载脂蛋白E与阿尔茨海默病:关联强度与发病年龄有关

D L Murman, N L Foster, S P Kilgore, C A McDonagh, J K Fink
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引用次数: 26

摘要

载脂蛋白E (apoE) epsilon 4等位基因频率在阿尔茨海默病(AD)患者中与对照组相比增加,并受到其他遗传因素和症状发作年龄的影响。我们通过比较正常老年对照受试者(n = 107)与AD患者(n = 123)的apoE epsilon 4等位基因频率来研究AD症状发病年龄与apoE之间的关系,并将其分为4个发病年龄期。此外,确定了携带apoE epsilon 4等位基因和不携带apoE epsilon 4等位基因的AD患者的症状发病年龄分布。我们观察到apoE epsilon 4等位基因频率在AD发病年龄55 - 75岁之间增加,但在发病年龄的极端(即45 - 54岁之间和75岁以后)没有增加。我们的数据表明,携带载脂蛋白ε 4等位基因会增加阿尔茨海默病患者在发病年龄中期出现症状的可能性。在AD发病年龄的极端情况下,非apoe因素,包括其他遗传因素和年龄,是AD发病风险的更重要决定因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Apolipoprotein E and Alzheimer's disease: strength of association is related to age at onset.

Apolipoprotein E (apoE) epsilon 4 allele frequency among Alzheimer's disease (AD) patients is increased compared to control subjects and is influenced by the presence of other genetic factors and age at symptom onset. We examined the relationship between age at AD symptom onset and apoE by comparing the apoE epsilon 4 allele frequency of normal, elderly control subjects (n = 107) to that in AD patients (n = 123), divided into four age-at-onset periods. Additionally, the distribution of symptom onset ages of AD patients with and without apoE epsilon 4 alleles was determined. We observed increased apoE epsilon 4 allele frequencies between the AD onset ages of 55 and 75 years, but not at the extremes of onset ages (i.e. onset between 45 and 54 years of age and after age 75). Our data suggests that having an apoE epsilon 4 allele increases the likelihood that AD patients will develop symptoms in the middle range of onset ages. At the extremes of AD onset ages, non-apoE factors, including other genetic factors and age, are more important determinants of risk of developing AD.

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