Kunduracıoğlu Ayperen, Karasu Işıl, Biçmen Can, Ozsöz Ayşe, Erbaycu Ahmet Emin
Dr. Suat Seren Chest Diseases and Surgery, Education and Research Hospital, Chest Diseases Clinic, Izmir, Turkey.
Mikrobiyol Bul. 2013 Jul;47(3):417-31. doi: 10.5578/mb.5728.
The aim of this study was to compare the results of nucleic acid amplification-based MTD (Mycobacterium tuberculosis direct test) Gene-Probe® method in samples obtained from acid-fast bacilli (ARB) smear-negative patients with suspected tuberculosis (TB), with the culture results obtained from automated BACTEC 960™ (MGIT) system and Löwenstein-Jensen (LJ) medium. In addition, the contribution of molecular methods in early diagnosis of pulmonary TB and the effect of radiological prevalence of the disease associated with or without cavity to the molecular diagnosis and/or growth time in culture media have been evaluated. A total of 107 patients (86 male, 21 female; mean age: 49.89 ± 17.1 years, age range: 18-81 years) who were clinically and radiologically suspected of having pulmonary TB and/or TB pleurisy, were included in the study. Of the samples 65 (60.7%) were sputum, 32 (29.9%) were bronchial aspiration, 5 (4.7%) were pleural fluid, and 5 (4.7%) were transthoracic fine needle aspiration biopsy materials. Patient samples were cultured in solid LJ media and liquid-based BACTEC 960 system (Becton Dickinson Co., USA) in the same working day. Meanwhile, MTD Gen-Probe test (Gen-Probe Inc., USA) was studied in two separate working days of the week as specified by the laboratory. The samples were incubated until positivity was determined in BACTEC 960 system and/or growth was detected in LJ medium. Negative cultures were incubated for 42 days and were finalized. When mycobacterial growth was determined in the culture, identification of M.tuberculosis complex (MTBC) and differentiation from nontuberculous mycobacteria were performed by conventional methods and BACTEC 460 NAP test. Forty five (42%) patients were diagnosed as pulmonary paranchimal TB (40 were active pulmonary TB, 1 was miliary TB and 4 were culture-negative pulmonary TB), while 4 (3.7%) patients diagnosed as extrapulmonary TB and 58 (57.9%) patients were diagnosed as other pulmonary diseases unrelated with TB. LJ cultures yielded positive results in 32 of 45 (71%) pulmonary TB patients, and BACTEC 960 were found positive in 84.4% (38/45) of those patients. On the other hand the positivity rate of MTD Gen-Probe test was detected as 37.4% (40/107). The sensitivity, specificity, positive and negative predictive values for MTD Gen-Probe test were estimated as 89%, 100%, 100% and 93%, respectively. Those values for BACTEC 960 system were found as 82%, 98%, 97% and 88%, and for LJ culture method as 71%, 100%, 100% and 83%, respectively. Average periods to make a decision for diagnosis of TB by MTD Gen-Probe, BACTEC 960 (MGIT) and LJ culture methods were calculated as 2.36 days, 20.11 days and 32.49 days, respectively. In comparison of the methods in terms of turnaround times, MTD Gen-Probe test was found superior to LJ culture method, however the turnaround times for BACTEC 960 and LJ culture methods were similar. When the clinical data were evaluated, no effect of radiological density of lesion was identified on the diagnosis time of molecular test and time of growth in liquid based automated BACTEC system and/or LJ culture method. However, LJ culture demonstrated earlier reactivity in patients with cavitary lesions. As a result, MTD Gene-Probe test was observed as a reliable and rapid method for the early diagnosis of pulmonary TB patients, early initiation of therapy, prevention of disease progression and transmission.
本研究旨在比较基于核酸扩增的结核分枝杆菌直接检测(MTD,Mycobacterium tuberculosis direct test)Gene-Probe®方法在疑似结核病(TB)的抗酸杆菌(ARB)涂片阴性患者样本中的检测结果,以及自动BACTEC 960™(MGIT)系统和罗-琴(LJ)培养基的培养结果。此外,还评估了分子方法在肺结核早期诊断中的作用,以及疾病有无空洞的影像学患病率对分子诊断和/或培养基中生长时间的影响。本研究共纳入107例临床和影像学上疑似患有肺结核和/或结核性胸膜炎的患者(86例男性,21例女性;平均年龄:49.89±17.1岁,年龄范围:18 - 81岁)。样本中,65份(60.7%)为痰液,32份(29.9%)为支气管吸出物,5份(4.7%)为胸腔积液,5份(4.7%)为经胸细针穿刺活检材料。患者样本在同一天在固体LJ培养基和液体BACTEC 960系统(美国BD公司)中进行培养。同时,按照实验室规定,在一周的两个不同工作日进行MTD Gen-Probe检测(美国Gen-Probe公司)。样本在BACTEC 960系统中培养至确定阳性和/或在LJ培养基中检测到生长。阴性培养物培养42天并得出最终结果。当在培养物中确定有分枝杆菌生长时,通过常规方法和BACTEC 460 NAP试验对结核分枝杆菌复合群(MTBC)进行鉴定并与非结核分枝杆菌进行区分。45例(42%)患者被诊断为肺实质结核(40例为活动性肺结核,1例为粟粒性结核,4例为培养阴性肺结核),4例(3.7%)患者被诊断为肺外结核,58例(57.9%)患者被诊断为与结核无关的其他肺部疾病。LJ培养在45例肺结核患者中的32例(71%)中得到阳性结果,BACTEC 960在这些患者中的阳性率为84.4%(38/45)。另一方面,MTD Gen-Probe检测的阳性率为37.4%(40/107)。MTD Gen-Probe检测的敏感性、特异性、阳性预测值和阴性预测值分别估计为89%、100%、100%和93%。BACTEC 960系统的这些值分别为82%、98%、97%和88%,LJ培养方法的这些值分别为71%、100%、100%和83%。通过MTD Gen-Probe、BACTEC 960(MGIT)和LJ培养方法诊断结核病的平均决策时间分别计算为2.36天、20.11天和32.49天。在周转时间方面比较这些方法时,发现MTD Gen-Probe检测优于LJ培养方法,然而BACTEC 960和LJ培养方法的周转时间相似。当评估临床数据时,未发现病变的放射学密度对分子检测诊断时间和液体自动BACTEC系统和/或LJ培养方法中的生长时间有影响。然而,LJ培养在有空洞病变的患者中显示出更早的反应性。结果表明,MTD Gene-Probe检测是一种可靠且快速的方法,可用于肺结核患者的早期诊断、早期开始治疗、预防疾病进展和传播。