Spatiotemporal characterization of value judgments and reward processing in the human brain
Lead Research Organisation:
University of Glasgow
Department Name: College of Medical, Veterinary, Life Sci
Abstract
The main goal of this project is to provide insights into how people make everyday value and preference judgments. For instance, how do we choose among different goods at the supermarket or how do we decide which mobile phone to purchase? How do we weigh the pros and cons of the various options to make our choices as rewarding as possible? How do we make use of our prior experience with the various alternatives to help us make better choices and obtain bigger rewards in the future? How do we learn, through trial and error, to update our future predictions in order to adapt and keep up with the competitive and ever-changing world around us? Importantly, we do not want to merely measure how people behave in some of these scenarios but we would also like to understand how the human brain processes the relevant information and how the outcome of that process ultimately cause one to express or externalize (i.e., by acting out) their preferred choice.
In recent years, modern neuroimaging methods have made it possible for researchers to "take a peak" into the human brain. Human electroencephalography (EEG) is a non-invasive method whereby electrodes placed on the surface of the scalp measure the brain's electrical activity. This technique provides precise information on when the brain processes information in time but cannot provide a clear picture of where in the brain this information is coming from. In contrast, functional magnetic resonance imaging (fMRI) measures (non-invasively in an MRI scanner) changes in the local blood flow in the brain as we process information. This in turn allows one to identify where in the brain this processing takes place but at the expense of poor precision in terms of when processing occurs in time. It is therefore easy to see that if these techniques were applied simultaneously, they could clearly compliment each other and help provide answers as to both when and where the brain processes information.
To perform concurrent EEG and fMRI experiments, however, one needs to overcome a series of technical challenges and devise an analysis methodology that will integrate the two datasets in a manner that circumvents the disparate space and time scales on which they are acquired. In collaboration between the Schools of Psychology and Physics at the University of Nottingham as well as our international partners (i.e., Department of Biomedical Engineering at Columbia University in New York), we have started to use some cutting-edge technology and analysis tools to overcome these challenges and make these simultaneous measurements possible. In this project we will recruit volunteers who will be asked to perform simple value and preference judgments while we simultaneously record EEG and fMRI data from them. We will then use the methodology we have recently devised to look at the data in an attempt to provide answers to the questions outlined above.
Crucially, understanding which brain areas are involved in value judgments, how they interact with one another and at which times can potentially lead to practical applications. For instance knowing how to tab into and monitor the various brain processes involved in value-based decision making can have applications in domains as diverse as economic and public policy analysis (e.g., when deciding on savings strategies and health behaviours) and marketing (e.g., when optimizing advertisement strategies and product design). In addition, improved understanding of the neurobiology of decision-making can potentially have applications in identifying prognostic indicators of normal and abnormal ageing or in defining precursors of disorders known to compromise ones decision-making faculties (e.g., autism, personality disorders, etc).
In recent years, modern neuroimaging methods have made it possible for researchers to "take a peak" into the human brain. Human electroencephalography (EEG) is a non-invasive method whereby electrodes placed on the surface of the scalp measure the brain's electrical activity. This technique provides precise information on when the brain processes information in time but cannot provide a clear picture of where in the brain this information is coming from. In contrast, functional magnetic resonance imaging (fMRI) measures (non-invasively in an MRI scanner) changes in the local blood flow in the brain as we process information. This in turn allows one to identify where in the brain this processing takes place but at the expense of poor precision in terms of when processing occurs in time. It is therefore easy to see that if these techniques were applied simultaneously, they could clearly compliment each other and help provide answers as to both when and where the brain processes information.
To perform concurrent EEG and fMRI experiments, however, one needs to overcome a series of technical challenges and devise an analysis methodology that will integrate the two datasets in a manner that circumvents the disparate space and time scales on which they are acquired. In collaboration between the Schools of Psychology and Physics at the University of Nottingham as well as our international partners (i.e., Department of Biomedical Engineering at Columbia University in New York), we have started to use some cutting-edge technology and analysis tools to overcome these challenges and make these simultaneous measurements possible. In this project we will recruit volunteers who will be asked to perform simple value and preference judgments while we simultaneously record EEG and fMRI data from them. We will then use the methodology we have recently devised to look at the data in an attempt to provide answers to the questions outlined above.
Crucially, understanding which brain areas are involved in value judgments, how they interact with one another and at which times can potentially lead to practical applications. For instance knowing how to tab into and monitor the various brain processes involved in value-based decision making can have applications in domains as diverse as economic and public policy analysis (e.g., when deciding on savings strategies and health behaviours) and marketing (e.g., when optimizing advertisement strategies and product design). In addition, improved understanding of the neurobiology of decision-making can potentially have applications in identifying prognostic indicators of normal and abnormal ageing or in defining precursors of disorders known to compromise ones decision-making faculties (e.g., autism, personality disorders, etc).
Technical Summary
In recent years the study of the neurobiological and computational basis of value-based decision making has received considerable attention and it provided the foundation upon which the field of neuroeconomics was built. Despite recent progress in understanding the neural correlates of value-based decisions, key questions pertaining to how value is computed at a mechanistic level remain. Specifically, it is unclear whether sensory regions are modulated by the value (or probabilistic evidence) conferred by different decision alternatives and how and where this information is combined to generate the value signal needed to make a decision. Another essential element of valuation pertains to how we process rewards to update future value expectations. Accurate reward representations associated with potential choices are critical for adaptive decision making. These representations can be acquired with reinforcement learning mechanisms, which use the prediction error (PE), the difference between expected and actual rewards, as a learning signal to update expectations. The spatiotemporal dynamics of the network associated with PE processing and the mechanisms by which PE valence and magnitude are used to update expectations and guide future choices remain inconclusive. In this project we will use state-of-the art neuroimaging to couple single-trial analysis of the EEG with simultaneously acquired fMRI to infer, with both high temporal and high spatial resolution information, the cascade of constituent cortical processes involved in value judgments and reward processing in humans. Our working hypothesis is that trial-to-trial variability in electrophysiologicaly-derived measures has information content that is meaningful in representing the dynamics of latent brain states that are unobservable via stimulus or behaviourally derived measures, which in conjunction with fMRI can be used to expose the cortical networks involved in value-based decision making.
