
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.

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.
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
Our lab is supported by



