首页> 外文期刊>Brain: A journal of neurology >Age, Alzheimer's disease and dementia in the Baltimore Longitudinal Study of Ageing.
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Age, Alzheimer's disease and dementia in the Baltimore Longitudinal Study of Ageing.

机译:巴尔的摩纵向老龄化研究中的年龄,阿尔茨海默氏病和痴呆症。

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Recent studies suggest that dementia in the most elderly (90 years of age and above) is only modestly related to Alzheimer's disease pathology. This raises the possibility that other, as yet unknown, disease processes may underlie dementia in this rapidly growing demographic group, and that efforts designed to combat Alzheimer's disease may not be appropriate for treating dementia in very elderly subjects. To study this question more closely, we examined the relationship between neocortical Alzheimer-type brain pathology and dementia in consecutive autopsies from 209 participants in the Baltimore Longitudinal Study of Ageing, a prospective longitudinal cohort study of the effect of ageing on cognition. Almost half of the cohort was older than 90 years of age at death. We found that several measures of neocortical Alzheimer's pathology, including the Consortium to Establish a Registry of Alzheimer's Disease neuritic plaque score and the Braak neurofibrillary tangle score, remained significant predictors of dementia, independent of age. In participants older than 90 years of age, intracranial atherosclerosis emerged as an important predictor of dementia in subjects with low Alzheimer's pathology scores, but did not mitigate the importance or population attributable risk of high Alzheimer's pathology scores on the odds of dementia. There was evidence that the threshold score for neurofibrillary pathology to cause dementia increased in the oldest subjects, but this was offset by an overall increase in neurofibrillary pathology in this age group. We conclude that neocortical Alzheimer's disease pathology remains significantly correlated with dementia, independent of age. In the most elderly, atherosclerosis also emerged as a cause of dementia in subjects with low Alzheimer's pathology scores. We found no evidence for a significant number of elderly subjects having dementia without an apparent cause.
机译:最近的研究表明,大多数老年人(90岁及以上)的痴呆仅与阿尔茨海默氏病的病理状况有一定关系。这增加了在这一迅速增长的人口群体中痴呆症可能是其他疾病过程(尚不清楚)的基础,而旨在对抗阿尔茨海默氏病的努力可能不适用于治疗老年患者的痴呆症。为了更仔细地研究这个问题,我们在巴尔的摩纵向老龄化研究中对209名参与者进行的连续尸检中检查了新皮质阿尔茨海默病型脑病理学与痴呆之间的关系,这是一项关于衰老对认知影响的前瞻性纵向队列研究。该队列中几乎有一半的人死于90岁以上。我们发现,新皮质阿尔茨海默氏病的多种测量指标,包括建立阿尔茨海默氏病神经病斑块评分和Braak神经原纤维缠结评分的联盟,仍然是老年痴呆症的重要预测指标,与年龄无关。在90岁以上的受试者中,颅内动脉粥样硬化已成为阿尔茨海默氏病病理评分较低的受试者痴呆的重要预测指标,但并未减轻痴呆几率对阿尔茨海默氏病病理评分较高的重要性或人群归因风险。有证据表明,在年龄最大的受试者中,引起痴呆的神经原纤维病理学阈值得分升高,但这一年龄组神经原纤维病理学总体升高抵消了这一得分。我们得出结论,新皮质阿尔茨海默氏病的病理学仍然与痴呆症显着相关,与年龄无关。在大多数老年人中,阿尔茨海默氏病病理评分较低的受试者中,动脉粥样硬化也成为痴呆的原因。我们没有证据表明大量老年痴呆症患者没有明显原因。

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