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利用血液 RNA 水平预测临床痴呆评定量表评分。

Predicting Clinical Dementia Rating Using Blood RNA Levels.

机构信息

Department of Biology, Brigham Young University, Provo, UT 84602, USA.

出版信息

Genes (Basel). 2020 Jun 26;11(6):706. doi: 10.3390/genes11060706.

Abstract

The Clinical Dementia Rating (CDR) is commonly used to assess cognitive decline in Alzheimer's disease patients and is included in the Alzheimer's Disease Neuroimaging Initiative (ADNI) dataset. We divided 741 ADNI participants with blood microarray data into three groups based on their most recent CDR assessment: cognitive normal (CDR = 0), mild cognitive impairment (CDR = 0.5), and probable Alzheimer's disease (CDR ≥ 1.0). We then used machine learning to predict cognitive status using only blood RNA levels. Only one probe for chloride intracellular channel 1 () was significant after correction. However, by combining individually nonsignificant probes with -values less than 0.1, we averaged 87.87% (s = 1.02) predictive accuracy for classifying the three groups, compared to a 55.46% baseline for this study due to unequal group sizes. The best model had an overall precision of 0.902, recall of 0.895, and a receiver operating characteristic (ROC) curve area of 0.904. Although we identified one significant probe in , levels alone were not sufficient to predict dementia status and cannot be used alone in a clinical setting. Additional analyses combining individually suggestive, but nonsignificant, blood RNA levels were significantly predictive and may improve diagnostic accuracy for Alzheimer's disease. Therefore, we propose that patient features that do not individually predict cognitive status might still contribute to overall cognitive decline through interactions that can be elucidated through machine learning.

摘要

临床痴呆评定量表(CDR)常用于评估阿尔茨海默病患者的认知能力下降,并且包含在阿尔茨海默病神经影像学倡议(ADNI)数据集中。我们根据最近的 CDR 评估将 741 名具有血液微阵列数据的 ADNI 参与者分为三组:认知正常(CDR=0)、轻度认知障碍(CDR=0.5)和可能的阿尔茨海默病(CDR≥1.0)。然后,我们仅使用血液 RNA 水平通过机器学习来预测认知状态。只有一个氯离子细胞内通道 1()的探针在经过校正后是显著的。然而,通过将个体上不显著的探针与小于 0.1 的 - 值结合起来,我们平均可以将三组分类的预测准确率提高到 87.87%(s=1.02),而由于组间大小不均,本研究的基线为 55.46%。最佳模型的整体精度为 0.902,召回率为 0.895,接收器操作特征(ROC)曲线面积为 0.904。尽管我们在中鉴定出一个显著的探针,但水平本身不足以预测痴呆状态,并且不能单独在临床环境中使用。结合个体上有提示但不显著的血液 RNA 水平的额外分析具有显著的预测性,并且可能提高阿尔茨海默病的诊断准确性。因此,我们提出,个体上不能预测认知状态的患者特征可能仍然通过可以通过机器学习阐明的相互作用对整体认知下降做出贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7991/7349260/897bb2fec0b1/genes-11-00706-g001.jpg

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