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基于三甲基化驱动基因的深度学习模型在人类免疫缺陷病毒合并感染和未合并感染患者中的结核病诊断应用。

A three-methylation-driven gene-based deep learning model for tuberculosis diagnosis in patients with and without human immunodeficiency virus co-infection.

机构信息

Drug Clinical Trial Center, Gansu Wuwei Tumor Hospital, Wuwei, Gansu, People's Republic of China.

出版信息

Microbiol Immunol. 2022 Jun;66(6):317-323. doi: 10.1111/1348-0421.12983. Epub 2022 May 27.

DOI:10.1111/1348-0421.12983
PMID:35510555
Abstract

Improved diagnostic tests for tuberculosis (TB) among people with human immunodeficiency virus (HIV) are urgently required. We hypothesized that methylation-driven genes (MDGs) of host blood could be used to diagnose patients co-infected with HIV/TB. In this study, we identified three MDGs among patients with HIV monoinfection and those with HIV/TB co-infection using the R package MethylMix. We then developed a deep learning model by screening these three MDGs, which distinguished HIV/TB co-infection from HIV monoinfection with a sensitivity of 95.2% and a specificity of 88.3%. On the two independent data sets, the sensitivity and specificity were 80%-92.8% and 72.7%-87.5%, respectively. Besides, our deep learning model accurately classified TB (sensitivity, 75.0%-100%; specificity, 91.3%-98.1%) and other respiratory disorders (sensitivity, 72.7%-75.0%; specificity, 70.9%-72.7%). This study will contribute to improve molecular diagnosis for HIV/TB co-infection.

摘要

迫切需要改进针对人类免疫缺陷病毒 (HIV) 感染者的结核病 (TB) 诊断检测方法。我们假设宿主血液的甲基化驱动基因 (MDG) 可用于诊断 HIV/TB 合并感染的患者。在这项研究中,我们使用 R 包 MethylMix 从 HIV 单一感染患者和 HIV/TB 合并感染患者中鉴定出三个 MDG。然后,我们通过筛选这三个 MDG 开发了一个深度学习模型,该模型能够以 95.2%的敏感性和 88.3%的特异性区分 HIV/TB 合并感染与 HIV 单一感染。在两个独立的数据集中,敏感性和特异性分别为 80%-92.8%和 72.7%-87.5%。此外,我们的深度学习模型能够准确地对 TB(敏感性为 75.0%-100%;特异性为 91.3%-98.1%)和其他呼吸道疾病(敏感性为 72.7%-75.0%;特异性为 70.9%-72.7%)进行分类。这项研究将有助于改善 HIV/TB 合并感染的分子诊断。

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