Evidence map›Paper›PMID 41101291›Full record

Observational studyMolecular genetics and metabolism2025

Functional ability profiles in beta-propeller protein-associated neurodegeneration (BPAN).

Francesco Gavazzi, Samuel R Pierce, Vanessa Smith, Eric Yang, Julie Skorup, Kristy Pucci, Emma Kotes, Allan M Glanzman, Stacy V Cusack, Todd Levy and 7 more

Abstract readObservational Study
In one paragraph

Observational study in Molecular genetics and metabolism, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

17 authors.

Francesco GavazziDivision of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA; Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA. Electronic address: gavazzif@chop.edu.
Samuel R PierceDepartment of Physical Therapy, Children's Hospital of Philadelphia, Philadelphia, PA, United States of America.
Vanessa SmithDivision of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Eric YangDivision of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Julie SkorupDepartment of Physical Therapy, Children's Hospital of Philadelphia, Philadelphia, PA, United States of America.
Kristy PucciDepartment of Occupational Therapy, Children's Hospital of Philadelphia, Philadelphia, PA, United States of America.
Emma KotesDivision of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Allan M GlanzmanDepartment of Physical Therapy, Children's Hospital of Philadelphia, Philadelphia, PA, United States of America.
Stacy V CusackDepartment of Occupational Therapy, Children's Hospital of Philadelphia, Philadelphia, PA, United States of America.
Todd LevyDepartment of Occupational Therapy, Children's Hospital of Philadelphia, Philadelphia, PA, United States of America.
Holly DubbsDivision of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Emma WienerDivision of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Sarah WoidillDivision of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Joseph VithayathilDivision of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Abbas JawadDepartment of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, United States of America.
Nivedita ThakurDepartment of Pediatrics, Division of Child and Adolescent Neurology, McGovern Medical School, UT-Houston Health Science Center, Houston, TX, USA.
Laura A AdangDivision of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA; Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Funding

Validation of the GMFC-MLDU54NS115052 · NINDS · CHILDREN'S HOSP OF PHILADELPHIA · PI Laura Ann Adang, FLORIAN S EICHLER · 2019 to 2026
$14.3M
NINDS NIH HHS U54 NS115052
6 · The paper itself

Abstract

backgroundBeta-propeller Protein-Associated Neurodegeneration (BPAN) is a rare neurodevelopmental degenerative disorder caused by pathogenic variants in WDR45 leading to brain iron accumulation. Its rarity and complex clinical course make it difficult to select appropriate clinical outcome assessments (COAs). This study evaluates established COAs for feasibility and effectiveness in capturing BPAN's functional ability profiles exploring cognitive, motor, and behavioral features.

methodsWe performed an observational study. Children were recruited as part of the Myelin Disorders Biorepository Project at the Children's Hospital of Philadelphia. We administered the Gross Motor Function Measure-88 (GMFM-88), the Leiter International Performance Scale (Leiter-3), and the Vineland Adaptive Behavior Scale (VABS-3). A Rasch validated version of the GMFM-88, the GMFM-66, was derived from the GMFM-88 data. Descriptive statistics and Spearman's rank correlation were used to compare assessments. Statistical analyses were performed to compare performance across cohorts and assess correlations, with significance defined as p < 0.05.

resultsFifty-three individuals (43 females, 10 males) with molecularly confirmed BPAN participated. The VABS-3 (n = 53) showed a decline in adaptive skills over time, with significant differences between Communication and Socialization Domain performance (Kruskal-Wallis test with Dunn's correction p < 0.0001). GMFM-88 assessments (n = 32) showed a median performance of 33.4 %. Patient participation/behavior affected data completeness. The more limited GMFM-66 correlated better with the VABS-3 Gross Motor subdomain than the GMFM-88 (r = 0.94, r = 0.73, respectively). The Leiter-3 (n = 36) demonstrated significant non-verbal cognitive impairment, although there were behavioral challenges which impacted implementation. Longitudinal VABS-3 data revealed a median - 2.9 points/year decline in Adaptive Behavior Composite scores, reflecting progressive functional loss. DISCUSSION: This study highlights key considerations for selecting COAs in BPAN. The panel of COAs should accommodate the behavioral challenges associated with BPAN that can limit participant compliance with testing. The abbreviated GMFM-66 was a more reliable tool to capture motor skills. Similarly, behavioral difficulties impacted Leiter-3 performance, which demonstrated general impairment in non-verbal cognitive skills. The VABS-3 effectively tracked adaptive function decline, demonstrating feasibility for longitudinal monitoring. Future studies should expand cohort size, refine assessment strategies, and align measures with disease progression to optimize clinical trial readiness.

Indexed as

Carrier ProteinsIron Metabolism DisordersNeuroaxonal DystrophiesAdolescentChildChild, PreschoolFemaleHumansMaleCarrier ProteinsWDR45 protein, humanAdaptive behaviorBPANIntellectual disabilityNeurodegenerationPediatricRare disorders

Identifiers

PMID41101291
PMCPMC13380170

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.