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Disease consequences of higher adiposity uncoupled from its adverse metabolic effects using Mendelian randomisation

Authors :
Susan, Martin
Jessica, Tyrrell
E Louise, Thomas
Matthew J, Bown
Andrew R, Wood
Robin N, Beaumont
Lam C, Tsoi
Philip E, Stuart
James T, Elder
Philip, Law
Richard, Houlston
Christopher, Kabrhel
Nikos, Papadimitriou
Marc J, Gunter
Caroline J, Bull
Joshua A, Bell
Emma E, Vincent
Naveed, Sattar
Malcolm G, Dunlop
Ian P M, Tomlinson
Sara, Lindström
Jimmy D, Bell
Timothy M, Frayling
Hanieh, Yaghootkar
Source :
eLife, Vol 11 (2022), eLife, Martin, S, Bull, C J, Bell, J A, Vincent, E E, Frayling, T, Yaghootkar, H & et, A 2022, ' Disease consequences of higher adiposity uncoupled from its adverse metabolic effects using Mendelian randomisation ', eLife, vol. 11, e72452, pp. 1-32 . https://doi.org/10.7554/eLife.72452, Martin, S, Tyrrell, J, Thomas, E L, Bown, M J, Wood, A R, Beaumont, R N, Tsoi, L C, Stuart, P E, Elder, J T, Law, P, Houlston, R, Kabrhel, C, Papadimitriou, N, Gunter, M J, Bull, C J, Bell, J A, Vincent, E E, Sattar, N, Dunlop, M G, Tomlinson, I P, Bell, J D, Frayling, T M & Yaghootkar, H 2022, ' Disease consequences of higher adiposity uncoupled from its adverse metabolic effects using Mendelian randomisation ', eLIFE, vol. 11 . https://doi.org/10.7554/eLife.72452
Publication Year :
2022
Publisher :
eLife Sciences Publications Ltd, 2022.

Abstract

Background:Some individuals living with obesity may be relatively metabolically healthy, whilst others suffer from multiple conditions that may be linked to adverse metabolic effects or other factors. The extent to which the adverse metabolic component of obesity contributes to disease compared to the non-metabolic components is often uncertain. We aimed to use Mendelian randomisation (MR) and specific genetic variants to separately test the causal roles of higher adiposity with and without its adverse metabolic effects on diseases.Methods:We selected 37 chronic diseases associated with obesity and genetic variants associated with different aspects of excess weight. These genetic variants included those associated with metabolically ‘favourable adiposity’ (FA) and ‘unfavourable adiposity’ (UFA) that are both associated with higher adiposity but with opposite effects on metabolic risk. We used these variants and two sample MR to test the effects on the chronic diseases.Results:MR identified two sets of diseases. First, 11 conditions where the metabolic effect of higher adiposity is the likely primary cause of the disease. Here, MR with the FA and UFA genetics showed opposing effects on risk of disease: coronary artery disease, peripheral artery disease, hypertension, stroke, type 2 diabetes, polycystic ovary syndrome, heart failure, atrial fibrillation, chronic kidney disease, renal cancer, and gout. Second, 9 conditions where the non-metabolic effects of excess weight (e.g. mechanical effect) are likely a cause. Here, MR with the FA genetics, despite leading to lower metabolic risk, and MR with the UFA genetics, both indicated higher disease risk: osteoarthritis, rheumatoid arthritis, osteoporosis, gastro-oesophageal reflux disease, gallstones, adult-onset asthma, psoriasis, deep vein thrombosis, and venous thromboembolism.Conclusions:Our results assist in understanding the consequences of higher adiposity uncoupled from its adverse metabolic effects, including the risks to individuals with high body mass index who may be relatively metabolically healthy.Funding:Diabetes UK, UK Medical Research Council, World Cancer Research Fund, National Cancer Institute.

Details

Language :
English
ISSN :
2050084X
Volume :
11
Database :
OpenAIRE
Journal :
eLife
Accession number :
edsair.doi.dedup.....eb327f7b668e8f6ab6b3c45d9b0c475d