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Research projects, funding, and publications

Our work spans blood-based biomarker trajectories, multi-omics discovery, and population differences in brain aging — supported by NIH and foundation funding.

Research focus areas

FOCUS 01

Longitudinal blood-based biomarkers and neurodegenerative outcomes

This research focus examines how plasma-based biomarkers — including markers of amyloid, tau, neurodegeneration, and neuroinflammation — change over time and how those trajectories relate to cerebrovascular and neurodegenerative outcomes.

FOCUS 02

Multi-omics discovery of ADRD mechanisms

This focus applies proteomic and genomic methods to identify novel biomarkers and mechanistic pathways underlying heterogeneity in ADRD. Current projects include plasma proteomic discovery analyses using high-throughput platforms (e.g., Olink / NULISA) and genetic analyses including Mendelian randomization to evaluate causal relationships between molecular exposures and ADRD-related outcomes.

FOCUS 03

Population differences in brain aging and health

This focus investigates biological and social determinants of Alzheimer’s disease and related dementias across diverse populations, with explicit attention to racial and ethnic heterogeneity, socioeconomic determinants, and vascular risk factors.

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What we are working on now

Genetic contributions of Alzheimer’s disease to cerebral small vessel disease

This project applies Mendelian randomization and related causal inference approaches to evaluate whether genetic liability for AD causally influences markers of cerebral small vessel disease (cSVD), including white matter hyperintensities.

NIH funded

Longitudinal changes in plasma proteomics and their associations with cerebral small vessel disease

This project characterizes the longitudinal trajectory of plasma proteomic markers — particularly in the context of oligodendrocytes/demyelination and the AT(N) framework — in relation to cSVD burden and progression, using mixed-effects models, generalized estimating equations, and trajectory-based analytic frameworks applied to deeply phenotyped cohort data.

BrightFocus Foundation funded

Neuropathologic heterogeneity in ADRD

We examine heterogeneity in neuropathologic findings at death and how distinct pathologic profiles correspond to antemortem cognitive impairment and trajectories of cognitive decline in autopsy-confirmed cohorts with rich longitudinal clinical data. We have a particular interest in the independent, additive, and interactive effects of vascular neuropathologies in the presence of co-pathologies, including Alzheimer’s disease neuropathologic change (ADNC), Lewy body disease (LBD), and TDP-43 pathology / limbic-predominant age-related TDP-43 encephalopathy neuropathologic change (LATE-NC).

Overlap of modifiable risk factors for dementia and cardiovascular disease

We investigate how hypertension, diabetes, obesity, and smoking contribute to brain aging and dementia risk. Our work examines how these vascular risk profiles are associated with cognitive performance, trajectories of cognitive decline, and dementia onset across the life course. We further evaluate their relationships with neurodegenerative and cerebrovascular pathology at death, as well as functional outcomes such as mobility and daily functioning. By integrating clinical, epidemiologic, and neuropathologic data, this line of research aims to clarify shared mechanisms linking cardiovascular health and dementia and to identify modifiable targets for prevention and intervention.

Selected recent work

A full, continuously updated record is available on Google Scholar and PubMed.

Journal of Alzheimer’s Disease

Article · 2026

Interleukin-6 is associated with white matter hyperintensities and cognition independent of Alzheimer’s disease plasma biomarkers — HABS-HD

Dharmapuri A, Chaudhuri S, Contreras JA, Hayes CA.

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Alzheimer’s & Dementia: DADM

Article · 2026

Associations of plasma p-Tau217 with cognitive domain performance in clinically unimpaired participants: evidence from HABS-HD

Najmi Z, Dharmapuri A, Contreras JA, Hayes CA*; HABS-HD Study Team.

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Alzheimer’s & Dementia: DADM

Article · February 2026

Plasma p-tau217 and cognitive impairment: evaluating biomarker equity across racial/ethnic groups in HABS-HD

Hayes CA#, Najmi Z, Contreras JA, Dharmapuri A, Winston C, HABS-HD Study Team.

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Neurology Open Communications

Article

APOE associations with longitudinal cerebrovascular disease neuroimaging biomarkers and brain imaging: The Strong Heart Study

Hayes CA#, Odden MC, Levendovszky SR, Buchwald DS, Verney S, Shibata DK, Zhang Y, Ali T, Suchy-Dicey A

Journal of Alzheimer’s Disease

Article · 2026

Independent associations of phosphorylated tau181 and neurofilament light with cognitive outcomes in the Health and Aging Brain Study–Health Disparities (HABS-HD)

Housini M, Contreras JA, Hayes CA.

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Alzheimer’s Research & Therapy

Article · 2025

Microinfarcts are associated with cognitive impairment in neurofibrillary tangle predominant decedents: evidence from the NACC autopsy cohort

Martinez NC, Bharani KL, Hasan S, Hayes CA.

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Alzheimer’s Research & Therapy

Article · 2025

Population intervention models of racial and ethnic disparities in cognitive outcomes from cardiometabolic risk factors — HABS-HD

Hayes CA#, Abdullah L, Gill J, Odden MC.

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Alzheimer’s & Dementia

Article · 2025

Targeting the cardiometabolic bottleneck to slow polypathology and cognitive decline

Hayes CA#, Younes K.

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Frontiers in Aging Neuroscience

Article · 2025

Sex differences in the association of cardiometabolic risk scores and blood pressure measurements with white matter hyperintensities in diverse older adults — HABS-HD

Hayes CA#, Vintimilla R, Chaudhuri S, Odden MC.

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Acta Neuropathologica Communications

Article · May 2025

Age-dependent interactions of APOE isoform 4 and Alzheimer’s disease neuropathology: findings from the NACC

Hayes CA#, Thorpe RJ Jr, Odden MC.

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Alzheimer’s & Dementia

Article · March 2025

The impact of arteriolosclerosis on cognitive impairment in decedents without severe dementia from the National Alzheimer’s Coordinating Center

Hayes CA#, Young CB, Abdelnour C, Reeves A, Odden MC, Nirschl J, Crane PK, Poston KL, Mormino EC, Younes K.

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Our lab is supported by

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