| Literature DB >> 34569937 |
Corrado Sandini1, Daniela Zöller1,2, Maude Schneider1,3, Anjali Tarun2, Marco Armando1, Barnaby Nelson4,5, Paul G Amminger4,5,6, Hok Pan Yuen4,5, Connie Markulev4,5, Monica R Schäffer5,6, Nilufar Mossaheb6, Monika Schlögelhofer6, Stefan Smesny6, Ian B Hickie7, Gregor Emanuel Berger8, Eric Yh Chen9, Lieuwe de Haan10, Dorien H Nieman11, Merete Nordentoft12, Anita Riecher-Rössler13, Swapna Verma14, Andrew Thompson4,5,15,16, Alison Ruth Yung4,5,17,18, Patrick D McGorry4,5, Dimitri Van De Ville2,19, Stephan Eliez1,20.
Abstract
Causal interactions between specific psychiatric symptoms could contribute to the heterogenous clinical trajectories observed in early psychopathology. Current diagnostic approaches merge clinical manifestations that co-occur across subjects and could significantly hinder our understanding of clinical pathways connecting individual symptoms. Network analysis techniques have emerged as alternative approaches that could help shed light on the complex dynamics of early psychopathology. The present study attempts to address the two main limitations that have in our opinion hindered the application of network approaches in the clinical setting. Firstly, we show that a multi-layer network analysis approach, can move beyond a static view of psychopathology, by providing an intuitive characterization of the role of specific symptoms in contributing to clinical trajectories over time. Secondly, we show that a Graph-Signal-Processing approach, can exploit knowledge of longitudinal interactions between symptoms, to predict clinical trajectories at the level of the individual. We test our approaches in two independent samples of individuals with genetic and clinical vulnerability for developing psychosis. Novel network approaches can allow to embrace the dynamic complexity of early psychopathology and help pave the way towards a more a personalized approach to clinical care.Entities:
Keywords: 22q11.2 deletion syndrome; affective pathway; human; medicine; network analysis; schizophrenia
Mesh:
Year: 2021 PMID: 34569937 PMCID: PMC8476129 DOI: 10.7554/eLife.59811
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140