Positive Clinical, Neuropsychological, and Metabolic Impact of Liver Transplantation in Patients With Argininosuccinate Lyase Deficiency

J Inherit Metab Dis. 2025 Jan;48(1):e12843. doi: 10.1002/jimd.12843.

Abstract

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.

Keywords: Argininosuccinate lyase deficiency; argininosuccinic acid; developmental/intellectual quotient; liver transplantation; quality of life.

MeSH terms

  • Adolescent
  • Argininosuccinate Lyase / genetics
  • Argininosuccinic Acid*
  • Argininosuccinic Aciduria*
  • Biomarkers / blood
  • Child
  • Child, Preschool
  • Female
  • Humans
  • Hyperammonemia
  • Infant
  • Liver Transplantation*
  • Male
  • Neuropsychological Tests
  • Treatment Outcome

Substances

  • Argininosuccinic Acid
  • Argininosuccinate Lyase
  • Biomarkers

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