Positive Clinical, Neuropsychological, and Metabolic Impact of Liver Transplantation in Patients With Argininosuccinate Lyase Deficiency
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.
Authors
- Benedetta Greco (ORCID: https://orcid.org/0000-0002-8598-2618)
- Chiara Parrillo (ORCID: https://orcid.org/0000-0001-6666-5601)
- Andrea Pietrobattista (ORCID: https://orcid.org/0000-0002-4426-0395)
- Sara Cairoli (ORCID: https://orcid.org/0000-0002-5925-0974)
- Roberta Taurisano
- Daniela Longo (ORCID: https://orcid.org/0000-0002-0097-736X)
- Gionata Spagnoletti (ORCID: https://orcid.org/0000-0003-2626-8147)
- Raffaele Simeoli (ORCID: https://orcid.org/0000-0002-3989-7703)
- Alessia Guarnera (ORCID: https://orcid.org/0000-0001-5529-7575)
- Lucilla Ravà (ORCID: https://orcid.org/0000-0002-3238-7807)
- Antonio Napolitano (ORCID: https://orcid.org/0000-0003-3258-6846)
- Barbara Siri (ORCID: https://orcid.org/0000-0002-2876-4745)
- Diego Martinelli (ORCID: https://orcid.org/0000-0002-9324-2871)
- Carlo Dionisi‐Vici (ORCID: https://orcid.org/0000-0002-0007-3379)
- Marco Spada (ORCID: https://orcid.org/0000-0002-8894-350X)
- Silvio Veraldi (ORCID: https://orcid.org/0000-0002-2509-9399)
Institutions
- Bambino Gesù Children's Hospital (IT)
- Istituti di Ricovero e Cura a Carattere Scientifico (IT)
Publication Details
- Journal
- Journal of Inherited Metabolic Disease
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1002/jimd.12843
- Citations
- 7
- Primary Topic
- Metabolism and Genetic Disorders
- Type
- article
- Field-Weighted Citation Impact
- 9.23
Funders
- Ospedale Pediatrico Bambino Gesù
- Ministero della Salute