Adrenoleukodystrophy National Registry Study
Study Details
Study Description
Brief Summary
The aim of this registry to understand the natural history and disease progression in ALD and potentially develop bio-markers using the biospecimens collected using this registry.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Detailed Description
This is a prospective, non-therapeutic protocol designed to create and maintain a registry of participants with Adrenoleukodystrophy (ALD) and known/presumed mutation for ALD. This study also involves maintaining a prospective biorepository to collect and store buccal swab, blood, stool and urine samples as well. In this protocol, pediatric (including infants), adolescents and adult patients with confirmed or presumed ALD (based on positive VLCFA testing and/or confirmed mutation) will be offered potential study participation. Additionally, presumed mutation for ALD (based on pedigree or confirmed mutation) will be offered potential study participation. After appropriate consent (online or in-person), subjects will be requested to provide a medical history (with authorization of release of medical records), longitudinal biospecimens, and permission to perform laboratory analyses on these samples. The overall goal is to understand the natural disease course in affected and unaffected patients (identified patients and relatives with a diagnosis of ALD), as well as women with ALD to assemble a resource of clinical, medical, and biological data from the participants. This study also aims to understand the outcomes of this disease, as well as possibly develop biomarkers to identify prognostic markers for disease progression, which may help develop effective interventions. The biospecimen bank and registry will provide access to samples and data for the ongoing studies as well as will provide an important resource for the future research.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Adrenoleukodystrophy All patients living in the United States diagnosed with adrenoleukodystrophy, either by newborn screen, based on family history or otherwise, are eligible to participate in this study. |
Other: Medical Record Abstraction
Collect clinical and epidemiological data through medical record abstraction and self-reported questionnaire survey semi-annually.
Other: Biospecimen Sample Collection
Collect research samples, when feasible for those diagnosed with ALD.
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Outcome Measures
Primary Outcome Measures
- Collect Clinical and Epidemiological Data [10 Years]
Collect clinical and epidemiological data through medical record abstraction and self-reported questionnaire survey semi-annually.
Eligibility Criteria
Criteria
Inclusion Criteria
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Age 0 - 100
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ALD patients or family member meeting any of the following criteria:
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Any patient diagnosed with ALD (confirmed by positive VLCFA testing and/or genetic mutation).
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Known or presumed mutation with ALD based on pedigree or confirmed mutation in ABCD1 gene
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Participants living in the United States and territories
Exclusion Criteria
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Patients diagnosed with ALD who lack the capacity to consent/assent AND do not have a designated legally authorized representative or guardian.
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Patients who have undergone BMT or other cellular therapy .
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Patients not fluent in English who are unable to consent in-person at the BMT Journey Clinic.
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Patients who are illiterate
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Patient determined by the PI or designee to be unlikely to complete required study components (due to language barriers, compliance issues, etc.)
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Masonic Cancer Center at University of Minnesota | Minneapolis | Minnesota | United States | 55455 |
Sponsors and Collaborators
- Masonic Cancer Center, University of Minnesota
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 2019NTLS027
- MT2019-01