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Genetic variant may increase risk for CTE severity among older individuals with repetitive head impacts

Date:
June 27, 2022
Source:
Boston University School of Medicine
Summary:
A new study reveals that a genetic variant plays a major role in determining CTE severity and that having that variant makes an individual 2.34 times more likely to develop a more severe form of CTE.
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How could two individuals who both played football for 10 years and developed CTE have different disease severity? How could some individuals develop dementia in their 50's while other never develop dementia at all? Perhaps the answer lies in their genes.

Repetitive head impact (RHI) exposure is the chief risk factor for chronic traumatic encephalopathy (CTE). However, the occurrence and severity of CTE varies widely among those with similar RHI exposure.

Now a new study from researchers from the BU CTE Center reveals that the genetic variant,APOEε4 plays a major role in determining CTE severity and that havingAPOEε4 makes an individual 2.34 times more likely to develop a more severe form of CTE.

"This study provides the most concrete evidence to date thatAPOEε4 is a risk factor for CTE-related pathological and clinical outcomes. Understanding genetic underpinnings of CTE pathology may provide insights into disease mechanism and offers a precision medicine approach to harm reduction, including guiding decisions regarding contact sport play and providing a target for therapies," explains corresponding author Jesse Mez, MD, MS, director of the BU Alzheimer's Disease Research Center Clinical Core and a BU CTE Center investigator.

The researchers studied the brains of deceased individuals exposed to RHI through contact sports or military service, 294 of whom developed CTE and 70 of whom did not. They then analyzed their neurological findings based on theirAPOEstatus and found thatAPOEε4 carriers were 2.34 times more likely to have more severe CTE than those without. More severe CTE was determined by both CTE Stage (I through IV) and a quantitative analysis of abnormaltauprotein burden.

"Our research team has shown that among football players, an individual's odds of developing a more severe stage of CTE double every additional 4.4 years of play. Specifically, for football players over age 65, havingAPOEε4 had an effect on CTE severity equivalent to playing an additional seven years of football, meaning it more than doubled risk," says Mez.

According to the researchers, these findings provide insight into how CTE progresses, which may provide new targets for developing treatments to slow or stop CTE progression.

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Materialsprovided byBoston University School of Medicine.Note: Content may be edited for style and length.


Journal Reference:

  1. Kathryn Atherton, Xudong Han, Jaeyoon Chung, Jonathan D. Cherry, Zachary Baucom, Nicole Saltiel, Evan Nair, Bobak Abdolmohammadi, Madeline Uretsky, Mohammed Muzamil Khan, Conor Shea, Shruti Durape, Brett M. Martin, Joseph N. Palmisano, Kurt Farrell, Christopher J. Nowinski, Victor E. Alvarez, Brigid Dwyer, Daniel H. Daneshvar, Douglas I. Katz, Lee E. Goldstein, Robert C. Cantu, Neil W. Kowall, Michael L. Alosco, Bertrand R. Huber, Yorghos Tripodis, John F. Crary, Lindsay Farrer, Robert A. Stern, Thor D. Stein, Ann C. McKee, Jesse Mez.Association of APOE Genotypes and Chronic Traumatic Encephalopathy.JAMA Neurology, 2022; DOI:10.1001/jamaneurol.2022.1634

Cite This Page:

Boston University School of Medicine. "Genetic variant may increase risk for CTE severity among older individuals with repetitive head impacts." ScienceDaily. ScienceDaily, 27 June 2022. .
Boston University School of Medicine. (2022, June 27). Genetic variant may increase risk for CTE severity among older individuals with repetitive head impacts.ScienceDaily. Retrieved June 21, 2023 from www.koonmotors.com/releases/2022/06/220627124634.htm
Boston University School of Medicine. "Genetic variant may increase risk for CTE severity among older individuals with repetitive head impacts." ScienceDaily. www.koonmotors.com/releases/2022/06/220627124634.htm (accessed June 21, 2023).

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