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Association of HLA-B∗35 and moderate or severe cutaneous reactions secondary to benznidazole treatment in chronic chagas disease.
Bosch-Nicolau, Pau; Salvador, Fernando; Sánchez-Montalvá, Adrián; Franco-Jarava, Clara; Arrese-Muñoz, Iria; Sulleiro, Elena; Roure, Silvia; Valerio, Lluis; Oliveira-Souto, Inés; Serre-Delcor, Núria; Pou, Diana; Treviño, Begoña; Aznar, María L; Espinosa-Pereiro, Juan; Molina, Israel.
Afiliação
  • Bosch-Nicolau P; Tropical Medicine & International Health Unit Vall D'Hebron-Drassanes, Infectious Diseases Department, PROSICS Barcelona, University Hospital Vall D'Hebron, Barcelona, Spain; Medicine Department, Universitat Autònoma de Barcelona, Barcelona, Spain. Electronic address: pbosch@vhebron.net.
  • Salvador F; Tropical Medicine & International Health Unit Vall D'Hebron-Drassanes, Infectious Diseases Department, PROSICS Barcelona, University Hospital Vall D'Hebron, Barcelona, Spain.
  • Sánchez-Montalvá A; Tropical Medicine & International Health Unit Vall D'Hebron-Drassanes, Infectious Diseases Department, PROSICS Barcelona, University Hospital Vall D'Hebron, Barcelona, Spain.
  • Franco-Jarava C; Immunology Department, University Hospital Vall D'Hebron, Barcelona, Spain.
  • Arrese-Muñoz I; Immunology Department, University Hospital Vall D'Hebron, Barcelona, Spain.
  • Sulleiro E; Microbiology Department, University Hospital Vall D'Hebron, Barcelona, Spain.
  • Roure S; North Metropolitan International Health Unit, PROSICS Metropolitana Nord, Badalona, Spain; Infectious Diseases Department, Germans Trias I Pujol University Hospital, Badalona, Spain.
  • Valerio L; North Metropolitan International Health Unit, PROSICS Metropolitana Nord, Badalona, Spain.
  • Oliveira-Souto I; Tropical Medicine & International Health Unit Vall D'Hebron-Drassanes, Infectious Diseases Department, PROSICS Barcelona, University Hospital Vall D'Hebron, Barcelona, Spain.
  • Serre-Delcor N; Tropical Medicine & International Health Unit Vall D'Hebron-Drassanes, Infectious Diseases Department, PROSICS Barcelona, University Hospital Vall D'Hebron, Barcelona, Spain.
  • Pou D; Tropical Medicine & International Health Unit Vall D'Hebron-Drassanes, Infectious Diseases Department, PROSICS Barcelona, University Hospital Vall D'Hebron, Barcelona, Spain.
  • Treviño B; Tropical Medicine & International Health Unit Vall D'Hebron-Drassanes, Infectious Diseases Department, PROSICS Barcelona, University Hospital Vall D'Hebron, Barcelona, Spain.
  • Aznar ML; Tropical Medicine & International Health Unit Vall D'Hebron-Drassanes, Infectious Diseases Department, PROSICS Barcelona, University Hospital Vall D'Hebron, Barcelona, Spain.
  • Espinosa-Pereiro J; Tropical Medicine & International Health Unit Vall D'Hebron-Drassanes, Infectious Diseases Department, PROSICS Barcelona, University Hospital Vall D'Hebron, Barcelona, Spain; Medicine Department, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Molina I; Tropical Medicine & International Health Unit Vall D'Hebron-Drassanes, Infectious Diseases Department, PROSICS Barcelona, University Hospital Vall D'Hebron, Barcelona, Spain; Medicine Department, Universitat Autònoma de Barcelona, Barcelona, Spain. Electronic address: imolina@vhebron.net.
Clin Microbiol Infect ; 28(6): 881.e1-881.e5, 2022 Jun.
Article em En | MEDLINE | ID: mdl-34863919
OBJECTIVES: Benznidazole is the first-line treatment for Chagas disease. Adverse events appear in more than 50% of patients, leading to discontinuation in approximately 15%. Cutaneous reactions are one of the most frequent adverse events. Human leucocyte antigen (HLA) genotyping studies identified an association between cutaneous reactions to benznidazole and carrying the specific allele HLA-B∗35:05. We designed the present study to prospectively confirm this association. METHODS: This is a prospective observational study including Chagas disease patients aged 18 years or more who accepted to receive benznidazole treatment following current guidelines. Allele genotyping of HLA-B was determined in all patients. Clinical and analytical follow up was performed at days 0, 7, 14, 30 and 60 of treatment. RESULTS: Two-hundred and seven individuals were included. Seventy per cent were female with a mean age of 45.1 (SD ± 9.86) years mainly from Bolivia (92.8%). In 102 (49.3%) cases a cutaneous reaction was diagnosed. Forty-eight (46.6%) were classified as mild, 37 (35.9%) as moderate and 18 (17.5%) as severe. Thirty-two (15.4%) patients had to definitively interrupt the treatment because of a cutaneous reaction. Female sex (OR 4.49; 95% CI 1.62-12.47), new-onset eosinophilia before cutaneous symptoms (OR 2.55; 95% CI 1.2-5.43) and carrying the HLA-B∗35 allelic group (OR 2.58; 95% CI 1.2-5.51) were all predictors of moderate to severe cutaneous reactions. No statistical significance was found when the specific allele HLA-B∗35:05 was analysed. CONCLUSIONS: Patients carrying the HLA-B∗35 allelic group are at higher risk of moderate to severe reactions when taking benznidazole treatment.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Antígenos HLA-B / Doença de Chagas / Hipersensibilidade Tardia / Nitroimidazóis Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Antígenos HLA-B / Doença de Chagas / Hipersensibilidade Tardia / Nitroimidazóis Idioma: En Ano de publicação: 2022 Tipo de documento: Article