Choudhary Hansraj, Malik Garima, Chauhan Devendra Singh, Bhalla Manpreet, Dusthackeer Azger, Desikan Prabha, Giri Sidhartha, Kumar Sandeep, Jayaprakasam Madhumathi, Singh Ajay Vir, Sethi Prabhpreet, Reza Md Shakir, Mythily V, Thiyagarajan V, Panwalkar Nikita, Tripathy Jyotismita, Mani Devdatt, Singh Diksha, Ramesh P M, Chalga Manjeet Singh, Rani Rajni, Gupta Nivedita, Pandey Ravindra Mohan, Singh Manjula
Division of Communicable Diseases, Indian Council of Medical Research, New Delhi, India.
Division of Delivery Research, Indian Council of Medical Research, New Delhi, India.
Indian J Med Res. 2025 May;161(5):482-490. doi: 10.25259/IJMR_824_2025.
Background & objectives Tuberculosis (TB) remains a major global health concern, with India accounting for 26 per cent of the global burden. Despite advances, access to rapid molecular diagnostics is limited, and the assays currently used in National TB Elimination Programme (NTEP) do not detect isoniazid (INH) resistance upfront. PathoDetect™ MTB RIF & INH is an indigenous closed-system assay that simultaneously detects Mycobacterium tuberculosis (MTB) and resistance to rifampicin (RIF) and INH. This study evaluated its diagnostic characteristics. Methods In this cross-sectional multicenter study conducted at six TB reference laboratories in India, 1039 participants were enrolled (718 presumptive pulmonary TB, 321 presumptive multidrug resistant TB; MDR-TB). PathoDetect™'s discriminatory ability was assessed using the measures sensitivity and specificity, and its diagnostic performance using positive predictive value (PPV) and negative predictive value (NPV). Liquid culture served as the reference standard for MTB detection, while phenotypic drug susceptibility testing (pDST) and line probe assay (LPA) as reference standards for RIF and INH resistance detection. Results For MTB detection in presumptive pulmonary TB (PTB), PathoDetect™ showed a sensitivity of 98.1 per cent [95% confidence interval (CI): 96.1-99.2], specificity of 94.2 per cent (95% CI: 91-96.5), PPV of 94.9 per cent (95% CI: 92.2-96.9), and NPV of 97.8 per cent (95% CI: 95.5-99.1) with near-perfect agreement with Truenat® (k=0.89). Among 514 confirmed TB cases, PathoDetect™ detected RIF resistance with a sensitivity of 86.5 per cent (95% CI: 80.2-91.5), specificity of 91.6 per cent (95% CI: 88.2-94.3), PPV of 82.3 per cent (95% CI: 75.6-87.8), and NPV of 93.8 per cent (95% CI: 90.7-96.1). For INH resistance, sensitivity was 88.9 per cent (95% CI: 84.1-92.6), specificity 87 per cent (95% CI: 82.4-90.8), PPV 85.6 per cent (95% CI: 80.5-89.8), and NPV 90 per cent (95% CI: 85.7-93.4) using pDST as reference. Truenat® MTB-RIF showed comparable performance for RIF resistance detection (k=0.75). Compared to line probe assay (LPA), PathoDetect™ demonstrated higher sensitivity (93.4 vs. 88.8%), specificity (98.2 vs. 93.9%), PPV (96.1 vs. 86.8%) and NPV (97 vs. 94.9%) for RIF resistance detection over Truenat®. Interpretation & conclusions PathoDetect™ is a reliable molecular diagnostic tool for detection of MTB and resistance to RIF & INH. The assay showed better RIF resistance detection compared to INH. Its high sensitivity and specificity indicate strong discriminatory ability, while PPV and NPV demonstrate reasonably good diagnostic performance in the study population. These findings support PathoDetect™ as a promising alternative for rapid TB diagnosis, particularly in high-burden settings.
结核病仍然是全球主要的健康问题,印度占全球负担的26%。尽管取得了进展,但快速分子诊断的可及性有限,目前国家结核病消除计划(NTEP)中使用的检测方法无法预先检测出异烟肼(INH)耐药性。PathoDetect™ MTB RIF & INH是一种国产封闭系统检测方法,可同时检测结核分枝杆菌(MTB)以及对利福平(RIF)和INH的耐药性。本研究评估了其诊断特征。方法:在印度的六个结核病参考实验室进行的这项横断面多中心研究中,招募了1039名参与者(718例疑似肺结核,321例疑似耐多药结核病;MDR-TB)。使用灵敏度和特异性评估PathoDetect™的鉴别能力,并使用阳性预测值(PPV)和阴性预测值(NPV)评估其诊断性能。液体培养作为MTB检测的参考标准,而表型药物敏感性试验(pDST)和线性探针分析(LPA)作为RIF和INH耐药性检测的参考标准。结果:对于疑似肺结核(PTB)中的MTB检测,PathoDetect™的灵敏度为98.1%[95%置信区间(CI):96.1-99.2],特异性为94.2%(95%CI:91-96.5),PPV为94.9%(95%CI:92.2-96.9),NPV为97.8%(95%CI:95.5-99.1),与Truenat®的一致性近乎完美(k=0.89)。在514例确诊的结核病病例中,PathoDetect™检测RIF耐药性的灵敏度为86.5%(95%CI:80.2-91.5),特异性为91.6%(95%CI:88.2-94.3),PPV为82.3%(95%CI:75.6-87.8),NPV为93.8%(95%CI:90.7-96.1)。对于INH耐药性,以pDST作为参考,灵敏度为88.9%(95%CI:84.1-92.6),特异性为87%(95%CI:82.4-90.8),PPV为85.6%(95%CI:80.5-89.8),NPV为90%(95%CI:85.7-93.4)。Truenat® MTB-RIF在RIF耐药性检测方面表现相当(k=0.75)。与线性探针分析(LPA)相比,PathoDetect™在RIF耐药性检测方面显示出更高的灵敏度(93.4%对88.8%)、特异性(98.2%对93.9%)、PPV(96.1%对86.8%)和NPV(97%对94.9%)。解读与结论:PathoDetect™是一种用于检测MTB以及对RIF和INH耐药性的可靠分子诊断工具。该检测方法在检测RIF耐药性方面比检测INH表现更好。其高灵敏度和特异性表明具有很强的鉴别能力,而PPV和NPV在研究人群中表现出相当好的诊断性能。这些发现支持PathoDetect™作为快速结核病诊断的一种有前景的替代方法,特别是在高负担地区。