阿尔茨海默病和其他神经病变与痴呆症患者和非痴呆症患者功能障碍的关系

Jose M Farfel, Ana W Capuano, Aron S Buchman, Julie A Schneider, David A Bennett
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摘要

背景 痴呆症是由多种神经病理变化引起的认知功能障碍,其严重程度足以影响功能状态。然而,这些病变和功能障碍在非痴呆症患者中也很常见。我们研究了注意力缺失症和其他多种神经病变与痴呆症患者和非痴呆症患者的工具性和基本日常生活活动之间的关系。方法 参与者是来自宗教团体研究(Religious Orders Study)或拉什记忆与衰老项目(Rush Memory and Aging Project)的 1,509 名逝者。除了四种非老年痴呆症神经退行性病变:脑淀粉样血管病(CAA)、海马硬化症、TDP-43和路易体,以及四种脑血管病变:大面积梗塞和微梗塞、动脉粥样硬化和动脉硬化,还对病理性老年痴呆症和其他三种老年痴呆症指数进行了检查。功能评估包括劳顿和卡茨指数器质性和基本日常生活活动(IADL 和 BADL)。使用调整了年龄、性别和教育程度的正回归模型来研究神经病变与 IADL 和 BADL 的关系。结果 除动脉粥样硬化和 CAA 与 BADL 无关外,AD 和其他神经病变均与 IADL 受损(Ps<0.001)和 BADL 受损(Ps<0.01)有关。大多数神经病变的影响主要受痴呆症的影响。然而,在对痴呆模型进行调整后,PHFtau缠结对IADL的影响仍然很小。在对痴呆模型进行调整后,粗梗塞对 IADL 和 BADL 的直接影响以及微梗塞对 BADL 的直接影响保持不变。结论 老年痴呆症和所有其他神经病变与功能障碍密切相关。除严重梗死和微梗死外,大多数神经病理与残疾的关系都因痴呆而消除或减弱。
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Association of Alzheimer’s Disease and Other Neuropathologies with Functional Disability in Persons With and Without Dementia
Background Dementia results from multiple neuropathologies causing cognitive impairment sufficiently severe to impact functional status. However, these pathologies and functional impairment are common in persons without dementia. We examined the association of AD and multiple other neuropathologies with instrumental and basic activities of daily living in persons with and without dementia. Methods Participants were 1,509 deceased from the Religious Orders Study or Rush Memory and Aging Project. Pathologic AD and three other AD indices were examined, in addition to four non-AD neurodegenerative pathologies: cerebral amyloid angiopathy (CAA), hippocampal sclerosis, TDP-43 and Lewy bodies, and four cerebrovascular pathologies: gross- and microinfarctions, athero- and arteriolosclerosis. Functional assessment included Lawton and Katz Index Instrumental and Basic Activities of Daily Living (IADL and BADL). Ordinal regression models adjusted for age, sex, and education were used to examine the association of neuropathologies with IADL and BADL. Results AD and the other neuropathologies were associated with impaired IADL (all Ps<0.001) and with impaired BADL (Ps<0.01), except for atherosclerosis and CAA which were not associated with BADL. The effects of most neuropathologies were largely affected by dementia. However, small effects on IADL remained for PHFtau tangles after adjusting models for dementia. Direct effects of gross infarcts on IADL and BADL, and of microinfarcts on BADL remained unchanged after adjusting the models for dementia. Conclusion AD and all other neuropathologies are strongly associated with functional disability. The association of most neuropathologies with disability was eliminated or attenuated by dementia, except for gross infarcts and microinfarcts.
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