Scacchi R, De Bernardini L, Mantuano E, Donini L M, Vilardo T, Corbo R M
Department of Genetics and Molecular Biology, University La Sapienza, Rome, Italy.
Neurosci Lett. 1995 Dec 15;201(3):231-4. doi: 10.1016/0304-3940(95)12190-0.
The Apolipoprotein E (APOE) epsilon 4 allele has been found to be strongly associated with Alzheimer's disease (AD) in most studies conducted up to now, though not all investigators have established a similar association with other forms of dementia, like vascular dementia. Our study examined the APOE polymorphism in a sample of 149 dementia patients, of which there were 80 with probable sporadic late-onset AD, 16 with a mixed form of dementia (MD), and 53 with vascular dementia (VD). An elderly control sample was composed of 126 subjects. The data obtained on the whole AD sample did not confirm the association already reported with APOE epsilon 4. A difference did emerge when the subjects were subdivided on the basis of age at the examination. AD patients aged < or = 80 years significantly differed from the correspondent elderly controls, while no difference was observed between the patients aged 81 years or older and controls. This pattern could be due to a previous disadvantageous effect of the epsilon 4 allele on the subjects bearing it. A substantially similar pattern was observed in the few MD patients, while no differences were found in the two VD subgroups. The odds ratio (OR) for AD associated with at least one epsilon 4 allele was significant and equal to 3.3 (95% CI = 1.2-9.1) for the < or = 80 age class, while it was not significant and equal to 1.1 (95% CI = 0.4-2.8) for the > 80 age class. Our data indicate that in AD patients aged less than 81 years, epsilon 4 is clearly associated with AD and that it can be considered a risk factor for AD chiefly before this age.
在迄今为止进行的大多数研究中,载脂蛋白E(APOE)ε4等位基因已被发现与阿尔茨海默病(AD)密切相关,不过并非所有研究人员都证实其与其他形式的痴呆(如血管性痴呆)存在类似关联。我们的研究检测了149例痴呆患者样本中的APOE多态性,其中80例为可能的散发性晚发型AD,16例为混合型痴呆(MD),53例为血管性痴呆(VD)。老年对照组样本由126名受试者组成。在整个AD样本中获得的数据并未证实已报道的与APOE ε4的关联。当根据检查时的年龄对受试者进行细分时,差异确实出现了。年龄≤80岁的AD患者与相应的老年对照组有显著差异,而81岁及以上的患者与对照组之间未观察到差异。这种模式可能是由于ε4等位基因对携带它的受试者先前存在不利影响。在少数MD患者中观察到了基本相似的模式,而在两个VD亚组中未发现差异。对于年龄≤80岁的人群,与至少一个ε4等位基因相关的AD优势比(OR)显著,等于3.3(95%置信区间=1.2 - 9.1),而对于年龄>80岁的人群,该优势比不显著,等于1.1(95%置信区间=0.4 - 2.8)。我们的数据表明,在年龄小于81岁的AD患者中,ε4与AD明显相关,并且主要在这个年龄之前它可被视为AD的一个危险因素。