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Neuroscientist Indira Turney unveils possible causes of racial disparities in brain aging

Why does dementia affect some populations more than others? Life experiences, chronic stressors and lack of health equity may be key to understanding, neuroscientist Indira Turney said during a Voices of Discovery lecture Monday.

Genetics play a role in whether we develop Alzheimer鈥檚 disease or other dementia, but the sum of our life experiences may have more influence on how our brains age, cognitive neuroscientist Indira Turney said during Monday鈥檚 lecture as part of the 2022-23 福利亚洲国产精品 Speaker Series, 鈥淟iving Well in a Changing World.鈥

Those experiences 鈥 chronic stressors, levels of income, access to healthy diets and activity 鈥 look different across demographics and may account for why Black Americans are more likely to develop dementia than their White, Hispanic or Asian American counterparts.

Indira Turney

鈥淎 lot of the reasons people develop dementia are things we can change,鈥 said Turney, an associate research scientist at Columbia University Medical Center. 鈥淎frican Americans have the highest rates of dementia across age groups, as early as 65. Asian Americans have the lowest mean, and White Americans are in the middle. The goal is for everyone to reach the Asian American rate as shown in the research, which would be health equity. To do that, we must first accurately identify the disparities, show they exist and what鈥檚 driving them.鈥

Turney鈥檚 presentation, 鈥淲eathering and Patterns of Brain Aging by Race and Ethnicity,鈥 outlined data and results from her research involving seniors and their children in New York City neighborhoods. Her appearance in McCrary Theatre was also part of Elon College, the College of Arts and Sciences鈥 Voices of Discovery speaker series.

Turney鈥檚 expertise is in studying Alzheimer鈥檚 disease, dementia and brain aging with a focus on understanding how racism affects the body, brain and health. She earned a doctorate in cognitive neuroscience from Pennsylvania State University and is a postdoctoral fellow at the Taub Institute for Research on Alzheimer鈥檚 Disease and the Aging Brain at Columbia University Medical Center. She hopes her work will improve the detection and treatment of Alzheimer鈥檚 and related dementias and develop prevention programs to target environmental, socio-cultural and biological mechanisms of change in at-risk populations.

As we age, our brains naturally lose mass and volume, but excessive loss of brain mass and structure is abnormal and may be indicative of dementia. Other signs of cognitive deterioration are white matter hyperintensities, often caused by tiny strokes occurring over time.

Turney鈥檚 research has shown that older Black adults have higher rates of white matter hyperintensities compared to White and Hispanic study participants. Even in midlife, Black people have more white matter hyperintensities than other races and ethnicities.

Her research has identified some possible causes of those disparities.

She focused much of the presentation on differences in biological age across race and ethnicity, studied by other researchers and which she uses as a hypothesis to explain her own work. A group of 30-year-olds may have the same chronological age, but the work they do, the conditions they live in and the levels of stress they are under cause 鈥渨ear and tear鈥 on the body. That can make people鈥檚 biological ages differ. For instance, Turney showed research data indicating that 30-year-old Black women have biological ages five to eight years older than their chronological age. Differences between chronological and biological ages in White men and women were 鈥渘egligible,鈥 she said.

鈥淭he cumulative impact of social, physical and economic adversities faced by African Americans leads to early health deterioration and advanced biological aging, which is believed to be caused by chronic or reoccurring stressors,鈥 Turney said.

Another study compared income levels across race and ethnicity with signs of cognitive decline, using New York City鈥檚 median annual income of $35,000 as a demarcation. Minorities were more likely to earn less than White residents, overall, and more likely to earn less than the $35,000 threshold. Preliminary data showed that MRIs of middle-aged Black Americans who earned less than that median wage showed greater levels of white matter hyperintensities in their brains.

鈥淭here was no relation to income in White individuals. In Hispanic individuals, there was a slight difference, but in Black people making less than $35,000 a year, they were more likely to have greater levels of brain aging,鈥 Turney said. 鈥淲e need to continue to look at why people with less income are at greater risk for developing dementia. Is it access to healthcare? Are there other underlying health conditions? Is current (income) more important than a family鈥檚 income during childhood?

鈥淲hat I actually found is that (family income during) childhood only matters for White individuals. In Black individuals, midlife income is more important.鈥

Throughout, Turney emphasized the need for more thorough data collection involving minority populations often underrepresented in studies. People who voluntarily present to a clinic for treatment or research may not represent the populations most affected or at-risk for certain conditions. Those at-risk may not even know their cognitive symptoms are abnormal, chalking them up to the standard effects of aging, she said.

鈥淚f we鈥檙e looking for a cure for Alzheimer鈥檚 disease, but we鈥檙e not studying the people who are most affected by it, if they鈥檙e not included in the study, we鈥檙e lacking answers in what鈥檚 causing Alzheimer鈥檚,鈥 she said. More thorough and targeted data collection could lead to the development of 鈥減recision treatments for all groups of people.鈥

She ended with a call for the next generation of cognitive neuroscientists to expand the search for the root causes of cognitive decline.

鈥淢y focus now is to get a more precise measure on how the body is aging, not just chronological aging, but to find out if life experiences are more important than chronological aging,鈥 Turney said. 鈥淲e also need to study adolescents and children to see how life experiences affect our genetic makeup to identify different critical timepoints or periods of susceptibility. Hopefully, one of you out there will start to study different generations so we can study causes across different groups of people at different life stages.鈥