| Literature DB >> 34239025 |
Rossana Santiago de Sousa Azulay1,2, Luís Cristóvão Porto3, Dayse Aparecida Silva4, Maria da Glória Tavares5,6, Roberta Maria Duailibe Ferreira Reis6, Gilvan Cortês Nascimento5,6, Sabrina da Silva Pereira Damianse5,6, Viviane Chaves de Carvalho Rocha5,6, Marcelo Magalhães6,7, Vandilson Rodrigues6, Paulo Ricardo Vilas Boas Carvalho3, Manuel Dos Santos Faria5,6,7, Marília Brito Gomes8.
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.Entities:
Year: 2021 PMID: 34239025 PMCID: PMC8266844 DOI: 10.1038/s41598-021-93691-x
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379