# Understanding Biological and Lifestyle Contributions to Alzheimer's Disease Pathology and Clinical Profiles in Black Women: Defining Prevention Targets in High Risk Groups

> **NIH NIH R01** · UNIVERSITY OF CALIFORNIA, SAN DIEGO · 2024 · $82,873

## Abstract

PROJECT SUMMARY/ABSTRACT
Women have higher rate of Alzheimer’s disease (AD) and tend to show a more aggressive profile of AD than
men, with greater pathological tau burden and steeper cognitive decline. The prevalence of AD also differs by
race with higher rates among Black versus White older adults. Yet, very little is known about AD in Black
individuals given their historical exclusion in research. Even less is known about the intersection of race and sex
in AD. In this proposal, we aim to study how sex- and/or race-disparate biological (inflammation, insulin
resistance [IR]) pathways and physical activity potentially contribute to tau accumulation and cognitive decline
specifically among older Black women at-risk for AD. We focus on potentially modifiable risk/protective factors
given the recent surge in evidence that modification of these factors can be highly effective in delaying or even
preventing cognitive decline. Our own preliminary work indicated that women may be more susceptible than men
to the adverse effect of inflammation on levels of phosphorylated tau (p-tau) and cognitive function. There is also
evidence that certain lifestyle factors, including physical activity, have a greater impact on AD-related outcomes
such as tau in women versus men. Given links between physical activity and inflammation, we propose to
investigate the interplay between inflammation and physical activity in their contributions to tau and cognitive
decline in older Black women at risk for AD. Since IR is a key driver of inflammation, and the rates of
prediabetes/diabetes are higher in Black adults, we will examine how IR impacts tau accumulation and cognitive
decline. It is critical to examine these relationships in the context of social determinants of health, which are a
driving factor in health outcomes such as inflammation and IR particularly in Black women. To achieve this, we
are conducting a prospective study that will assess all variables of interest and their interactive pathways. The
study will build upon an ongoing pilot study that will collect these variables in 30 White women by study end
(June, 2022), but will represent a more targeted and less invasive study in order to enhance recruitment in the
understudied yet higher risk group of older Black women. We will recruit Black women at two sites, one
leveraging an existing research registry of Black women in Los Angeles, and the other leveraging local
community connections and previous research experience to create a new cohort in San Diego. We will use a
community-based participatory research approach to recruitment that involves decision making at each level
involving a Community Advisory Board. We will measure inflammatory markers in blood, IR, physical activity and
the Area Deprivation Index as our primary social determinant of interest in 100 Black women at-risk for AD and
relate these measures to changes in cognitive function and accumulation of tau, measured in plasma, over a
two-year pe...

## Key facts

- **NIH application ID:** 10877463
- **Project number:** 3R01AG077579-02S1
- **Recipient organization:** UNIVERSITY OF CALIFORNIA, SAN DIEGO
- **Principal Investigator:** SARAH BANKS
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2024
- **Award amount:** $82,873
- **Award type:** 3
- **Project period:** 2022-12-15 → 2027-11-30

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10877463

## Citation

> US National Institutes of Health, RePORTER application 10877463, Understanding Biological and Lifestyle Contributions to Alzheimer's Disease Pathology and Clinical Profiles in Black Women: Defining Prevention Targets in High Risk Groups (3R01AG077579-02S1). Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/grant/nih/10877463. Licensed CC0.

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