Brain Structure and Neurocognitive Development in Sickle Cell Disease; a Longitudinal Cohort Study (BRICK Study)
Study Details
Study Description
Brief Summary
Sickle cell disease (SCD) is an autosomal recessive red blood cell blood disorder. One especially vital organ affected in SCD is the brain. Individuals with SCD have an increased risk of both overt cerebral infarctions and silent infarctions. The latter are brain lesions without apparent neurological sequelae. Since cortical neurons in the brain lack the ability to regenerate, tissue damage accumulates throughout the already shortened lifespan of individuals with SCD, resulting in far-reaching consequences such as significant cognitive impairment. Currently, only hematological stem cell transplantation can halt the multiorgan tissue damage. However, the criteria to determine the timing of curative therapy do not center the brain, despite that subtle anomalies of this critical organ can have long-lasting consequences. Since it is not yet known whether brain tissue damage precedes, parallels, or lags behind non-brain tissue damage, it is critical to map these effects in youth with SCD. While importantly comparing images with a healthy reference population. Understanding how the brain is affected is critical for clinical decision making, such as timing of potentially curative interventions but also, to prevent long term irreversible brain damage in youth with SCD. In this study, a cohort of 84 SCD patients between the ages of 6 and 18 at baseline, will undergo MR imaging, neurological examination, neuropsychological assessment and blood sampling three times in total, with intervals of two years; results will be innovatively compared with children included in the Generation R population study (±8000 MRIs children and (young)adults) 6-20 years of age). Our hypothesis, based on the inability of the brain to generate new cortical neurons following cell death, is that brain function is impaired earlier than other organ systems and that there is an age-dependent limit in the brain's ability to remodel itself based on neuroplasticity.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Detailed Description
Objective: The primary objective is to evaluate longitudinal developmental changes in brain structure in patients aged 6-18 years with SCD. The secondary objective is to analyze the longitudinal relations between biomarkers, demographic characteristics, brain structure, neurocognitive functioning, behavioral functioning and developmental changes in brain structure.
Study Design: Longitudinal cohort study (BRICK) with a duration of 4 years. Study population:
Children and adolescents with sickle cell disease (SCD) of all genotypes (e.g. HbSS, HbSβº, HbSβ+, and HbSC) aged 6 -18 years. This will be compared to a cohort of healthy children and adolescents from Generation R.
Primary study endpoint:
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Total white matter volume increase in children and adolescents with SCD Secondary study endpoints
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Neurocognitive functioning (intelligence, specific neurocognitive functions, network organization)
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Incidence of stroke
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Other forms complications due to SCD
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Amount of hospital admissions, day care admissions (adult care only), crises at home, contact moments with the sickle cell center, ER visits
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Biomarkers for anemia, hemolysis, inflammation and endothelial activation.
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Behavioral functioning Nature and extent of the burden and risk associated with participation, benefit and group relatedness: By creating an advanced model for structural neurological, neurocognitive functioning in SCD, we will gain more insight into the pathophysiological origins and risk factors for SCD-related brain abnormalities. This will support development of preventive and supportive strategies as well as the initiation and evaluation of therapeutic interventions. Previous experience with the performance of brain MRI scans combined with recent research, indicates that the emotional burden placed on young children when undergoing a brain MR scan, are proportionate to the emotional burden placed on adults when they undergo a brain MR-scan. Furthermore, children will be offered the opportunity to become acquainted with the research procedure by witnessing an MRI scan session prior before participation.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Severe SCD genotypes Children between 6 and 18 years of age of genotypes HbSS, HbSβº |
Diagnostic Test: MR scan of the brain
Subjects will undergo MRI of the head, blood sampling and neurological examination on the same day or spread over 2 days. On a separate day from blood sampling and undergoing an MRI scan, the neuropsychological assessment will take place. The interval between the MRI scan and the neuropsychological assessment will be a maximum of 2 months. These measurements will be performed a total of 3 times with an interval of 2 years.
