# Alzheimer’s disease plasma biomarkers are associated with cognitive performance among Hispanic/Latino adults

**Authors:** Freddie Márquez, Wassim Tarraf, Sayaka Kuwayama, Deisha F. Valencia, Ariana M. Stickel, Richard B. Lipton, Fernando D. Testai, Natasha Z. Anita, Kevin A. Gonzalez, Robert Kaplan, Carmen R. Isasi, Gregory A. Talavera, Martha Daviglus, Jianwen Cai, Haibo Zhou, Douglas Galasko, Linda C. Gallo, Charles DeCarli, Bharat Thyagarajan, Hector M. González

PMC · DOI: 10.1038/s43856-025-01295-7 · Communications Medicine · 2025-12-15

## TL;DR

This study shows that blood-based Alzheimer’s biomarkers are linked to lower cognitive performance in Hispanic/Latino adults, suggesting potential for early detection.

## Contribution

The study is the first to show associations between Alzheimer’s plasma biomarkers and cognitive performance in a large, diverse Hispanic/Latino population.

## Key findings

- Higher levels of phosphorylated tau-181 and neurofilament light chain are linked to worse global cognitive performance.
- Lower amyloid-beta 42/40 ratios are associated with poorer verbal fluency.
- Glial fibrillary acidic protein levels are not significantly linked to cognitive performance.

## Abstract

Blood-based biomarkers hold promise as a minimally invasive tool for identifying early signs of Alzheimer’s disease pathology and neurodegeneration. We investigated associations between plasma biomarkers of amyloid-beta, tau, neuroaxonal injury, and glial activation with cognitive performance among community-dwelling Hispanic/Latino adults in the United States.

We analyzed cross-sectional data from 5730 adults aged 50 years and older (unweighted; mean [SD], 63.5 [8.2] years) in the Study of Latinos-Investigation of Neurocognitive Aging (SOL-INCA; 2016–2018). Plasma concentrations of amyloid-beta (Aβ42/40), phosphorylated tau-181 (pTau-181), neurofilament light chain (NfL), and glial fibrillary acidic protein (GFAP) were quantified (Quanterix Simoa HD-X) and log-transformed (ln). Cognitive performance was assessed across domain-specific scores (learning, memory, verbal fluency, and executive functioning/processing speed) used to calculate global cognitive performance. Survey-weighted linear regression models were used to examine associations between plasma biomarkers and cognitive performance, adjusting for sociodemographic, cardiometabolic, kidney, and APOE ε4 covariates.

Here we show higher ln(pTau-181) and ln(NfL) are associated with lower global cognitive performance (bpTau-181 = −0.06; 95%CI = [−0.12;−0.01]; p = 0.022; bNfL = −0.07; 95%CI = [−0.12;−0.02]; p = 0.005). Lower ln(Aβ42/40) is associated with poorer verbal fluency, higher ln(pTau-181) is associated with poorer learning and memory, and higher ln(NfL) is associated with learning and executive functioning/processing speed. We find ln(GFAP) is not significantly associated with cognitive performance.

Plasma biomarkers related to Alzheimer’s disease pathophysiology and broader neurodegenerative processes are associated with cognitive performance among Hispanic/Latino adults. These findings highlight the potential utility of blood-based biomarkers for identifying early cognitive vulnerability in this population.

This study looked at how certain substances in the blood, called biomarkers, are linked to thinking and memory abilities in Hispanic/Latino adults aged 50 and older in the United States. These biomarkers can reflect changes in the brain related to Alzheimer’s disease and other conditions that affect cognition. Researchers tested blood samples from over 5700 adults aged 50 and older and compared the results with their performance on memory and thinking tests. They found that people with higher levels of certain biomarkers had lower cognitive scores. This research helps us understand how blood tests might one day help detect early brain changes in diverse communities. It also highlights the importance of including underrepresented populations in aging and brain health research.

Márquez et al. examine associations between blood-based biomarkers of neurodegenerative processes and cognitive performance in over 5,700 Hispanic/Latino adults in the United States. They find that higher levels of phosphorylated tau and neurofilament light are linked to poorer cognitive performance.

## Linked entities

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

## Full-text entities

- **Genes:** 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}, GFAP (glial fibrillary acidic protein) [NCBI Gene 2670] {aka ALXDRD}, NEFL (neurofilament light chain) [NCBI Gene 4747] {aka CMT1F, CMT2E, CMTDIG, NF-L, NF68, NFL}, APOE (apolipoprotein E) [NCBI Gene 348] {aka AD2, APO-E, ApoE4, LDLCQ5, LPG}
- **Diseases:** Alzheimer's disease (MESH:D000544), injury (MESH:D014947), neurodegeneration (MESH:D019636), poorer learning and memory (MESH:D007859)

## Full text

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## Figures

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## References

6 references — full list in the complete paper: https://tomesphere.com/paper/PMC12815935/full.md

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Source: https://tomesphere.com/paper/PMC12815935