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Published on: April 9, 2012
PCR targeting IS6110 in diagnosing tuberculosis in children in comparison to MGIT culture
Rajeshwar Dayal1, Dipti Agarwal2, Harish Pathak3
1Professor and Head, Department of Pediatrics, Sarojini Naidu Medical College, Agra, India.
Insights
Polymerase chain reaction (PCR) targeting IS6110 demonstrates superior sensitivity for diagnosing pediatric tuberculosis (TB), including extrapulmonary TB, compared to MGIT 960 culture. This molecular test offers improved diagnostic efficiency in children.
Area of Science:
- Pediatric Infectious Diseases
- Molecular Diagnostics
- Microbiology
Background:
- Diagnosing tuberculosis (TB) in children, particularly extrapulmonary TB (EPTB), presents significant challenges.
- Accurate and timely diagnosis is crucial for effective treatment and disease control in pediatric populations.
Purpose of the Study:
- To evaluate the diagnostic utility of polymerase chain reaction (PCR) targeting the IS6110 insertion sequence for TB detection in children.
- To compare the performance of IS6110 PCR against MGIT 960 culture and conventional microscopy in pediatric TB cases.
Main Methods:
- A study involving 142 pediatric patients (<15 years) with suspected TB (50 pulmonary, 92 extrapulmonary).
- Clinical specimens were analyzed using Ziehl-Neelsen staining (ZN), MGIT 960 TB culture, and IS6110-targeted PCR.
- Sensitivity and specificity of PCR were assessed and compared with MGIT culture results.
Main Results:
- IS6110 PCR exhibited a significantly higher sensitivity (69.01%) than MGIT culture (47.41%) (p<0.05).
- Sensitivity for PCR in extrapulmonary specimens (65.21%) was comparable to pulmonary specimens (76%), with no statistical significance (p>0.05).
Conclusions:
- The diagnostic efficacy of IS6110 PCR was consistent across both pulmonary and extrapulmonary TB in children.
- PCR utilizing the IS6110 primer demonstrated superior diagnostic efficiency compared to MGIT culture for pediatric TB.
Background:
Diagnosis of tuberculosis (TB) in children is difficult in children especially in extrapulmonary tuberculosis (EPTB). This study was conducted to evaluate the use of polymerase chain reaction (PCR) targeting IS6110 in the diagnosis of TB in children with pulmonary TB and EPTB and also to compare its performance with MGIT 960 culture and conventional microscopy.
Methods:
A total of 142 cases (50 pulmonary, 92 extrapulmonary) of suspected TB patients <15 years of age were included in the study. The clinical specimens obtained from these cases were subjected to Ziehl-Neelsen staining (ZN), MGIT 960 TB culture and PCR targeting insertion sequence IS6110. Sensitivity and specificity of PCR were calculated in pulmonary and extrapulmonary specimens. The results were compared to MGIT culture.
Results:
PCR targeting IS6110 sequence had sensitivity of 69.01% in various clinical specimens which was significantly more than MGIT culture showing a sensitivity of 47.41% (p<0.05). Sensitivity of PCR IS6110 in extrapulmonary specimens was 65.21% which was lower than sensitivity in pulmonary specimens (76%) but was not statistically significant (p>0.05).
Conclusions:
Diagnostic efficacy of PCR IS6110 in pulmonary and extrapulmonary TB cases was similar. PCR using IS6110 primer had significantly better efficiency than MGIT culture in diagnosing TB in children.
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