FP6Individual fellowship2005–2007

EMOTION · Controlling attention to emotional stimuli: a combined functional neuroimaging and functional genomics approach

FP6 — Marie Curie Actions (Human Resources and Mobility)

Duration
2005-04-01 → 2007-09-30
EU contribution
€209,467
Participants
2
Scheme
OIF

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Results in brief

Final Activity Report Summary - EMOTION (Controlling attention to emotional stimuli: a combined functional neuroimaging and functional genomics approach)

Problems in controlling attention to emotional stimuli have long been recognised to play a central role in anxiety. However, the relative role of brain mechanisms involved in controlling attention, in particular the lateral prefrontal cortex, versus that of brain mechanisms involved in detecting the presence of negative or 'threat-related' emotional stimuli, in particular the amygdale, has been fairly poorly understood. The undertaken research attempted to examine these issues. In particular, the following questions were addressed: - Are prefrontal cortical brain mechanisms recruited when we try to control our attention and ignore emotional but task-irrelevant stimuli? - Is this only the case when 'distractor' stimuli are negative and signal potential threat or is this also the case when they are positive and signal potential reward? - Do anxious individuals show poorer recruitment of these mechanisms? - Can we identify common genetic variations which influence the activation of these brain regions? - In addition, is the amygdala specifically responsive to the presence of threat-related stimuli? - Is this response greater in anxious individuals? - Is it influenced by how attentionally demanding the task to be performed is made? - Are there genetic variants which influence activity in this brain region in response to threat-related stimuli? The research supported by this fellowship produced a number of important results. Firstly, it appeared that when the task engaged in was highly attentionally demanding, even anxious people did not show an amygdala response to negative stimuli that signalled potential threat. This had a number of important implications. It suggested that being overly involved in a given task might lead us to miss genuine signals of danger. Secondly, aiding anxious individuals to engage in tasks more effectively might be one way to help them to prevent their attention being captured by threat cues which low anxious individuals were able to ignore. Through combining genotyping with functional Magnetic resonance imaging (MRI), I was also able to investigate the impact of specific genes upon brain activity linked to attentional capture by emotional stimuli. This helped us to identity specific genetic variants or 'polymorphisms' that influenced the neural mechanisms of relevance. More specifically, this research showed that a polymorphism in the Catechol-o-methyltransferase (COMT) gene influenced activity in the prefrontal mechanisms that helped us to control our attention to emotional stimuli as well as to perform demanding cognitive tasks. In addition, it produced promising initial findings suggesting that a polymorphism in the serotonin transporter (5HTT) gene influenced how strongly the amygdala responded to threat-related distractors. Hopefully in future work, we could examine how these genetic variants interact to jointly influence recruitment of the brain regions that help us control our attention to emotional stimuli. The hope was that through this we might begin to build up a model of the genes that lead some people to be more vulnerable to anxiety than others.

Data: CORDIS, © European Union

Project objective

Problems in controlling attention to negative and positive stimuli have been associated with anxiety disorders and addiction, respectively. Few studies have attempted to delineate the neural mechanisms underlying attentional control over emotional stimuli.The first phase of the proposed research has two main objectives:1) to investigate the involvement of lateral prefrontal cortex (LPFC) and anterior cingulated cortex (ACC) in the 'top-down' control of attention over emotional stimuli;2) to investigate the role of the amygdala and nucleus accumbens in the processing of negative and positive stimuli and in the 'bottom up' modulation of attention by emotional stimuli.Functional magnetic resonance imaging (fMRI) studies varying the valence and intensity of distracting stimuli and the attentional demands of the primary task will examine the factors influencing recruitment of these neural structures. Two combined fMRI/functional genomic studies will examine whether genetic polymorphisms associated with alterations in central monoamine activity influence recruitment of the neural circuitry underlying attentional control over emotional stimuli. Participants will be split into groups according to their COMT Val158 Met and 5-HTTLPR genotypes.Here, the objectives a re to establish whether:1) the COMT Val158 Met polymorphism influences recruitment of LPFC and ACC mechanisms supporting the `top-down¿ regulation of attention and2) the 5-HTTLPR polymorphism influences amygdala activation associated with the 'bottom-up' modulation of attention by emotional stimuli.Integrating genetic and cognitive neuroscience methodologies to examine neuro-cognitive mechanisms of relevance to anxiety and addiction is in line with the FP6 Call: 'Life Sciences, Genomics and Biotechnology for Health'. Research in this specific area is at an early stage - this project will both promote European excellence in this field and aid my career, helping me obtain the training needed for independence.

Original text from CORDIS.

Participants

Links

Data: CORDIS, © European Union