The open-access library for brain clearance, BAT Levels, and biological drift.

Contents


BAT Testing and BATCheck

Quantifying brain clearance with plasma biomarkers

BAT Testing and BATCheck work together to measure and interpret clearance efficiency, the brain’s ability to regulate and clear Beta-Amyloid (Aβ) and Tau (T) proteins. BAT Testing focuses on validated plasma assays, Aβ42/40, pTau-181, pTau-217. BATCheck adds upstream context, inflammation, metabolic state, circadian alignment, to identify drivers of biological drift.

Why this matters

Traditional methods detect change after symptoms. This framework supports preventive action by tracking clearance rhythm early, in a real-world, repeatable way. The intent is educational and observational, not diagnostic or treatment-oriented.

How the system fits together

ComponentWhat it doesPublic-health role
BAT TestingMeasures Aβ42/40 and pTau (181 or 217) via CLIA-certified labsEstablishes clearance baseline and trend
BATCheckEvaluates inflammation, metabolic friction, circadian alignmentFlags upstream influences on drift
BATScoreConverts longitudinal data into a single indexEnables population-level tracking
BATResetShort cycle to re-stabilize clearance rhythm under clinician oversightSupports maintenance, not disease modification
BATWatch RegistryAggregates de-identified lab and context dataReal-world evidence for quantitative prevention

Key points

  • Uses plasma biomarkers with growing validation in large research cohorts.
  • Adds upstream context to explain change, not just measure it.
  • Designed for repeated monitoring, population analysis, and neutral reporting.
  • Frames outcomes as observational and exploratory, consistent with public-health goals.

Alignment

The approach aligns with WHO dementia prevention priorities, CDC Healthy Brain Initiative, and NIH translational goals for scalable biomarkers. 

Reference:

BATWatch Research Group (2025). Quantifying Brain Clearance Through BAT Testing and BATChecks.  Zenodo.  http://doi.org/10.5281/zenodo.17524148

DOI: 10.5281/zenodo.17524148
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