Nowadays, sports betting has become increasingly available and easy to engage in. Here we examined the neural responses to stimuli that represent sporting events available for betting as compared to sporting events without a gambling opportunity. We used a cue exposure task in which football (soccer) fans (N = 42) viewed cues depicting scheduled football games that would occur shortly after the scanning session. In the “betting” condition, participants were instructed to choose, at the end of each block, the game (and the team) they wanted to bet on. In the “watching” condition, participants chose the game they would prefer to watch. After the scanning session, participants completed posttask rating questionnaires assessing, for each cue, their level of confidence about the team they believed would win and how much they would enjoy watching the game. We found that stimuli representing sport events available for betting elicited higher fronto-striatal activation, as well as higher insular cortex activity and functional connectivity, than sport events without a gambling opportunity. Moreover, games rated with more confidence towards the winning team resulted in greater brain activations within regions involved in affective decision-making (ventromedial prefrontal cortex), cognitive inhibitory control (medial and superior frontal gyri) and reward processing (ventral and dorsal striatum). Altogether, these novel findings offer a sensible simulation of how the high availability of sports betting in today’s environment impacts on the reward and cognitive control systems. Future studies are needed to extend the present findings to a sample of football fans that includes a samilar proportion of female and male participants.
There has been a rapid proliferation of both online and brick-and-motor sports betting venues that are readily available and easy to engage with. This all-time gambling availability is likely to be a key environmental factor in triggering the need for or temptation to gamble (Shaffer et al., 2004). With an easy access from a computer, tablet or phone, it is possible to bet everywhere, at every moment, such as before or during a game in play, while simultaneously using different platforms (James, O’Malley, & Tunney, 2016). Since every sporting event is available to bet on, merely viewing cues related to sporting events (e.g., advertisements featuring betting odds) has the potential to drastically increase gambling temptation (e.g., Dwyer, Shapiro, & Drayer, 2017; Dwyer & Weiner, 2018; Hing, Li, Vitartas, & Russell, 2017a; Hing, Russell, & Browne, 2017b; Hing, Russell, Lamont, & Vitartas, 2017c). In other words, exposure to sports betting stimuli might not simply involve perceiving salient cues, but should also trigger more advanced motivational and (monetary) decision-making processes.
The impact of reward availability on neural processes has been previously examined in neuroimaging studies on tobacco and food (for reviews, see Jasinska, Stein, Kaiser, Naumer, & Yalachkov, 2014; Wilson & Sayette, 2015; Yalachkov, Kaiser, & Naumer, 2012). Hayashi, Ko, Strafella, and Dagher (2013) found that when cigarettes were immediately available, subjective craving was higher and was associated with increased activation within the dorsolateral prefrontal cortex (DLPFC). This region is activated during experimental tasks that involve strategic decision-making and high-order cognitive functions, such as working memory, planning, and inhibitory control (Bechara, 2005; Bickel et al., 2007; McClure & Bickel, 2014; Metcalfe & Mischel, 1999). Consistent with Hayashi et al., smokers who expected imminent access to cigarettes showed greater activation in bilateral DLPFC to smoking-related cues over neutral cues, as compared to those who did not expect such access (McBride, Barrett, Kelly, Aw, & Dagher, 2006; Wilson, Sayette, Delgado, & Fiez, 2005; Wilcox, Teshiba, Merideth, Ling, & Mayer, 2011; Zelle, Gates, Fiez, Sayette, & Wilson, 2017). In a recent study, Blechert, Klackl, Miedl, and Wilhelm (2016) showed that available foods, as compared to unavailable ones, elicited higher palatability ratings, as well as stronger neural activation in the orbitofrontal cortex, amygdala, caudate nucleus, and anterior cingulate cortex. These are all structures that are commonly activated during experimental paradigms that involve motivation and reward-related decision-making (e.g., Bechara, 2005).
Comparable patterns of activations have been observed by previous neuroimaging studies on problem gambling—that is, when samples of problem gamblers viewed casino-related or gambling-related pictures (Crockford, Goodyear, Edwards, Quickfall, & el-Guebaly, 2005; Goudriaan, de Ruiter, van den Brink, Oosterlaan, & Veltman, 2010; Limbrick-Oldfield et al., 2017). Nevertheless, viewing gambling pictures in these studies was not directly linked to an opportunity to gamble during or after the experiment. In some cases, the neural responses associated with cue exposure may have also been mixed with unrelated motor processes, (e.g., such as in Goudriaan et al., 2010, in which subjects pressed a response button when a face appeared on a picture). Hence, although these studies have laid important groundwork for understanding the brain systems underlying gambling cue responding, they did not explicitly model the impact of availability during gambling picture viewing. Moreover, these studies recruited problem gamblers from addiction treatment centers. This could have lowered the motivational saliency of gambling cues in these populations (e.g., Brevers et al., 2017; Jasinska et al., 2014; van Holst, van Holstein, van den Brink, Veltman, & Goudriaan, 2012a). Specifically, it is possible that both the nonavailability of gambling cues and the quitting motivation of abstinent gamblers could lower the motivational salience of gambling cues during cue exposure tasks.
