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与高龄老人阿尔茨海默病神经病理改变缺失相关的病史:90岁以上研究

Medical Histories Associated With Absence of Alzheimer Disease Neuropathologic Changes in the Oldest-Old: The 90+ Study.

作者信息

Lee Sean, Rajmohan Ravi, Al-Darsani Zeinah, Paganini-Hill Annlia, Montine Thomas J, Corrada Maria M, Kawas Claudia

机构信息

From the Departments of Neurology (S.L., R.R., A.P.-H., M.M.C., C.K.) and Epidemiology and Biostatistics (M.M.C.), and the Institute for Memory Impairments and Neurological Disorders (Z.A.-D., M.M.C., C.K.), University of California, Irvine; Department of Epidemiology and Biostatistics, Temple University College of Public Health, Philadelphia, PA; and Pathology (T.J.M.), Stanford University, CA.

出版信息

Neurology. 2025 Jan 14;104(1):e210107. doi: 10.1212/WNL.0000000000210107. Epub 2024 Dec 12.

Abstract

OBJECTIVES

Exploration of medical histories and medications associated with Alzheimer disease neuropathologic change (ADNC) absence and potential resistance may identify protective factors against ADNC. This was a retrospective examination of data from participants age ≥90 years who enrolled in , a longitudinal study based in California. Participants underwent neuropathologic analysis for the presence of neuritic amyloid plaques (NPs) (any), beta amyloid plaques (Thal phase > 0), and neurofibrillary tangles (>2). Odds ratios (ORs) for the presence of pathologic changes to genotype, self-reported medical histories, and medication use were estimated by logistic regression and (a)djusted for sex, age at death (continuous), and education.

RESULTS

We examined 267 participants; 75% were female, with a mean age at death of 98 (± 3.5) years. Variables associated with ADNC absence/presence were for NPs: heart disease (adjusted OR [aOR] = 0.46), -ε4 (aOR = 3.48), angiotensin-converting enzyme (ACE) inhibitors (aOR = 0.46), cataracts (aOR = 0.26), and beta-blockers (aOR = 0.51); for Aβ: heart disease (aOR = 0.33) and -ε4 (aOR = 8.10); and for neurofibrillary tangles: ACE inhibitors (aOR = 0.46), glaucoma (aOR = 0.29), HTN (aOR = 0.44), seizures (aOR = 0.16), -ε2 presence (aOR = 0.39), and vasodilators (aOR = 0.36). These observations would not survive multiple comparison corrections.

DISCUSSION

Cataract formation, status, ACE inhibitors, and beta-blockers may be associated with ADNC absence because of differential lipid trafficking. Survival bias and type 1 errors warrant consideration.

摘要

目的

探究与阿尔茨海默病神经病理改变(ADNC)缺失及潜在抗性相关的病史和药物,可能会识别出针对ADNC的保护因素。这是一项对年龄≥90岁的参与者的数据进行的回顾性研究,这些参与者来自加利福尼亚州的一项纵向研究。参与者接受了神经病理分析,以检测是否存在神经炎淀粉样斑块(NPs)(任何情况)、β淀粉样斑块(Thal分期>0)和神经原纤维缠结(>2)。通过逻辑回归估计病理改变与基因型、自我报告的病史和药物使用之间的比值比(OR),并对性别、死亡年龄(连续变量)和教育程度进行(校正)调整。

结果

我们检查了267名参与者;75%为女性,平均死亡年龄为98(±3.5)岁。与ADNC缺失/存在相关的变量,对于NPs而言:心脏病(校正后OR[aOR]=0.46)、-ε4(aOR=3.48)、血管紧张素转换酶(ACE)抑制剂(aOR=0.46)、白内障(aOR=0.26)和β受体阻滞剂(aOR=0.51);对于Aβ而言:心脏病(aOR=0.33)和-ε4(aOR=8.10);对于神经原纤维缠结而言:ACE抑制剂(aOR=0.46)、青光眼(aOR=0.29)、高血压(aOR=0.44)、癫痫(aOR=0.16)、-ε2存在(aOR=0.39)和血管扩张剂(aOR=0.36)。这些观察结果在多次比较校正后不成立。

讨论

白内障形成、 状态、ACE抑制剂和β受体阻滞剂可能因脂质转运差异而与ADNC缺失相关。生存偏差和I类错误值得考虑。

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