N-PhenoGENICS: Neurocognitive-Phenome, Genome, Epigenome and Nutriome In Childhood Leukemia Survivors
NCT ID: NCT01913093
Last Updated: 2020-10-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
204 participants
OBSERVATIONAL
2013-07-31
2019-06-30
Brief Summary
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Detailed Description
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Objectives
1. To identify TRANCE phenotypes of the childhood leukemia survivors.
2. To characterize the folate and vitamin B12 levels of these children
3. To identify DNA methylation patterns associated with TRANCE trait in the leukemia survivors
4. To identify SNPs associated with the TRANCE trait in the leukemia survivors.
5. To identify the "deficit genotype" associated only with the TRANCE leukemia survivors, but not with general population children who show developmental phenotypes similar to TRANCE: TRANCE-unique deficit variant
6. To replicate the association between the TRANCE-unique deficit variants and the TRANCE trait in a population of childhood leukemia survivors.
7. To evaluate the importance of rare genetic variants in the TRANCE trait in the leukemia survivors.
Study design: A case-control study of leukemia survivors
Analyses
1. Leukemia survivors will be characterized by their status of neurocognitive function, and categorized into the Deficit case and the non-deficit Control case.
2. They will be also characterized by the following attributes
1. Pathway-based genetic variant status (folate and PK-related genes)
2. Folate and vitamin B12 status
3. Epigenetic markers
3. Comparative analyses between neuro-cognitiive deficit phenotype (TRANCE) and Control on those parameters
Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Leukemia survivors with neurocognitive deficit
Leukemia survivors with neuro-cognitive deficit phenotype. Based on DIVERGET and other phenotyping tools, we will identify those with the deficit phenotype. This will be treated as "case".
No interventions assigned to this group
Leukemia survivors without neurocognitive deficit
Leukemia survivors who did not show impaired neurocognitive function, compared to the Control group defined above.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* 8 years : 0 months - 20 years : 11 months old at the time of their study visit
* At least 2 years : 0 months from the last treatment for acute lymphoblastic leukemia at the time of their study visit
* Continuous complete remission and undergone no bone marrow transplantation or cranial radiation therapy
* Fluent in English (a subject and one parent) for test completion
* Signed informed consent
Exclusion Criteria
* Down Syndrome diagnosis
8 Years
20 Years
ALL
No
Sponsors
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Canadian Institutes of Health Research (CIHR)
OTHER_GOV
Canadian Cancer Society (CCS)
OTHER
C17 Council
OTHER
Garron Family Cancer Centre
OTHER
Pediatric Oncology Group of Ontario
OTHER
The Hospital for Sick Children
OTHER
Responsible Party
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Shinya Ito
Division Head, Clinical Pharmacology and Toxicology
Principal Investigators
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Dr. Shinya Ito, MD
Role: PRINCIPAL_INVESTIGATOR
The Hospital for Sick Children
Dr. Sharon Guger
Role: PRINCIPAL_INVESTIGATOR
The Hospital for Sick Children
Dr. Johann Hitzler
Role: PRINCIPAL_INVESTIGATOR
The Hospital for Sick Children
Dr. Deborah L O'Connor
Role: PRINCIPAL_INVESTIGATOR
The Hospital for Sick Children
Dr. Russell Schachar
Role: PRINCIPAL_INVESTIGATOR
The Hospital for Sick Children
Dr. Brenda Spiegler
Role: PRINCIPAL_INVESTIGATOR
The Hospital for Sick Children
Dr. Rosanna Weksberg
Role: PRINCIPAL_INVESTIGATOR
The Hospital for Sick Children
Locations
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The Hospital for Sick Children
Toronto, Ontario, Canada
Countries
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Other Identifiers
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1000033923
Identifier Type: -
Identifier Source: org_study_id
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