July 23, 2025 • 2 mins
New research from the Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN). This summary is based on a paper published in the Journal of Inherited Metabolic Disease on June 2, 2025, titled "Characterizing Diagnostic Delays in Metachromatic Leukodystrophy: A Real-World Data Approach."
Read the paper here.
Learn more about GLIA-CTN.
Transcript:
New research from the Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN), a research group of the Rare Diseases Clinical Research Network.
Characterizing Diagnostic Delays in Metachromatic Leukodystrophy.
This summary is based on a paper published in the Journal of Inherited Metabolic Disease on June 2, 2025.
Metachromatic leukodystrophy (MLD) is a rare inherited disorder that causes progressive damage to the nervous system. The subtypes of MLD are defined by the onset of neurodegeneration, but less is known about the earliest features of this inborn error in metabolism.
In this study, researchers found that many children experience subtle early features in the months to years prior to diagnosis. The early medical journeys of children were mapped using two independent payor-system databases. Every medical encounter prior to diagnosis was captured. Across these cohorts, they found that children frequently presented within the medical system with signs and symptoms of disease, including early developmental delay, feeding issues, gallbladder problems, and abnormal eye movements. This work was complemented by similar findings from an MLD natural history study, which is supported through the GLIA-CTN.
Authors note that this study highlights early features of MLD and defines barriers to diagnosis, further supporting the need for early screening. By better understanding the barriers to diagnosis and characterizing how MLD begins, we can better define clinical monitoring guidelines in presymptomatic children and define ideal windows for intervention to improve outcomes. This work underscores the critical need for newborn screening to definitively diagnose children prior to disease onset.
Read the paper here.
Learn more about GLIA-CTN.
Transcript:
New research from the Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN), a research group of the Rare Diseases Clinical Research Network.
Characterizing Diagnostic Delays in Metachromatic Leukodystrophy.
This summary is based on a paper published in the Journal of Inherited Metabolic Disease on June 2, 2025.
Metachromatic leukodystrophy (MLD) is a rare inherited disorder that causes progressive damage to the nervous system. The subtypes of MLD are defined by the onset of neurodegeneration, but less is known about the earliest features of this inborn error in metabolism.
In this study, researchers found that many children experience subtle early features in the months to years prior to diagnosis. The early medical journeys of children were mapped using two independent payor-system databases. Every medical encounter prior to diagnosis was captured. Across these cohorts, they found that children frequently presented within the medical system with signs and symptoms of disease, including early developmental delay, feeding issues, gallbladder problems, and abnormal eye movements. This work was complemented by similar findings from an MLD natural history study, which is supported through the GLIA-CTN.
Authors note that this study highlights early features of MLD and defines barriers to diagnosis, further supporting the need for early screening. By better understanding the barriers to diagnosis and characterizing how MLD begins, we can better define clinical monitoring guidelines in presymptomatic children and define ideal windows for intervention to improve outcomes. This work underscores the critical need for newborn screening to definitively diagnose children prior to disease onset.
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