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Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome

Authors :
National Institutes of Health (US)
Lundbeck Foundation
German Research Foundation
Royal Netherlands Academy of Arts and Sciences
National Science Centre (Poland)
National Institute for Health and Care Research (US)
NIHR Biomedical Research Centre (UK)
Jain, Pritesh
Miller-Fleming, Tyne
Topaloudi, Apostolia
Yu, Dongmei
Drineas, Petros
Georgitsi, Marianthi
Yang, Zhiyu
Rizzo, Renata
Müller-Vahl, Kirsten R.
Tumer, Zeynep
Mol Debes, Nanette
Hartmann, Andreas
Depienne, Christel
Worbe, Yulia
Mir, Pablo
Cath, Danielle
Boomsma, Dorret I.
Roessner, Veit
Wolańczyk, Tomasz
Janik, Piotr
Szejko, Natalia
Zekanowski, Cezary
Barta, Csaba
Nemoda, Zsofia
Tarnok, Zsanett
Buxbaum, Joseph D.
Grice, Dorothy
Glennon, Jeffrey
Stefansson, Hreinn
Hengerer, Bastian
Benaroya‑Milshtein, Noa
Cardona, Francesco
Hedderly, Tammy
Heyman, Isobel
Huyser, Chaim
Morer, Astrid
Mueller, Norbert
Münchau, Alexander
Plessen, Kerstin J.
Porcelli, Cesare
Walitza, Susanne
Schrag, Anette
Martino, Davide
The Psychiatric Genomics Consortium Tourette Syndrome Working Group (PGC-TS)
The EMTICS collaborative group
Dietrich, Andrea
The TS-EUROTRAIN Network
Mathews, Carol A.
Scharf, Jeremiah M.
Hoekstra, Pieter J.
Davis, Lea K.
Paschou, Peristera
National Institutes of Health (US)
Lundbeck Foundation
German Research Foundation
Royal Netherlands Academy of Arts and Sciences
National Science Centre (Poland)
National Institute for Health and Care Research (US)
NIHR Biomedical Research Centre (UK)
Jain, Pritesh
Miller-Fleming, Tyne
Topaloudi, Apostolia
Yu, Dongmei
Drineas, Petros
Georgitsi, Marianthi
Yang, Zhiyu
Rizzo, Renata
Müller-Vahl, Kirsten R.
Tumer, Zeynep
Mol Debes, Nanette
Hartmann, Andreas
Depienne, Christel
Worbe, Yulia
Mir, Pablo
Cath, Danielle
Boomsma, Dorret I.
Roessner, Veit
Wolańczyk, Tomasz
Janik, Piotr
Szejko, Natalia
Zekanowski, Cezary
Barta, Csaba
Nemoda, Zsofia
Tarnok, Zsanett
Buxbaum, Joseph D.
Grice, Dorothy
Glennon, Jeffrey
Stefansson, Hreinn
Hengerer, Bastian
Benaroya‑Milshtein, Noa
Cardona, Francesco
Hedderly, Tammy
Heyman, Isobel
Huyser, Chaim
Morer, Astrid
Mueller, Norbert
Münchau, Alexander
Plessen, Kerstin J.
Porcelli, Cesare
Walitza, Susanne
Schrag, Anette
Martino, Davide
The Psychiatric Genomics Consortium Tourette Syndrome Working Group (PGC-TS)
The EMTICS collaborative group
Dietrich, Andrea
The TS-EUROTRAIN Network
Mathews, Carol A.
Scharf, Jeremiah M.
Hoekstra, Pieter J.
Davis, Lea K.
Paschou, Peristera
Publication Year :
2023

Abstract

Tourette Syndrome (TS) is a complex neurodevelopmental disorder characterized by vocal and motor tics lasting more than a year. It is highly polygenic in nature with both rare and common previously associated variants. Epidemiological studies have shown TS to be correlated with other phenotypes, but large-scale phenome wide analyses in biobank level data have not been performed to date. In this study, we used the summary statistics from the latest meta-analysis of TS to calculate the polygenic risk score (PRS) of individuals in the UK Biobank data and applied a Phenome Wide Association Study (PheWAS) approach to determine the association of disease risk with a wide range of phenotypes. A total of 57 traits were found to be significantly associated with TS polygenic risk, including multiple psychosocial factors and mental health conditions such as anxiety disorder and depression. Additional associations were observed with complex non-psychiatric disorders such as Type 2 diabetes, heart palpitations, and respiratory conditions. Cross-disorder comparisons of phenotypic associations with genetic risk for other childhood-onset disorders (e.g.: attention deficit hyperactivity disorder [ADHD], autism spectrum disorder [ASD], and obsessive-compulsive disorder [OCD]) indicated an overlap in associations between TS and these disorders. ADHD and ASD had a similar direction of effect with TS while OCD had an opposite direction of effect for all traits except mental health factors. Sex-specific PheWAS analysis identified differences in the associations with TS genetic risk between males and females. Type 2 diabetes and heart palpitations were significantly associated with TS risk in males but not in females, whereas diseases of the respiratory system were associated with TS risk in females but not in males. This analysis provides further evidence of shared genetic and phenotypic architecture of different complex disorders.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1431966705
Document Type :
Electronic Resource