Neurologic outcome following liver transplantation for methylmalonic aciduria

Author:

Martinelli Diego1ORCID,Catesini Giulio1ORCID,Greco Benedetta12ORCID,Guarnera Alessia3ORCID,Parrillo Chiara4ORCID,Maines Evelina15ORCID,Longo Daniela3ORCID,Napolitano Antonio4ORCID,De Nictolis Francesca1,Cairoli Sara1ORCID,Liccardo Daniela6ORCID,Caviglia Stefania2ORCID,Sidorina Anna1ORCID,Olivieri Giorgia1ORCID,Siri Barbara1ORCID,Bianchi Roberto7ORCID,Spagnoletti Gionata8ORCID,Dello Strologo Luca9ORCID,Spada Marco8ORCID,Dionisi‐Vici Carlo1ORCID

Affiliation:

1. Division of Metabolism, Department of Pediatric Subspecialties Bambino Gesù Children's Hospital Rome Italy

2. Clinical Psychology Unit, Department of Neuroscience Bambino Gesù Children's Hospital, IRCCS Rome Italy

3. Neuroradiology Unit, Imaging Department Bambino Gesù Children's Hospital, IRCCS Rome Italy

4. Medical Physics Unit, Risk Management Enterprise Bambino Gesù Children's Hospital, IRCCS Rome Italy

5. Pediatric Department S.Chiara Hospital of Trento Trento Italy

6. Division of Hepatology, Gastroenterology and Nutrition, Department of Pediatric Subspecialties Bambino Gesù Children's Hospital, IRCCS Rome Italy

7. Department of Anesthesiology Bambino Gesù Children's Hospital, IRCCS Rome Italy

8. Unit of Hepato‐Biliary‐Pancreatic Surgery, Department of Surgery Bambino Gesù Children's Hospital, IRCCS Rome Italy

9. Renal Transplant Unit Bambino Gesù, Children's Hospital, IRCCS Rome Italy

Abstract

AbstractLiver 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.

Funder

Ministero della Salute

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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