyase deficiency (ASLD) has a more complex phenotype than other UCDs, with long-term neurocognitive deficits. Therefore, the role of LTx in ASLD is still debated. The impact of LTx on nine patients with early-onset ASLD was assessed through pre- and post-LTx clinical, neuropsychological, MRI and biochemical evaluations. After LTx, no episodes of metabolic decompensations were reported. Neuropsychological evaluations documented significant improvement in cognitive/developmental functioning especially in patients transplanted in early childhood. Improvements were also highlighted in daily living skills and emotional-behavioral problems, with a reduction in attention disturbances and somatic complaints. Movement disorders resolved after LTx in patient transplanted in early childhood. Any patients developed epilepsy with stability of EEG alterations after LTx. A positive effect of LTx on other disease-related outcomes such as growth, diet, medications, hospitalizations, and long-term ASLD-related complications was highlighted. The primary biomarker argininosuccinic acid dramatically reduced in plasma after transplantation with a decreasing trend in CSF at long-term follow-up. Moreover, health-related quality of life improved after LTx, especially when assessed through MetabQoL, a tool designed for intoxication diseases such as ASLD. In conclusion, our study showed a global beneficial impact of LTx in early-onset ASLD patients to avoid episodes of hyperammonemia, and improve neurocognitive outcome, adaptive and behavioral deficits when performed in early childhood with a dramatic benefit in terms of quality of life.
肝移植(LTx)越来越多地用于尿素循环障碍(UCDs),以预防复发性高氨血症及相关的不可逆神经损伤。在UCDs中,精氨琥珀酸裂解酶缺乏症(ASLD)的表型比其他UCDs更为复杂,存在长期神经认知缺陷。因此,肝移植在ASLD中的作用仍存在争议。通过肝移植前后的临床、神经心理学、MRI和生化评估,评估了肝移植对9例早发型ASLD患者的影响。肝移植后,未报告代谢失代偿事件。神经心理学评估表明,认知/发育功能有显著改善,尤其是在幼儿期接受移植的患者中。日常生活技能和情绪行为问题也有改善,注意力障碍和躯体不适减少。幼儿期接受移植的患者肝移植后运动障碍得到解决。肝移植后,没有患者发生癫痫,脑电图改变保持稳定。肝移植对其他疾病相关结局,如生长、饮食、药物治疗、住院次数和长期ASLD相关并发症也有积极影响。主要生物标志物精氨琥珀酸在移植后血浆中显著降低,长期随访时脑脊液中有下降趋势。此外,肝移植后健康相关生活质量得到改善,尤其是通过MetabQoL评估时,MetabQoL是一种针对ASLD等中毒性疾病设计的工具。总之,我们的研究表明,肝移植对早发型ASLD患者具有全面的有益影响,可避免高氨血症发作,改善神经认知结局、适应性和行为缺陷,在幼儿期进行肝移植对生活质量有显著益处。