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Abstract
We present the results of a GWAS of food liking conducted on 161,625 participants from the UK-Biobank. Liking was assessed over 139 specific foods using a 9-point scale. Genetic correlations coupled with structural equation modelling identified a multi-level hierarchical map of food-liking with three main dimensions: “Highly-palatable”, “Acquired” and “Low-caloric”. The Highly-palatable dimension is genetically uncorrelated from the other two, suggesting that independent processes underlie liking high reward foods. This is confirmed by genetic correlations with MRI brain traits which show with distinct associations. Comparison with the corresponding food consumption traits shows a high genetic correlation, while liking exhibits twice the heritability. GWAS analysis identified 1,401 significant food-liking associations which showed substantial agreement in the direction of effects with 11 independent cohorts. In conclusion, we created a comprehensive map of the genetic determinants and associated neurophysiological factors of food-liking.
Genetic determinants of food consumption and food liking are likely to be distinct, although it has not been well studied. Here, the authors identify genetic variants associated with food-liking, finding that different food-liking traits correlate with different brain areas and other food consumption traits.
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1 University of Edinburgh, Centre for Global Health Research, Usher Institute, Edinburgh, UK (GRID:grid.4305.2) (ISNI:0000 0004 1936 7988)
2 University of North Carolina at Chapel Hill, Department of Genetics, Chapel Hill, USA (GRID:grid.10698.36) (ISNI:0000000122483208); University of North Carolina at Chapel Hill, UNC Neuroscience Center, Chapel Hill, USA (GRID:grid.10698.36) (ISNI:0000000122483208)
3 University of Bristol, Population Health Sciences, Bristol Medical School, Bristol, UK (GRID:grid.5337.2) (ISNI:0000 0004 1936 7603); Medical Research Council (MRC) Integrative Epidemiology Unit (IEU) at the University of Bristol, Bristol, UK (GRID:grid.5337.2)
4 Vrije Universiteit Amsterdam, Dept of Biological Psychology, FGB, Amsterdam, The Netherlands (GRID:grid.12380.38) (ISNI:0000 0004 1754 9227)
5 Institute for Maternal and Child Health—IRCCS, Burlo Garofolo, Trieste, Italy (GRID:grid.418712.9) (ISNI:0000 0004 1760 7415)
6 King’s College London, Department of Twin Research and Genetic Epidemiology, London, UK (GRID:grid.13097.3c) (ISNI:0000 0001 2322 6764); NIHR Biomedical Research Centre at Guy’s and St Thomas’ Foundation Trust, London, UK (GRID:grid.420545.2) (ISNI:0000 0004 0489 3985)
7 King’s College London, Department of Twin Research and Genetic Epidemiology, London, UK (GRID:grid.13097.3c) (ISNI:0000 0001 2322 6764)
8 Institute for Maternal and Child Health—IRCCS, Burlo Garofolo, Trieste, Italy (GRID:grid.418712.9) (ISNI:0000 0004 1760 7415); University of Trieste, Department of Medicine, Surgery and Health Sciences, Trieste, Italy (GRID:grid.5133.4) (ISNI:0000 0001 1941 4308)
9 Mersin University, Department of Anatomy, Faculty of Medicine, Mersin, Turkey (GRID:grid.411691.a) (ISNI:0000 0001 0694 8546)
10 Vrije Universiteit Amsterdam, Dept of Biological Psychology, FGB, Amsterdam, The Netherlands (GRID:grid.12380.38) (ISNI:0000 0004 1754 9227); Amsterdam Public Health research institute, Amsterdam, The Netherlands (GRID:grid.16872.3a) (ISNI:0000 0004 0435 165X)
11 University of Edinburgh, Centre for Global Health Research, Usher Institute, Edinburgh, UK (GRID:grid.4305.2) (ISNI:0000 0004 1936 7988); University of Edinburgh, MRC Human Genetics Unit, Institute of Genetics and Cancer, Edinburgh, UK (GRID:grid.4305.2) (ISNI:0000 0004 1936 7988)
12 University of Edinburgh, Centre for Global Health Research, Usher Institute, Edinburgh, UK (GRID:grid.4305.2) (ISNI:0000 0004 1936 7988); Human Technopole, Milan, Italy (GRID:grid.510779.d) (ISNI:0000 0004 9414 6915)