Amerindian ancestry proportion as a risk factor for inflammatory bowel diseases: results from a Latin American Andean cohort

dc.contributor.affiliationPontificia Universidad Catolica de Chile
dc.contributor.affiliationUniversidad de Chile
dc.contributor.affiliationLa Jolla Institute for Immunology
dc.contributor.affiliationMRC Biostatistics Unit
dc.contributor.affiliationUniversity of Cambridge
dc.contributor.affiliationUniversidad de Las Americas - Chile
dc.contributor.affiliationKarolinska Institutet
dc.contributor.affiliationKarolinska University Hospital
dc.contributor.affiliationUniversity of California System
dc.contributor.affiliationUniversity of California San Diego
dc.contributor.authorPerez-Jeldres, Tamara
dc.contributor.authorMagne, Fabien
dc.contributor.authorAscui, Gabriel
dc.contributor.authorAlvares, Danilo
dc.contributor.authorOrellana, Matias
dc.contributor.authorAlvarez-Lobos, Manuel
dc.contributor.authorHernandez-Rocha, Cristian
dc.contributor.authorAzocar, Lorena
dc.contributor.authorAguilar, Nataly
dc.contributor.authorEspino, Alberto
dc.contributor.authorEstela, Ricardo
dc.contributor.authorEscobar, Sergio
dc.contributor.authorZazueta, Alejandra
dc.contributor.authorBaez, Pablo
dc.contributor.authorSilva, Veronica
dc.contributor.authorla Vega, Andres de
dc.contributor.authorArriagada, Elizabeth
dc.contributor.authorPavez-Ovalle, Carolina
dc.contributor.authorDiaz-Asencio, Alejandro
dc.contributor.authorTravisany, Dante
dc.contributor.authorMiquel, Juan Francisco
dc.contributor.authorVillablanca, Eduardo J.
dc.contributor.authorKronenberg, Mitchell
dc.contributor.authorBustamante, Maria Leonor
dc.date.accessioned2024-09-03T19:17:45Z
dc.date.available2024-09-03T19:17:45Z
dc.date.issued2023-10-27
dc.description.abstractBackground 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.
dc.description.sponsorshipThe author(s) declare financial support was received for the research, authorship, and/or publication of this article. TP-J was supported by the ANID, Chile. Project Fondecyt Initiation (grant number 11220147). DA was supported by the UKRI Medical Research; ANID, Chile [11220147]; Project Fondecyt Initiation [MC_UU_00002/5]; UKRI Medical Research Council [1211344]; Project Fondecyt Regular; Medical Research Council [MC_UU_00002/5] Funding Source: researchfish; The author(s) declare financial support was received for the research, authorship, and/or publication of this article. TP-J was supported by the ANID, Chile. Project Fondecyt Initiation (grant number 11220147). DA was supported by the UKRI Medical Research Council (grant number MC_UU_00002/5). MA-L was supported by the ANID, Chile. Project Fondecyt Regular (grant number 1211344).r The author(s) declare financial support was received for the research, authorship, and/or publication of this article. TP-J was supported by the ANID, Chile. Project Fondecyt Initiation (grant number 11220147). DA was supported by the UKRI Medical Research Council (grant number MC_UU_00002/5). MA-L was supported by the ANID, Chile. Project Fondecyt Regular (grant number 1211344).
dc.format.mimetypeapplication/pdf
dc.identifier.citationFrontiers in Medicine, 10, 1258395. https://doi.org/10.3389/fmed.2023.1258395
dc.identifier.doihttps://doi.org/10.3389/fmed.2023.1258395
dc.identifier.folio11220147
dc.identifier.folio1211344
dc.identifier.issn2296-858X
dc.identifier.orcidhttps://orcid.org/0009-0002-6622-056X
dc.identifier.orcidhttps://orcid.org/0000-0002-0526-4377
dc.identifier.orcidhttps://orcid.org/0000-0001-9071-2463
dc.identifier.orcidhttps://orcid.org/0000-0002-8210-4561
dc.identifier.orcidhttps://orcid.org/0000-0001-5707-6290
dc.identifier.orcidhttps://orcid.org/0000-0002-2545-176X
dc.identifier.orcidhttps://orcid.org/0000-0001-9018-4242
dc.identifier.pmid37964883
dc.identifier.researcheridAAT-6078-2021
dc.identifier.researcheridIXD-3497-2023
dc.identifier.researcheridHKV-9453-2023
dc.identifier.researcheridH-3728-2014
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dc.identifier.researcheridK-6310-2014
dc.identifier.researcheridAAO-6491-2021
dc.identifier.researcheridF-1393-2014
dc.identifier.researcheridNRY-8803-2025
dc.identifier.researcheridJUV-6790-2023
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dc.identifier.scopusauthorid57188686509
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dc.identifier.urihttps://repositorio.udla.cl/handle/udla/1356
dc.language.isoeng
dc.publisherFRONTIERS MEDIA SA
dc.relation.fundingAgencia Nacional de Investigación y Desarrollo, ANID
dc.relation.fundingFondecyt Initiation, (11220147)
dc.relation.fundingMedical Research Council, MRC, (MC_UU_00002/5)
dc.relation.fundingMedical Research Council, MRC
dc.relation.fundingFondecyt Regular, (1211344)
dc.relation.fundingThe author(s) declare financial support was received for the research, authorship, and/or publication of this article. TP-J was supported by the ANID, Chile. Project Fondecyt Initiation (grant number 11220147). DA was supported by the UKRI Medical Research
dc.relation.fundingANID, Chile [11220147]
dc.relation.fundingProject Fondecyt Initiation [MC_UU_00002/5]
dc.relation.fundingUKRI Medical Research Council [1211344]
dc.relation.fundingProject Fondecyt Regular
dc.relation.fundingMedical Research Council [MC_UU_00002/5] Funding Source: researchfish
dc.relation.isindexedbyWeb of Science
dc.relation.issn2296-858X
dc.rightsCreative Commons Attribution 4.0 International
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceFRONTIERS IN MEDICINE
dc.source.urihttps://doi.org/10.3389/fmed.2023.1258395
dc.subjectinflammatory bowel disease
dc.subjectsingle nucleotide polymorphism (SNP)
dc.subjectancestry
dc.subjectLatin American
dc.subjectgenetics
dc.subject.lcshEnfermedades inflamatorias del intestino
dc.subject.lcshAscendencia
dc.subject.lcshAmérica Latina
dc.subject.lcshGenética
dc.titleAmerindian ancestry proportion as a risk factor for inflammatory bowel diseases: results from a Latin American Andean cohort
dc.title.alternativeAmerindian ancestry proportion as a risk factor for inflammatory bowel diseases: results from a Latin American Andean cohort.
dc.typejournal article
dc.type.coarhttp://purl.org/coar/resource_type/c_6501
dc.type.driverinfo:eu-repo/semantics/article
dc.udla.catalogadorCBM
oaire.citation.titleFRONTIERS IN MEDICINE
oaire.citation.volume10
oaire.fundingReference.awardNumber11220147
oaire.fundingReference.awardNumber1211344
oaire.fundingReference.funderNameAgencia Nacional de Investigación y Desarrollo (ANID)
udla.curacion.controljmvg
udla.oecd.area1 Ciencias Naturales
udla.oecd.discipline1.6.9 Genética y Herencia
udla.oecd.subarea1.6 Ciencias Biológicas

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