首页> 外文期刊>Alzheimer’s & dementia: the journal of the Alzheimer’s Association >Predicting sporadic Alzheimer's disease progression via inherited Alzheimer's disease‐informed machine‐learning
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Predicting sporadic Alzheimer's disease progression via inherited Alzheimer's disease‐informed machine‐learning

机译:通过遗传的阿尔茨海默病的机器学习预测孢子素阿尔茨海默病进展

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Abstract Introduction Developing cross‐validated multi‐biomarker models for the prediction of the rate of cognitive decline in Alzheimer's disease (AD) is a critical yet unmet clinical challenge. Methods We applied support vector regression to AD biomarkers derived from cerebrospinal fluid, structural magnetic resonance imaging (MRI), amyloid‐PET and fluorodeoxyglucose positron‐emission tomography (FDG‐PET) to predict rates of cognitive decline. Prediction models were trained in autosomal‐dominant Alzheimer's disease (ADAD, n = 121) and subsequently cross‐validated in sporadic prodromal AD (n = 216). The sample size needed to detect treatment effects when using model‐based risk enrichment was estimated. Results A model combining all biomarker modalities and established in ADAD predicted the 4‐year rate of decline in global cognition (R 2 = 24%) and memory (R 2 = 25%) in sporadic AD. Model‐based risk‐enrichment reduced the sample size required for detecting simulated intervention effects by 50%–75%. Discussion Our independently validated machine‐learning model predicted cognitive decline in sporadic prodromal AD and may substantially reduce sample size needed in clinical trials in AD.
机译:摘要介绍开发交叉验证的多生物标志物模型,用于预测阿尔茨海默病(AD)的认知下降率(广告)是一个关键但未得到满足的临床挑战。方法施用支持向量回归到来自脑脊髓液,结构磁共振成像(MRI),淀粉样蛋白和氟脱氧葡萄糖正电子排放断层扫描(FDG-PET)的AD生物标志物,以预测认知下降的速度。预测模型在常染色体显性阿尔茨海默病(Adad,N = 121)中受过培训,随后在散摩生品Ad(n = 216)中交叉验证。估计基于模型的风险富集时检测治疗效果所需的样品大小。结果组合所有生物标志物的模型和在Adad中建立的模型预测了零星广告中全球认知(R 2 = 24%)和内存(R 2 = 25%)的4年下降率。基于模型的风险富集降低了检测模拟干预效果所需的样品尺寸50%-75%。讨论我们独立验证的机器学习模型预测散发性前甲态广告中的认知下降,可大大降低广告中临床试验所需的样本大小。

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