Planned Impact
The potential impact of the developments supported by this application could address several of BBSRC's new strategic priorities (e.g. economic, social and public policy impact, cognitive ageing, systems approach to biological research).
Economic, social and public policy impact: In our everyday lives we constantly engage in value and preference judgments to make choices that are more likely to lead to desirable outcomes. Knowing how to tab into and monitor the various brain processes involved in value-based decision making can have applications in domains as diverse as economic and public policy analysis (e.g. to inform decisions on health behaviours and savings strategies) and marketing (e.g. to help optimize advertisement strategies and product design).
Imagine for instance having to make a choice between a high-calorie strawberry smoothie and a healthy alternative such as a fruit salad. Obesity is a growing problem in the western world and can have direct and severe consequences on people's health as well as indirect costs on a nation's health care system. A more thorough characterization of the cortical networks underlying preference judgments and reinforcement-guided decision making can potentially lead to ways of enhancing the value of less-preferred choices (in this example low-caloric foods), possibly through feedback protocols that make use of incentive motivation to reinforce and promote optimum (here healthier) behaviour.
Another translational aspect of this work relates to the newly developed field of neuromarketing. For example, how does one develop an effective and influential advertisement campaign (e.g. to promote a new product or service and raise public awareness for key health and socioeconomic issues such the one outlined above)? Traditional marketing techniques rely heavily on market research through cumbersome approaches (e.g. through surveys and questionnaires) that can suffer experimenter biases and that are often hard to quantify. In contrast, neural signatures of value can provide a true quantitative measure of internal preference and as such can be used to triage through various advertisement pieces and product designs.
Cognitive ageing and disorders: In normal and abnormal cognitive ageing even simple decision making is effected, as evidenced by changes in behavioural measures such as accuracy and response time. A number of disorders known to compromise ones decision-making faculties (e.g. autism, personality disorders) can also lead to similar behavioural changes. The imaging tools and methods proposed here could potentially be used to characterize the neural changes that are causal to these behavioural changes. As such this work can lead to the development of new methods for identifying diagnostic and prognostic indicators of cognitive deficits, as well as more directed behavioural and pharmacological treatments.
Systems approaches to biological research: This work also addresses BBSRC's priority on "exploiting new ways of working". It is practically axiomatic that new tools, particularly in neuroimaging, lead to new observations and more fundamental understanding of the processes under observation. For decision making some of the neural processes underlying it can only be observed via trial-to-trial electrophysiological variability. All fMRI studies of decision making to date, more-or-less, look at mean changes and do not consider trial-to-trial changes (other than those that can be measured behaviourally). Here, we will develop a new methodology that exploits trial-to-trial changes in EEG (via multivariate analysis techniques) to drive the analysis of simultaneously acquired fMRI data in order to identify latent brain states associated with value-based decisions. Here, this new approach will be used to address issues in some of BBSRC's priority areas (as outlined above) but at the same time has the potential to become a powerful new tool in cognitive neuroscience in general
Economic, social and public policy impact: In our everyday lives we constantly engage in value and preference judgments to make choices that are more likely to lead to desirable outcomes. Knowing how to tab into and monitor the various brain processes involved in value-based decision making can have applications in domains as diverse as economic and public policy analysis (e.g. to inform decisions on health behaviours and savings strategies) and marketing (e.g. to help optimize advertisement strategies and product design).
Imagine for instance having to make a choice between a high-calorie strawberry smoothie and a healthy alternative such as a fruit salad. Obesity is a growing problem in the western world and can have direct and severe consequences on people's health as well as indirect costs on a nation's health care system. A more thorough characterization of the cortical networks underlying preference judgments and reinforcement-guided decision making can potentially lead to ways of enhancing the value of less-preferred choices (in this example low-caloric foods), possibly through feedback protocols that make use of incentive motivation to reinforce and promote optimum (here healthier) behaviour.
Another translational aspect of this work relates to the newly developed field of neuromarketing. For example, how does one develop an effective and influential advertisement campaign (e.g. to promote a new product or service and raise public awareness for key health and socioeconomic issues such the one outlined above)? Traditional marketing techniques rely heavily on market research through cumbersome approaches (e.g. through surveys and questionnaires) that can suffer experimenter biases and that are often hard to quantify. In contrast, neural signatures of value can provide a true quantitative measure of internal preference and as such can be used to triage through various advertisement pieces and product designs.
Cognitive ageing and disorders: In normal and abnormal cognitive ageing even simple decision making is effected, as evidenced by changes in behavioural measures such as accuracy and response time. A number of disorders known to compromise ones decision-making faculties (e.g. autism, personality disorders) can also lead to similar behavioural changes. The imaging tools and methods proposed here could potentially be used to characterize the neural changes that are causal to these behavioural changes. As such this work can lead to the development of new methods for identifying diagnostic and prognostic indicators of cognitive deficits, as well as more directed behavioural and pharmacological treatments.
Systems approaches to biological research: This work also addresses BBSRC's priority on "exploiting new ways of working". It is practically axiomatic that new tools, particularly in neuroimaging, lead to new observations and more fundamental understanding of the processes under observation. For decision making some of the neural processes underlying it can only be observed via trial-to-trial electrophysiological variability. All fMRI studies of decision making to date, more-or-less, look at mean changes and do not consider trial-to-trial changes (other than those that can be measured behaviourally). Here, we will develop a new methodology that exploits trial-to-trial changes in EEG (via multivariate analysis techniques) to drive the analysis of simultaneously acquired fMRI data in order to identify latent brain states associated with value-based decisions. Here, this new approach will be used to address issues in some of BBSRC's priority areas (as outlined above) but at the same time has the potential to become a powerful new tool in cognitive neuroscience in general
People |
ORCID iD |
Marios G Philiastides (Principal Investigator) |
Publications

Delis I
(2016)
Space-by-time decomposition for single-trial decoding of M/EEG activity.
in NeuroImage

Fouragnan E
(2015)
Two spatiotemporally distinct value systems shape reward-based learning in the human brain
in Nature Communications

Fouragnan E
(2017)
Spatiotemporal neural characterization of prediction error valence and surprise during reward learning in humans.
in Scientific reports

Fouragnan E
(2018)
Separate neural representations of prediction error valence and surprise: Evidence from an fMRI meta-analysis.
