Major Depressive Disorder and Lifestyle: Correlated Genetic Effects in Extended Twin Pedigrees

In recent years, evidence has accumulated with regard to the ubiquity of pleiotropy across the genome, and shared genetic etiology is thought to play a large role in the widespread comorbidity among psychiatric disorders and risk factors. Recent methods investigate pleiotropy by estimating genetic c...

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Main Authors: Floris Huider, Yuri Milaneschi, Matthijs D. van der Zee, Eco J. C. de Geus, Quinta Helmer, Brenda W. J. H. Penninx, Dorret I. Boomsma
Format: Article
Language:English
Published: MDPI AG 2021-09-01
Series:Genes
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Online Access:https://www.mdpi.com/2073-4425/12/10/1509
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author Floris Huider
Yuri Milaneschi
Matthijs D. van der Zee
Eco J. C. de Geus
Quinta Helmer
Brenda W. J. H. Penninx
Dorret I. Boomsma
author_facet Floris Huider
Yuri Milaneschi
Matthijs D. van der Zee
Eco J. C. de Geus
Quinta Helmer
Brenda W. J. H. Penninx
Dorret I. Boomsma
author_sort Floris Huider
collection DOAJ
description In recent years, evidence has accumulated with regard to the ubiquity of pleiotropy across the genome, and shared genetic etiology is thought to play a large role in the widespread comorbidity among psychiatric disorders and risk factors. Recent methods investigate pleiotropy by estimating genetic correlation from genome-wide association summary statistics. More comprehensive estimates can be derived from the known relatedness between genetic relatives. Analysis of extended twin pedigree data allows for the estimation of genetic correlation for additive and non-additive genetic effects, as well as a shared household effect. Here we conduct a series of bivariate genetic analyses in extended twin pedigree data on lifetime major depressive disorder (MDD) and three indicators of lifestyle, namely smoking behavior, physical inactivity, and obesity, decomposing phenotypic variance and covariance into genetic and environmental components. We analyze lifetime MDD and lifestyle data in a large multigenerational dataset of 19,496 individuals by variance component analysis in the ‘Mendel’ software. We find genetic correlations for MDD and smoking behavior (<i>r</i><sub>G</sub> = 0.249), physical inactivity (<i>r</i><sub>G</sub> = 0.161), body-mass index (<i>r</i><sub>G</sub> = 0.081), and obesity (<i>r</i><sub>G</sub> = 0.155), which were primarily driven by additive genetic effects. These outcomes provide evidence in favor of a shared genetic etiology between MDD and the lifestyle factors.
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spelling doaj.art-3f629d5bba8c4328b57d295e83b67ec82023-11-22T18:21:03ZengMDPI AGGenes2073-44252021-09-011210150910.3390/genes12101509Major Depressive Disorder and Lifestyle: Correlated Genetic Effects in Extended Twin PedigreesFloris Huider0Yuri Milaneschi1Matthijs D. van der Zee2Eco J. C. de Geus3Quinta Helmer4Brenda W. J. H. Penninx5Dorret I. Boomsma6Department of Biological Psychology, Vrije Universiteit, 1081 BT Amsterdam, The NetherlandsAmsterdam Public Health (APH) Research Institute, Amsterdam, The NetherlandsDepartment of Biological Psychology, Vrije Universiteit, 1081 BT Amsterdam, The NetherlandsDepartment of Biological Psychology, Vrije Universiteit, 1081 BT Amsterdam, The NetherlandsDepartment of Biological Psychology, Vrije Universiteit, 1081 BT Amsterdam, The NetherlandsAmsterdam Public Health (APH) Research Institute, Amsterdam, The NetherlandsDepartment of Biological Psychology, Vrije Universiteit, 1081 BT Amsterdam, The NetherlandsIn recent years, evidence has accumulated with regard to the ubiquity of pleiotropy across the genome, and shared genetic etiology is thought to play a large role in the widespread comorbidity among psychiatric disorders and risk factors. Recent methods investigate pleiotropy by estimating genetic correlation from genome-wide association summary statistics. More comprehensive estimates can be derived from the known relatedness between genetic relatives. Analysis of extended twin pedigree data allows for the estimation of genetic correlation for additive and non-additive genetic effects, as well as a shared household effect. Here we conduct a series of bivariate genetic analyses in extended twin pedigree data on lifetime major depressive disorder (MDD) and three indicators of lifestyle, namely smoking behavior, physical inactivity, and obesity, decomposing phenotypic variance and covariance into genetic and environmental components. We analyze lifetime MDD and lifestyle data in a large multigenerational dataset of 19,496 individuals by variance component analysis in the ‘Mendel’ software. We find genetic correlations for MDD and smoking behavior (<i>r</i><sub>G</sub> = 0.249), physical inactivity (<i>r</i><sub>G</sub> = 0.161), body-mass index (<i>r</i><sub>G</sub> = 0.081), and obesity (<i>r</i><sub>G</sub> = 0.155), which were primarily driven by additive genetic effects. These outcomes provide evidence in favor of a shared genetic etiology between MDD and the lifestyle factors.https://www.mdpi.com/2073-4425/12/10/1509major depressive disorderlifestyleextended twin pedigreevariance decompositionMendelgenetic correlation
spellingShingle Floris Huider
Yuri Milaneschi
Matthijs D. van der Zee
Eco J. C. de Geus
Quinta Helmer
Brenda W. J. H. Penninx
Dorret I. Boomsma
Major Depressive Disorder and Lifestyle: Correlated Genetic Effects in Extended Twin Pedigrees
Genes
major depressive disorder
lifestyle
extended twin pedigree
variance decomposition
Mendel
genetic correlation
title Major Depressive Disorder and Lifestyle: Correlated Genetic Effects in Extended Twin Pedigrees
title_full Major Depressive Disorder and Lifestyle: Correlated Genetic Effects in Extended Twin Pedigrees
title_fullStr Major Depressive Disorder and Lifestyle: Correlated Genetic Effects in Extended Twin Pedigrees
title_full_unstemmed Major Depressive Disorder and Lifestyle: Correlated Genetic Effects in Extended Twin Pedigrees
title_short Major Depressive Disorder and Lifestyle: Correlated Genetic Effects in Extended Twin Pedigrees
title_sort major depressive disorder and lifestyle correlated genetic effects in extended twin pedigrees
topic major depressive disorder
lifestyle
extended twin pedigree
variance decomposition
Mendel
genetic correlation
url https://www.mdpi.com/2073-4425/12/10/1509
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