Sescousse, Barbalat, Domenech, and Dreher (2013) explicitly examined the impact of gambling availability on neural processes. This fMRI study highlighted that (non-treatment-following) problem gamblers, as compared to nongambler healthy controls, exhibited higher ventral–striatal activation when viewing cues that signal the probabilistic occurrence of an upcoming monetary rewards. Importantly, problem gamblers exhibit blunted neural responses when viewing cues that signal the occurrence of another type of rewards (i.e., erotic content pictures). These findings further outline the importance of examining the impact of gambling availability, as well as the relative attractiveness of the gambling cue on the neural response (see also Limbrick-Oldfield et al., 2017).
Therefore, the main goal of this study was to evaluate the availability of gambling cues on neural cue reactivity in football fans. Specifically, we reasoned that making gambling cues available for participants to bet on would represent a sensible simulation of the high availability of ready-to-gamble offers in today’s environments. Through this experimental manipulation we aimed to identify the neural correlates of sports betting availability by football fans. Moreover, we also wanted to examine how brain activation was modulated by participants’ level of interest (i.e., degree of confidence toward the winning team; and degree of enjoyment directed toward a game) toward each cue presented during the experiment.
Another aim of the present study was to examine the effect of sports betting availability on insular-cortex-centered psycho-physiological interaction. Indeed, activation of the insula has been shown to vary according to the levels of uncertainty or saliency attached to a stimulus (e.g., Burke & Tobler, 2011; Grosenick, Greer, & Knutson, 2008; Knutson, Rick, Wimmer, Prelec, & Loewenstein, 2007; Paulus & Frank, 2006; B. W. Smith et al., 2009; Symmonds, Wright, Bach, & Dolan, 2011; Wu, Bossaerts, & Knutson, 2011; Wu, Sacchet, & Knutson, 2012). The insula has also been identified as an integrative interoceptive site connecting autonomic, affective, and cognitive processing (for reviews, see Craig, 2009; Droutman, Bechara, & Read, 2015a; Droutman, Read, & Bechara, 2015b). Specifically, a growing body of research has indicated that the insula plays a key role in altering the balance between the automatic and deliberative systems (Addicott, Sweitzer, Froeliger, Rose, & McClernon, 2015; Janes et al., 2010; Naqvi & Bechara, 2009, 2010; Naqvi, Gaznick, Tranel, & Bechara, 2014; Noël, Brevers, & Bechara, 2013a, 2013b) and could initiate network switching between the default (ventromedial prefrontal cortex [VMPFC] and posterior cingulate cortex) and central executive (DLPFC and posterior parietal cortex) modes during the identification of salient stimuli (Addicott et al., 2015; Chang, Yarkoni, Khaw, & Sanfey, 2013; Droutman et al. 2015a, b; Menon & Uddin, 2010). Hence, examining insular-centered psycho-physiological interaction should offer a fine-grained analysis of the neural processes triggered by cues that signal gambling availability.
Forty-two football (i.e., soccer) fans participated in this study (38 males and four females, mean age 23.42 years). All participants gave written informed consent to the experimental procedure, which was approved by the Ghent University Institutional Review Board. This study was performed strictly in accordance with the approved guidelines. All participants were right-handed and had normal or corrected-to-normal vision. They were advised to avoid alcoholic drinks in the 24 h prior to testing.
Participants were recruited on the Internet through advertisements displayed on social media. The ads asked for football fans (i.e., individuals who like watching European Football) to participate in a neuroimaging study on sports betting. Individuals who were interested then had to complete an online survey. This online prescreening tool aimed to assess individuals’ (1) frequency of football game watching, (2) frequency of football game betting, (3) knowledge of teams from the main European Football League, and (4) level of interest attached to each main European Football League. All participants were judged to be physically healthy on the basis of their answers on an MRI screening form, enclosed to the online survey. The prescreening tool was also used to exclude any participant who reported having used mood stabilizers, antidepressants, antipsychotics, sleep medications, morphine, cocaine, or heroine or having regularly used cannabis in the past 12 months. The online prescreening tool is accessible through the following link: www.panlablimesurvey.ugent.be/PAN200/index.php/477436/lang-nl.