in Human brain mapping

Kayser SJ
(2017)
Sounds facilitate visual motion discrimination via the enhancement of late occipital visual representations.
in NeuroImage

Philiastides MG
(2021)
Inferring Macroscale Brain Dynamics via Fusion of Simultaneous EEG-fMRI.
in Annual review of neuroscience

Philiastides MG
(2014)
Human scalp potentials reflect a mixture of decision-related signals during perceptual choices.
in The Journal of neuroscience : the official journal of the Society for Neuroscience

Pisauro MA
(2017)
Neural correlates of evidence accumulation during value-based decisions revealed via simultaneous EEG-fMRI.
in Nature communications

Queirazza F
(2019)
Neural correlates of weighted reward prediction error during reinforcement learning classify response to cognitive behavioral therapy in depression.
in Science advances
Related Projects
Project Reference | Relationship | Related To | Start | End | Award Value |
---|---|---|---|---|---|
BB/J015393/1 | 12/11/2012 | 30/08/2013 | £397,955 | ||
BB/J015393/2 | Transfer | BB/J015393/1 | 31/08/2013 | 29/02/2016 | £260,142 |
Title | Short video animation about reward learning |
Description | An animation video presenting our recent work on decision making and learning for a lay audience. |
Type Of Art | Film/Video/Animation |
Year Produced | 2017 |
Impact | The video was added to our lab's YouTube channel and was made publically available to engage the non-experts with the work we carry out in the lab. |
URL | https://www.youtube.com/watch?v=CasPtVhDW2E&t=5s |
Title | Trigger Productions |
Description | PI interview with Davey Anderson and Gary McNair from Trigger Productions on "How To Choose?". Segments of the interview were later integrated into a theatrical play designed to take a critical look on human choice behaviour at The Arches Theatre in Glasgow. |
Type Of Art | Performance (Music, Dance, Drama, etc) |
Year Produced | 2014 |
Impact | Engaging with the general public in an interactive way to convey information on the inner workings of the human brain during decision making. |
URL | https://soundcloud.com/trigger-stuff/episode-9-brain-scanner?in=trigger-stuff/sets/how-to-choose |
Description | Imagine picking wild berries in a forest when suddenly a swarm of bees flies out from behind a bush. In a split second, your motor system has already reacted to flee the swarm. This automatic response constitutes a powerful survival mechanism that allows efficient behaviour switching to run away from a threat. In turn, a separate and more deliberate process of learning to avoid similar situations will also occur, rendering future berry picking attempts less appealing. This example highlights that avoiding repeated mistakes and learning to reinforce rewarding decisions is critical for human survival and adaptive actions. Yet, the neural underpinnings of the value systems that encode different decision outcomes remain elusive. Here, coupling single-trial electroencephalography (EEG) with simultaneously acquired functional magnetic resonance imaging (fMRI). An EEG machine records brain activity with high temporal precision ("when" things are happening in the brain) while functional MRI provides information on the location of this activity ("where" things are happening in the brain). To date, "when" and "where" questions have largely been studied separately, using each technique in isolation. Here, by combining the two techniques we uncovered the spatiotemporal dynamics of two separate but interacting value systems encoding decision-outcomes. Consistent with a role in regulating alertness and switching behaviours, an early system is activated only by negative outcomes and engages arousal-related and motor-preparatory brain structures. Consistent with a role in motivational learning and updating value representations associated with future choices, a later system differentially suppresses or activates regions of the human reward network in response to negative and positive outcomes, respectively. Following negative outcomes, the early system interacts and down-regulates the late system, through a thalamic interaction with the ventral striatum. Critically, the strength of this coupling predicts participants' switching behaviour and avoidance learning, directly implicating the thalamostriatal pathway in reward-based learning. Reward learning depends on accurate reward associations with potential choices. These associations can be attained with reinforcement learning mechanisms using a reward prediction error (RPE) signal (the difference between actual and expected rewards) for updating future reward expectations. Despite an extensive body of literature on the influence of RPE on learning, little has been done to investigate the potentially separate contributions of RPE valence (positive or negative) and surprise (absolute degree of deviation from expectations). In this BBSRC funded work, we coupled single-trial electroencephalography with simultaneously acquired fMRI, during a probabilistic reversal-learning task, to offer evidence of temporally overlapping but largely distinct spatial representations of RPE valence and surprise. Electrophysiological variability in RPE valence correlated with activity in regions of the human reward network promoting approach or avoidance learning. Electrophysiological variability in RPE surprise correlated primarily with activity in regions of the human attentional network controlling the speed of learning. Crucially, despite the largely separate spatial extend of these representations our EEG-informed fMRI approach uniquely revealed a linear superposition of the two RPE components in a smaller network encompassing visuo-mnemonic and reward areas. Activity in this network was further predictive of stimulus value updating indicating a comparable contribution of both signals to reward learning. Another main aim of this work was to use the same state-of-the-art neuroimaging approach (simultaneous EEG-fMRI) to characterise the spatiotemporal dynamics of the decision making process itself during preference- and value-based decision making. Current computational work suggests that value and preference-based decisions involve an integrative mechanism in which subjective value information supporting different decision alternatives accumulates over time to an internal decision boundary. However, the neurobiological validity of this proposition remains unclear. In this work we were able to capture this process of evidence accumulation as it unfolded in time using our EEG signals. We subsequently exploited these signals and used them as predictors for the fMRI data that were recorder simultaneously and uncovered a, previously overlooked, region of the posteriomedial prefrontal cortex that appears to be responsible for implementing the temporal integration of value information in order to drive the decision. Consistent with integrating the evidence for the decision, this region also exhibited task-dependent coupling with the ventromedial prefrontal cortex and the striatum, brain areas known to encode the subjective value of the decision alternatives. These results further endorse the proposition of an evidence accumulation process during value-based decisions in humans and implicate the posterior-medial frontal cortex in this process. Despite a long literature implicating certain regions of the prefrontal and ventromedial parietal cortex in encoding the subjective value assigned to different choices, no previous study has been able to reliably identify the brain centre responsible for processing this information to drive the decision. Crucially, we also confirmed that the main findings of this work would have been missed using stand-alone EEG or fMRI measurements. We clearly demonstrated that it is the combination of the two brain imaging modalities that enabled the developments described above. This finding is important as it suggests that the data acquisition and analysis methodology we developed in this work can become a power new tool in cognitive neuroscience. |
