Lee Sean, Rajmohan Ravi, Al-Darsani Zeinah, Paganini-Hill Annlia, Montine Thomas J, Corrada Maria M, Kawas Claudia
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.
Neurology. 2025 Jan 14;104(1):e210107. doi: 10.1212/WNL.0000000000210107. Epub 2024 Dec 12.
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.
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.
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.
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。
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。
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。