Genetic vulnerability following traumatic brain injury: the role of apolipoprotein E

被引:69
作者
Nathoo, N
Chetty, R
van Dellen, JR
Barnett, GH
机构
[1] Cleveland Clin Fdn, Dept Neurosurg, Cleveland, OH 44195 USA
[2] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON M5G 2M9, Canada
[3] Charing Cross Hosp, Imperial Coll Sch Med, London W6 8RF, England
[4] Charing Cross Hosp, W London Neurosci Ctr, London W6 8RF, England
来源
JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY | 2003年 / 56卷 / 03期
关键词
D O I
10.1136/mp.56.3.132
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Apolipoprotein E (APOE) is thought to be responsible for the transportation of lipids within the brain, maintaining structural integrity of the microtubule within the neurone, and assisting with neural transmission. Possession of the APOE epsilon4 allele has also been shown to influence neuropathological findings in patients who die from traumatic brain injury, including the accumulation of amyloid beta protein. Previous clinical studies reporting varying outcome severities of traumatic brain injury, including cognitive and functional recovery, all support the notion that APOE epsilon4 allele possession is associated with an unfavourable outcome. Evidence from experimental and clinical brain injury studies confirms that APOE plays an important role in the response of the brain to injury.
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页码:132 / 136
页数:5
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