The screening procedure identified participants who watched football frequently and who maintained a high level of knowledge and interest in European Football Leagues. With regard to the frequency of football betting, the participants ranged from nonbettors to high-frequent bettors. Specifically, six participants reported having “not previously” bet on football, three participants reported their frequency of football betting as “very seldom,” three participants reported it as “seldom,” 13 participants reported betting “sometimes” on football, 12 participants reported betting “frequently” on football, and four participants reported betting “very frequently” on football. Importantly, the participants with no experience in sports betting reported that they could be potentially interested by betting on football. This additional question was added to the online screening tool in order to avoid recruiting individuals with some reluctance to bet on football.
Severity of problem gambling (Problem Gambling Severity Index; PGSI; Ferris & Wynne, 2001), and of alcohol use (Alcohol Use Disorders Identification Test; AUDIT; Saunders, Aasland, Babor, de la Fuente, & Grant, 1993) was screened on the day of the study. On the PGSI, 27 participants reported no gambling problem; ten participants reported a moderate problem (score of 3 to 7); and five participants reported a high level of gambling problems (score of 8 or more). On the AUDIT, 18 participants reported no or low risk of alcohol use disorders (score between 0 and 7), 16 participants reported a medium risk (score between 8 and 15), and nine reported high risk (score between 16 and 19).
Participants received a fixed amount of €50 for their participation, plus the money won with the sports betting game (up to €20).
Experimental task and MRI procedure
We used a cue exposure task (adapted from Blechert et al., 2016; see Fig. 1) in which cues depicting football games appeared on a screen (stimulus presentation length = 5 s, jittered intertrial interval [ITI] = 1.8 to 3 s, task length ≈ 16 min 45 s). More specifically, each cue depicted a football game from a European league (i.e., English Premiere League, German Bundesliga, Italian Calcio, French Ligue 1, Spanish Liga, Portuguese Primeira Liga, Netherlandse Eredivisie, and Belgian Pro League) that would occur either the day of (but after the scanning session) or the day following the scanning session. This procedure was adopted in order to reinforce the perceived availability of the event that appeared during the cue exposure task. This also required that different games be displayed as stimuli for each separate day of scanning. As a result, all participants were scanned on a Saturday (from 9 a.m. to 5 p.m.; seven to ten participants were scanned on the same day). Five Saturday sessions were undertaken in total (weekly from August 19 to September 23, 2017).
Prior to positioning in the scanner, participants received task instructions. They were asked to look attentively at each cue and were informed that there were two types of blocks of trials: a betting and a watching block. Each block consisted of ten football games (i.e., ten trials). In the “betting” block, each football game (showing the logos of the teams that would be playing against each other) was displayed on the screen for 5 s each (jittered ITI = 1.8 to 3 s). Participants were informed that when ten games were shown, they could bet on their chosen game and team at the end of the block. Specifically, an overview slide appeared for 10 s, after the betting block, displaying all ten cues (games) that had just been presented. During this phase, participants orally reported the number of the game and the team that they wanted to bet on (e.g., “One, FC Barcelona”) via intercom to the experimenter. Participants were also informed that they would receive the betting money once the sports event that he or she had bet on had taken place (€4 in case of a win, €2 in case of a draw, €0 in case of a loss). In the “watching” block, participants viewed the game cues as before; however, they were instructed to identify the game they would enjoy watching the most and the team they thought would win the game. This implied that the cue exposure attached to the watching condition was not associated with the prospect of getting a monetary reward. Finally, participants were informed that there were five “betting” and five “watching” blocks displaying the same 50 games (but presented in a different pseudorandom order; 100 trials in total); that they could win an amount ranging from €0 (i.e., in the case of five losing bets) to €20 (i.e., in the case of five winning bets); that the two types of conditions would be presented in an alternating order; that there would be a 10-s interval (white screen) between blocks; that the task could start with either a “betting” or a “watching” block; and that all the games depicted during the experiment would occur the same weekend as the scanning session.
Directly after the scanning session, participants completed posttask rating questionnaires. Specifically, for all 50 games that had been depicted during the cue exposure task, participants were asked to indicate which team they thought would win the game (by circling the team) and how sure they were that this team would win (1 = not at all, 2 = very little, 3 = somewhat, 4 = to a great extent). Next, they were asked to report, for the same 50 games, how much they would enjoy watching the game (1 = not at all, 2 = very little, 3 = somewhat, 4 = to a great extent). Then participants completed the AUDIT and PGSI and wrote down their bank account number for receiving the payment attached to their betting choices (i.e., we had to wait until the games were played before being able to remunerate the participant).
