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CHI3L1 variant association with AD progression in human patients

active
experiment Created: 2026-04-10T22:32:22 By: etl-v1-backfill Quality: 50% ✓ SciDEX ID: exp-73e6f43d-a179-4e2d-955a-ae0f60d77cef
🧫 Experiment Protocol ExploratoryAlzheimer's diseaseCHI3L1human patientsproposed
A genetic association study examining the relationship between CHI3L1 gene variants and Alzheimer's disease progression in human patients. The study focused on variants that result in decreased cerebrospinal fluid YKL-40 expression and their impact on disease progression rates. This clinical genetic analysis aimed to understand how genetic variation in CHI3L1 affects AD pathogenesis and clinical outcomes in real patients.
PRIMARY OUTCOME
AD progression rate
EXPECTED OUTCOMES
1. The intervention targeting CHI3L1 shifts AD progression rate in the predicted direction relative to the matched control arm. 2. Secondary disease-relevant readouts in Alzheimer's disease remain directionally concordant with the primary endpoint rather than showing isolated single-assay effects. 3. The effect persists after adjustment for baseline covariates, batch effects, or repeated-measures structure used in the study design.
SUCCESS CRITERIA
- Prespecified primary endpoint (AD progression rate) improves versus control with p < 0.05 or an equivalent corrected threshold used by the study. - The effect size is biologically meaningful and reproduced across technical/biological replicates or the validation subset. - Safety, data quality, and missingness remain within protocol-defined bounds so the result is interpretable rather than driven by attrition or assay failure.
PROTOCOL
1. Establish human patients cohorts for Alzheimer's disease and predefine inclusion, exclusion, and quality-control criteria before intervention. 2. Apply the experimental manipulation described for CHI3L1, alongside matched control or comparator arms, and document dose, exposure window, and sample timing in a locked protocol log. 3. Measure AD progression rate together with orthogonal secondary readouts such as molecular, imaging, behavioral, or safety endpoints that are appropriate to the title and study design. 4. Use blinded outcome assessment where feasible, prespecified statistical analysis, and replicate the core readout across biological replicates or an independent validation subset. 5. Interpret results against the baseline study rationale: A genetic association study examining the relationship between CHI3L1 gene variants and Alzheimer's disease progression in human patients. The study focused on variants that result in decreased cerebrospinal fluid YKL-40 expression and their impact on disease
🧫 Experiment Extras
PATHWAY
neuroinflammation
MARKET PRICE
$0.50
STATUS
proposed
Metadataorigin_type: v1_polymorphic_backfill
origin_typev1_polymorphic_backfill
source_tableexperiments
_schema_version1
📊 Evidence Profile
Evidence Balance
+0%
Certainty
0%
Debates
0
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Outgoing
0
0 supporting 0 contradicting 0 neutral
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