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Genetic influence on within-person longitudinal change in anthropometric traits in the UK Biobank.
Kemper, Kathryn E; Sidorenko, Julia; Wang, Huanwei; Hayes, Ben J; Wray, Naomi R; Yengo, Loic; Keller, Matthew C; Goddard, Michael; Visscher, Peter M.
Afiliação
  • Kemper KE; Institute for Molecular Bioscience, University of Queensland, Brisbane, QLD, Australia. k.kemper@uq.edu.au.
  • Sidorenko J; Institute for Molecular Bioscience, University of Queensland, Brisbane, QLD, Australia.
  • Wang H; Institute for Molecular Bioscience, University of Queensland, Brisbane, QLD, Australia.
  • Hayes BJ; Queensland Alliance for Agriculture and Food Innovation, University of Queensland, Brisbane, QLD, Australia.
  • Wray NR; Institute for Molecular Bioscience, University of Queensland, Brisbane, QLD, Australia.
  • Yengo L; Department of Psychiatry, University of Oxford, Oxford, UK.
  • Keller MC; Institute for Molecular Bioscience, University of Queensland, Brisbane, QLD, Australia.
  • Goddard M; Institute for Behavioral Genetics, University of Colorado, Boulder, CO, USA.
  • Visscher PM; Faculty of Veterinary and Agricultural Science, University of Melbourne, Parkville, VIC, Australia.
Nat Commun ; 15(1): 3776, 2024 May 06.
Article em En | MEDLINE | ID: mdl-38710707
ABSTRACT
The causes of temporal fluctuations in adult traits are poorly understood. Here, we investigate the genetic determinants of within-person trait variability of 8 repeatedly measured anthropometric traits in 50,117 individuals from the UK Biobank. We found that within-person (non-directional) variability had a SNP-based heritability of 2-5% for height, sitting height, body mass index (BMI) and weight (P ≤ 2.4 × 10-3). We also analysed longitudinal trait change and show a loss of both average height and weight beyond about 70 years of age. A variant tracking the Alzheimer's risk APOE- E 4 allele (rs429358) was significantly associated with weight loss ( ß = -0.047 kg per yr, s.e. 0.007, P = 2.2 × 10-11), and using 2-sample Mendelian Randomisation we detected a relationship consistent with causality between decreased lumbar spine bone mineral density and height loss (bxy = 0.011, s.e. 0.003, P = 3.5 × 10-4). Finally, population-level variance quantitative trait loci (vQTL) were consistent with within-person variability for several traits, indicating an overlap between trait variability assessed at the population or individual level. Our findings help elucidate the genetic influence on trait-change within an individual and highlight disease risks associated with these changes.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Apolipoproteínas E / Estatura / Índice de Massa Corporal / Polimorfismo de Nucleotídeo Único / Locos de Características Quantitativas Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Apolipoproteínas E / Estatura / Índice de Massa Corporal / Polimorfismo de Nucleotídeo Único / Locos de Características Quantitativas Idioma: En Ano de publicação: 2024 Tipo de documento: Article