Amerindian mtDNA haplogroups and celiac disease risk HLA haplotypes in mixed-blood Latin American patients
Author
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Parada, Alejandra
Author
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Araya, Magdalena
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Pérez Bravo, Francisco
Author
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Méndez, Marco
Author
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Mimbacas, Adriana
Author
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Motta, Patricia
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Martín, Gabriela
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Botero, Jorge
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Espinosa, Nelly
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Alarcon, Teresa
Author
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Canales, Paulina
Admission date
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2019-03-18T11:59:42Z
Available date
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2019-03-18T11:59:42Z
Publication date
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2011
Cita de ítem
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Journal of Pediatric Gastroenterology and Nutrition, Volumen 53, Issue 4, 2018, Pages 429-434
Identifier
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15364801
Identifier
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02772116
Identifier
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10.1097/MPG.0b013e31821de3fc
Identifier
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https://repositorio.uchile.cl/handle/2250/167241
Abstract
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Background and Objective: Risk haplotypes have been described in celiac disease (CD), but the influence of native genes on CD in Hispanic Americans is unknown. The aim of the study was to measure the frequency of Amerindian mitochondrial DNA (mtDNA) haplogroups (inherited by the maternal line) in mixed-blood patients with CD from Chile, Argentina, and Uruguay, and to assess the relation between these and human leukocyte antigen (HLA) alleles and haplotypes and clinical presentations. Patients and Methods: Clinical history, histological data, and genetic studies were conducted following 2 protocols: a case-control study of 72 Chilean patients with CD and controls, and an assessment of 43 (additional) samples of celiac patients from Chile, 96 from Argentina, and 57 from Uruguay, compared with the mtDNA frequency in the corresponding country. HLA typing was performed by a commercial kit, and mtDNA was determined by means of polymerase chain reaction and restriction fragment length polymor