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Assessing Changes in Synaptic Plasticity Using an Awake Closed-Head Injury Model of Mild Traumatic Brain Injury
Published on: January 20, 2023
Mild Traumatic Brain Injury Does Not Significantly Affect Midlife Cognitive Functioning Within the General
Alice Theadom1, Suzanne Barker-Collo, Varsha Parag
1Author Affiliations: Traumatic Brain Injury Network (TBIN), School of Clinical Sciences, Faculty of Health and Environment Sciences, Auckland University of Technology, Auckland, New Zealand (Dr Theadom); School of Psychology, University of Auckland, Auckland, New Zealand (Dr Barker-Collo); National Institute for Health Innovation, University of Auckland, Auckland, New Zealand (Dr Parag); Dunedin Multidisciplinary Health & Development Research Unit, University of Otago, Otago, New Zealand (Mr Hogan and Drs Ramrakha and Poulton); and Department of Psychology and Neuroscience, Duke University, Durham, North Carolina (Drs Caspi and Moffitt).
Objective:
To determine whether differences exist in mid-adulthood cognitive functioning in people with and without history of mild traumatic brain injury (mTBI).
Setting:
Community-based study.
Participants:
People born between April 1, 1972, and March 31, 1973, recruited into the Dunedin Multidisciplinary Health and Development Longitudinal Study, who completed neuropsychological assessments in mid-adulthood. Participants who had experienced a moderate or severe TBI or mTBI in the past 12 months were excluded.
Design:
Longitudinal, prospective, observational study.
Main Measures:
Data were collected on sociodemographic characteristics, medical history, childhood cognition (between 7 and 11 years), and alcohol and substance dependence (from 21 years of age). mTBI history was determined from accident and medical records (from birth to 45 years of age). Participants were classified as having 1 mTBI and more in their lifetime or no mTBI. The Wechsler Adult Intelligence Scale (WAIS-IV) and Trail Making Tests A and B (between 38 and 45 years of age) were used to assess cognitive functioning. T tests and effect sizes were used to identify any differences on cognitive functioning domains between the mTBI and no mTBI groups. Regression models explored the relative contribution of number of mTBIs and age of first mTBI and sociodemographic/lifestyle variables on cognitive functioning.
Results:
Of the 885 participants, 518 (58.5%) had experienced at least 1 mTBI over their lifetime, with a mean number of 2.5 mTBIs. The mTBI group had significantly slower processing speed ( P < .01, d = 0.23) in mid-adulthood than the no TBI controls, with a medium effect size. However, the relationship no longer remained significant after controlling for childhood cognition, sociodemographic and lifestyle factors. No significant differences were observed for overall intelligence, verbal comprehension, perceptual reasoning, working memory, attention, or cognitive flexibility. Childhood cognition was not linked to likelihood of sustaining mTBI later in life.
Conclusion:
mTBI histories in the general population were not associated with lower cognitive functioning in mid-adulthood once sociodemographic and lifestyle factors were taken into account.
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