Scientific Reports (Jul 2021)

Genetic ancestry inferred from autosomal and Y chromosome markers and HLA genotypes in Type 1 Diabetes from an admixed Brazilian population

  • Rossana Santiago de Sousa Azulay,
  • Luís Cristóvão Porto,
  • Dayse Aparecida Silva,
  • Maria da Glória Tavares,
  • Roberta Maria Duailibe Ferreira Reis,
  • Gilvan Cortês Nascimento,
  • Sabrina da Silva Pereira Damianse,
  • Viviane Chaves de Carvalho Rocha,
  • Marcelo Magalhães,
  • Vandilson Rodrigues,
  • Paulo Ricardo Vilas Boas Carvalho,
  • Manuel dos Santos Faria,
  • Marília Brito Gomes

DOI
https://doi.org/10.1038/s41598-021-93691-x
Journal volume & issue
Vol. 11, no. 1
pp. 1 – 12

Abstract

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Abstract This study aimed to investigate the relationship between genetic ancestry inferred from autosomal and Y chromosome markers and HLA genotypes in patients with Type 1 Diabetes from an admixed Brazilian population. Inference of autosomal ancestry; HLA-DRB1, -DQA1 and -DQB1 typifications; and Y chromosome analysis were performed. European autosomal ancestry was about 50%, followed by approximately 25% of African and Native American. The European Y chromosome was predominant. The HLA-DRB1*03 and DRB1*04 alleles presented risk association with T1D. When the Y chromosome was European, DRB1*03 and DRB1*04 homozygote and DRB1*03/DRB1*04 heterozygote genotypes were the most frequent. The results suggest that individuals from Maranhão have a European origin as their major component; and are patrilineal with greater frequency from the R1b haplogroup. The predominance of the HLA-DRB1*03 and DRB1*04 alleles conferring greater risk in our population and being more frequently related to the ancestry of the European Y chromosome suggests that in our population, the risk of T1D can be transmitted by European ancestors of our process miscegenation. However, the Y sample sizes of Africans and Native Americans were small, and further research should be conducted with large mixed sample sizes to clarify this possible association.