Genome-Wide and Abdominal MRI Data Provide Evidence That a Genetically Determined Favorable Adiposity Phenotype Is Characterized by Lower Ectopic Liver Fat and Lower Risk of Type 2 Diabetes, Heart Disease, and Hypertension

Author:

Ji Yingjie1,Yiorkas Andrianos M.23,Frau Francesca4,Mook-Kanamori Dennis56,Staiger Harald789,Thomas E. Louise10,Atabaki-Pasdar Naeimeh11,Campbell Archie1213,Tyrrell Jessica1,Jones Samuel E.1,Beaumont Robin N.1,Wood Andrew R.1,Tuke Marcus A.1,Ruth Katherine S.1,Mahajan Anubha14,Murray Anna1,Freathy Rachel M.1,Weedon Michael N.1,Hattersley Andrew T.15,Hayward Caroline16,Machann Jürgen78,Häring Hans-Ulrich7817,Franks Paul111819,de Mutsert Renée5,Pearson Ewan20,Stefan Norbert7817,Frayling Timothy M.1,Allebrandt Karla V.4,Bell Jimmy D.10,Blakemore Alexandra I.23,Yaghootkar Hanieh1ORCID

Affiliation:

1. Genetics of Complex Traits, University of Exeter Medical School, University of Exeter, Royal Devon and Exeter Hospital, Exeter, U.K.

2. Section of Investigative Medicine, Imperial College London, London, U.K.

3. Department of Life Sciences, Brunel University London, Uxbridge, U.K.

4. Translational Medicine and Early Development, TMED Translational Informatics, Sanofi, Frankfurt am Main, Germany

5. Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, the Netherlands

6. Department of Public Health and Primary Care, Leiden University Medical Center, Leiden, the Netherlands

7. Institute for Diabetes Research and Metabolic Diseases of the Helmholtz Center Munich at the University of Tübingen, Tübingen, Germany

8. German Center for Diabetes Research (DZD), Tübingen, Germany

9. Institute of Pharmaceutical Sciences, Department of Pharmacy and Biochemistry, Eberhard Karls University Tübingen, Tübingen, Germany

10. Research Centre for Optimal Health, School of Life Sciences, University of Westminster, London, U.K.

11. Department of Clinical Sciences, Genetic and Molecular Epidemiology Unit, Lund University, Skåne University Hospital Malmö, Malmö, Sweden

12. Generation Scotland, Centre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, U.K.

13. Usher Institute for Population Health Sciences and Informatics, University of Edinburgh, Edinburgh, U.K.

14. Wellcome Centre for Human Genetics, University of Oxford, Oxford, U.K.

15. Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, U.K.

16. Medical Research Council Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, U.K.

17. Department of Internal Medicine IV, Division of Endocrinology, Diabetology, Angiology, Nephrology and Clinical Chemistry, Eberhard Karls University Tübingen, Tübingen, Germany

18. Department of Public Health & Clinical Medicine, Umeå University, Umeå, Sweden

19. Department of Nutrition, Harvard School of Public Health, Boston, MA

20. Division of Molecular and Clinical Medicine, University of Dundee, Ninewells Hospital, Dundee, U.K.

Abstract

Recent genetic studies have identified alleles associated with opposite effects on adiposity and risk of type 2 diabetes. We aimed to identify more of these variants and test the hypothesis that such favorable adiposity alleles are associated with higher subcutaneous fat and lower ectopic fat. We combined MRI data with genome-wide association studies of body fat percentage (%) and metabolic traits. We report 14 alleles, including 7 newly characterized alleles, associated with higher adiposity but a favorable metabolic profile. Consistent with previous studies, individuals carrying more favorable adiposity alleles had higher body fat % and higher BMI but lower risk of type 2 diabetes, heart disease, and hypertension. These individuals also had higher subcutaneous fat but lower liver fat and a lower visceral-to-subcutaneous adipose tissue ratio. Individual alleles associated with higher body fat % but lower liver fat and lower risk of type 2 diabetes included those in PPARG, GRB14, and IRS1, whereas the allele in ANKRD55 was paradoxically associated with higher visceral fat but lower risk of type 2 diabetes. Most identified favorable adiposity alleles are associated with higher subcutaneous and lower liver fat, a mechanism consistent with the beneficial effects of storing excess triglycerides in metabolically low-risk depots.

Funder

Wellcome Trust and Royal Society

European Research Council

Diabetes UK RD Lawrence fellowship

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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