Exploitation Route | Our general research approach (simultaneous EEG-fMRI and corresponding analysis methods) as well as our scientific findings open up new avenues for the investigation of the neural systems underlying value- and reward-based decision making in humans. Crucially, our findings have the potential to further our understanding of how everyday responses to rewarding or stressful events can affect our capacity to make optimal decisions, as well as facilitate the study of how mental disorders - such as chronic stress, obsessive-compulsive-disorder, post-traumatic disorder and depression - affect learning and strategic planning. Correspondingly, our work can lead to the development of new methods for identifying diagnostic and prognostic indicators of cognitive deficits in disease, as well as more directed behavioural and pharmacological treatments. It is also likely that our results can have significant impact on how artificial neural networks are trained and adapted to learn to deal with an ever-increasing number of online "big data" applications. We have made two full EEG-fMRI datasets fully available on openneuro.org to inspire the development of future fusion methodologies for EEG and fMRI data and to encourage others to either re-analyse the data (aiming at reproducibility) or use them to address new and novel questions. Furthermore, we utilised the outcome of this work to inform the development of novel biomarkers in Psychiatry. Specifically, we have used the paradigms and neural signatures developed through this work (neural correlates of prediction error processing in particular) to demonstrate that brain activation patterns in a sample of depressed patients undergoing scanning prior to commencing treatment (Cognitive Behavioural Therapy) were predictive of the subsequent success or failure of the treatment. Our findings offer a paradigm shift in Psychiatry and enable a potentially significant and far-reaching impact on the way patients are triaged and treated for mental health problems. This work has only recently been completed and we are currently in the process of replicating and validating the findings in a larger sample of patients. Completing this next step successfully would pave the way for introducing our predictive biomarkers in a day-to-day clinical practice. |
Sectors | Communities and Social Services/Policy Creative Economy Education Healthcare Government Democracy and Justice Pharmaceuticals and Medical Biotechnology |
Description | There are currently no reliable clinical markers for predicting treatment response in major depressive disorder (MDD) and trial and error is the basis of clinical practice. A clinically meaningful predictor of treatment response should ideally be treatment-specific and predict differential outcome to either medications or psychotherapy. We have been able to use the framework we have developed to study reward learning in the human brain to predict the likelihood of treatment response in MDD (more reliably that standard behavioural assessments currently obtained in the clinic). New findings indicate that this brain-informed approach has the potential to become a clinically viable predictors of response to CBT and antidepressant treatment for MDD in order to inform the development of a stratified medicine approach to psychiatric clinical practice. More specifically, to discriminate response to computerised Cognitive Behavioural Therapy (CBT) in a sample of 37 unmedicated depressed subjects we modelled the online appraisal of feedback information during a probabilistic learning task employing a dynamic learning rate. First, using computational modelling we showed between-group differences in the learning style. Second, using functional magnetic resonance imaging (fMRI), we leverage the pre-treatment neural encoding of the dynamic learning rate in the dorsomedial prefrontal cortex and show between-group differences in BOLD activity following negative probabilistic feedback. Our findings provide novel and important insights into the putative cognitive mechanisms underpinning response to cCBT and lend support to the feasibility and validity of neurocomputational approaches to treatment prediction research in psychiatry. [Update 2020] We have now had a chance to utilise the outcome of this work to inform the development of novel biomarkers in Psychiatry. Specifically, we have used the paradigms and neural signatures developed through this work (neural correlates of prediction error processing in particular) to demonstrate that brain activation patterns in a sample of depressed patients undergoing scanning prior to commencing treatment (Cognitive Behavioural Therapy) were predictive of the subsequent success or failure of the treatment. Our findings offer a paradigm shift in Psychiatry and enable a potentially significant and far-reaching impact on the way patients are triaged and treated for mental health problems. This work has only recently been completed and we are currently in the process of replicating and validating the findings in a larger sample of patients. Completing this next step successfully would pave the way for introducing our predictive biomarkers in a day-to-day clinical practice. This work has the potential to transform clinical practice in the field of Psychiatry and in particular the way depressed patients are being assessed and assigned to treatment. Specifically, our approach has the potential to predict the efficacy of different treatment protocols *prior* to the deployment of treatment via the use of predictive imaging biomarkers. Critically, these biomarkers offer additional predictive power, over and above what could be inferred by standard clinical assessment tools alone). As such, our approach can optimise both the outcome and time-to-outcome, while at the same time minimize the use of valuable NHS resources. Finally, since our approach allows us to model the mechanisms behind treatment response, it can lead to the identification of novel target sites for future drug development. |
First Year Of Impact | 2017 |
Sector | Communities and Social Services/Policy,Creative Economy,Education,Healthcare,Government, Democracy and Justice,Pharmaceuticals and Medical Biotechnology |
Impact Types | Societal Economic Policy & public services |
Description | Summer School on Brain Imaging |
Geographic Reach | Multiple continents/international |
Policy Influence Type | Influenced training of practitioners or researchers |
Impact | We have been developing an international summer school on advanced brain imaging methods that will run on a yearly basis at the Centre for Cognitive Neuroimaging at the University Glasgow starting in 2016. |
Description | Dynamic Network Reconstruction of Human Perceptual and Reward Learning via Multimodal Data Fusion |
Amount | € 2,000,000 (EUR) |
Funding ID | 865003 |
Organisation | European Research Council (ERC) |
Sector | Public |
Country | Belgium |
Start | 08/2020 |
End | 08/2025 |
Description | Improving the prediction of treatment response in Major Depression using brain imaging (MRC/PsyStar) |
Amount | £376,000 (GBP) |
Organisation | Medical Research Council (MRC) |
Sector | Public |
Country | United Kingdom |
Start | 07/2014 |
End | 08/2017 |
