Evidence map›Paper›PMID 39135350›Full record

ArticleJournal of inherited metabolic disease2025

Long-term neurodevelopmental outcomes following liver transplantation for metabolic disease-a single centre experience.

Catherine Patterson, Anna Gold, Stephanie So, Leila Kahnami, Michaela Dworsky-Fried, Eva Mamak, Alaine Rogers, Andreas Schulze, Birgit Ertl-Wagner, Vicky Ng and 1 more

Abstract read
In one paragraph

Article in Journal of inherited metabolic disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Catherine PattersonDepartment of Rehabilitation Services, The Hospital for Sick Children, Toronto, Ontario, Canada.ORCID 0000-0002-0765-5144
Anna GoldDepartment of Psychology, The Hospital for Sick Children, Toronto, Ontario, Canada.ORCID 0000-0002-7719-5673
Stephanie SoDepartment of Rehabilitation Services, The Hospital for Sick Children, Toronto, Ontario, Canada.ORCID 0009-0004-1548-4105
Leila KahnamiDepartment of Psychology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Michaela Dworsky-FriedDepartment of Psychology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Eva MamakDepartment of Psychology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Alaine RogersDepartment of Rehabilitation Services, The Hospital for Sick Children, Toronto, Ontario, Canada.
Andreas SchulzeDepartment of Occupational Therapy, University of Toronto, Toronto, Ontario, Canada.
Birgit Ertl-WagnerDepartment of Diagnostic and Interventional Radiology, Hospital for Sick Children, Toronto, Ontario, Canada.ORCID 0000-0002-7896-7049
Vicky NgDivision of Gastroenterology, Hepatology and Nutrition, The Hospital for Sick Children, Toronto, Ontario, Canada.ORCID 0000-0002-9998-5692
Yaron AvitzurDivision of Gastroenterology, Hepatology and Nutrition, The Hospital for Sick Children, Toronto, Ontario, Canada.ORCID 0000-0002-8072-5727

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study describes the neurodevelopmental outcome of children with urea cycle disorders (UCD) and organic acidemias (OA) preliver transplant (LT), 1-year, and 3-years post-LT. We performed a retrospective chart review of children with OA or UCD transplanted between January 2014 and December 2021. Standardized motor and cognitive assessment scores were collected from children who had ≥1 motor/cognitive assessment at any timepoint. Pre-LT brain magnetic resonance imaging (MRI) was graded. Associations between demographic/medical variables and neurodevelopmental outcomes were explored. Twenty-six children (64% male) underwent LT at a median age of 1.4 (interquartile range 0.71, 3.84) years. Fifteen (58%) had a UCD diagnosis, 14 (54%) required dialysis for hyperammonemia, and 10 (42%) had seizures typically around diagnosis. The proportion of children with gross motor scores >1 standard deviation (SD) below the mean increased across timepoints, and ≥50% demonstrated general intellect scores >2 SD below the mean at each timepoint. The following significant associations were noted: UCD diagnoses with lower general intellect scores (p = 0.019); arginosuccinate lyase deficiency diagnosis with lower visual motor scores at 3-years post-LT (p = 0.035); a history of seizures pre-LT with lower general intellect (>2SD below the mean) at 3-years post-LT (p = 0.020); dialysis pre-LT with lower motor scores (>1 SD below the mean) at 1-year post-LT (p = 0.039); pre-emptive LT with higher general intellect scores at 3-years post-LT (p = 0.001). MRI gradings were not associated with developmental scores. In our single centre study, children with UCD or OA had a higher prevalence of developmental impairment post-LT compared to population norms. Earlier screening, pre-emptive transplant, and rehabilitation may optimize long-term outcomes.

Indexed as

Liver TransplantationAmino Acid Metabolism, Inborn ErrorsChildChild, PreschoolFemaleHumansInfantMagnetic Resonance ImagingMaleNeurodevelopmental DisordersRetrospective StudiesTreatment OutcomeUrea Cycle Disorders, Inborncognitive developmentliver transplantmotor developmentorganic acidemiapediatricurea cycle

Identifiers

PMID39135350
PMCPMC11670442

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.