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Title: | Interaction between the FTO gene, body mass index and depression: meta-analysis of 13701 individuals. |
Authors: | Rivera, Margarita Locke, Adam E Corre, Tanguy Czamara, Darina Wolf, Christiane Ching-Lopez, Ana Milaneschi, Yuri Kloiber, Stefan Cohen-Woods, Sarah Rucker, James Aitchison, Katherine J Bergmann, Sven Boomsma, Dorret I Craddock, Nick Gill, Michael Holsboer, Florian Hottenga, Jouke-Jan Korszun, Ania Kutalik, Zoltan Lucae, Susanne Maier, Wolfgang Mors, Ole Müller-Myhsok, Bertram Owen, Michael J Penninx, Brenda W J H Preisig, Martin Rice, John Rietschel, Marcella Tozzi, Federica Uher, Rudolf Vollenweider, Peter Waeber, Gerard Willemsen, Gonneke Craig, Ian W Farmer, Anne E Lewis, Cathryn M Breen, Gerome McGuffin, Peter |
metadata.dc.subject.mesh: | Alleles Alpha-Ketoglutarate-Dependent Dioxygenase FTO Body Mass Index Case-Control Studies Comorbidity Depressive Disorder, Major Genetic Predisposition to Disease Humans Obesity Polymorphism, Genetic |
Issue Date: | 22-Jun-2017 |
Abstract: | BackgroundDepression and obesity are highly prevalent, and major impacts on public health frequently co-occur. Recently, we reported that having depression moderates the effect of the FTO gene, suggesting its implication in the association between depression and obesity.AimsTo confirm these findings by investigating the FTO polymorphism rs9939609 in new cohorts, and subsequently in a meta-analysis.MethodThe sample consists of 6902 individuals with depression and 6799 controls from three replication cohorts and two original discovery cohorts. Linear regression models were performed to test for association between rs9939609 and body mass index (BMI), and for the interaction between rs9939609 and depression status for an effect on BMI. Fixed and random effects meta-analyses were performed using METASOFT.ResultsIn the replication cohorts, we observed a significant interaction between FTO, BMI and depression with fixed effects meta-analysis (β = 0.12, P = 2.7 × 10-4) and with the Han/Eskin random effects method (P = 1.4 × 10-7) but not with traditional random effects (β = 0.1, P = 0.35). When combined with the discovery cohorts, random effects meta-analysis also supports the interaction (β = 0.12, P = 0.027) being highly significant based on the Han/Eskin model (P = 6.9 × 10-8). On average, carriers of the risk allele who have depression have a 2.2% higher BMI for each risk allele, over and above the main effect of FTOConclusionsThis meta-analysis provides additional support for a significant interaction between FTO, depression and BMI, indicating that depression increases the effect of FTO on BMI. The findings provide a useful starting point in understanding the biological mechanism involved in the association between obesity and depression. |
URI: | http://hdl.handle.net/10668/11335 |
metadata.dc.identifier.doi: | 10.1192/bjp.bp.116.183475 |
Appears in Collections: | Producción 2020 |
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