SAMENTA - Santé Mentale et Addictions

Biomarkers of social sensitivity in major depression – SENSO

Toward a biological diagnosis of major depression

The main goal of that project is to define biological and brain imaging biomarkers of major depression. To identify these biomarkers of depression we will use a multidisciplinary approach combining functional magnetic resonance imaging, immunological, virtual reality, and behavioral performance assessments in depressed patients.

Assessment of sensitivity to social signal in major depression

Major Depressive Disorder (MDD) is a highly prevalent disorder. The diagnosis of MDD is usually based on clinical interview with collection of symptoms affecting cognition, emotion and behavior. In order to improve early diagnosis and to define homogeneous group of patients better suited for treatment, we clearly need diagnosis of mental disorders based upon pathophysiologic processes. Genetic and environmental factors influence the onset, maintenance and longitudinal course of MDD. Among these environmental factors, interpersonal stress and life-events involving social rejection may precipitate depressive episodes. This suggests MDD has tight links with social functioning. Moreover it has recently been emphasized that social abilities are good predictors of functional and social outcome of depressed patients. Neurobiological mechanisms of social difficulties of depressed patients are unknown. The main objectives of this project are to define social related biomarkers of MDD. SENSO will specifically focus on social inclusion and exclusion and other forms of social-psychological threats to define related biomarkers for early diagnosis and follow-up of patients with MDD.


This project uses a multidisciplinary approach combining brain imaging, immunological, virtual reality and cognitive experiments to study the biological bases of social impairment in MDD. Moreover we will create a new animal model assessing social exclusion and social cooperation in rats. SENSO will bring expertise from cognitive-social psychology, cognitive neuroscience, immunology, animal models and clinical psychiatry to define new pathophysiologic pathways.
Our main hypothesis is that depressed patients showed heightened sensitivity to social signal reflecting impairment in basic social processes that monitor social acceptance.

The project will include 60 depressed patients and 110 healthy controls. Patients and controls will be simultaneously examined with multiple experimental tasks. The project is composed of 5 experimental sets that evaluate behavior, cognitive, biological and neural biomarkers of sensitivity to social signal in MDD.
Throughout the project patients and controls will participate to experimental tasks assessing sensitivity to dynamic social signal, social attention, sensitivity to criticism or approbation from others, social exclusion and abilities to socially reconnect after exclusion.
Cognitive performance, EEG and functional MRI, behavior and relationships between pro-inflammatory cytokines and social stress will be systematically assessed in depressed patients and controls.


- We have recently shown - using statistical analyses of published fMRI data in healthy volunteers – that social exlusion and social threat activate brain regions, namely ventral anterior cingulate, involved in depression. This result is consistent with our general hypothesis that major depression is associated with impairment in brain regions evaluation social links and social acceptance.
- We also have elaborated a theoretical Framework emphasizing the role of dedicated brain and biological system for monitoring social acceptance. In this model, self-esteem plays a major role in evaluating social acceptance. Impairment in different components of this model in major depression will be assessed

Our multitasking approach will provide the opportunity for a better definition of phenotypes of MDD associated with social impairment. Additional possible output of the project also includes the development of specific devices and tools for cognitive and social remediation.
Overall this project contributes to the development of personalized medicine tailored to the specific needs of patients suffering from major depression.

- Courgeon, M., Rautureau, G., Martin, J.C., Grynszpan, O. Joint attention simulation using Eye-Tracking and virtual humans, IEEE Transactions on Affective Computing, 2014.

- Rotge, J.Y., Lemogne, C., Hinfray, S., Huguet, P., Grynszpan, O., Tartour, E., George, N., Fossati P. A méta-analysis of anterior cingulate contribution to social pain. Social Cognitive and Affective Neuroscience, in review.

Major Depressive Disorder (MDD) is a highly prevalent disorder. The diagnosis of MDD is usually based on clinical interview with collection of symptoms affecting cognition, emotion and behavior. In order to improve early diagnosis and to define homogeneous group of patients better suited for
treatment, we clearly need diagnosis of mental disorders based upon pathophysiologic processes. Genetic and environmental factors influence the onset, maintenance and longitudinal course of MDD. Among these environmental factors, interpersonal stress and life-events involving social rejection may precipitate depressive episodes. MDD is also associated with disengagement from professional and vocational commitments. This suggests MDD has tight links with social functioning. Moreover it has recently been emphasized that social cognition is a good predictor of functional and social outcome of depressed patients.
Neurobiological mechanisms of social difficulties of depressed patients are unknown. The main objectives of SENSO are to define social related biomarkers of MDD. SENSO will specifically focus on social inclusion and exclusion and other forms of social-psychological threats to define related biomarkers for early diagnosis and follow-up of patients with MDD.
This project uses a multidisciplinary approach combining brain imaging, immunological, virtual reality and cognitive experiments to study the biological bases of social impairment in MDD. SENSO will bring expertise from cognitive-social psychology, cognitive neuroscience, immunology and clinical psychiatry to define new pathophysiologic pathways.
Our main hypothesis is that depressed patients showed heightened sensitivity to social signal reflecting impairment in basic social processes that monitor social acceptance.
The project will include 60 depressed patients and 150 healthy controls. Patients and controls will be simultaneously examined with multiple experimental tasks. The project is composed of 5 workpackages that evaluate behavior, cognitive, biological and neural biomarkers of sensitivity to social signal in MDD.
Throughout the project patients and controls will participate to experimental tasks assessing sensitivity to dynamic social signal, social attention, sensitivity to criticism or approbation from others, social exclusion and abilities to socially reconnect after exclusion.
Cognitive performance, EEG and functional MRI, behavior and relationships between pro-inflammatory cytokines and social stress will be systematically assessed in depressed patients and controls.
Our multitasking approach will provide the opportunity for a better definition of phenotypes of MDD associated with social impairment. Additional possible output of the project also includes the development of specific devices and tools for cognitive and social remediation.
Overall this project contributes to the development of personalized medicine tailored to the specific needs of patients suffering from major depression.

Project coordination

Philippe Fossati (Centre émotion-remédiation et réalité virtuelle) – philippe.fossati@psl.aphp.fr

The author of this summary is the project coordinator, who is responsible for the content of this summary. The ANR declines any responsibility as for its contents.

Partner

LPC Laboratoire de Psychologie Cognitive
CERRV Centre émotion-remédiation et réalité virtuelle
Centre de Recherche en Psychiatrie et Neurosciences - Equipe Vulnérabilité aux troubles psychiatriques et addictifs
Service d'immunologie Biologique
UMR 7225

Help of the ANR 564,955 euros
Beginning and duration of the scientific project: August 2012 - 42 Months

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