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Genomic Regions 10q22.2, 17q21.31, and 2p23.1 Can Contribute to a Lower Lung Function in African Descent Populations.
Fonseca, Héllen; da Silva, Thiago M; Saraiva, Mariana; Santolalla, Meddly L; Sant'Anna, Hanaisa P; Araujo, Nathalia M; Lima, Natália P; Rios, Raimon; Tarazona-Santos, Eduardo; Horta, Bernardo L; Cruz, Alvaro; Barreto, Mauricio L; Figueiredo, Camila A.
Affiliation
  • Fonseca H; Programa de Pós Graduação em Imunologia (PPGIm), Instituto de Ciências da Saúde, Universidade Federal da Bahia (UFBA), Salvador 40140-100, BA, Brazil.
  • da Silva TM; Departamento de Ciências Biológicas, Universidade Estadual do Sudoeste da Bahia, Jequié 45206-190, BA, Brazil.
  • Saraiva M; Programa de Pós Graduação em Imunologia (PPGIm), Instituto de Ciências da Saúde, Universidade Federal da Bahia (UFBA), Salvador 40140-100, BA, Brazil.
  • Santolalla ML; Departamento de Genética, Ecologia e Evolução, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte 31270-901, Brazil.
  • Sant'Anna HP; Departamento de Genética, Ecologia e Evolução, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte 31270-901, Brazil.
  • Araujo NM; Departamento de Genética, Ecologia e Evolução, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte 31270-901, Brazil.
  • Lima NP; Programa de Pós-Graduação em Epidemiologia, Universidade Federal de Pelotas, Pelotas 96020-220, Rio Grande do Sul, Brazil.
  • Rios R; Programa de Pós Graduação em Imunologia (PPGIm), Instituto de Ciências da Saúde, Universidade Federal da Bahia (UFBA), Salvador 40140-100, BA, Brazil.
  • Tarazona-Santos E; Departamento de Genética, Ecologia e Evolução, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte 31270-901, Brazil.
  • Horta BL; Programa de Pós-Graduação em Epidemiologia, Universidade Federal de Pelotas, Pelotas 96020-220, Rio Grande do Sul, Brazil.
  • Cruz A; ProAR, Faculdade de Medicina, Universidade Federal da Bahia (UFBA), Salvador 40060-330, BA, Brazil.
  • Barreto ML; Centro de Integração de dados e Conhecimentos para Saúde (CIDACS), Fiocruz, Salvador 41745-715, BA, Brazil.
  • Figueiredo CA; Departamento de Bio-Regulação, Instituto de Ciências da Saúde, Universidade Federal da Bahia (UFBA), Salvador 40110-902, BA, Brazil.
Genes (Basel) ; 11(9)2020 09 04.
Article in En | MEDLINE | ID: mdl-32899814
ABSTRACT
Accumulated evidence supports the contribution of genetic factors in modulating airway function, especially ancestry. We investigated whether genetic polymorphisms can affect lung function in a mixed Brazilian child population using the admixture mapping strategy through RFMix software version 1.5.4 (Stanford University, Stanford, CA, USA), followed by fine mapping, to identify regions whereby local African or European ancestry is associated with lung function measured by the forced expiratory volume in the first second (FEV1)/forced vital capacity (FVC) ratio, an indicator of airway obstruction. The research cohort included 958 individuals aged 4 to 11 years enrolled in the SCAALA (Social Change, Asthma, Allergy in Latin America) Program. We identified that African ancestry at 17q21.31, 10q22.2, and 2p23.1 regions was associated with lower lung function measured by FEV1/FVC p < 1.9 × 10-4. In contrast, European ancestry at 17q21.31 showed an opposite effect. Fine mapping pointed out 5 single nucleotide polymorphisms (SNPs) also associated in our replication cohort (rs10999948, rs373831475, rs8068257, rs6744555, and rs1520322). Our results suggest that genomic regions associated with ancestry may contribute to differences in lung function measurements in African American children in Brazil replicated in a cohort of Brazilian adults. The analysis strategy used in this work is especially important for phenotypes, such as lung function, which has considerable disparities in terms of measurements across different populations.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Black or African American / Chromosomes, Human, Pair 2 / Chromosomes, Human, Pair 10 / Chromosomes, Human, Pair 17 / Polymorphism, Single Nucleotide / Quantitative Trait Loci / Lung Diseases Type of study: Prognostic_studies Limits: Humans Country/Region as subject: America do sul / Brasil Language: En Journal: Genes (Basel) Year: 2020 Document type: Article Affiliation country: Brasil

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Black or African American / Chromosomes, Human, Pair 2 / Chromosomes, Human, Pair 10 / Chromosomes, Human, Pair 17 / Polymorphism, Single Nucleotide / Quantitative Trait Loci / Lung Diseases Type of study: Prognostic_studies Limits: Humans Country/Region as subject: America do sul / Brasil Language: En Journal: Genes (Basel) Year: 2020 Document type: Article Affiliation country: Brasil
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