MRI brain volumetric analysis of type II GM1 gangliosidosis patients treated with gene therapy

Motivation: Type II GM1 gangliosidosis is a rare disease that lacks reliable quantitative neural biomarkers to monitor disease progression. Goal(s): With the advent of gene therapy in treating GM1, we sought to quantify volumetrics of different brain regions known to be affected in GM1 patients. Approach: We quantified and tracked brain volumetric changes longitudinally on specific brain structures at different timepoints using MRI to evaluate disease progression/regression in GM1 patients treated with gene therapy and compared them to untreated patients and healthy controls. Results: We demonstrated the utility of brain volumetrics in assessing longitudinal brain region changes in gene therapy treated GM1 patients. Impact: Our study addressed the need for quantitative neural biomarkers in type II GM1 gangliosidosis which correlated with clinical markers. Through longitudinal brain volumetric analysis using MRI, we demonstrated the efficacy of gene therapy in monitoring disease progression/regression in GM1 patients.

Authors

Publication Details

Journal
Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
Published
2025-09-16
DOI
https://doi.org/10.58530/2025/2413
Primary Topic
Lysosomal Storage Disorders Research
Type
article
Field-Weighted Citation Impact
0.00
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article

MRI brain volumetric analysis of type II GM1 gangliosidosis patients treated with gene therapy

Maria Acosta, Srinivasan Vedantham, Mohammed Salman Shazeeb, Precilla D’Souza et al.
Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
Lysosomal Storage Disorders Research
article

MRI brain volumetric analysis of type II GM1 gangliosidosis patients treated with gene therapy

Maria Acosta, Srinivasan Vedantham, Mohammed Salman Shazeeb, Precilla D’Souza, Asma Hader, Jean M. Johnston, Cynthia J. Tifft, Catherine A. Lebel, Behroze Vachha, Anna Luisa Kühn, Clifford Lindsay, R King, Connor Lewis, Josephine Kolstad, Heather Gray‐Edwards, Zubir Rentiya, Ahmet Peker, Zeynep Vardar, Christopher Zoppo, Hakki Celik
article en

Abstract

Motivation: Type II GM1 gangliosidosis is a rare disease that lacks reliable quantitative neural biomarkers to monitor disease progression. Goal(s): With the advent of gene therapy in treating GM1, we sought to quantify volumetrics of different brain regions known to be affected in GM1 patients. Approach: We quantified and tracked brain volumetric changes longitudinally on specific brain structures at different timepoints using MRI to evaluate disease progression/regression in GM1 patients treated with gene therapy and compared them to untreated patients and healthy controls. Results: We demonstrated the utility of brain volumetrics in assessing longitudinal brain region changes in gene therapy treated GM1 patients. Impact: Our study addressed the need for quantitative neural biomarkers in type II GM1 gangliosidosis which correlated with clinical markers. Through longitudinal brain volumetric analysis using MRI, we demonstrated the efficacy of gene therapy in monitoring disease progression/regression in GM1 patients.

Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
Openalex Percentile: Top 69%
Lysosomal Storage Disorders Research
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