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Genetics of cognitive trajectory in Brazilians: 15 years of follow-up from the Bambuí-Epigen Cohort Study of Aging.
Gouveia, Mateus H; Cesar, Cibele C; Santolalla, Meddly L; Anna, Hanaisa P Sant; Scliar, Marilia O; Leal, Thiago P; Araújo, Nathalia M; Soares-Souza, Giordano B; Magalhães, Wagner C S; Mata, Ignacio F; Ferri, Cleusa P; Castro-Costa, Erico; Mbulaiteye, Sam M; Tishkoff, Sarah A; Shriner, Daniel; Rotimi, Charles N; Tarazona-Santos, Eduardo; Lima-Costa, Maria Fernanda.
Afiliação
  • Gouveia MH; Fundação Oswaldo Cruz, Instituto de Pesquisas René Rachou, Belo Horizonte, Brazil. mateus.gouveia@nih.gov.
  • Cesar CC; Departamento de Genética, Ecologia e Evolução, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, 31270-901, Brazil. mateus.gouveia@nih.gov.
  • Santolalla ML; Center for Research on Genomics and Global Health, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America. mateus.gouveia@nih.gov.
  • Anna HPS; Universidade Federal de Minas Gerais, Faculdade de Ciências Econômicas, Belo Horizonte, Brazil.
  • Scliar MO; Departamento de Genética, Ecologia e Evolução, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, 31270-901, Brazil.
  • Leal TP; Departamento de Genética, Ecologia e Evolução, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, 31270-901, Brazil.
  • Araújo NM; Melbourne Integrative Genomics, The University of Melbourne, Melbourne, VIC, 3052, Australia.
  • Soares-Souza GB; Departamento de Genética, Ecologia e Evolução, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, 31270-901, Brazil.
  • Magalhães WCS; Departamento de Genética, Ecologia e Evolução, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, 31270-901, Brazil.
  • Mata IF; Fundação Oswaldo Cruz, Instituto de Pesquisas René Rachou, Belo Horizonte, Brazil.
  • Ferri CP; Departamento de Genética, Ecologia e Evolução, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, 31270-901, Brazil.
  • Castro-Costa E; Departamento de Genética, Ecologia e Evolução, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, 31270-901, Brazil.
  • Mbulaiteye SM; Departamento de Genética, Ecologia e Evolução, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, 31270-901, Brazil.
  • Tishkoff SA; Núcleo de Ensino e Pesquisa - NEP, Instituto Mário Penna, Rua Gentios, Terceiro Andar, Belo Horizonte, Minas Gerais, 3052, Brazil.
  • Shriner D; Lerner Research Institute, Genomic Medicine, Cleveland Clinic Foundation, Cleveland, OH, USA.
  • Rotimi CN; Universidade Federal de São Paulo, Department of Psychiatry, São Paulo, Brazil.
  • Tarazona-Santos E; Fundação Oswaldo Cruz, Instituto de Pesquisas René Rachou, Belo Horizonte, Brazil.
  • Lima-Costa MF; Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
Sci Rep ; 9(1): 18085, 2019 12 02.
Article em En | MEDLINE | ID: mdl-31792241
ABSTRACT
Age-related cognitive decline (ACD) is the gradual process of decreasing of cognitive function over age. Most genetic risk factors for ACD have been identified in European populations and there are no reports in admixed Latin American individuals. We performed admixture mapping, genome-wide association analysis (GWAS), and fine-mapping to examine genetic factors associated with 15-year cognitive trajectory in 1,407 Brazilian older adults, comprising 14,956 Mini-Mental State Examination measures. Participants were enrolled as part of the Bambuí-Epigen Cohort Study of Aging. Our admixture mapping analysis identified a genomic region (3p24.2) in which increased Native American ancestry was significantly associated with faster ACD. Fine-mapping of this region identified a single nucleotide polymorphism (SNP) rs142380904 (ß = -0.044, SE = 0.01, p = 7.5 × 10-5) associated with ACD. In addition, our GWAS identified 24 associated SNPs, most in genes previously reported to influence cognitive function. The top six associated SNPs accounted for 18.5% of the ACD variance in our data. Furthermore, our longitudinal study replicated previous GWAS hits for cognitive decline and Alzheimer's disease. Our 15-year longitudinal study identified both ancestry-specific and cosmopolitan genetic variants associated with ACD in Brazilians, highlighting the need for more trans-ancestry genomic studies, especially in underrepresented ethnic groups.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Envelhecimento / Polimorfismo de Nucleotídeo Único / Disfunção Cognitiva Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged País como assunto: America do sul / Brasil Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Envelhecimento / Polimorfismo de Nucleotídeo Único / Disfunção Cognitiva Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged País como assunto: America do sul / Brasil Idioma: En Ano de publicação: 2019 Tipo de documento: Article