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利用机器学习和细胞因子枢纽对长新冠进行诊断并与慢性莱姆病进行区分。

Long COVID diagnostic with differentiation from chronic lyme disease using machine learning and cytokine hubs.

机构信息

IncellDx Inc, 30920 Huntwood Ave, San Carlos, Hayward, CA, 94544, USA.

Lab of Tumor Chemosensitivity, Faculty of Microbiology, CIET/CICICA, Universidad de Costa Rica, San José, Costa Rica.

出版信息

Sci Rep. 2024 Aug 26;14(1):19743. doi: 10.1038/s41598-024-70929-y.

Abstract

The absence of a long COVID (LC) or post-acute sequelae of COVID-19 (PASC) diagnostic has profound implications for research and potential therapeutics given the lack of specificity with symptom-based identification of LC and the overlap of symptoms with other chronic inflammatory conditions. Here, we report a machine-learning approach to LC/PASC diagnosis on 347 individuals using cytokine hubs that are also capable of differentiating LC from chronic lyme disease (CLD). We derived decision tree, random forest, and gradient-boosting machine (GBM) classifiers and compared their diagnostic capabilities on a dataset partitioned into training (178 individuals) and evaluation (45 individuals) sets. The GBM model generated 89% sensitivity and 96% specificity for LC with no evidence of overfitting. We tested the GBM on an additional random dataset (106 LC/PASC and 18 Lyme), resulting in high sensitivity (97%) and specificity (90%) for LC. We constructed a Lyme Index confirmatory algorithm to discriminate LC and CLD.

摘要

缺乏长新冠(LC)或新冠后急性后遗症(PASC)的诊断,这对研究和潜在治疗方法产生了深远的影响,因为基于症状的 LC 识别缺乏特异性,而且症状与其他慢性炎症性疾病存在重叠。在这里,我们报告了一种使用细胞因子枢纽的机器学习方法,对 347 个人进行 LC/PASC 诊断,这些枢纽还能够区分 LC 和慢性莱姆病(CLD)。我们得出了决策树、随机森林和梯度提升机(GBM)分类器,并比较了它们在数据集上的诊断能力,该数据集分为训练(178 个人)和评估(45 个人)集。GBM 模型对 LC 的敏感性为 89%,特异性为 96%,没有过度拟合的证据。我们在另一个随机数据集(106 个 LC/PASC 和 18 个莱姆)上测试了 GBM,结果显示 LC 的敏感性(97%)和特异性(90%)都很高。我们构建了一个莱姆指数确认算法来区分 LC 和 CLD。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aadf/11347643/fd10a6802191/41598_2024_70929_Fig1_HTML.jpg

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