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  Composite trait Mendelian randomization reveals distinct metabolic and lifestyle consequences of differences in body shape

Sulc, J., Sonrel, A., Mounier, N., Auwerx, C., Marouli, E., Darrous, L., et al. (2021). Composite trait Mendelian randomization reveals distinct metabolic and lifestyle consequences of differences in body shape. Communications Biology, 4: 1064. doi:10.1038/s42003-021-02550-y.

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 Urheber:
Sulc, Jonathan1, 2, Autor
Sonrel, Anthony2, 3, Autor
Mounier, Ninon1, 2, Autor
Auwerx, Chiara1, 2, 4, Autor
Marouli, Eirini5, 6, Autor
Darrous, Liza1, 2, Autor
Draganski, Bogdan7, 8, Autor           
Kilpeläinen, Tuomas O.9, Autor
Joshi, Peter10, Autor
Loos, Ruth J. F.11, 12, 13, Autor
Kutalik, Zoltán1, 2, 14, Autor
Affiliations:
1Center for Primary Care and Public Health, University of Lausanne, Switzerland, ou_persistent22              
2Swiss Institute of Bioinformatics, University of Lausanne, Switzerland, ou_persistent22              
3Department of Molecular Life Sciences, University of Zurich, Switzerland, ou_persistent22              
4Center for Integrative Genomics, University of Lausanne, Switzerland, ou_persistent22              
5William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, London, United Kingdom, ou_persistent22              
6Centre for Genomic Health, Queen Mary University of London, United Kingdom, ou_persistent22              
7Département des Neurosciences Cliniques, Laboratoire de Recherche en Neuroimagerie (LREN), Centre hospitalier universitaire vaudois, Lausanne, Switzerland, ou_persistent22              
8Department Neurology, MPI for Human Cognitive and Brain Sciences, Max Planck Society, ou_634549              
9Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Denmark, ou_persistent22              
10Usher Institute, University of Edinburgh, United Kingdom, ou_persistent22              
11Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA, ou_persistent22              
12Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA, ou_persistent22              
13Department of Environmental Medicine and Public Health, Icahn School of Medicine at Mount Sinai, New York, NY, USA, ou_persistent22              
14Genetics of Complex Traits, Medical School, University of Exeter, United Kingdom, ou_persistent22              

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Schlagwörter: Obesity; Risk factors
 Zusammenfassung: Obesity is a major risk factor for a wide range of cardiometabolic diseases, however the impact of specific aspects of body morphology remains poorly understood. We combined the GWAS summary statistics of fourteen anthropometric traits from UK Biobank through principal component analysis to reveal four major independent axes: body size, adiposity, predisposition to abdominal fat deposition, and lean mass. Mendelian randomization analysis showed that although body size and adiposity both contribute to the consequences of BMI, many of their effects are distinct, such as body size increasing the risk of cardiac arrhythmia (b = 0.06, p = 4.2 ∗ 10-17) while adiposity instead increased that of ischemic heart disease (b = 0.079, p = 8.2 ∗ 10-21). The body mass-neutral component predisposing to abdominal fat deposition, likely reflecting a shift from subcutaneous to visceral fat, exhibited health effects that were weaker but specifically linked to lipotoxicity, such as ischemic heart disease (b = 0.067, p = 9.4 ∗ 10-14) and diabetes (b = 0.082, p = 5.9 ∗ 10-19). Combining their independent predicted effects significantly improved the prediction of obesity-related diseases (p < 10-10). The presented decomposition approach sheds light on the biological mechanisms underlying the heterogeneity of body morphology and its consequences on health and lifestyle.

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 Datum: 2021-06-032021-08-122021-09-13
 Publikationsstatus: Online veröffentlicht
 Seiten: -
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: -
 Identifikatoren: DOI: 10.1038/s42003-021-02550-y
PMID: 34518635
PMC: PMC8438050
 Art des Abschluß: -

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Grant ID : 31003A-143914, 310030-189147, 32003B_135679, 32003B_159780, 324730_192755, and CRSK-3_190185
Förderprogramm : -
Förderorganisation : Swiss National Science Foundation
Projektname : -
Grant ID : NNF17OC0026848, NNF18CC0034900
Förderprogramm : -
Förderorganisation : Novo Nordisk Foundation

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Titel: Communications Biology
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: London : Springer Nature
Seiten: - Band / Heft: 4 Artikelnummer: 1064 Start- / Endseite: - Identifikator: ISSN: 2399-3642
CoNE: https://pure.mpg.de/cone/journals/resource/2399-3642