Evidence map›Paper›PMID 41332681›Full record

ArticlebioRxiv : the preprint server for biology2025

Longitudinal Exploration of Auditory Sensory-Perceptual Processing in CLN3 Disease (Juvenile Neuronal Ceroid Lipofuscinosis (Batten disease)): A High-Density Auditory Evoked Potential (AEP) Study.

Erin K Bojanek, Eve R Lang, Heather R Adams, Jennifer Vermilion, Erika F Augustine, Tufikameni Brima, Shahzoda Nasimjonova, Edward G Freedman, John J Foxe

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

9 authors.

Erin K BojanekThe Frederick J. and Marion A. Schindler Cognitive Neurophysiology Laboratory, Department of Neuroscience, University of Rochester School of Medicine and Dentistry, The Del Monte Institute for Neuroscience, Rochester, New York 14642, USA.ORCID 0000-0002-7390-5463
Eve R LangThe Frederick J. and Marion A. Schindler Cognitive Neurophysiology Laboratory, Department of Neuroscience, University of Rochester School of Medicine and Dentistry, The Del Monte Institute for Neuroscience, Rochester, New York 14642, USA.ORCID 0009-0009-3406-2131
Heather R AdamsThe Golisano Intellectual and Developmental Disabilities Institute, Department of Neuroscience, University of Rochester School of Medicine and Dentistry, Rochester, New York 14642, USA.ORCID 0000-0002-6980-3309
Jennifer VermilionThe Golisano Intellectual and Developmental Disabilities Institute, Department of Neuroscience, University of Rochester School of Medicine and Dentistry, Rochester, New York 14642, USA.ORCID 0000-0003-3893-2922
Erika F AugustineKennedy Krieger Institute, Baltimore, Maryland 21205, USA.ORCID 0000-0001-7257-8985
Tufikameni BrimaThe Frederick J. and Marion A. Schindler Cognitive Neurophysiology Laboratory, Department of Neuroscience, University of Rochester School of Medicine and Dentistry, The Del Monte Institute for Neuroscience, Rochester, New York 14642, USA.ORCID 0000-0002-3116-226X
Shahzoda NasimjonovaThe Frederick J. and Marion A. Schindler Cognitive Neurophysiology Laboratory, Department of Neuroscience, University of Rochester School of Medicine and Dentistry, The Del Monte Institute for Neuroscience, Rochester, New York 14642, USA.
Edward G FreedmanThe Frederick J. and Marion A. Schindler Cognitive Neurophysiology Laboratory, Department of Neuroscience, University of Rochester School of Medicine and Dentistry, The Del Monte Institute for Neuroscience, Rochester, New York 14642, USA.ORCID 0000-0001-8570-6325
John J FoxeThe Frederick J. and Marion A. Schindler Cognitive Neurophysiology Laboratory, Department of Neuroscience, University of Rochester School of Medicine and Dentistry, The Del Monte Institute for Neuroscience, Rochester, New York 14642, USA.ORCID 0000-0002-4300-3098

Funding

University of Rochester Intellectual and Developmental Disabilities Research CenterP50HD103536 · NICHD · UNIVERSITY OF ROCHESTER · PI Leona Ashley Oakes · 2020 to 2026
$9.8M
Meaningful Outcomes and Multi-Site Readiness for Clinical Trials in Juvenile Neuronal Ceroid LipofuscinosisU01NS101946 · NINDS · UNIVERSITY OF ROCHESTER · PI AUGUSTINE, ERIKA · 2019 to 2024
$3.7M
NICHD NIH HHS P50 HD103536NINDS NIH HHS U01 NS101946
6 · The paper itself

Abstract

Background: There is currently limited information about sensory and perceptual abilities across the progression of CLN3 disease (Juvenile Neuronal Ceroid Lipofuscinosis; Batten disease), a recessively inherited lysosomal storage disorder and a leading cause of childhood neurodegeneration. Clinical symptoms include vision loss, motor impairments, and cognitive challenges, making it difficult to accurately assess neurocognitive and perceptual abilities. Thus, there is a critical need to identify objective biomarkers that can be used to inform disease progression and track treatment response in this population. Methods: This exploratory study investigates longitudinal changes in auditory sensory perceptual processing in a small sample of individuals with genetically confirmed CLN3 disease (N=4; 3 male) compared to a cross-sectional sample of 60 neurotypical (NT) controls using high-density electroencephalography (EEG). We utilized a duration mismatch negativity (MMN) paradigm, identical to what has been used in our previous cross-sectional study. We examined the auditory evoked potentials (AEPs) of the standard tones across three different stimulus onset asynchrony conditions and examined the N1 and P2 components of the AEP. Results: We found age related differences in the amplitudes of the N1 and P2 components in individuals with CLN3 disease relative to NT controls. These amplitude differences were most notable in CLN3 disease when participants were presented with standard tones that had the slowest presentation rate. Specifically, N1 and P2 amplitudes were more negative than NT controls in childhood and adolescence and as CLN3 disease participants aged, the amplitude of the AEPs was greater than controls. Further, a more positive N1 amplitude during the longest stimulus presentation condition was associated with both reduced verbal intelligence and working memory abilities in CLN3 disease participants. Conclusions: Our preliminary findings parallel recently published work in a mouse model of CLN3 disease that showed both sex- and age-dependent disruptions in central auditory processing. Taken together, we demonstrate the utility of auditory EEG measures as a sensitive, objective and translational measure in CLN3 disease that may serve as a potential outcome measure useful in tracking disease progression. Continued work is needed in humans focused on sex-based differences and longitudinal changes of auditory processing in CLN3 disease.

Identifiers

PMID41332681
PMCPMC12667938

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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.