# Neuroimaging correlates and biomarker performance of a fully automated plasma p‐tau217/Aβ42 ratio assay in a clinical cohort with Alzheimer's disease

**Authors:** Yoo Hyun Um, Paul Wynveen, Mark Holland, Kinal Bhatt, Zivjena Vucetic, Brian Engel, Corey Carlson, Andrew Becker, Irene B. Meier, Vaibhav A. Narayan, Sheng‐Min Wang, Dong Woo Kang, Sunghwan Kim, Suhyung Kim, Donghyeon Kim, Yeong Sim Choe, Regina E. Y. Kim, Seunggyun Ha, Hyun Kook Lim

PMC · DOI: 10.1002/alz.70942 · Alzheimer's & Dementia · 2025-11-24

## TL;DR

A new blood test for Alzheimer's disease shows high accuracy in detecting brain changes linked to the condition.

## Contribution

This is the first validation of a fully automated plasma p-tau217/Aβ42 ratio assay for Alzheimer's detection.

## Key findings

- The p-tau217/Aβ42 ratio had the highest diagnostic accuracy for amyloid PET positivity with an area under curve of 0.943.
- The biomarker correlated strongly with tau PET and brain atrophy across Alzheimer's disease stages.
- Glial fibrillary acidic protein reflected astrocytic activation, offering complementary diagnostic value.

## Abstract

Blood‐based biomarkers offer scalable, non‐invasive tools for Alzheimer's disease (AD) detection. We investigated the performance of plasma biomarkers associated with AD on the automated Beckman Coulter Access DxI 9000 analyzer.

This cross‐sectional study included 262 individuals from across the AD continuum. Plasma phosphorylated tau at threonine 217 (p‐tau217), amyloid beta (Aβ)42, and their ratio were measured. Diagnostic accuracy for amyloid positron emission tomography (PET) positivity (Centiloid > 20), using a dual cutoff approach, was assessed via receiver operative characteristic curve. Associations with tau PET (n = 76) were also assessed.

The p‐tau217/Aβ42 ratio showed the highest diagnostic accuracy for amyloid PET positivity (area under curve = 0.943) and the smallest indeterminate zone (8.0%). It correlated strongly and consistently with tau PET across Braak stages and with AD‐related cortical atrophy.

The p‐tau217/Aβ42 ratio was the most reliable plasma biomarker, closely tracking tau PET. It has potentials for clinical use in diagnosis and treatment monitoring.

This is the first validation of the Beckman Coulter plasma immunoassay.The plasma phosphorylated tau at threonine 217 amyloid beta 42 ratio showed the highest accuracy across the full Alzheimer's disease (AD) spectrum.Plasma biomarkers correlated with tau positron emission tomography and AD‐related brain atrophy.Glial fibrillary acidic protein offered complementary value reflecting astrocytic activation.

This is the first validation of the Beckman Coulter plasma immunoassay.

The plasma phosphorylated tau at threonine 217 amyloid beta 42 ratio showed the highest accuracy across the full Alzheimer's disease (AD) spectrum.

Plasma biomarkers correlated with tau positron emission tomography and AD‐related brain atrophy.

Glial fibrillary acidic protein offered complementary value reflecting astrocytic activation.

## Linked entities

- **Diseases:** Alzheimer's disease (MONDO:0004975)

## Full-text entities

- **Genes:** GFAP (glial fibrillary acidic protein) [NCBI Gene 2670] {aka ALXDRD}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}
- **Diseases:** atrophy (MESH:D001284), brain atrophy (MESH:C566985), AD (MESH:D000544), amyloid (MESH:C000718787)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12644925/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12644925/full.md

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Source: https://tomesphere.com/paper/PMC12644925