Liver and liver/kidney transplantation are increasingly used in methylmalonic aciduria, but little is known on their impact on CNS. The effect of transplantation on neurological outcome was prospectively assessed in six patients pre- and post-transplant by clinical evaluation and by measuring disease biomarkers in plasma and CSF, in combination with psychometric tests and brain MRI studies. Primary (methylmalonic- and methylcitric acid) and secondary biomarkers (glycine and glutamine) significantly improved in plasma, while they remained unchanged in CSF. Differently, biomarkers of mitochondrial dysfunction (lactate, alanine, and related ratios) significantly decreased in CSF. Neurocognitive evaluation documented significant higher post-transplant developmental/cognitive scores and maturation of executive functions corresponding to improvement of brain atrophy, cortical thickness, and white matter maturation indexes at MRI. Three patients presented post-transplantation reversible neurological events, which were differentiated, by means of biochemical and neuroradiological evaluations, into calcineurin inhibitor-induced neurotoxicity and metabolic stroke-like episode. Our study shows that transplantation has a beneficial impact on neurological outcome in methylmalonic aciduria. Early transplantation is recommended due to the high risk of long-term complications, high disease burden, and low quality of life.

Martinelli, D., Catesini, G., Greco, B., Guarnera, A., Parrillo, C., Maines, E., Longo, D., Napolitano, A., De Nictolis, F., Cairoli, S., Liccardo, D., Caviglia, S., Sidorina, A., Olivieri, G., Siri, B., Bianchi, R., Spagnoletti, G., Dello Strologo, L., Spada, M., Dionisi-Vici, C., Neurologic outcome following liver transplantation for methylmalonic aciduria, <<JOURNAL OF INHERITED METABOLIC DISEASE>>, 2023; 46 (3): 450-465. [doi:10.1002/jimd.12599] [https://hdl.handle.net/10807/288300]

Neurologic outcome following liver transplantation for methylmalonic aciduria

Spagnoletti, Gionata;Dello Strologo, Luca;
2023

Abstract

Liver and liver/kidney transplantation are increasingly used in methylmalonic aciduria, but little is known on their impact on CNS. The effect of transplantation on neurological outcome was prospectively assessed in six patients pre- and post-transplant by clinical evaluation and by measuring disease biomarkers in plasma and CSF, in combination with psychometric tests and brain MRI studies. Primary (methylmalonic- and methylcitric acid) and secondary biomarkers (glycine and glutamine) significantly improved in plasma, while they remained unchanged in CSF. Differently, biomarkers of mitochondrial dysfunction (lactate, alanine, and related ratios) significantly decreased in CSF. Neurocognitive evaluation documented significant higher post-transplant developmental/cognitive scores and maturation of executive functions corresponding to improvement of brain atrophy, cortical thickness, and white matter maturation indexes at MRI. Three patients presented post-transplantation reversible neurological events, which were differentiated, by means of biochemical and neuroradiological evaluations, into calcineurin inhibitor-induced neurotoxicity and metabolic stroke-like episode. Our study shows that transplantation has a beneficial impact on neurological outcome in methylmalonic aciduria. Early transplantation is recommended due to the high risk of long-term complications, high disease burden, and low quality of life.
2023
Inglese
Martinelli, D., Catesini, G., Greco, B., Guarnera, A., Parrillo, C., Maines, E., Longo, D., Napolitano, A., De Nictolis, F., Cairoli, S., Liccardo, D., Caviglia, S., Sidorina, A., Olivieri, G., Siri, B., Bianchi, R., Spagnoletti, G., Dello Strologo, L., Spada, M., Dionisi-Vici, C., Neurologic outcome following liver transplantation for methylmalonic aciduria, <<JOURNAL OF INHERITED METABOLIC DISEASE>>, 2023; 46 (3): 450-465. [doi:10.1002/jimd.12599] [https://hdl.handle.net/10807/288300]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10807/288300
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