Millar K, Nicoll J A R, Thornhill S, Murray G D, Teasdale G M
Division of Behavioural Medicine, Department of Psychological Medicine, University of Glasgow, Gartnavel Royal Hospital, Glasgow, Scotland, UK.
J Neurol Neurosurg Psychiatry. 2003 Aug;74(8):1047-52. doi: 10.1136/jnnp.74.8.1047.
Existing evidence suggests that some patients who sustain a head injury suffer cognitive decline many years later, and that head injury and possession of the APOE epsilon 4 allele are each risk factors for Alzheimer's disease.
To determine whether late cognitive decline after head injury is more prevalent among carriers of APOE epsilon 4.
A database of head injured patients was used. Initial assessment was at the time of their injury, between 1968 and 1985, and outcome data at six months were available. Their ages at the time of injury ranged between 2 and 70 years. A cohort of 396 subjects was reassessed at a mean of 18 years later, with determination of APOE genotype and detailed neuropsychological testing.
Judging by the Glasgow outcome scale, twice as many patients had deteriorated as improved between six months after injury and the late assessment; 22.2% of APOE epsilon 4 carriers had a good late outcome compared with 30.5% of non-carriers (95% confidence interval for the difference, -0.7% to 17.2%; p = 0.084). There were no clear differences between epsilon 4 carriers and non-carriers in detailed neuropsychological assessments.
Although this study provides additional evidence that a late decline may occur after head injury, there was no clear relation to APOE genotype. Despite the follow up interval of 15 to 25 years, the cohort is still too young (mean age 42.1 years) to assess the risk of Alzheimer's disease.
现有证据表明,一些头部受伤的患者多年后会出现认知能力下降,并且头部受伤和携带APOE ε4等位基因均为阿尔茨海默病的危险因素。
确定APOE ε4携带者中头部受伤后晚期认知能力下降是否更为普遍。
使用头部受伤患者数据库。初始评估在其受伤时进行,时间为1968年至1985年之间,且可获得六个月时的结局数据。他们受伤时的年龄在2岁至70岁之间。对396名受试者组成的队列在平均18年后进行重新评估,确定APOE基因型并进行详细的神经心理学测试。
根据格拉斯哥结局量表判断,从受伤后六个月到晚期评估期间,病情恶化的患者数量是病情改善患者数量的两倍;22.2%的APOE ε4携带者晚期结局良好,而非携带者为30.5%(差异的95%置信区间为-0.7%至17.2%;p = 0.084)。在详细的神经心理学评估中,ε4携带者和非携带者之间没有明显差异。
尽管本研究提供了更多证据表明头部受伤后可能会出现晚期衰退,但与APOE基因型并无明确关联。尽管随访间隔为15至25年,但该队列仍然过于年轻(平均年龄42.1岁),无法评估患阿尔茨海默病的风险。