## Abstract The diagnosis of American tegumentary leishmaniasis (ATL) is based on the visualization or isolation of the parasite, which is a time‐consuming and poorly sensitive method. In this study, we evaluated the accuracy and reliability of ELISA for the diagnosis of ATL using soluble (SF) and
Comparative study of amplification systems in immunoenzyme assays for the diagnosis of American tegumentary leishmaniasis
✍ Scribed by Lílian Dias Nascimento; Sonia Regina Lambert Passos; Eliame Mouta-Confort; Marta de Almeida Santiago; Andreia Silva Alves; Maria de Fátima Madeira; Armando de Oliveira Schubach; Mauro Célio de Almeida Marzochi
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 111 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0887-8013
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✦ Synopsis
Abstract
We compared the accuracy and reliability of three amplification systems for enzyme immunoassays in the detection of specific IgG antibodies for the diagnosis of cutaneous leishmaniasis caused by Leishmania (Viannia) braziliensis in patients from an endemic area in Rio de Janeiro, Brazil. Partially soluble antigens obtained from the promastigote forms of L. (V.) braziliensis were used. For development of the reaction, two chromogens, 1,2‐orthophenylenediamine (OPD) and 3,3′,5,5′‐tetramethylbenzidine (TMB), and a fluorogen, 4‐methylumbelliferylphosphate (MUP), were tested. The performance of each system was compared using the following parameters: accuracy, intraclasscorrelation coefficient (ICC), and area under the receiver operating characteristic (ROC) curve. Sensitivity was the same (97.4%) for all systems. The reliability was excellent (ICC=98.6, 98.7, and 99.1%) and specificity was 93.7, 95.8, and 97.4% for OPD, MUP, and TMB, respectively, showing no statistical significance. Despite the absence of differences in the performance of the three systems, the use of TMB is suggested because of its operational advantages, such as low cost compared with fluorogens, easy manipulation, greater stability, and lower toxicity. J. Clin. Lab. Anal. 23:152–156, 2009. © 2009 Wiley‐Liss, Inc.
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