Diagnostic Test: Blood work
Lab work for current lab values and biobanking
Diagnostic Test: Neurological examination
Classical neurological examination
Diagnostic Test: Neuropsychological assessment
Overview of standard neurocognitive assessment tools in BRICK study Children and adolescents (Young) Adults
Wechsler Intelligence Test for Children- Fifth edition (WISC-V) (6-16 YOA) Wechsler Adult Intelligence Scale- Fourth edition WAIS-IV (16-24 YOA)
A Developmental NEuroPSYchological Assessment, Second Edition (NEPSY-II)
Narrative memory
Word fluency
Route finding NEPSY-II
World Fluency
Additional Questionnaires (6-18 years):
Child Behavior Checklist (CBCL)
Teacher Report Form (TRF)
Youth Self Report (YSR)
Behavior Rating Inventory of Executive Function (BRIEF), parent- and teacher-report)
Conners-3® • Additional Questionnaires (18+ years):
Adult Self-Report (ASR) / Adult Behavior Checklist (ABCL) (in case of IQ<70)
Behavior Rating Inventory of Executive Function Adult version (BRIEF-A), self-report / informant-report (in case of IQ<70)
Conners' Adult ADHD Rating Scales (CAARS)
Emma toolbox
|
| Not severe SCD genotypes Children between 6 and 18 years of age of genotypes HbSβ+, and HbSC and more |
Diagnostic Test: MR scan of the brain
Subjects will undergo MRI of the head, blood sampling and neurological examination on the same day or spread over 2 days. On a separate day from blood sampling and undergoing an MRI scan, the neuropsychological assessment will take place. The interval between the MRI scan and the neuropsychological assessment will be a maximum of 2 months. These measurements will be performed a total of 3 times with an interval of 2 years.
Diagnostic Test: Blood work
Lab work for current lab values and biobanking
Diagnostic Test: Neurological examination
Classical neurological examination
Diagnostic Test: Neuropsychological assessment
Overview of standard neurocognitive assessment tools in BRICK study Children and adolescents (Young) Adults
Wechsler Intelligence Test for Children- Fifth edition (WISC-V) (6-16 YOA) Wechsler Adult Intelligence Scale- Fourth edition WAIS-IV (16-24 YOA)
A Developmental NEuroPSYchological Assessment, Second Edition (NEPSY-II)
Narrative memory
Word fluency
Route finding NEPSY-II
World Fluency
Additional Questionnaires (6-18 years):
Child Behavior Checklist (CBCL)
Teacher Report Form (TRF)
Youth Self Report (YSR)
Behavior Rating Inventory of Executive Function (BRIEF), parent- and teacher-report)
Conners-3® • Additional Questionnaires (18+ years):
Adult Self-Report (ASR) / Adult Behavior Checklist (ABCL) (in case of IQ<70)
Behavior Rating Inventory of Executive Function Adult version (BRIEF-A), self-report / informant-report (in case of IQ<70)
Conners' Adult ADHD Rating Scales (CAARS)
Emma toolbox
|
Outcome Measures
Primary Outcome Measures
- mm3/time unit [4 years]
Total white matter volume increase in children and adolescents with SCD
Secondary Outcome Measures
- Full scale IQ (FSIQ) [4 years]
Neurocognitive functioning (intelligence, specific neurocognitive functions, network organization)
- Incidence of stroke [4 years]
- Other forms complications due to SCD [4 years]
- Amount of hospital admissions [4 years]
- Ld, bilirubin [4 years]
Hemolysis biomarkers
- Times/year [4 years]
ER visits
- Hb, Ht [4 years]
Biomarkers for anemia
- T score metric: a score of 50 represents the mean score of a reference population and 10 is the standard deviation. [4 years]
Patient-Reported Outcomes Measurement Information System® (PROMIS) within domains such as fatigue, pain behavior, depression, anxiety
Eligibility Criteria
Criteria
Inclusion Criteria:
- Patients with SCD of all genotype between 6 and 18 at baseline
Exclusion Criteria:
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Parents/ guardians (in case of minors) or patients themselves (>16 years) unable to make an informed decision on participating in this study.
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An abnormal brain MRI prior to initiation of the study due to non-SCD related causes.
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Contraindications for brain MRI per protocol
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Erasmus MC | Rotterdam | South Holland | Netherlands | 3000 CA |
| 2 | Amsterdam University Medical Center | Amsterdam | Netherlands |
Sponsors and Collaborators
- Dr. Marjon H. Cnossen MD PhD
- Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- MEC-25022-0004