Apolipoprotein e (APOE) ε4 genotype influences memory performance following remote traumatic brain injury in U.S. military service members and veterans.
Genetics
Head injury
Military
Neurocognition
Neuropsychological assessment
TBI
Verbal memory
Journal
Brain and cognition
ISSN: 1090-2147
Titre abrégé: Brain Cogn
Pays: United States
ID NLM: 8218014
Informations de publication
Date de publication:
11 2021
11 2021
Historique:
received:
19
03
2021
revised:
27
08
2021
accepted:
29
08
2021
pubmed:
7
9
2021
medline:
5
11
2021
entrez:
6
9
2021
Statut:
ppublish
Résumé
The purpose of this study was to examine the association between the apolipoprotein E (APOE) ε4 allele and neurocognitive functioning following traumatic brain injury (TBI) in military service members and veterans (SMVs). Participants included 176 SMVs with a history of remote TBI (≥1 year post-injury), categorized into mild (n = 100), moderate (n = 40), and severe (n = 36) TBI groups. Participants completed a neuropsychological assessment and APOE genotyping (n = 46 ε4+, n = 130 ε4-). Neurocognitive composite scores representing memory, executive functioning, and visual processing speed were computed. ANCOVAs adjusting for race, education, combat exposure, and PTSD symptom severity showed a significant main effect of ε4 on the memory composite, such that ε4+ SMVs exhibited poorer memory performance than ε4- SMVs. When ε2 allele carriers were removed from the analyses, associations with memory were strengthened, demonstrating a possible protective effect of the ε2 allele. No main effect of TBI group was identified on any cognitive composite, nor were there any significant TBI group × ε4 status interactions for any cognitive composite. Future studies with larger samples are needed to verify these findings, but our results suggest an important relationship between ε4 status and memory functioning following remote TBI of all severities.
Identifiants
pubmed: 34487993
pii: S0278-2626(21)00110-X
doi: 10.1016/j.bandc.2021.105790
pii:
doi:
Substances chimiques
ApoE protein, human
0
Apolipoprotein E4
0
Apolipoproteins E
0
Types de publication
Journal Article
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
105790Subventions
Organisme : CSRD VA
ID : IK2 CX001952
Pays : United States
Informations de copyright
Published by Elsevier Inc.