RT Journal Article T1 European Multicentre Tics in Children Studies (EMTICS): protocol for two cohort studies to assess risk factors for tic onset and exacerbation in children and adolescents. A1 Schrag, Anette A1 Martino, Davide A1 Apter, Alan A1 Ball, Juliane A1 Bartolini, Erika A1 Benaroya-Milshtein, Noa A1 Buttiglione, Maura A1 Cardona, Francesco A1 Creti, Roberta A1 Efstratiou, Androulla A1 Gariup, Maria A1 Georgitsi, Marianthi A1 Hedderly, Tammy A1 Heyman, Isobel A1 Margarit, Immaculada A1 Mir, Pablo A1 Moll, Natalie A1 Morer, Astrid A1 Müller, Norbert A1 Müller-Vahl, Kirsten A1 Münchau, Alexander A1 Orefici, Graziella A1 Plessen, Kerstin J A1 Porcelli, Cesare A1 Paschou, Peristera A1 Rizzo, Renata A1 Roessner, Veit A1 Schwarz, Markus J A1 Steinberg, Tamar A1 Tagwerker Gloor, Friederike A1 Tarnok, Zsanett A1 Walitza, Susanne A1 Dietrich, Andrea A1 Hoekstra, Pieter J A1 EMTICS Collaborative Group, K1 Genetics K1 Longitudinal K1 Obsessive–compulsive disorder K1 Streptococcal infection K1 Stress K1 Tourette syndrome AB Genetic predisposition, autoimmunity and environmental factors [e.g. pre- and perinatal difficulties, Group A Streptococcal (GAS) and other infections, stress-inducing events] might interact to create a neurobiological vulnerability to the development of tics and associated behaviours. However, the existing evidence for this relies primarily on small prospective or larger retrospective population-based studies, and is therefore still inconclusive. This article describes the design and methodology of the EMTICS study, a longitudinal observational European multicentre study involving 16 clinical centres, with the following objectives: (1) to investigate the association of environmental factors (GAS exposure and psychosocial stress, primarily) with the onset and course of tics and/or obsessive-compulsive symptoms through the prospective observation of at-risk individuals (ONSET cohort: 260 children aged 3-10 years who are tic-free at study entry and have a first-degree relative with a chronic tic disorder) and affected individuals (COURSE cohort: 715 youth aged 3-16 years with a tic disorder); (2) to characterise the immune response to microbial antigens and the host's immune response regulation in association with onset and exacerbations of tics; (3) to increase knowledge of the human gene pathways influencing the pathogenesis of tic disorders; and (4) to develop prediction models for the risk of onset and exacerbations of tic disorders. The EMTICS study is, to our knowledge, the largest prospective cohort assessment of the contribution of different genetic and environmental factors to the risk of developing tics in putatively predisposed individuals and to the risk of exacerbating tics in young individuals with chronic tic disorders. YR 2018 FD 2018-07-07 LK http://hdl.handle.net/10668/12692 UL http://hdl.handle.net/10668/12692 LA en DS RISalud RD Apr 17, 2025