巴基斯坦AJK地区MTB/RIF专家检测中分子探针的流行病学研究

Jahan Zeb Baber, Imran Ali, Z. Qasim, Noore Saba, Sara Akram, Muhammad Nouman, U. Waheed, Akhlaaq Wazeer
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引用次数: 0

摘要

目的:本研究旨在检测利福平耐药结核病病例,并评估在巴基斯坦阿扎德查谟和克什米尔(AJK)不同研究人群中缺失探针的频率。方法:本研究在AJK米尔布尔区总部教学医院的国家结核病参考实验室进行。2016年3月至2019年8月期间收集的2790份标本进行了分析。肺结核(PTB)占病例的94%,而6%被归类为肺外病例。所有呼吸道和非呼吸道样本均采用荧光涂片镜检(AFB)和实时PCR检测(Xpert MTB/RIF法)检测结核分枝杆菌(MTB)和利福平耐药性。结果:在2790例疑似结核分枝杆菌患者中,734例(26%)通过Xpert MTB/RIF检测确诊为结核分枝杆菌,564例(20%)通过荧光显微镜检测呈阳性。在mtb阳性患者中,720例(98%)被诊断为肺结核,14例(2%)被诊断为肺外结核。66例(9%)患者检测到利福平耐药(RR),其中97%为肺部耐药,3%为肺外耐药。缺失最多的探针是E(密码子529-533),占34%,其次是探针D(密码子523-529),占26%。最不常见的缺失探针是C(密码子523-529),仅占3%。探针B(密码子512-518)缺失占15.4%,探针A(密码子518-523)缺失占9.4%。结论:利用分子诊断技术,如Xpert MTB/RIF试验,可以快速鉴定MTB并检测利福平耐药性。该研究为rpoB基因81 bp突变的患病率提供了有价值的基线数据,强调了进一步评估AJK突变模式的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epidemiology of Molecular Probes in Xpert MTB/RIF Assay in AJK, Pakistan
Objective: This study aimed to detect rifampicin-resistant tuberculosis cases and assess the frequency of missing probes in different study populations in Azad Jammu and Kashmir (AJK), Pakistan. Methodology: The study was conducted at the State TB Reference Laboratory, District Headquarters Teaching Hospital, Mirpur, AJK. A total of 2,790 specimens collected between March 2016 to August 2019 were analyzed. Pulmonary TB (PTB) accounted for 94% of the cases, while 6% were classified as extra-pulmonary cases. All respiratory and non-respiratory samples underwent fluorescence smear microscopy (AFB) and a real-time PCR test (Xpert MTB/RIF assay) to detect Mycobacterium tuberculosis (MTB) and rifampicin resistance. Results: Among the 2,790 suspected MTB patients, 734 (26%) were confirmed to have MTB using the Xpert MTB/RIF assay, while 564 (20%) tested positive by fluorescence microscopy. Of the MTB-positive patients, 720 (98%) were diagnosed with pulmonary TB, and 14 (2%) had extra-pulmonary TB. Rifampicin resistance (RR) was detected in 66 (9%) cases, with 97% of the resistant cases being pulmonary and 3% extra-pulmonary. The most frequently missing probe was E (Codon 529-533), accounting for 34% of the cases, followed by probe D (Codon 523-529) at 26%. The least frequently missing probe was C (Codon 523-529), observed in 3% of the cases. Probe B (Codon 512-518) was missing in 15.4% of cases, while probe A (Codon 518-523) was missing in 9.4% of cases. Conclusion: The utilization of molecular diagnostic techniques, such as the Xpert MTB/RIF assay, enables rapid identification of MTB and detection of rifampicin resistance. This study provides valuable baseline data on the prevalence of 81 bp mutations in the rpoB gene, highlighting the need for further evaluation of mutation patterns in AJK.
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