The role of apolipoprotein E episilon (ɛ)-4 allele on outcome following traumatic brain injury: A systematic review

DW Lawrence, P Comper, MG Hutchison, B Sharma - Brain injury, 2015 - Taylor & Francis
Brain injury, 2015Taylor & Francis
Background: The apolipoprotein E gene (APOE) has emerged as a candidate for
prognosticating traumatic brain injury (TBI) recovery, with APOE ɛ 4 identified as a
susceptibility marker for poor outcome, despite large discrepancy in its reported influence
post-TBI. Methods: A systematic review was conducted, including all primary articles
investigating the role of APOE ɛ 4 on TBI outcome. A total of 65 studies were included,
including 24 predominantly investigating mild (mTBI), seven moderate (modTBI) and 33 …
Abstract
Background: The apolipoprotein E gene (APOE) has emerged as a candidate for prognosticating traumatic brain injury (TBI) recovery, with APOEɛ4 identified as a susceptibility marker for poor outcome, despite large discrepancy in its reported influence post-TBI.
Methods: A systematic review was conducted, including all primary articles investigating the role of APOEɛ4 on TBI outcome. A total of 65 studies were included, including 24 predominantly investigating mild (mTBI), seven moderate (modTBI) and 33 severe (sTBI); severity was not reported in one study.
Results: In mTBI studies, the association between APOEɛ4 and post-TBI outcome was concluded as non-contributory in 14 studies (58.3%), hazardous in nine (37.5%) and protective in one (4.2%). In sTBI studies, the role of APOEɛ4 was hazardous in 21 (63.6%), non-contributory in nine (27.3%) and protective in three (9.1%). Of the seven studies investigating dementia outcomes, four observed a hazardous association with APOEɛ4, while three reported no association. Six studies examined Alzheimer’s dementia pathology, of which three reported a hazardous influence of APOEɛ4.
Conclusions: The influence of APOEɛ4 on neuropsychological testing, functional outcome and in paediatric populations was incongruous. This review supports the majority of research indicating APOEɛ4 adversely influences recovery following TBI, particularly with respect to dementia-related outcomes and outcomes following sTBI.
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