Contribution of health history and neuropathologic changes to the likelihood of dementia in those with intermediate/high Alzheimer’s pathology: findings from The 90 + Study

IF 10.3 1区 医学 Q1 CLINICAL NEUROLOGY
Zarui A. Melikyan, Zeinah Al-darsani, Luohua Jiang, Katherine A. Colcord, Annlia Paganini-Hill, Syed A. Bukhari, Thomas J. Montine, Claudia H. Kawas, María M. Corrada
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引用次数: 0

Abstract

Although intermediate/high Alzheimer’s Disease Neuropathologic Change (ADNC) is associated with dementia in many older adults, some remain cognitively normal and are often referred to as resilient to ADNC. We aim to examine health, lifestyle, and neuropathologic factors that distinguish older adults with dementia vs. normal cognition in the presence of intermediate/high ADNC. Participants were from The 90 + Study, a longitudinal study of aging in southern California. This cross-sectional analysis included participants with an intermediate/high ADNC on neuropathologic exam and normal cognition or dementia diagnosis on case conference. We analyzed 11 neuropathologic changes, both vascular and neurodegenerative, dichotomized as present/absent, and the total number of neuropathologies. To examine the association of health and lifestyle factors and neuropathologic changes (predictors) with cognitive diagnosis at consensus case conference, dementia vs. normal cognition, (outcome), we used logistic regression adjusted for demographics. Among 235 participants (mean age at death = 98 years, 70% women), 33% maintained normal cognition. Participants with heart disease (OR = 0.45; 95% CI = 0.25, 0.81) and hypertension (OR = 0.53; 95% CI = 0.29, 0.95) had lower likelihood of dementia. In contrast, participants with a history of transient ischemic attacks (OR = 3.00; 95% CI = 1.46, 6.18), Lewy Body Disease (OR = 2.73; 95% CI = 1.14, 6.58), hippocampal sclerosis (OR = 2.70; 95% CI = 1.06, 6.86), Limbic-predominant Age-related TDP-43 Encephalopathy neuropathologic change (OR = 2.80; 95% CI = 1.53, 5.12), and a high number of non-ADNCs (OR = 4.46; 95% CI = 2.01, 9.92) had higher likelihood of dementia. Arteriolosclerosis, atherosclerosis, cerebral amyloid angiopathy, and microvascular lesions were not associated with dementia. In this study, the presence of neurodegenerative neuropathologic changes other than ADNC and the absence of hypertension distinguish oldest old individuals with dementia from those with normal cognition. Understanding mechanisms underlying normal cognition in those with ADNC may provide important clues to prevention and resilience to the effects of AD neuropathology.

健康史和神经病理改变对中重度阿尔茨海默病患者痴呆可能性的贡献:来自90 +研究的发现
虽然中/高度阿尔茨海默病神经病理改变(ADNC)与许多老年人的痴呆症有关,但一些老年人仍保持认知正常,通常被认为对ADNC具有弹性。我们的目的是检查健康、生活方式和神经病理因素,以区分老年痴呆症患者与中/高ADNC存在的正常认知。参与者来自“90 +研究”,这是南加州一项关于老龄化的纵向研究。该横断面分析纳入了神经病理学检查中/高ADNC和病例会议中认知正常或痴呆诊断的参与者。我们分析了11种神经病理改变,包括血管和神经退行性改变,分为存在/不存在,以及神经病理的总数。为了检查健康和生活方式因素和神经病理改变(预测因子)与共识病例会议上认知诊断的关系,痴呆与正常认知,(结果),我们使用了人口统计学调整的逻辑回归。在235名参与者中(平均死亡年龄为98岁,70%为女性),33%保持正常认知。患有心脏病(OR = 0.45; 95% CI = 0.25, 0.81)和高血压(OR = 0.53; 95% CI = 0.29, 0.95)的参与者患痴呆的可能性较低。相比而言,有短暂性脑缺血发作(OR = 3.00; 95% CI = 1.46, 6.18)、路易体病(OR = 2.73; 95% CI = 1.14, 6.58)、海马硬化症(OR = 2.70; 95% CI = 1.06, 6.86)、边缘区显性年龄相关TDP-43脑病神经病理改变(OR = 2.80; 95% CI = 1.53, 5.12)和大量非adnc (OR = 4.46; 95% CI = 2.01, 9.92)病史的参与者患痴呆的可能性更高。小动脉硬化、动脉粥样硬化、脑淀粉样血管病和微血管病变与痴呆无关。在本研究中,存在除ADNC以外的神经退行性神经病理改变和没有高血压将老年痴呆患者与认知正常的患者区分开来。了解ADNC患者正常认知的机制可能为AD神经病理学的预防和恢复提供重要线索。
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来源期刊
Acta Neuropathologica
Acta Neuropathologica 医学-病理学
CiteScore
23.70
自引率
3.90%
发文量
118
审稿时长
4-8 weeks
期刊介绍: Acta Neuropathologica publishes top-quality papers on the pathology of neurological diseases and experimental studies on molecular and cellular mechanisms using in vitro and in vivo models, ideally validated by analysis of human tissues. The journal accepts Original Papers, Review Articles, Case Reports, and Scientific Correspondence (Letters). Manuscripts must adhere to ethical standards, including review by appropriate ethics committees for human studies and compliance with principles of laboratory animal care for animal experiments. Failure to comply may result in rejection of the manuscript, and authors are responsible for ensuring accuracy and adherence to these requirements.
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