Souza E Silva Bruno Oliveira, Tolentino Júnior Dilceu Silveira, Miranda Silvana Spíndola, Pascoal Xavier Marcelo Antônio, Cunha Cury Geraldo
Federal University of the Jequitinhonha and Mucuri Valleys, Diamantina, Minas Gerais, Brazil.
Postgraduate Program in Collective Health, Oswaldo Cruz Foundation, René Rachou Institute, Belo Horizonte, Minas Gerais, Brazil.
Sci Rep. 2025 Apr 11;15(1):12537. doi: 10.1038/s41598-025-97714-9.
Leprosy is an infectious and chronic dermatoneurological disease, considered the most frequent cause of physical disabilities worldwide. It remains a major challenge for public health in Brazil, which is classified as a country with a high burden of the disease and ranks second in number of cases among all nations. Laboratory tests are important tools to complement the clinical-epidemiological evaluation, and molecular techniques emerged in the hope of reducing the limitations existing in the laboratory diagnosis of leprosy. We aimed to evaluate the accuracy of real-time polymerase chain reaction (qPCR) in the detection of Mycobacterium leprae in direct intradermal scrapings (swabs) and smears from bacilloscopy slides. This is an observational and cross-sectional study to evaluate diagnostic tests, which used bacilloscopy as the gold standard. Participants with epidemiological and/or clinical suspicion of leprosy from the northeastern region of Minas Gerais, referred to the Macroregional Laboratory of Teófilo Otoni for collection of intradermal scrapings from the earlobes, right elbow, left elbow or suspicious lesion were included. Bacilloscopy was performed according to the Technical Procedures Guide of the Ministry of Health and the DNA samples, after extraction and quantification, were subjected to qPCR with primers specific for the RLEP region of Mycobacterium leprae. The study obtained the number of 45 samples collected from suspected cases of leprosy in the period between May/2022 and February/2023. Descriptive, comparative and accuracy statistical analyses were performed using Minitab 17 and GraphPad Prism version 6.00 software. The sensitivity of qPCR on direct intradermal scraping samples (swabs) and smear slides, compared with bacilloscopy, was 100%. The specificity was higher for qPCR on swab samples (64.3%) than on smear slides (53.8%). The performance of qPCR on intradermal scraping swab samples and smear slides indicated accuracies of 82.10 and 76.9%, respectively. The results of the comparison of the proportions of qPCR positivity of the two samples showed a statistically significant association (P-value = 0.005), with a degree of agreement of 55% (Kappa = 0.55). Taken together, the results of the performance and comparative analyses of qPCR on intradermal scraping swabs and smear slides showed good accuracy in relation to bacilloscopy and moderate agreement between these different qPCR strategies.
麻风病是一种传染性慢性皮肤神经疾病,被认为是全球身体残疾最常见的原因。在巴西,它仍然是公共卫生面临的一项重大挑战,巴西被列为麻风病高负担国家,在所有国家中病例数排名第二。实验室检测是补充临床流行病学评估的重要工具,分子技术的出现是为了减少麻风病实验室诊断中存在的局限性。我们旨在评估实时聚合酶链反应(qPCR)在检测直接皮内刮片(拭子)和细菌学检查玻片涂片上的麻风分枝杆菌时的准确性。这是一项观察性横断面研究,用于评估诊断试验,该研究将细菌学检查作为金标准。纳入了来自米纳斯吉拉斯州东北部、因流行病学和/或临床怀疑患有麻风病而被转诊至特奥菲洛·奥托尼大区实验室进行耳垂、右肘、左肘或可疑病变皮内刮片采集的参与者。细菌学检查按照卫生部的技术程序指南进行,DNA样本经提取和定量后,使用针对麻风分枝杆菌RLEP区域的特异性引物进行qPCR。该研究在2022年5月至2023年2月期间从疑似麻风病病例中采集了45份样本。使用Minitab 17和GraphPad Prism 6.00版软件进行描述性、比较性和准确性统计分析。与细菌学检查相比,qPCR对直接皮内刮片样本(拭子)和涂片玻片的敏感性为100%。qPCR对拭子样本的特异性(64.3%)高于涂片玻片(53.8%)。qPCR对皮内刮片拭子样本和涂片玻片的性能表明准确性分别为82.10%和76.9%。两个样本qPCR阳性比例比较结果显示存在统计学显著关联(P值 = 0.005),一致性程度为55%(Kappa = 0.55)。综合来看,qPCR对皮内刮片拭子和涂片玻片的性能及比较分析结果显示,与细菌学检查相比具有良好的准确性,且这些不同qPCR策略之间具有中等一致性。