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Search for DQ2 5 and DQ8 alleles using a lower cost technique in patients with type 1 diabetes and celiac disease in a population of southern Brazil
Bastos, Marília D; Kowalski, Thayne W; Puñales, Márcia; Tschiedel, Balduíno; Mariath, Luiza M; Pires, Ana Luiza G; Faccini, Lavínia S; Silveira, Themis R.
  • Bastos, Marília D; Universidade Federal do Rio Grande do Sul. Porto Alegre. BR
  • Kowalski, Thayne W; Universidade Federal do Rio Grande do Sul. Porto Alegre. BR
  • Puñales, Márcia; Universidade Federal do Rio Grande do Sul. Porto Alegre. BR
  • Tschiedel, Balduíno; Universidade Federal do Rio Grande do Sul. Porto Alegre. BR
  • Mariath, Luiza M; Universidade Federal do Rio Grande do Sul. Porto Alegre. BR
  • Pires, Ana Luiza G; Universidade Federal do Rio Grande do Sul. Porto Alegre. BR
  • Faccini, Lavínia S; Universidade Federal do Rio Grande do Sul. Porto Alegre. BR
  • Silveira, Themis R; Universidade Federal do Rio Grande do Sul. Porto Alegre. BR
Arch. endocrinol. metab. (Online) ; 61(6): 550-555, Dec. 2017. tab
Artículo en Inglés | LILACS | ID: biblio-887614
ABSTRACT
ABSTRACT Objective To evaluate the frequency of DQ2.5 and DQ8 alleles using the Tag-single-nucleotide polymorphism (Tag-SNP) technique in individuals with type 1 diabetes mellitus (T1DM) and celiac disease (CD) in southern Brazil. Materials and methods In a prospective design, we performed the search for DQA1*0501 and DQB1*0201 alleles for DQ2.5 and DQB1*0302 for DQ8 through Real-Time Polymerase Chain Reaction (RT-PCR) technique, using TaqMan Genotyping Assays (Applied Biosystems, USA). The diagnosis of CD was established by duodenal biopsy and genotypic determination performed by StepOne Software v2.3. Allelic and genotypic frequencies were compared between groups using Chi-square and Fisher's exact tests and the multiple comparisons using Finner's adjustment. Results Three hundred and sixty two patients with a median age of 14 years were divided into 3 groups T1DM without CD (264); T1DM with CD (32) and CD without T1DM (66). In 97% of individuals with T1DM and CD and 76% of individuals with CD without T1DM, respectively, the alleles DQ2.5 and/or DQ8 were identified (p < 0.001). DQ2.5 was more common in individuals with CD (p = 0.004) and DQ8 was more common in individuals with type 1 diabetes (p = 0.008). Conclusions The evaluation of the alleles for DQ2.5 and DQ8 by Tag-SNP technique showed a high negative predictive value among those with T1DM, similar to that described by the conventional technique. The high frequency of DQ8 alleles in individuals with T1DM did not allow differentiating those at higher risk of developing T1DM.
Asunto(s)


Texto completo: Disponible Índice: LILACS (Américas) Asunto principal: Enfermedad Celíaca / Predisposición Genética a la Enfermedad / Diabetes Mellitus Tipo 1 / Frecuencia de los Genes Tipo de estudio: Estudio de etiología / Evaluación Económica en Salud / Estudio observacional / Estudio pronóstico / Factores de riesgo Límite: Femenino / Humanos / Masculino País/Región como asunto: America del Sur / Brasil Idioma: Inglés Revista: Arch. endocrinol. metab. (Online) Asunto de la revista: Endocrinologia / Metabolismo Año: 2017 Tipo del documento: Artículo País de afiliación: Brasil Institución/País de afiliación: Universidade Federal do Rio Grande do Sul/BR

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Texto completo: Disponible Índice: LILACS (Américas) Asunto principal: Enfermedad Celíaca / Predisposición Genética a la Enfermedad / Diabetes Mellitus Tipo 1 / Frecuencia de los Genes Tipo de estudio: Estudio de etiología / Evaluación Económica en Salud / Estudio observacional / Estudio pronóstico / Factores de riesgo Límite: Femenino / Humanos / Masculino País/Región como asunto: America del Sur / Brasil Idioma: Inglés Revista: Arch. endocrinol. metab. (Online) Asunto de la revista: Endocrinologia / Metabolismo Año: 2017 Tipo del documento: Artículo País de afiliación: Brasil Institución/País de afiliación: Universidade Federal do Rio Grande do Sul/BR