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Amerindian ancestry proportion as a risk factor for inflammatory bowel diseases: results from a Latin American Andean cohort.
Pérez-Jeldres, Tamara; Magne, Fabien; Ascui, Gabriel; Alvares, Danilo; Orellana, Matias; Alvarez-Lobos, Manuel; Hernandez-Rocha, Cristian; Azocar, Lorena; Aguilar, Nataly; Espino, Alberto; Estela, Ricardo; Escobar, Sergio; Zazueta, Alejandra; Baez, Pablo; Silva, Verónica; De La Vega, Andres; Arriagada, Elizabeth; Pavez-Ovalle, Carolina; Díaz-Asencio, Alejandro; Travisany, Dante; Miquel, Juan Francisco; Villablanca, Eduardo J; Kronenberg, Mitchell; Bustamante, María Leonor.
Afiliación
  • Pérez-Jeldres T; Department of Gastroenterology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Magne F; Department of Gastroenterology, Hospital San Borja Arriarán, Santiago, Chile.
  • Ascui G; Department of Microbiology, Faculty of Medicine, Institute of Biomedical Sciences (ICBM), Universidad de Chile, Santiago, Chile.
  • Alvares D; La Jolla Institute for Immunology, San Diego, CA, United States.
  • Orellana M; MRC Biostatistics Unit, University of Cambridge, Cambridge, United Kingdom.
  • Alvarez-Lobos M; Department of Computer Science, Faculty of Physical Sciences and Mathematics, Universidad de Chile, Santiago, Chile.
  • Hernandez-Rocha C; Department of Gastroenterology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Azocar L; Department of Gastroenterology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Aguilar N; Department of Gastroenterology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Espino A; Department of Gastroenterology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Estela R; Department of Gastroenterology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Escobar S; Department of Gastroenterology, Hospital San Borja Arriarán, Santiago, Chile.
  • Zazueta A; Department of Gastroenterology, Hospital San Borja Arriarán, Santiago, Chile.
  • Baez P; Department of Microbiology, Faculty of Medicine, Institute of Biomedical Sciences (ICBM), Universidad de Chile, Santiago, Chile.
  • Silva V; Center of Medical Informatics and Telemedicine, University of Chile, Santiago, Chile.
  • De La Vega A; Department of Gastroenterology, Hospital San Borja Arriarán, Santiago, Chile.
  • Arriagada E; Department of Gastroenterology, Hospital San Borja Arriarán, Santiago, Chile.
  • Pavez-Ovalle C; Department of Gastroenterology, Hospital San Borja Arriarán, Santiago, Chile.
  • Díaz-Asencio A; Department of Gastroenterology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Travisany D; Department of Gastroenterology, Hospital San Borja Arriarán, Santiago, Chile.
  • Miquel JF; Núcleo de Investigación en Data Science, Facultad de Ingeniería y Negocios, Universidad de las Américas, Santiago, Chile.
  • Villablanca EJ; Department of Gastroenterology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Kronenberg M; Division of Immunology and Allergy, Department of Medicine, Solna, Karolinska Institutet and University Hospital, Stockholm, Sweden.
  • Bustamante ML; La Jolla Institute for Immunology, San Diego, CA, United States.
Front Med (Lausanne) ; 10: 1258395, 2023.
Article en En | MEDLINE | ID: mdl-37964883
ABSTRACT
Background and

aims:

Latin American populations remain underrepresented in genetic studies of inflammatory bowel diseases (IBDs). Most genetic association studies of IBD rely on Caucasian, African, and Asian individuals. These associations have yet to be evaluated in detail in the Andean region of South America. We explored the contribution of IBD-reported genetic risk variants to a Chilean cohort and the ancestry contribution to IBD in this cohort.

Methods:

A total of 192 Chilean IBD patients were genotyped using Illumina's Global Screening Array. Genotype data were combined with similar information from 3,147 Chilean controls. The proportions of Aymara, African, European, and Mapuche ancestries were estimated using the software ADMIXTURE. We calculated the odds ratios (ORs) and 95% confidence intervals (CIs) for gender, age, and ancestry proportions. We also explored associations with previously reported IBD-risk variants independently and in conjunction with genetic ancestry.

Results:

The first and third quartiles of the proportion of Mapuche ancestry in IBD patients were 24.7 and 34.2%, respectively, and the corresponding OR was 2.30 (95%CI 1.52-3.48) for the lowest vs. the highest group. Only one variant (rs7210086) of the 180 reported IBD-risk SNPs was associated with IBD risk in the Chilean cohort (adjusted P = 0.01). This variant is related to myeloid cells.

Conclusion:

The type and proportion of Native American ancestry in Chileans seem to be associated with IBD risk. Variants associated with IBD risk in this Andean region were related to myeloid cells and the innate immune response.
Palabras clave

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Front Med (Lausanne) Año: 2023 Tipo del documento: Article País de afiliación: Chile

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Front Med (Lausanne) Año: 2023 Tipo del documento: Article País de afiliación: Chile