Schellenberg G D, Boehnke M, Wijsman E M, Moore D K, Martin G M, Bird T D
Division of Neurology, University of Washington, Seattle 98195.
Ann Neurol. 1992 Feb;31(2):223-7. doi: 10.1002/ana.410310214.
We previously reported a genetic association between the 3.5 kb (F) Taq I restriction fragment length polymorphism allele of the apolipoprotein CII gene on chromosome 19 and familial Alzheimer's disease. Here, we report an additional analysis of this association performed on an expanded and better defined data set of 23 families with familial Alzheimer's disease. The F allele frequency in affected family members in the expanded set was 0.62 +/- 0.06 (mean +/- standard error, n = 51 subjects), which differed significantly from a frequency of 0.39 +/- 0.02 (n = 226) for unrelated control subjects (Z = 3.75, p less than 0.0002). These results are consistent with our previous findings and suggest an association between the F allele of apolipoprotein CII and familial Alzheimer's disease. When the apolipoprotein CII locus was tested for linkage to familial Alzheimer's disease, LOD scores summed for the complete group of families were negative and close linkage was excluded. Close linkage was also excluded for early-onset families (mean onset age less than or equal to 60 years), but small positive LOD scores were obtained for late-onset kindreds.
我们先前报道过,位于19号染色体上的载脂蛋白CII基因的3.5 kb (F) Taq I限制性片段长度多态性等位基因与家族性阿尔茨海默病之间存在遗传关联。在此,我们报告了对这一关联的进一步分析,该分析是在一个经过扩充且定义更明确的数据集上进行的,该数据集包含23个患有家族性阿尔茨海默病的家庭。在扩充后的数据集里,患病家庭成员中的F等位基因频率为0.62±0.06(均值±标准误,n = 51名受试者),这与无关对照受试者的频率0.39±0.02(n = 226)有显著差异(Z = 3.75,p < 0.0002)。这些结果与我们之前的发现一致,表明载脂蛋白CII的F等位基因与家族性阿尔茨海默病之间存在关联。当对载脂蛋白CII基因座进行与家族性阿尔茨海默病的连锁分析时,所有家庭的LOD分数总和为阴性,排除了紧密连锁。早发型家庭(平均发病年龄小于或等于60岁)也排除了紧密连锁,但晚发型亲属获得了小的正LOD分数。