作为结核病诊断生物标记物的循环血脂:多队列、多组学数据整合分析

Nguyen Tran Nam Tien, Nguyen Thi Hai Yen, Nguyen Ky Phat, Nguyen Ky Anh, Nguyen Quang Thu, Eunsu Cho, Ho-Sook Kim, Dinh Hoa Vu, Duc Ninh Nguyen, Dong Hyun Kim, Jee Youn Oh, Nguyen Phuoc Long
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引用次数: 0

摘要

摘要背景:循环免疫代谢生物标志物有望用于结核病(TB)的诊断和治疗监测。然而,能将肺结核与非结核分枝杆菌(NTM)感染、潜伏肺结核感染(LTBI)和其他肺部疾病(ODx)区分开来的生物标志物尚未阐明。本研究采用多队列、多组学方法并结合预测建模来鉴定、验证和优先选择用于诊断活动性肺结核的生物标记物。研究方法从两个发现队列(76 名 TB-NTM 队列患者和 72 名 TB-LTBI-ODx 队列患者)和一个验证队列(68 名 TB 患者和 30 名 LTBI 患者)中收集功能组学数据。通过多组学综合分析,确定了血浆多组学生物特征。然后应用基于机器学习的预测模型来评估这些生物特征的性能,并优先选择最有希望的候选特征。结果免疫图谱和代谢组学的常规统计分析显示,活动性肺结核组和非肺结核组之间的差异很小,而脂质组则出现了显著变化。突变组学综合分析发现了三个能区分活动性肺结核和非肺结核的多组生物特征,其性能良好,在发现组和验证组中各组的 ROC 曲线下面积(AUC)值均为 0.7-0.9。脂质 PC(14:0_22:6)是区分活动性肺结核和非肺结核对照组的最重要的预测因子,与对照组相比,活动性肺结核组的脂质 PC(14:0_22:6)水平一直较低。使用两个独立的外部数据集进行的进一步验证显示,AUC 为 0.77-1.00,证实了生物标记物在区分结核病与其他非结核病组方面的功效:结论:我们的综合多组学研究揭示了结核病的重大免疫代谢变化。预测模型表明,脂质是结核病-非结核病鉴别诊断和结核病-创伤性脑损伤-ODx诊断的有前途的生物标志物。外部验证进一步表明,PC(14:0_22:6)是结核病潜在的候选诊断标志物。
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Circulating Lipids as Biomarkers for Diagnosis of Tuberculosis: A Multi-cohort, Multi-omics Data Integration Analysis
ABSTRACT Background: Circulating immunometabolic biomarkers show promise for the diagnosis and treatment monitoring of tuberculosis (TB). However, biomarkers that can distinguish TB from nontuberculous mycobacteria (NTM) infections, latent tuberculosis infection (LTBI), and other lung diseases (ODx) have not been elucidated. This study utilized a multi-cohort, multi-omics approach combined with predictive modeling to identify, validate, and prioritize biomarkers for the diagnosis of active TB. Methods: Functional omics data were collected from two discovery cohorts (76 patients in the TB-NTM cohort and 72 patients in the TB-LTBI-ODx cohort) and one validation cohort (68 TB patients and 30 LTBI patients). An integrative multi-omics analysis was performed to identify the plasma multi-ome biosignatures. Machine learning-based predictive modeling was then applied to assess the performance of these biosignatures and prioritize the most promising candidates. Results: Conventional statistical analyses of immune profiling and metabolomics indicated minor differences between active TB and non-TB groups, whereas the lipidome showed significant alteration. Muti-omics integrative analysis identified three multi-ome biosignatures that could distinguish active TB from non-TB with promising performance, achieving area under the ROC curve (AUC) values of 0.7-0.9 across groups in both the discovery and validation cohorts. The lipid PC(14:0_22:6) emerged as the most important predictor for differentiating active TB from non-TB controls, consistently presenting at lower levels in the active TB group compared with counterparts. Further validation using two independent external datasets demonstrated AUCs of 0.77-1.00, confirming the biomarkers' efficacy in distinguishing TB from other non-TB groups. Conclusion: Our integrative multi-omics reveals significant immunometabolic alteration in TB. Predictive modeling suggests lipids as promising biomarkers for TB-NTM differential diagnosis and TB-LTBI-ODx diagnosis. External validation further indicates PC(14:0_22:6) as a potential diagnostic marker candidate for TB.
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