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Performance of QuantiFERON-TB Gold In-Tube (QFTGIT) for the diagnosis of Mycobacterium tuberculosis (Mtb) infection in Afar Pastoralists, Ethiopia

机译:QuantiFERON-TB金管(QFTGIT)在埃塞俄比亚远方牧民中诊断结核分枝杆菌(Mtb)感染的性能

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Background Currently, T-cell based gamma interferon (IFNγ) release assays (IGRAs) are acknowledged as the best methods available for the screening of latent tuberculosis infection (LTBI) and also as aid for the diagnosis of active tuberculosis (TB). To our information, the performance of these diagnostic tests has not been evaluated in Ethiopia. Therefore, the intent of this study was to evaluate the performance of QuantiFERON-TB Gold In-Tube (QFTGIT) in patients clinically suspected of active pulmonary TB (PTB) as well as in healthy subjects prior to its utilization for the epidemiological study of active TB and LTBI in Afar pastoralists. Methods The sensitivity of QFTGIT was evaluated in 140 subjects who were clinically suspected of PTB using the cut-off value recommended by the manufacturer (≥ 0.35 IU/ml) and disease-specific cut-off value. Sputum culture result was used as a gold standard. The specificity of the test was evaluated both in patients and in 55 tuberculin skin test (TST) negative healthy subjects. Results Out of the 140 study participants, 37 (26.4%) were positive for active PTB by culture. Out of the 37 subjects who had positive results by culture, 6 individuals were HIV-seropositive. Out of the 103 subjects who were negative by culture, 6 subjects had indeterminate results and 21 were HIV-seropositive. The performance of the test was assessed using data from 107 (31 culture positive and 76 culture negative) individuals who were clinically suspected of PTB and HIV-seronegatives. Using the manufacturer recommended cut-off value, the sensitivity of the test was 64.5% (20/31), while its specificity was 36.8% (28/76). The sensitivity of the test was increased to 77.4%, while the specificity was reduced to 23.7% using a cut-off value ≥ 0.1 IU/ml of IFNγ as disease-specific cut-off value. In TST negative healthy subjects, the specificity of the test was 58.2%. Conclusion Our findings revealed a low sensitivity of QFTGIT in the diagnosis of Mycobacterium tuberculosis (Mtb) infection in the present study area using the cut-off value recommended by the manufacturer. Nevertheless, the sensitivity increased from 64.5% to 77.4% by lowering the cut-off value recommended by the manufacturer to ≥ 0.1 IU/ml of IFNγ level. Hence, it is of practical importance to evaluate the performance of QFTGIT in population under different settings prior to its application either for the diagnosis of active TB or LTBI.
机译:背景技术目前,基于T细胞的γ干扰素(IFNγ)释放测定(IGRA)被公认为是筛查潜伏性结核感染(LTBI)的最佳方法,也有助于诊断活动性结核(TB)。据我们所知,埃塞俄比亚尚未评估这些诊断测试的性能。因此,本研究的目的是评估QuantiFERON-TB黄金管(QFTGIT)在临床怀疑患有活动性肺结核(PTB)的患者以及健康受试者中的性能,然后再将其用于活动性流行病学研究。 Afar牧民中的TB和LTBI。方法使用制造商推荐的临界值(≥0.35 IU / ml)和特定疾病的临界值,对140名临床上怀疑患有PTB的受试者进行QFTGIT敏感性评估。痰培养结果用作金标准。在患者和55名结核菌素皮肤试验(TST)阴性健康受试者中均评估了该试验的特异性。结果在140名研究参与者中,有37名(26.4%)的培养阳性PTB阳性。在通过文化获得阳性结果的37位受试者中,有6位是HIV血清阳性。在文化阴性的103名受试者中,有6名受试者的结果不确定,而21名HIV血清阳性。使用来自107名临床怀疑为PTB和HIV血清阴性药物的个体(31名培养阳性和76名培养阴性)的数据评估了测试的性能。使用制造商建议的临界值,测试的灵敏度为64.5%(20/31),而特异性为36.8%(28/76)。使用≥0.1 IU / mlIFN​​γ的临界值作为疾病特异性的临界值,测试的灵敏度提高到77.4%,而特异性降低到23.7%。在TST阴性健康受试者中,测试的特异性为58.2%。结论我们的发现表明,使用制造商建议的临界值,QFTGIT在当前研究区对结核分枝杆菌(Mtb)感染的诊断中敏感性较低。但是,通过将制造商推荐的临界值降低到≥0.1 IU / mlIFN​​γ水平,灵敏度从64.5%提高到77.4%。因此,在将QFTGIT用于活动性结核病或LTBI的诊断之前,评估QFTGIT在不同环境下人群的表现具有实际意义。

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