Description | Neural correlates of learning and confidence during decision making and their utility in developing "intelligent" information technologies |
Amount | £597,000 (GBP) |
Funding ID | ES/L012995/1 |
Organisation | Economic and Social Research Council |
Sector | Public |
Country | United Kingdom |
Start | 01/2015 |
End | 01/2018 |
Description | fMRI signatures of depression and response to antidepressants in first episode psychosis |
Amount | £200,000 (GBP) |
Organisation | Royal College of Physicians of Edinburgh |
Sector | Academic/University |
Country | United Kingdom |
Start | 12/2019 |
End | 12/2021 |
Title | EEG-informed fMRI analysis tool |
Description | We developed a multivariate single-trial analysis framework for integrating simultaneously acquired EEG and whole-brain fMRI data. Specifically, we exploit trial-to-trial variability of electrophysiologically derived measures to inform the subsequent analysis of the simultaneously acquired fMRI data, to tease apart the cascade of constituent cortical processes involved in value-based decision making. |
Type Of Material | Improvements to research infrastructure |
Provided To Others? | No |
Impact | Our analysis techniques can be used in way that supersedes what is currently considered common analysis practice in the human neuroimaging literature. Our analysis framework has the potential to open new avenues in analysing human neuroimaging data in ways that help identify latent brain states that would otherwise be missed using more conventional analysis tools to independently analyse EEG and fMRI data. We plan to make our analysis tools freely available upon completion of the project and submission of all relevant work for publication. |
Title | Combined EEG/fMRI datasets - Confidence & Learning |
Description | Combined measurements of electroencephalographic (EEG) and functional magnetic resonance imaging (fMRI) data from 25 healthy participants performing two different tasks designed to probe the neural correlates of perceptual learning and the role of confidence during perceptual decisions. |
Type Of Material | Database/Collection of data |
Year Produced | 2017 |
Provided To Others? | Yes |
Impact | Combined EEG and fMRI measurements offer an opportunity to gain important new insights into human brain function that cannot be obtained using either modality alone (e.g. revealing latent brain states). Our ESRC funded work clearly demonstrated this in the context of studying perceptual learning and confidence during perceptual decisions (publications in preparation). Importantly, collecting this database allowed us to develop novel techniques to analyse the acquired data in way that supersedes what is currently considered common analysis practice in the human neuroimaging literature. We plan to make the database and our analysis tools fully available upon completion of the project and submission of all relevant work for publication. |
URL | https://openneuro.org/datasets/ds001512/versions/2.0.0 |
Title | Combined EEG/fMRI datasets - Value & Reward Learning |
Description | Combined measurements of electroencephalographic (EEG) and functional magnetic resonance imaging (fMRI) data from 24 healthy participants performing two different tasks designed to probe the neural correlates of value-based decision making and the role of learning during reward-based decisions. |
Type Of Material | Database/Collection of data |
Year Produced | 2017 |
Provided To Others? | No |
Impact | Combined EEG and fMRI measurements offer an opportunity to gain important new insights into human brain function that cannot be obtained using either modality alone (e.g. revealing latent brain states). Our current BBSRC funded work clearly demonstrated this in the context of studying learning during value- and reward-based decision making. Importantly, collecting this database allowed us to develop novel techniques to analyse the acquired data in way that supersedes what is currently considered common analysis practice in the human neuroimaging literature. The database and our analysis tools are fully available upon request. |
URL | https://openneuro.org/datasets/ds001219/versions/1.0.0 |
Description | Brain computer interfaces for augmenting decision making |
Organisation | Columbia University |
Country | United States |
Sector | Academic/University |
PI Contribution | Agreement established in October 2014. Collaboration will commence in early 2015. We will be providing insights into the behavioural and neurobiological origins of decision making and learning as these have been (and continue to be) developed through our BBSRC (BB/J015393/1-2) and ESRC (ES/L012995/1) awards. The collaboration will focus on the development of cognitive interfaces (brain-computer interfaces) that exploit decision correlates to optimise human performance in dealing with problems relating to security (e.g. optimise target/threat detection), global economy (e.g. optimising marketing strategies) and health and wellbeing (e.g. identifying prognostic indicators of cognitive ageing and disorders known to compromise ones decision-making faculties). |
Collaborator Contribution | Our partner at Columbia University is an expert in the development of brain computer interface (BCI) systems and will take the lead in developing the actual BCI platform required for the project as highlighted above. |
Impact | Disciplines involved: neuroscience, psychology, engineering, computer science |
Start Year | 2014 |
Description | Influence of branding on consumer decision making |
Organisation | Ohio State University |
Country | United States |
Sector | Academic/University |
PI Contribution | Building on insights gained on the behavioural and mechanistic details of value and preference based decision making (through BBSRC award, BB//1-2) we collected additional behavioural and eye-tracking data to investigate the role of branding on consumer choices. Analysed and modelled the behavioural data. This work has led to a publication in Psychological Science (Marios G. Philiastides, Roger Ratcliff (2013), "Influence of branding on preference-based decision making", Psychological Science, 24 (7): 1208-1215). |
Collaborator Contribution | Our partners at OSU are experts in computational modelling and analysis of eye-tracking data. They are currently analysing the eye-tracking data results from the work described above. We are hoping to provide additional insights into how consumers make purchasing decisions and the role of spatial attention (through eye-movement analysis) plays in these decisions. |
Impact | One publication: Marios G. Philiastides, Roger Ratcliff (2013), "Influence of branding on preference-based decision making", Psychological Science, 24 (7): 1208-1215). Disciplines involved: psychology, computational neuroscience |
Start Year | 2013 |
Description | Reward learning in depression |
Organisation | University of Dundee |
Country | United Kingdom |
Sector | Academic/University |
PI Contribution | Developed a new framework for understanding changes in neuronal activity during reward learning in humans that are characterised both in time and space. |
Collaborator Contribution | Offering access to a clinical group (depression) with surgical lesions to the mid-cingulate cortex to formally test the causal role of this region in reward learning using the framework developed by our research team. |
Impact | MRC grant application submitted in early 2016. |
Start Year | 2015 |
Description | Berlin School of Mind and Brain 2015 |
Form Of Engagement Activity | A formal working group, expert panel or dialogue |
Part Of Official Scheme? | No |
Geographic Reach | International |
