TY - JOUR
T1 - Long-term cognitive correlates of traumatic brain injury across adulthood and interactions with APOE genotype, Sex, and age cohorts
AU - Eramudugolla, Ranmalee
AU - Bielak, Allison A.M.
AU - Bunce, David
AU - Easteal, Simon
AU - Cherbuin, Nicolas
AU - Anstey, Kaarin J.
PY - 2014/4
Y1 - 2014/4
N2 - There is continuing debate about long-term effects of brain injury. We examined a range of traumatic brain injury (TBI) variables (TBI history, severity, frequency, and age of injury) as predictors of cognitive outcome over 8 years in an adult population, and interactions with apolipoprotein E (APOE) genotype, sex, and age cohorts. Three randomly sampled age cohorts (20-24, 40-44, 60-64 years at baseline; N = 6333) were each evaluated three times over 8 years. TBI variables, based on self-report, were separately modeled as predictors of cognitive performance using linear mixed effects models. TBI predicted longitudinal cognitive decline in all three age groups. APOE 4 + genotypes in the young and middle-aged groups predicted lower baseline cognitive performance in the context of TBI. Baseline cognitive performance was better for young females than males but this pattern reversed in middle age and old age. The findings suggest TBI history is associated with long-term cognitive impairment and decline across the adult lifespan. A role for APOE genotype was apparent in the younger cohorts but there was no evidence that it is associated with impairment in early old age. The effect of sex and TBI on cognition varied with age cohort, consistent with a proposed neuroprotective role for estrogen. (JINS, 2014, 20, 444-454)
AB - There is continuing debate about long-term effects of brain injury. We examined a range of traumatic brain injury (TBI) variables (TBI history, severity, frequency, and age of injury) as predictors of cognitive outcome over 8 years in an adult population, and interactions with apolipoprotein E (APOE) genotype, sex, and age cohorts. Three randomly sampled age cohorts (20-24, 40-44, 60-64 years at baseline; N = 6333) were each evaluated three times over 8 years. TBI variables, based on self-report, were separately modeled as predictors of cognitive performance using linear mixed effects models. TBI predicted longitudinal cognitive decline in all three age groups. APOE 4 + genotypes in the young and middle-aged groups predicted lower baseline cognitive performance in the context of TBI. Baseline cognitive performance was better for young females than males but this pattern reversed in middle age and old age. The findings suggest TBI history is associated with long-term cognitive impairment and decline across the adult lifespan. A role for APOE genotype was apparent in the younger cohorts but there was no evidence that it is associated with impairment in early old age. The effect of sex and TBI on cognition varied with age cohort, consistent with a proposed neuroprotective role for estrogen. (JINS, 2014, 20, 444-454)
KW - Cognitive decline
KW - Dementia
KW - Epidemiology
KW - Head injury
KW - Prospective study
UR - http://www.scopus.com/inward/record.url?scp=84897057556&partnerID=8YFLogxK
U2 - 10.1017/S1355617714000174
DO - 10.1017/S1355617714000174
M3 - Article
SN - 1355-6177
VL - 20
SP - 444
EP - 454
JO - Journal of the International Neuropsychological Society
JF - Journal of the International Neuropsychological Society
IS - 4
ER -