Affiliation:
1. Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Incheon St Mary´s Hospital, Republic of Korea
2. Department of Laboratory Medicine, Seoul St Mary´s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea
Abstract
BACKGROUND: We investigated the feasibility of early line-probe assay (LPA) using remnant DNA of Mycobacterium tuberculosis from polymerase chain reaction (PCR) test.METHODS: M. tuberculosis DNA specimens with cycle threshold (Ct) values reported and
collected from patients with known results for both LPA with culture isolates and phenotype drug susceptibility testing (pDST) were selected. The diagnostic performance of DNA-based LPA according to the Ct value was investigated.RESULTS: A total of 143 respiratory specimens were
included. For isoniazid resistance, the accuracy in subgroups with Ct value <25, 25–29 and ≥29 was respectively 96.8%, 65.7% and 13.3%. For rifampicin resistance, accuracy in subgroups with Ct values <29 and ≥29 was respectively 87.8% and 13.3%. When compared to the pDST
results, sensitivity, specificity, positive predictive value and negative predictive value in specimens with Ct values <25 was respectively 1.00 (95% CI 0.69–1.00), 0.95 (95% CI 0.76–1.00), 0.91 (95% CI 0.59–1.00) and 1.00 (95% CI 0.83–1.00) for isoniazid resistance.
For rifampicin resistance, corresponding values in subgroups with Ct values <29 were respectively 0.89 (95% CI 0.52–1.00), 0.98 (95% CI 0.91–1.00), 0.80 (95% CI 0.50–0.94) and 0.99 (95% CI 0.92–1.00).CONCLUSIONS: DNA-based early LPA with remnant DNA from
respiratory samples was feasible and accurate when the Ct values were low.
Publisher
International Union Against Tuberculosis and Lung Disease
Subject
Infectious Diseases,Pulmonary and Respiratory Medicine