Primary Audience | Other audiences |
Results and Impact | Workshop with an international audience of academic peers (academic staff, students and research assistants), on current state of the art in multimodal brain imaging. Presentation followed by questions and discussion and , hand-on exercises . |
Year(s) Of Engagement Activity | 2015 |
Description | Bristol University Visit, 2013 |
Form Of Engagement Activity | A talk or presentation |
Part Of Official Scheme? | Yes |
Geographic Reach | Local |
Primary Audience | Other academic audiences (collaborators, peers etc.) |
Results and Impact | Talk to an audience of academic peers (academic staff, students and research assistants), which sparked questions and discussion afterwards. Requests for further information on the topic presented and a request for a future collaboration utilising the new research tools we have been developing in relation to the BBSRC award (analysis of combined EEG/fMRI data). New experimental designs are currently under development. |
Year(s) Of Engagement Activity | 2013 |
Description | CBU Seminar Cambridge University |
Form Of Engagement Activity | A talk or presentation |
Part Of Official Scheme? | No |
Geographic Reach | International |
Primary Audience | Other audiences |
Results and Impact | Research talk on value based decision making and learning, perceptual learning and decision confidence. |
Year(s) Of Engagement Activity | 2018 |
Description | Cutting edge EEG Workkhop |
Form Of Engagement Activity | A formal working group, expert panel or dialogue |
Part Of Official Scheme? | No |
Geographic Reach | International |
Primary Audience | Postgraduate students |
Results and Impact | I organised a four day event in Glasgow to discuss and showcase the most up-to-date developments in EEG research. The event included plenary talks and hands-on workshops. 300 people attended the event (postgraduate students, postdocs, faculty) from more than 100 institutions worldwide. In addition to organising the event I also presented our lab's work during one of the plenary sessions. |
Year(s) Of Engagement Activity | 2017 |
URL | http://cuttingeeg.ccni.gla.ac.uk |
Description | FENS Brain Conference Talk |
Form Of Engagement Activity | A talk or presentation |
Part Of Official Scheme? | No |
Geographic Reach | International |
Primary Audience | Other audiences |
Results and Impact | Research talk on value based decision making and learning, perceptual learning and decision confidence. |
Year(s) Of Engagement Activity | 2018 |
URL | https://www.fens.org/Meetings/The-Brain-Conferences/The-Computational-Neuroscience-of-Prediction/ |
Description | Flip Side series: How to Choose. |
Form Of Engagement Activity | A press release, press conference or response to a media enquiry/interview |
Part Of Official Scheme? | Yes |
Geographic Reach | National |
Primary Audience | Public/other audiences |
Results and Impact | Discussed how people make decisions from a neurobiological prospective for a large audience of the general public. Topics included current theories of decision making and neurobiological evidence supporting preference and value-based decisions in the human brain. Information on the technologies and research tools we use to study the brain was also provided. Sample audio track can be found here: https://soundcloud.com/trigger-stuff/sets/how-to-choose We received additional media requests, including the BBC, for short interviews on the neurobiology of decision making. |
Year(s) Of Engagement Activity | 2014 |
URL | http://www.triggerstuff.co.uk/theatre/how-to-choose/ |
Description | Keynote lecture at University of Tuebingen |
Form Of Engagement Activity | A talk or presentation |
Part Of Official Scheme? | No |
Geographic Reach | International |
Primary Audience | Postgraduate students |
Results and Impact | A research talk on decision making and learning to a group of academic peers (research staff, students) followed by questions and discussion. |
Year(s) Of Engagement Activity | 2017 |
URL | http://meg.medizin.uni-tuebingen.de/2017/ |
Description | Neuroeconomics Society, Annual Conference 2013 |
Form Of Engagement Activity | Scientific meeting (conference/symposium etc.) |
Part Of Official Scheme? | Yes |
Type Of Presentation | poster presentation |
Geographic Reach | International |
Primary Audience | Other academic audiences (collaborators, peers etc.) |
Results and Impact | Shared initial results of BBSRC funded work on the role of learning in economic decision (see abstract below) with a wide range of academic attendees (including post-graduate students and junior postdoctoral fellows). Objective: Adaptive decisions depend on accurate reward representations associated with potential choices. These representations can be acquired with reinforcement learning mechanisms that use the prediction error (PE) - the difference between expected and actual rewards - as a learning signal to update reward expectations. To date, most studies used fMRI and EEG independently to either identify brain regions or activation latencies associated with PE signals. The goal of this study is to couple high temporal resolution, single-trial EEG with simultaneously acquired fMRI to infer the full spatiotemporal dynamics of the brain networks involved in PE processing. Methods: Twenty-four subjects participated in the study. They performed a probabilistic reversal-learning task while we simultaneously collected concurrent EEG/fMRI data. Single-trial multivariate discriminant analysis was used to identify linear spatial weightings of the EEG sensors to find speci?c temporal windows, which optimally discriminated between trials conditioned along different PE valence and magnitude dimensions. The resulting single-trial discriminant component amplitudes were used to build EEG-informed fMRI regressors to identify brain regions correlating with the trial-by-trial variance in PE valence and magnitude. For comparison, a more conventional fMRI analysis was carried out whereby behaviorally derived, model-based regressors were used instead. Results: We confirmed our previous, stand-alone, EEG work by providing a temporal account of PE processing. Specifically, 220 ms after feedback, outcomes are initially evaluated categorically with respect to their valence (positive vs. negative). Around 300 ms and parallel to a second valence-evaluation, the brain also represents quantitative information about PE magnitude. We are currently using trial-by-trial variability intrinsic to these temporally-distinct neural representations to map out the spatial characteristics of PE processing and provide a mechanistic and causal account of the neural networks involved in learning reward contingencies and guiding future actions. Conclusions: Our results suggest that the temporal brain dynamics of PE processing can be inferred reliably using single-trial EEG acquired inside an MR-scanner. Crucially, to provide a complete spatiotemporal characterization of the underlying networks, single-trial EEG estimates associated with PE valence and magnitude can be used to inform the analysis of simultaneously acquired fMRI data. We propose that EEG-informed fMRI has the potential to expose latent brain states - that could otherwise go astray using conventional model-based fMRI - by exploiting trial-by-trial variability in electrophysiologically- rather than behaviorally-derived measures. Presenting at this conference sparked later exchange with academic colleagues in related disciplines (e.g. in the form of requests for additional information on the work and invitation for seminar talks for the PI and lead postdoctoral fellow). |
Year(s) Of Engagement Activity | 2013 |
