Evidence map›Paper›PMID 39920752›Full record

ArticleOrphanet journal of rare diseases2025

Clinically meaningful improvements after gene therapy for aromatic L-amino acid decarboxylase deficiency (AADCd) in the Peabody Developmental Motor Scale, Second Edition (PDMS-2) and correlation with Bayley-III scores and motor milestones.

Wuh-Liang Hwu, Hui-Min Lee, John Devin Peipert, Rongrong Zhang, Christian Werner, J Rafael Sierra, Thomas O'Connell, Jonathan J Woolley, Marjorie Crowell, Antonia Wang and 1 more

Abstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
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.

Wuh-Liang HwuDepartment of Medical Genetics and Pediatrics, National Taiwan University Hospital, National Taiwan University College of Medicine, Taipei, Taiwan.
Hui-Min LeeDepartment of Medical Genetics and Pediatrics, National Taiwan University Hospital, National Taiwan University College of Medicine, Taipei, Taiwan.
John Devin PeipertCentre for Patient Reported Outcomes Research, Department of Applied Health Sciences, University of Birmingham, Birmingham, UK.
Rongrong ZhangPTC Therapeutics Sweden AB, Askim, Sweden.
Christian WernerPTC Therapeutics Germany GmbH, Frankfurt am Main, Germany.
J Rafael SierraPTC Therapeutics, 500 Warren Corporate Center Drive, Warren, NJ, 07059, USA.
Thomas O'ConnellMedicus Economics, Boston, MA, USA.
Jonathan J WoolleyMedicus Economics, Boston, MA, USA.
Marjorie CrowellMedicus Economics, Boston, MA, USA.
Antonia WangPTC Therapeutics, 500 Warren Corporate Center Drive, Warren, NJ, 07059, USA.
Ioannis TomazosPTC Therapeutics, 500 Warren Corporate Center Drive, Warren, NJ, 07059, USA. ytomazos@ptcbio.com.ORCID http://orcid.org/0000-0003-0290-4583

Funding

PTC Therapeutics PTC Therapeutics
6 · The paper itself

Abstract

backgroundAromatic L-amino acid decarboxylase deficiency (AADCd) is a rare genetic disorder characterized by movement disorders, motor and autonomic dysfunction, and developmental delays. The gene therapy eladocagene exuparvovec has become available in some regions; pooled clinical trial results demonstrate continuous long-term improvement in motor development and cognitive function. We sought to characterize clinically meaningful change in motor function, as measured by Total Peabody Developmental Motor Scales-Second Edition (PDMS-2) score, and assess correlations with cognition and language domains of the Bayley-III and motor milestone (MM) achievement.

methodsData from N = 30 patients from three single-arm clinical studies of eladocagene exuparvovec were analyzed. Anchor-based estimation of the meaningful score difference (MSD) of Total PDMS-2 score was conducted using mean-difference and receiver operating characteristic curve (ROC) approaches. MM achievement served as the anchor defining meaningful change.

resultsAn MSD of 40 points for Total PDMS-2 score was selected for analysis as it yielded specificity > 0.95 using the ROC approach, and generally aligned with the mean-difference approach. Cumulative incidence analysis reflected that 50% of patients treated with eladocagene exuparvovec may achieve the MSD of 40-point change in Total PDMS-2 score at 6 months, and 86% at 18 months. Correlations between measures were of large magnitude and improved over time (Month 6: r = 0.599 [p = 0.0032]; Month 18: r = 0.796 [p = 0.0002]; Month 60: r = 0.861 [p = 0.0007]).

conclusionsThe MSD of 40 points for Total PDMS-2 score enables the interpretation of changes observed in patients with AADCd, and suggests that treatment with eladocagene exuparvovec leads to significant improvements in motor and cognitive function.

Indexed as

Amino Acid Metabolism, Inborn ErrorsAromatic-L-Amino-Acid DecarboxylasesGenetic TherapyChildChild, PreschoolFemaleHumansInfantMaleAromatic-L-Amino-Acid DecarboxylasesAromatic L-amino acid decarboxylase deficiencyCognitive functionGene therapyMotor function

Identifiers

PMID39920752
PMCPMC11806574

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.