van Duijn C M, Farrer L A, Cupples L A, Hofman A
Department of Epidemiology and Biostatistics, Erasmus University Medical School, Rotterdam, The Netherlands.
J Med Genet. 1993 Aug;30(8):640-6. doi: 10.1136/jmg.30.8.640.
We evaluated age at onset and transmission patterns of Alzheimer's disease (AD) in families of 198 patients who had onset of symptoms before the age of 65 years and were diagnosed before the age of 70 years. Patients were ascertained in a population based study in The Netherlands. The results suggest that the risk of AD by the age of 90 in first degree relatives is 39% (95% confidence interval 27 to 51). By the age of 90, this risk is 2.8 (95% confidence interval 1.5-5.2) times greater than the corresponding risk of 14% among relatives of age and sex matched control subjects. Segregation analysis indicated that patterns of familial clustering are best explained by transmission of a major autosomal dominant gene with reduced penetrance and a multifactorial component. However, the single major locus model could be rejected in favour of the mixed model only when a cohort effect for heritability was allowed for. The frequency of the AD susceptibility allele was estimated to be 0.48% in the single major locus model and 0.31% in the mixed model. Although our study confirms that a dominant major gene is implicated in early onset AD, the results suggest that other genetic or perhaps non-genetic factors may account for the disease in a considerable number of patients.
我们评估了198例在65岁前出现症状且在70岁前被诊断为阿尔茨海默病(AD)的患者家庭中AD的发病年龄和遗传模式。这些患者是在荷兰一项基于人群的研究中确定的。结果表明,一级亲属在90岁时患AD的风险为39%(95%置信区间27%至51%)。到90岁时,这一风险比年龄和性别匹配的对照受试者亲属中相应的14%的风险高2.8倍(95%置信区间1.5 - 5.2)。分离分析表明,家族聚集模式最好由一个具有降低外显率的主要常染色体显性基因的传递和一个多因素成分来解释。然而,只有当考虑到遗传力的队列效应时,单一位点模型才可能被拒绝而支持混合模型。在单一位点模型中,AD易感等位基因的频率估计为0.48%,在混合模型中为0.31%。尽管我们的研究证实了一个显性主要基因与早发性AD有关,但结果表明,其他遗传因素或可能的非遗传因素可能在相当数量的患者中导致了这种疾病。