Kukull Walter A, Higdon Roger, Bowen James D, McCormick Wayne C, Teri Linda, Schellenberg Gerard D, van Belle Gerald, Jolley Lance, Larson Eric B
National Alzheimer Coordinating Center, Department of Epidemiology, Box 357236, School of Public Health and Community Medicine, University of Washington, Seattle, WA 98195-7236, USA.
Arch Neurol. 2002 Nov;59(11):1737-46. doi: 10.1001/archneur.59.11.1737.
Age-specific incidence rates for dementia and Alzheimer disease (AD) are important for research and clinical practice. Incidence estimates for the United States are few and vary with the population sampled and study design; we present data that will contribute to a consensus of these rates.
To provide age-specific incidence estimates for dementia and AD and to estimate the association of sex, educational level, and apolipoprotein E genotype with onset.
Prospective cohort study; begun in 1994 with follow-up interviews every 2 years.
Members of community-based, large health maintenance organization with demographics consistent with the surrounding base population; diagnostic evaluation by university-based study clinicians.
Random sample of subjects aged 65 years or older from the base population; dementia free, nonnursing home residents. Of 5422 who were eligible, 2581 were enrolled, and 2356 had at least 1 follow-up evaluation (10 591 person-years of observation).
Dementia and Alzheimer disease diagnoses were based on standard criteria. Age-specific incidence rates were calculated using a person-years approach with Poisson distribution confidence intervals. Cox proportional hazards model analysis was used to examine other factors.
Two hundred fifteen cases of dementia and 151 cases of AD were diagnosed. Incidence rates for dementia and AD increase across the 5-year age groups; AD rates rise from 2.8 per 1000 person-years (age group, 65-69 years) to 56.1 per 1000 person-years in the older than 90-year age group. The rates nearly triple from the 75-to-79-year and 80-to-84-year age groups, but the relative increase is much less thereafter. Sex was not associated with AD onset. Educational level (>15 years vs <12 years) was associated with a decreased risk of AD; however, the association was also dependent on the baseline cognitive screening test score.
Our dementia and AD incidence rates are consistent with recent US and European cohort studies, providing clinicians and researchers new information concerning the reproducibility of incidence estimates across settings. Increased risk was associated with age and the apolipoprotein E genotype; also with a low baseline cognitive screening test score. Educational level was inversely associated with the risk of dementia and positively associated with the baseline cognitive test score; thus, detection of AD by the screening test could also be influenced by educational level.
痴呆症和阿尔茨海默病(AD)的年龄特异性发病率对于研究和临床实践很重要。美国的发病率估计数据较少,且因抽样人群和研究设计的不同而有所差异;我们提供的数据将有助于就这些发病率达成共识。
提供痴呆症和AD的年龄特异性发病率估计,并评估性别、教育程度和载脂蛋白E基因型与发病的关联。
前瞻性队列研究;始于1994年,每2年进行一次随访访谈。
以社区为基础的大型健康维护组织的成员,其人口统计学特征与周边基础人群一致;由大学研究临床医生进行诊断评估。
从基础人群中随机抽取的65岁及以上的受试者;无痴呆症,非养老院居民。在5422名符合条件的人中,2581人被纳入研究,2356人至少接受了1次随访评估(共10591人年的观察)。
痴呆症和AD的诊断基于标准标准。采用人年法并结合泊松分布置信区间计算年龄特异性发病率。使用Cox比例风险模型分析来研究其他因素。
诊断出215例痴呆症和151例AD。痴呆症和AD的发病率在5岁年龄组中呈上升趋势;AD发病率从每1000人年2.8例(年龄组为65 - 69岁)上升至90岁以上年龄组的每1000人年56.1例。在75 - 79岁和80 - 84岁年龄组中,发病率几乎增加了两倍,但此后相对增幅要小得多。性别与AD发病无关。教育程度(>15年与<12年)与AD风险降低相关;然而,这种关联也取决于基线认知筛查测试分数。
我们的痴呆症和AD发病率与近期美国和欧洲的队列研究结果一致,为临床医生和研究人员提供了关于不同环境下发病率估计可重复性的新信息。风险增加与年龄和载脂蛋白E基因型有关;也与较低的基线认知筛查测试分数有关。教育程度与痴呆症风险呈负相关,与基线认知测试分数呈正相关;因此,筛查测试对AD的检测也可能受教育程度的影响。