Description | Neuroeconomics Society, Annual Conference 2014 |
Form Of Engagement Activity | Scientific meeting (conference/symposium etc.) |
Part Of Official Scheme? | Yes |
Type Of Presentation | poster presentation |
Geographic Reach | International |
Primary Audience | Other academic audiences (collaborators, peers etc.) |
Results and Impact | Shared initial results of BBSRC funded work on the role of the role of spatial attention (eye-movements) on consumer decision making (see abstract below) with a wide range of academic attendees (including post-graduate students and junior postdoctoral fellows). Objective: Product branding is a crucial dimension of consumer choices. Recent work has suggested that branding information and subjective product preference may be integrated into a single source of evidence in the decision-making process. Here we investigate how exactly these two sources of information are combined, by employing the attentional drift-diffusion model (aDDM) to relate choices and reaction times to the relative gaze time on the two products and their brands. Methods: We carried out an experiment in which subjects made a series of hypothetical preference decisions between two items of clothing paired with different designer brands. In control trials subjects also made preference-based clothing decisions, but with phase-scrambled brand images. While subjects made these choices, we tracked their eye-movements. Beforehand we also collected separate individual ratings for each clothing item and brand. We then used subjects' ratings and gaze patterns as inputs to the aDDM to test whether these measures alone could account for subjects' choices and reaction times. Results: Using the aDDM we were able to accurately predict the influence of gaze time on the probability of choosing the left or right item. Comparing the intact brand trials to the scrambled control trials, we find that subjects spent more time looking at the brand information, took longer to make their decisions, and were more likely to choose an item if it was paired with a preferred brand. Furthermore, we were able to use the aggregate fraction of time spent looking at the brands to predict the average influence of the brand ratings on subjects' choices. This relationship was further established with a significant across-subject correlation between brand gaze time and brand weight in their utility functions. Finally, consistent with previous aDDM findings, we observed no correlation between item or brand ratings and gaze duration. Conclusions: Our results indicate that branding information and subjective product preference are combined together in a multi-attribute drift-diffusion model, where the relative weights on the two attributes are determined by the gaze time on the product vs. brand. These findings lend further support to the aDDM as a common mechanism underlying value-based decisions and are consistent with the hypothesis that in binary choice, attention leads to preference, and not vice-versa. Presentation sparked later exchange with academic colleagues in related disciplines (e.g. in the form of requests for additional information on the work and requests for potential collaborators). |
Year(s) Of Engagement Activity | 2014 |
Description | Open Days, Studying decision making using brain imaging, 2016 |
Form Of Engagement Activity | Participation in an open day or visit at my research institution |
Part Of Official Scheme? | No |
Geographic Reach | International |
Primary Audience | Public/other audiences |
Results and Impact | Open Days, University of Glasgow. The event is designed to inform prospective students and their families about ongoing research activities in our department. We used this opportunity to present our work to the general public. |
Year(s) Of Engagement Activity | 2016 |
Description | Organisation of Human Brain Mapping, Annual Meeting 2014 |
Form Of Engagement Activity | Scientific meeting (conference/symposium etc.) |
Part Of Official Scheme? | Yes |
Type Of Presentation | poster presentation |
Geographic Reach | International |
Primary Audience | Other academic audiences (collaborators, peers etc.) |
Results and Impact | Shared initial results of BBSRC funded work on the role of learning in economic decision (see abstract below) with a wide range of academic attendees (including post-graduate students and junior postdoctoral fellows) as well as a small number of the general public. Introduction: Adaptive decisions depend on accurate reward representations associated with potential choices. These representations can be acquired with reinforcement learning mechanisms that use the prediction error (PE) - the difference between expected and actual outcomes - as a learning signal to update expectations [1]. To date, most studies used fMRI and EEG independently to either identify brain regions or activation latencies associated with PE signals [2, 3]. The goal of this study is to couple high temporal resolution, single-trial EEG with simultaneously acquired fMRI to infer the full spatiotemporal dynamics of the brain networks involved in PE processing. Methods: Twenty-four subjects participated in the study (9 males, 24yrs±3). Data were acquired on a 3T Philips MR scanner and 64-channel Brain Products EEG system. Subjects performed a probabilistic reversal-learning task while we collected, simultaneously, EEG and fMRI data. Single-trial multivariate discriminant analysis was used to identify linear spatial weightings of the EEG sensors to find speci?c temporal windows, which optimally discriminated between trials conditioned along different PE valence and magnitude dimensions [4]. EEG-informed fMRI regressors were built from the resulting single-trial discriminant component amplitudes and employed in a random-effects GLM analysis to identify brain regions correlating with the trial-by-trial variance in PE valence and magnitude. For comparison, a more conventional fMRI analysis was carried out whereby behaviorally derived, model-based regressors were used in the analysis instead. Results: We provide additional support to our previous, stand-alone, EEG work [3] by characterizing the temporal dynamics of PE processing. Specifically, 220 ms after feedback, outcomes are initially evaluated categorically with respect to their valence (positive vs. negative). Around 300 ms and parallel to a second valence-evaluation, the brain also represents quantitative information about PE magnitude, which is partially correlated with the trial-by-trial changes in model-based PE magnitude (r ¯ = 0.3, p<.001). Importantly, we also show that unaccounted variance in single-trial EEG amplitudes has additional predictive power in explaining fMRI data and we have begun to identify brain regions correlating with each of our temporally-specific EEG components. Additionally, we expect that activations traditionally absorbed by a single regressor in a model-based analysis (e.g. for PE valence) will now be distributed across regressors from temporally distinct components, thereby allowing us to begin making causal inferences about the underlying network. Conclusions: Our results suggest that the temporal dynamics of PE processing can be inferred reliably using single-trial EEG during simultaneous fMRI. Crucially, to provide a complete spatiotemporal characterization of the underlying networks, single-trial EEG estimates associated with PE valence and magnitude can be used to inform the analysis of the fMRI data. These results extend previous findings and allow us to begin mapping the spatiotemporal profile of PE processing, providing the first instance of a mechanistic and causal account of the network involved in learning reward contingencies. We propose that EEG-informed fMRI has the potential to expose latent brain states - that could otherwise go astray using conventional model-based fMRI - by exploiting trial-by-trial variability in electrophysiologically- rather than behaviorally-derived measures. Presenting at this conference sparked later exchange with academic colleagues in related disciplines (e.g. in the form of requests for additional information on the work and invitation for seminar talks for the PI and lead postdoctoral fellow). |
