Suppr超能文献

评估结核分枝杆菌来源的无细胞 DNA 用于胸腔积液和配对血浆样本在胸腔结核诊断中的应用。

Evaluation of Mycobacterium tuberculosis derived cell-free DNA using pleural fluid and paired plasma samples for the diagnosis of pleural tuberculosis.

机构信息

Department of Experimental Medicine and Biotechnology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Department of Medical Microbiology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

出版信息

Tuberculosis (Edinb). 2023 Sep;142:102369. doi: 10.1016/j.tube.2023.102369. Epub 2023 Jul 8.

Abstract

Pleural tuberculosis (pTB) is a grave clinical challenge. A novel cell-free M. tuberculosis DNA (cfM.tb-DNA) probe-based-qPCR assay was developed for the diagnosis of pTB. Total cell-free DNA was extracted from pleural fluid (PF) and paired plasma samples and cfM.tb-DNA was quantified by probe-based qPCR targeting devR (109-bp) gene of M. tuberculosis in patients with pleural effusion. Patient categorization was done using 'Composite-Reference-Standard' formulated for the study. Assay cut-offs were determined from samples in the 'Development set' (n = 17; 'Definite & Probable' pTB; n = 9 and 'Non-TB'; n = 8) by ROC-curve analysis and applied to 'Validation set' (n = 112; 'Definite' pTB; n = 8, 'Probable' pTB; n = 34, 'Possible' pTB; n = 28 and 'Non-TB'; n = 42). cfM.tb-DNA qPCR had a sensitivity of 62.5% (95%CI; 24.4,91.4) in 'Definite' pTB category and 59.5% (95%CI; 43.2,74.3) in 'Definite & Probable' pTB category with 95.2% (95%CI; 83.8,99.4) specificity using PF. In plasma (n = 85), the assay had a sub-optimal sensitivity of 7.6% (95%CI; 0.95,25.1) with 88.2% (95%CI; 72.5,96.7) specificity in 'Definite & Probable' pTB group. Xpert MTB/RIF assay detected only six-samples in the 'Validation set'. Logistic regression analysis indicated that PF-cfM.tb-DNA qPCR provided incremental advantage over existing pTB diagnostic algorithms. To the best of our knowledge, this is the first report describing the utility of cfM.tb-DNA for pTB diagnosis in India.

摘要

结核性胸膜炎(pTB)是一个严峻的临床挑战。本研究开发了一种新型的无细胞结核分枝杆菌 DNA(cfM.tb-DNA)探针 qPCR 检测方法,用于诊断 pTB。从胸腔积液(PF)和配对血浆样本中提取总无细胞 DNA,并使用针对结核分枝杆菌 devR(109-bp)基因的探针 qPCR 定量 cfM.tb-DNA。采用为该研究制定的“综合参考标准”对患者进行分类。通过 ROC 曲线分析从“开发集”(n=17;“确诊”和“可能”pTB;n=9 和“非结核”;n=8)中的样本确定检测限,并应用于“验证集”(n=112;“确诊”pTB;n=8,“可能”pTB;n=34,“可疑”pTB;n=28 和“非结核”;n=42)。在“确诊”pTB 组中,cfM.tb-DNA qPCR 的敏感性为 62.5%(95%CI;24.4,91.4),在“确诊”和“可能”pTB 组中为 59.5%(95%CI;43.2,74.3),PF 的特异性为 95.2%(95%CI;83.8,99.4)。在血浆(n=85)中,该检测在“确诊”和“可能”pTB 组中的敏感性为 7.6%(95%CI;0.95,25.1),特异性为 88.2%(95%CI;72.5,96.7)。Xpert MTB/RIF 检测仅在“验证集”中检测到 6 个样本。逻辑回归分析表明,PF-cfM.tb-DNA qPCR 比现有 pTB 诊断算法提供了额外的优势。据我们所知,这是首次在印度报道使用 cfM.tb-DNA 诊断 pTB 的研究。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验