Algorithm Predicts Psychosis Risk for At-Risk Kids - Technology Networks

Teams from the UNIGE and EPFL have used for the first time the method of longitudinal network analysis applied to children, in order to detect the symptoms that herald the development of psychotic illness in the future.

One third of children with a microdeletion of chromosome 22 will later develop a psychotic illness such as schizophrenia. But how do we know which of these children might be affected? Today, various studies have contributed to the understanding of the neurobiological mechanisms that are associated with the development of psychotic illnesses. The problem is that the ability to identify those at risk and adapt their treatment accordingly remains limited. Indeed, many variables - other than neurobiological - contribute to their development. This is why a team from the University of Geneva has joined forces with a team from the EPFL to use in a longitudinal manner an artificial intelligence tool:  the network analysis method. This algorithm correlates many variables from different backgrounds - neurobiological, psychological, cognitive, etc. - over a period of twenty years, in order to determine which current symptoms are predictive of a psychotic illness in the child's future developmental trajectory. These results, to be read in the journal eLife, will enable early treatment of children deemed to be at risk of developing psychological disorders, with the aim of preventing or even avoiding them.

One in 4,000 people have a microdeletion of chromosome 22, which can lead to the development of psychotic illnesses, such as schizophrenia, in adolescence. However, only one third of them will eventually be affected by a psychotic disorder. How can we determine which ones? "For the time being, the analyses are looking at the neurobiological mechanisms involved in psychological disorders, as well as the presence of certain symptoms that are assimilated to a psychological illness, without knowing which are the most relevant", explains Corrado Sandini, a researcher at the Department of Psychiatry of the University of Geneva   Faculty of Medicine, to the Fondation Pôle Autisme and first author of the study.

Not being able to take into account the degree of importance of each symptom can be problematic in predicting the course of the disease and providing the most appropriate treatment for the patient. "This is why we thought of using the network analysis method", he continues. This methodology, which is currently used on adults, makes it possible to combine variables from completely different worlds in the same analysis space, while considering them individually. "Since the development of psychotic illnesses depends on many variables other than purely neurobiological ones, this algorithm would make it possible to highlight the most important symptoms to alert about the potential risks of a child becoming schizophrenic, for example", says Stéphan Eliez, professor in the Department of Psychiatry at the University of Geneva Faculty of Medicine and to the Fondation Pôle Autisme.

Finding the predictive symptoms

The Geneva team has joined forces with researchers at EPFL to develop this methodology and apply it to a cohort of children and adolescents suffering from a microdeletion of chromosome 22, some of whom have been followed for more than twenty years. "The aim is to adapt network analysis by tailoring it to young patients in a longitudinal manner, in order to obtain insightful statistics on highly intertwined variables throughout the child's developmental trajectory", emphasises Dimitri Van De Ville, a professor in the Department of Radiology and Medical Informatics at the University of Geneva Faculty bof Medicine and at the EPFL Institute of Bioengineering. The aim is to find the variables in childhood that will foresay the development of psychotic illnesses. "We will therefore know which battle to fight, thanks to key factors that will enable us to act where and, above all, when it is necessary", explains Stéphan Eliez. "If we can identify them, we can try to regulate the symptom to reduce the risk of developing a psychotic illness later on."

To test the methodology, 40 variables were taken into account for 70 children suffering from a microdeletion of chromosome 22, observed every three years from childhood to adulthood. "These variables included hallucinations, general mood, feelings of guilt and the management of daily stress", explains Corrado Sandini. Questionnaires completed by parents also provided valuable data. Visual representations then shed light/highlighted/determined the most important variables that predict the development of psychological problems three years later. "We found that an anxious 10-year-old whose anxiety turns into an inability to cope with stress in adolescence is likely to develop a psychological illness. The evolution of anxiety is therefore a significant warning signal", continues the Geneva researcher. Similarly, sadness, which over time becomes a feeling of guilt, is also a very important symptom.

A personalised method for each child

In order to confirm the results of their algorithm, the researchers applied it to other cohorts vulnerable to psychotic illnesses that have been followed for many years, and were thus able to confirm that the computer tool works. The aim is now to use it as a predictive tool, but also to refine it by integrating other variables, such as weight, to contribute to the clinical assessment. Finally, the interest of this method is obviously the prediction, with the aim of avoiding the disease, but above all its fully personalised quality that studies the developmental trajectory specific to each child.

Reference:

Sandini C, Zöller D, Schneider M, et al. Characterization and prediction of clinical pathways of vulnerability to psychosis through graph signal processing. Shackman A, Ivry RB, eds. eLife. 2021;10:e59811. doi:10.7554/eLife.59811

This article has been republished from the following materials. Note: material may have been edited for length and content. For further information, please contact the cited source.

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