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Neuropsychiatric Symptoms and Alzheimer's Disease Biomarkers Predict Driving Decline: Brief Report

机译:神经精神症状和阿尔茨海默病生物标志物预测驾驶衰退:简要报道

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We examined whether neuropsychiatric symptoms (NPS) interact with cerebrospinal fluid (CSF) biomarkers (amyloid-beta(42) [A beta(42)], tau, phosphorylated tau(181) [ptau(181)], tau/A beta(42), and ptau(181)/A beta(42)) of Alzheimer's disease pathology to predict driving decline among cognitively-normal older adults (N= 116) aged >= 65. Cox proportional hazards models examined time to receiving a rating of marginal or fail on the driving test. Age, education, and gender were adjusted in the models. Participants with more abnormal CSF (A beta(42), tau/A beta(42), ptau(181)/A beta(42)) and NPS were faster to receive a marginal/fail on the road test compared to those without NPS. NPS interact with abnormal CSF biomarkers to impact driving performance among cognitively-normal older adults.
机译:我们检查神经精神症状(NPS)是否与脑脊液(CSF)生物标志物相互作用(淀粉样蛋白β(42)[β(42)],Tau,磷酸化Tau(181)[Ptau(181)],Tau /Aβ( 42)和Ptau(181)/Aβ(42))阿尔茨海默病病理学,以预测认知性普通成年人(n = 116)的驾驶下降(n = 116),年龄> = 65. Cox比例危险模型检查了收到评级的时间 在驾驶考试中的边缘或失败。 在模型中调整了年龄,教育和性别。 与没有NPS的人相比,具有更多异常CSF(β(42),TAU /Aβ(42),PTAU(181)/Aβ(42))和NPS的速度较快,以在道路测试中获得边际/失败的速度更快 。 NPS与异常CSF生物标志物相互作用,以影响认知性普通成年人之间的驾驶性能。

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