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Epidemiological, clinical and immune factors that influence the persistence of antiphospholipid antibodies in leprosy
Ribeiro, Sandra Lúcia Euzébio; Pereira, Helena Lúcia Alves; Boechat, Antonio Luiz; Silva, Neusa Pereira; Sato, Emilia Ionue; Cunha, Maria das Graças Souza; Passos, Luiz Fernando de Souza; Dos-Santos, Maria Cristina.
Afiliación
  • Ribeiro, Sandra Lúcia Euzébio; Federal University of Amazonas. Faculty of Health Sciences. Department of Clinical Medicine. Manaus. BR
  • Pereira, Helena Lúcia Alves; Federal University of Amazonas. Faculty of Health Sciences. Department of Clinical Medicine. Manaus. BR
  • Boechat, Antonio Luiz; Federal University of Amazonas. Immunochemistry Laboratory. Department of Parasitology. Manaus. BR
  • Silva, Neusa Pereira; Federal University of São Paulo. Escola Paulista de Medicina. Division of Rheumatology. São Paulo. BR
  • Sato, Emilia Ionue; Federal University of São Paulo. Escola Paulista de Medicina. Division of Rheumatology. São Paulo. BR
  • Cunha, Maria das Graças Souza; Alfredo da Matta Foundation. Manaus. BR
  • Passos, Luiz Fernando de Souza; Federal University of Amazonas. Faculty of Health Sciences. Department of Clinical Medicine. Manaus. BR
  • Dos-Santos, Maria Cristina; Federal University of Amazonas. Immunochemistry Laboratory. Department of Parasitology. Manaus. BR
Adv Rheumatol ; 59: 52, 2019. tab, graf
Article en En | LILACS | ID: biblio-1088611
Biblioteca responsable: BR1.1
ABSTRACT
Abstract

Introduction:

Antiphospholipid antibodies (aPL) are described in individuals with leprosy without the clinical features of antiphospholipid antibody syndrome (APS), a condition involving thromboembolic phenomena. We have described the persistence of these antibodies for over 5 years in patients with leprosy after specific treatment.

Objectives:

To determine whether epidemiological, clinical and immunological factors played a role in the longterm persistence of aPL antibodies in leprosy patients after multidrug therapy (MDT) had finished.

Methods:

The study sample consisted of 38 patients with a diagnosis of leprosy being followed up at the Dermatology and Venereology Outpatient Department at the Alfredo da Matta Foundation (FUAM) in Manaus, AM. ELISA was used to detect anticardiolipin (aCL) and anti-β2 glycoprotein I (anti-β2GPI) antibodies. Patients were reassessed on average of 5 years after specific treatment for the disease (MDT) had been completed.

Results:

Persistence of aPL antibodies among the 38 leprosy patients was 84% (32/38), and all had the IgM isotype. Mean age was 48.1 ± 15.9 years, and 23 (72.0%) were male. The lepromatous form (LL) of leprosy was the most common (n = 16, 50%). Reactional episodes were observed in three patients (9.4%). Eighteen (47.37%) were still taking medication (prednisone and/or thalidomide). Mean IgM levels were 64 U/mL for aCL and 62 U/mL for anti-β2GPI. In the multivariate binary logistic regression the following variables showed a significant association age (p = 0.045, OR = 0.91 and CI 95% 0.82-0.98), LL clinical presention (p = 0.034; OR = 0.02 and CI 95% = 0.0-0.76) and bacterial index (p = 0.044; OR = 2.74 and CI 95% = 1.03-7.33). We did not find association between prednisone or thalidomide doses and positivity for aPL (p = 0.504 and p = 0.670, respectively). No differences in the variables vascular thrombosis, pregnancy morbidity, diabetes, smoking and alcoholism were found between aPL-positive and aPL-negative patients.

Conclusion:

Persistence of positivity for aPL antibodies was influenced by age, clinical presentation and bacterial index. However, further studies are needed to elucidate the reason for this persistence, the role played by aPL antibodies in the disease and the B cell lineages responsible for generation of these antibodies.
Asunto(s)

Texto completo: 1 Índice: LILACS Asunto principal: Lepra Límite: Humans Idioma: En Revista: Adv Rheumatol Asunto de la revista: Artrite / Reumatologia Año: 2019 Tipo del documento: Article

Texto completo: 1 Índice: LILACS Asunto principal: Lepra Límite: Humans Idioma: En Revista: Adv Rheumatol Asunto de la revista: Artrite / Reumatologia Año: 2019 Tipo del documento: Article