Year(s) Of Engagement Activity | 2014 |
Description | Oxford University Visit 2012 |
Form Of Engagement Activity | A talk or presentation |
Part Of Official Scheme? | Yes |
Geographic Reach | Local |
Primary Audience | Other academic audiences (collaborators, peers etc.) |
Results and Impact | Talk to an audience of academic peers (academic staff, students and research assistants), which sparked questions and discussion afterwards. asdsad |
Year(s) Of Engagement Activity | 2012 |
Description | Presentation at Human Brain Project Summit |
Form Of Engagement Activity | A talk or presentation |
Part Of Official Scheme? | No |
Geographic Reach | International |
Primary Audience | Public/other audiences |
Results and Impact | Presented our recent work on value-based decision making and learning and the importance of multimodal neuroimaging in enabling new neuroscientific discoveries. The event was designed to showcase recent neuroscience developments to the general public and expert professional. The audience was comprised of about 300 people of all ages and ranging in expertise as expected (general public to the neuroscience professional). |
Year(s) Of Engagement Activity | 2017 |
URL | https://www.humanbrainproject.eu/en/follow-hbp/news/5th-annual-human-brain-project-summit/ |
Description | Press release - NatComms |
Form Of Engagement Activity | A press release, press conference or response to a media enquiry/interview |
Part Of Official Scheme? | No |
Geographic Reach | International |
Primary Audience | Media (as a channel to the public) |
Results and Impact | Press release on the outcome of our Nature Communication paper (Fouragnan et al., 2015) highlighting the main findings and the potential implications and practical applications of the work. |
Year(s) Of Engagement Activity | 2015 |
URL | http://www.gla.ac.uk/news/headline_418740_en.html |
Description | Press release - NatComms - BBSRC Tumblr |
Form Of Engagement Activity | A press release, press conference or response to a media enquiry/interview |
Part Of Official Scheme? | No |
Geographic Reach | International |
Primary Audience | Media (as a channel to the public) |
Results and Impact | Press release on the outcome of our Nature Communication paper (Fouragnan et al., 2015) highlighting the main findings and the potential implications and practical applications of the work. |
Year(s) Of Engagement Activity | 2015 |
URL | http://bbsrc.tumblr.com/post/130123515646/mapping-the-consequences-of-our-decisions-in-the |
Description | Science Slam, Studying decision Making using brain imaging, 2016 |
Form Of Engagement Activity | A talk or presentation |
Part Of Official Scheme? | No |
Geographic Reach | International |
Primary Audience | Public/other audiences |
Results and Impact | Science Slam IV, Glasgow. The event encourages PhD students to present their research in creative ways and to do something the audience has never seen before. We used this opportunity to present our ongoing research activities to the general public. |
Year(s) Of Engagement Activity | 2016 |
Description | Scottish Neuroscience Meeting, 2014 |
Form Of Engagement Activity | Scientific meeting (conference/symposium etc.) |
Part Of Official Scheme? | Yes |
Type Of Presentation | keynote/invited speaker |
Geographic Reach | National |
Primary Audience | Other academic audiences (collaborators, peers etc.) |
Results and Impact | Presented a summary of our recent work on the neurobiology of decision making to academic colleagues (neuroscientists) from throughout Scotland as well as a small number of members of the general public. Increased in requests for additional information, further participation in our study and scientific involved in our lab (e.g. postdoc and studentship requests). |
Year(s) Of Engagement Activity | 2014 |
Description | Swansea Visit, 2013 |
Form Of Engagement Activity | A talk or presentation |
Part Of Official Scheme? | Yes |
Geographic Reach | Local |
Primary Audience | Other academic audiences (collaborators, peers etc.) |
Results and Impact | Talk to an audience of academic peers (academic staff, students and research assistants), which sparked questions and discussion afterwards. Further requests for additional information from academic colleagues. |
Year(s) Of Engagement Activity | 2014 |
Description | TEDx Talk 2020 |
Form Of Engagement Activity | A talk or presentation |
Part Of Official Scheme? | No |
Geographic Reach | International |
Primary Audience | Public/other audiences |
Results and Impact | Invited to give a TEDx talk in Glasgow on our recent work on multimodal brain imaging of human decision making and learning. The talk focused on the latest technologies used for brain imaging and their application on mental health - more specifically, their role in diagnostic stratification and predicting treatment response in depression, enabling early intervention and more favourable patient outcomes. TED is one of the most recognised brands worldwide, focusing on "ideas worth sharing" that have potential for significant impact. TED talks freely available online on TED and TEDx youtube channels, totalling more than 40 million subscribers across the globe. Therefore the impact of this talk is presumably far reaching. |
Year(s) Of Engagement Activity | 2020 |
Description | Talk at Oxford University - Functional Neurosurgery Unit 2016 |
Form Of Engagement Activity | A talk or presentation |
Part Of Official Scheme? | No |
Geographic Reach | National |
Primary Audience | Other audiences |
Results and Impact | A research talk on decision making and learning to a group of academic peers (research staff, students) and clinicians followed by questions and discussion. Plans for future collaborations (looking at clinical groups) made. |
Year(s) Of Engagement Activity | 2016 |
Description | Talk at the British Association for Cognitive Neuroscience |
Form Of Engagement Activity | A talk or presentation |
Part Of Official Scheme? | No |
Geographic Reach | International |
Primary Audience | Postgraduate students |
Results and Impact | A research talk on decision making and learning to a group of academic peers (research staff, students) followed by questions and discussion. |
Year(s) Of Engagement Activity | 2017 |
Description | University of Leuven Visit, 2015 |
Form Of Engagement Activity | A talk or presentation |
Part Of Official Scheme? | No |
Geographic Reach | International |
Primary Audience | Other audiences |
Results and Impact | Research talk on decision making and learning to an audience of academic peers (research staff, students) followed by questions and discussion. |
Year(s) Of Engagement Activity | 2015 |
Description | University of Zurich Visit, 2014 |
Form Of Engagement Activity | A talk or presentation |
Part Of Official Scheme? | No |
Geographic Reach | International |
Primary Audience | Other audiences |
Results and Impact | A research talk on decision making and learning to a group of academic peers (research staff, students) followed by questions and discussion. |
Year(s) Of Engagement Activity | 2014 |