TY - JOUR KW - Adolescent KW - Adult KW - Aged KW - Aged, 80 and over KW - Antigens, Bacterial KW - Brazil KW - Case-Control Studies KW - Child KW - Child, Preschool KW - Chromatography, Affinity KW - Female KW - Glycolipids KW - Humans KW - Immunoassay KW - Immunoglobulin Isotypes KW - leprosy KW - Male KW - Middle Aged KW - Mycobacterium leprae KW - Nepal KW - Predictive Value of Tests KW - Reagent Kits, Diagnostic KW - Sensitivity and Specificity KW - Young Adult AU - Stefani MMA AU - Grassi AB AU - Sampaio LH AU - Sousa ALOM AU - Costa MB AU - Scheelbeek PF D AU - Neupane KD AU - Hagge D AU - Macdonald M AU - Cho S AU - Oskam L AU - Bührer-Sékula S AB -

The diagnosis of leprosy continues to be based on clinical symptoms and early diagnosis and treatment are critical to preventing disability and transmission. Sensitive and specific laboratory tests are not available for diagnosing leprosy. Despite the limited applicability of anti-phenolic glycolipid-I (PGL-I) serology for diagnosis, it has been suggested as an additional tool to classify leprosy patients (LPs) for treatment purposes. Two formats of rapid tests to detect anti-PGL-I antibodies [ML immunochromatography assay (ICA) and ML Flow] were compared in different groups, multibacillary patients, paucibacillary patients, household contacts and healthy controls in Brazil and Nepal. High ML Flow intra-test concordance was observed and low to moderate agreement between the results of ML ICA and ML Flow tests on the serum of LPs was observed. LPs were "seroclassified" according to the results of these tests and the seroclassification was compared to other currently used classification systems: the World Health Organization operational classification, the bacilloscopic index and the Ridley-Jopling classification. When analysing the usefulness of these tests in the operational classification of PB and MB leprosy for treatment and follow-up purposes, the ML Flow test was the best point-of-care test for subjects in Nepal and despite the need for sample dilution, the ML ICA test yielded better performance among Brazilian subjects. Our results identified possible ways to improve the performance of both tests.

BT - Memorias do Instituto Oswaldo Cruz C1 - http://www.ncbi.nlm.nih.gov/pubmed/23283463?dopt=Abstract CN - STEFANI 2012 DA - 2012 Dec DO - 10.1590/s0074-02762012000900019 J2 - Mem. Inst. Oswaldo Cruz LA - eng N2 -

The diagnosis of leprosy continues to be based on clinical symptoms and early diagnosis and treatment are critical to preventing disability and transmission. Sensitive and specific laboratory tests are not available for diagnosing leprosy. Despite the limited applicability of anti-phenolic glycolipid-I (PGL-I) serology for diagnosis, it has been suggested as an additional tool to classify leprosy patients (LPs) for treatment purposes. Two formats of rapid tests to detect anti-PGL-I antibodies [ML immunochromatography assay (ICA) and ML Flow] were compared in different groups, multibacillary patients, paucibacillary patients, household contacts and healthy controls in Brazil and Nepal. High ML Flow intra-test concordance was observed and low to moderate agreement between the results of ML ICA and ML Flow tests on the serum of LPs was observed. LPs were "seroclassified" according to the results of these tests and the seroclassification was compared to other currently used classification systems: the World Health Organization operational classification, the bacilloscopic index and the Ridley-Jopling classification. When analysing the usefulness of these tests in the operational classification of PB and MB leprosy for treatment and follow-up purposes, the ML Flow test was the best point-of-care test for subjects in Nepal and despite the need for sample dilution, the ML ICA test yielded better performance among Brazilian subjects. Our results identified possible ways to improve the performance of both tests.

PY - 2012 SP - 124 EP - 31 T2 - Memorias do Instituto Oswaldo Cruz TI - Comparison of two rapid tests for anti-phenolic glycolipid-I serology in Brazil and Nepal. UR - http://www.scielo.br/pdf/mioc/v107s1/19.pdf VL - 107 Suppl 1 SN - 1678-8060 ER -