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GWAS Study

Genetic determinants of serum bilirubin using inferred native American gene variants in Chilean adolescents.

Miranda JP, Pereira A, Corvalán C et al.

38826804 PubMed ID
GWAS Study Type
707 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

MJ
Miranda JP
PA
Pereira A
CC
Corvalán C
MJ
Miquel JF
AG
Alberti G
GJ
Gana JC
SJ
Santos JL
Chapter II

Abstract

Summary of the research findings

Gene variants in the UGT1A1 gene are strongly associated with circulating bilirubin levels in several populations, as well as other variants of modest effect across the genome. However, the effects of such variants are unknown regarding the Native American ancestry of the admixed Latino population. Our objective was to assess the Native American genetic determinants of serum bilirubin in Chilean admixed adolescents using the local ancestry deconvolution approach. We measured total serum bilirubin levels in 707 adolescents of the Chilean Growth and Obesity Cohort Study (GOCS) and performed high-density genotyping using the Illumina-MEGA array (>1.7 million genotypes). We constructed a local ancestry reference panel with participants from the 1000 Genomes Project, the Human Genome Diversity Project, and our GOCS cohort. Then, we inferred and isolated haplotype tracts of Native American, European, or African origin to perform genome-wide association studies. In the whole cohort, the rs887829 variant and others near UGT1A1 were the unique signals achieving genome-wide statistical significance (b = 0.30; p = 3.34 × 10-57). After applying deconvolution methods, we found that significance is also maintained in Native American (b = 0.35; p = 3.29 × 10-17) and European (b = 0.28; p = 1.14 × 10-23) ancestry components. The rs887829 variant explained a higher percentage of the variance of bilirubin in the Native American (37.6%) compared to European ancestry (28.4%). In Native American ancestry, carriers of the TT genotype of this variant averaged 4-fold higher bilirubinemia compared to the CC genotype (p = 2.82 × 10-12). We showed for the first time that UGT1A1 variants are the primary determinant of bilirubin levels in Native American ancestry, confirming its pan-ethnic relevance. Our study illustrates the general value of the local ancestry deconvolution approach to assessing isolated ancestry effects in admixed populations.

707 Chilean ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

707
Total Participants
GWAS
Study Type
No
Replicated
Hispanic or Latin American
Ancestry
Chile
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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