Associations Between Traumatic Brain Injury and Cognitive Decline Among Older Male Veterans: A Twin Study.

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Date

2023-10

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Abstract

Background and objectives

Traumatic brain injuries (TBIs) are associated with increased risk of dementia, but whether lifetime TBI influences cognitive trajectories in later life is less clear. Cognitive interventions after TBI may improve cognitive trajectories and delay dementia. Because twins share many genes and environmental factors, we capitalize on the twin study design to examine the association between lifetime TBI and cognitive decline.

Methods

Participants were members of the National Academy of Sciences-National Research Council's Twin Registry of male veterans of World War II with self or proxy-reported history of TBI and with up to 4 observations over 12 years of the modified Telephone Interview for Cognitive Status (TICS-m). We used linear random-effects mixed models to analyze the association between TBI and TICS-m in the full sample and among co-twins discordant for TBI. Additional TBI predictor variables included number of TBIs, severity (loss of consciousness [LOC]), and age of first TBI (age <25 vs 25+ years [older age TBI]). Models were adjusted for age (centered at 70 years), age-squared, education, wave, twin pair, lifestyle behaviors, and medical conditions.

Results

Of 8,662 participants, 25% reported TBI. History of any TBI (β = -0.56, 95% CI -0.73 to -0.39), TBI with LOC (β = -0.51, 95% CI -0.71 to -0.31), and older age TBI (β = -0.66, 95% CI -0.90 to -0.42) were associated with lower TICS-m scores at 70 years. TBI with LOC (β = -0.03, 95% CI -0.05 to -0.001), more than one TBI (β = -0.05, 95% CI -0.09 to -0.002,), and older age TBI (β = -0.06, 95% CI -0.09 to -0.03) were associated with faster cognitive decline. Among monozygotic pairs discordant for TBI (589 pairs), history of any TBI (β = -0.55, 95% CI -0.91 to -0.19) and older age TBI (β = -0.74, 95% CI -1.22 to -0.26) were associated with lower TICS-m scores at 70 years. Those with more than one TBI (β = -0.13, 95% CI -0.23 to -0.03) and older age TBI (β = -0.07, 95% CI -0.13 to -0.002) showed greater cognitive decline compared with their co-twin without TBI.

Discussion

These findings support an association of the effect of TBI on cognitive score and the rapidity of cognitive decline in later life. The results in monozygotic pairs, who share all genes and many exposures, particularly in early life, provide additional evidence of a causal relationship between TBI and poorer late-life cognitive outcomes.

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Humans, Dementia, Unconsciousness, Adult, Aged, Veterans, Male, Cognitive Dysfunction, Brain Injuries, Traumatic

Citation

Published Version (Please cite this version)

10.1212/wnl.0000000000207819

Publication Info

Chanti-Ketterl, Marianne, Carl F Pieper, Kristine Yaffe and Brenda L Plassman (2023). Associations Between Traumatic Brain Injury and Cognitive Decline Among Older Male Veterans: A Twin Study. Neurology, 101(18). pp. e1761–e1770. 10.1212/wnl.0000000000207819 Retrieved from https://hdl.handle.net/10161/33790.

This is constructed from limited available data and may be imprecise. To cite this article, please review & use the official citation provided by the journal.

Scholars@Duke

Chanti-Ketterl

Marianne Chanti-Ketterl

Assistant Professor in Psychiatry and Behavioral Sciences

I am a geroscientist and epidemiologist with expertise in cognitive health and neurodegenerative conditions, particularly Alzheimer’s disease and related dementias. My research program examines how the exposome influences brain health throughout the lifespan, with a specific focus on environmental exposures, alongside social, behavioral, and biological factors. My work has investigated traumatic brain injury, metabolic biomarkers, resilience, and cognitive training. Through these efforts, I aim to identify modifiable pathways that promote healthy cognitive aging, reduce risk, and delay disease progression across diverse aging populations.

 

A central focus of my scholarship is to improve the inclusiveness, reach, and translational impact of aging and brain health research. My work addresses persistent gaps in participation and representation among older adults from communities historically under-engaged in scientific studies, to ensure that research findings are generalizable, equitable, and relevant to the broader U.S. population. In parallel with my research program, I serve as Faculty Operational Director for the North Carolina Registry for Brain Health, where I lead statewide initiatives to expand research engagement, strengthen community and institutional partnerships, and connect older adults with brain health studies. I also coordinate the Duke Aging Center’s T32 fellowship program and am deeply committed to mentoring students, postdoctoral fellows, and early-career investigators. Across these roles, I aim to advance rigorous, community-informed science while cultivating the next generation of scholars prepared to address the complex needs of an aging society.

 



Pieper

Carl F. Pieper

Professor Emeritus of Biostatistics & Bioinformatics

Analytic Interests.

1) Issues in the Design of Medical Experiments: I explore the use of reliability/generalizability models in experimental design. In addition to incorporation of reliability, I study powering longitudinal trials with multiple outcomes and substantial missing data using Mixed models.

2) Issues in the Analysis of Repeated Measures Designs & Longitudinal Data: Use of Hierarchical Linear Models (HLM) or Mixed Models in modeling trajectories of multiple variables over time (e.g., physical and cognitive functioning and Blood Pressure). My current work involves methodologies in simultaneous estimation of trajectories for multiple variables within and between domains, modeling co-occuring change.

Areas of Substantive interest: (1) Experimental design and analysis in gerontology and geriatrics, and psychiatry,
(2) Multivariate repeated measures designs,

Plassman

Brenda Lee Plassman

Professor in Psychiatry and Behavioral Sciences

My research interests include the following areas:
1) Epidemiological studies to examine the prevalence and incidence of dementia and cognitive impairment, not dementia (CIND)
2) Studies examining risk and protective factors for dementia and CIND
3) Behavioral genetics of aging and dementia with an emphasis on twin studies
4) Long term outcomes of traumatic brain injury
5) Oral health and cognition in later life


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