98%
921
2 minutes
20
Background: A history of traumatic brain injury (TBI) is associated with an increased risk of developing neurodegenerative disorders, including Parkinson's Disease (PD). However, TBI's influences on disease progression remain underassessed. This study explored whether a history of TBI influences the progression of pathological and clinical outcomes up to 5 years of follow-up in individuals with early PD.
Methods: Longitudinal data were extracted from the Parkinson's Progression Markers Initiative (PPMI) and the PostCEPT observational study. Participants in PostCEPT had complete head injury data, while PPMI participants were eligible if they completed the head injury section of the PD Risk Factor Questionnaire (n = 208). Principal component analysis was used to derive composite scores of cognitive ability and mood dysfunction, with motor outcomes calculated using the Movement Disorders Society Unified Parkinson's Disease Rating Scale. Progression of clinical and pathological outcomes up to 5 years and 4 years following study entry were compared, including subset analyses in PPMI examining injury severity.
Results: Individuals with a history of TBI in the PPMI dataset exhibited a younger age of onset; however, a history of TBI did not affect progression rates of any assessed variables across both cohorts. Exploratory analysis determined that injury severity significantly predicted striatal dopamine transporter binding but accounted for only a small portion of outcome variance.
Conclusion: While the history of TBI was associated with earlier PD onset, it did not correspond to a differential disease course. However, given differences in TBI characterisation between cohorts, additional research must be conducted to validate these findings.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11926254 | PMC |
http://dx.doi.org/10.1111/ene.70090 | DOI Listing |
Neurotrauma Rep
August 2025
Department of Neurological Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
The sports medicine community and society at large have recognized traumatic brain injury (TBI) as a major public health concern. It is estimated that more than 150 million youths have played football in the United States. As an alternative to blood, sweat is a potential source for protein biomarkers, providing a non-invasive method for objective measurements for head safety guidelines.
View Article and Find Full Text PDFNeurotrauma Rep
August 2025
Department of Rehabilitation and Human Performance, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Recent investments in large-scale mortem tissue collection have accelerated opportunities to understand the neuropathology of traumatic brain injury (TBI) and post-traumatic neurodegeneration (PTND). Clinicopathological correlation requires ante-mortem clinical information. Post-mortem family interviews (PFIs) are an established method to capture comprehensive ante-mortem clinical information.
View Article and Find Full Text PDFAlcohol Res
September 2025
Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, Washington.
Purpose: Alcohol use disorder (AUD) and mild traumatic brain injury (mTBI) have a bidirectional, synergistic, and complicated relationship. Although it is difficult to definitively say that mTBI causes AUD, certain biological mechanisms that occur after trauma are also associated with hazardous alcohol use. Hazardous drinking is defined as any quantity or pattern of alcohol consumption that places people at risk for physical and/or psychological harm.
View Article and Find Full Text PDFClinical apathy might result from either a diminished willingness to exert effort for known rewards or from reduced motivation to explore potentially beneficial future opportunities. To identify the underlying cognitive and neural bases of apathy, we used task-based fMRI to examine motivated choice computations in patients with chronic traumatic brain injury (TBI)-a condition frequently associated with apathy-and compared their behavior and neural activity to that of healthy controls (CTRLs). Participants performed two choice tasks involving distinct types of motivational tradeoffs: i) An effort-value tradeoff task (the 'Apples Task') requiring them to decide how much physical effort they were willing to exert for varying reward magnitudes, and ii) An explore-exploit tradeoff task (the 'Novelty-Bandit Task') requiring them to choose between exploiting options with a known history of reward or exploring novel options with uncertain but potentially higher future value.
View Article and Find Full Text PDFCureus
July 2025
Department of Neuroanesthesiology and Neurocritical Care, National Institute of Mental Health and Neurosciences, Bengaluru, IND.
A 38-year-old man sustained a traumatic brain injury (TBI) following a road traffic accident, presenting unconscious with vomiting and right ear bleeding. He had a prior history of head trauma with cranioplasty. On admission, he was deeply unconscious (Glasgow Coma Scale (GCS) E1VTM3) with unequal non-reactive pupils.
View Article and Find Full Text PDF