The stimulus presentation and timing of all events were achieved using Python 2.7.13 and Pygame 1.9.3 on an IBM-compatible PC.
All fMRI imaging was conducted in a 3-T Siemens MAGNETOM Prisma scanner at the GIfMI Center, UZ Gent, Gent University. Functional scanning used a z-shim gradient-echo echoplanar imaging (EPI) sequence with prospective acquisition correction (PACE). This specific sequence is dedicated to reducing signal loss in the prefrontal and orbitofrontal areas. The PACE option can help reduce the impact of head motion during data acquisition. The parameters were: TR = 2,000 ms; TE = 25 ms; flip angle = 90°; 64 × 64 matrix size with resolution 3 × 3 mm2. Thirty-one 3.5-mm axial slices were used to cover the whole cerebral cortex and most of the cerebellum with no gap. The slices were tilted about 30 deg clockwise along the AC–PC plane in order to obtain better signals in the orbitofrontal cortex. A 180-slice MPRAGE structural sequence was acquired (TI = 800 ms; TR = 2,530 ms; TE = 3.1 ms; flip angle 10°; 208 sagittal slices; 256 × 256 matrix size with spatial resolution as 1 × 1 × 1 mm3) for registering each participant’s functional data to standard space. Prior to the EPI sequence, standard Siemens magnetic field maps were collected with the same slice prescription as the functional scans using a multi-echo gradient-echo acquisition (effective EPI echo spacing = 0.5 ms, EPI TE = 25 ms, percent signal loss threshold = 10). This field map was used for correction of geometric distortions in the EPI data caused by magnetic field inhomogeneity.
The functional data for each participant were motion-corrected using rigid-body registration, implemented in FSL’s linear registration tool, MCFLIRT (Jenkinson, Bannister, Brady, & Smith, 2002). Image preprocessing was carried out using the FMRI Expert Analysis Tool (version 6.00), part of the FSL package (FMRIB Software Library, version 5.0.9; www.fmrib.ox.ac.uk/fsl). All participants demonstrated less than 1.0 mm of either absolute or relative motion. Hence, no participant was excluded due to head motion. After motion correction and temporal low-pass filtering, each time series was corrected for geometric distortions caused by magnetic field inhomogeneity (Jenkinson, 2004). The first three volumes of each participant’s functional data were discarded in order to allow the magnetic resonance signal to reach a steady state. The data were spatially smoothed using a 5-mm full-width-at-half-maximum (FWHM) Gaussian kernel. The data were filtered in the temporal domain using a nonlinear high-pass filter with a 116-s cutoff. A three-step registration procedure was used, whereby the EPI images were registered first to the matched-bandwidth high-resolution scan, then to the MPRAGE structural image, and finally into standard MNI space, using FLIRT (Jenkinson et al., 2002; Jenkinson & Smith, 2001). The registration from MPRAGE structural image to standard space was further refined using FNIRT nonlinear registration (Andersson, Jenkinson, & Smith, 2007a, b). Statistical analyses were performed in the native image space, with the statistical maps normalized to the standard space prior to higher-level analysis.
Betting versus watching trials
To identify brain regions involved in the cue exposure of football games available for betting, we examined the neural activity during stimulus presentation. Specifically, we compared blood oxygen level-dependent (BOLD) activity, during the onset of “betting” trials, in which participants viewed football games available for betting, with activity during the onset of “watching trials,” in which participants viewed games when reflecting on whether they would be interested in potentially watching it. The brain-imaging data were modeled using an event-related general linear model (GLM) within FSL’s FILM module using FEAT. First-level statistical analysis included the “betting” trials and the “watching” trials as regressors (i.e., two conditions of interest). The event onsets (duration of each event = 5 s) were convolved with a canonical hemodynamic response function (HRF, double-gamma) to generate regressors used in the GLM. Null events were not explicitly modeled and therefore constituted an implicit baseline. An additional 24 motion regressors were added (six motion parameters, the derivatives of these motion parameters, the squares of the motion parameters, and the squares of the derivatives; comprising FSL’s standard + extended set of motion parameters). For each participant, we computed the following contrast images: (1) betting trials minus watching trials and (2) watching trials minus betting trials. These were then input into a random-effect model for group analysis using nonparametric permutation analyses (FSL Randomize, with 10,000 random permutations of the data), with a height threshold of z > 3.1 and a cluster probability of p < .05, family-wise error [FWE] corrected for multiple comparisons across the whole brain.
Brain activation as a function of parametric increases of confidence and enjoyment
The event-related whole-brain GLM analyses were also used to perform parametric contrasts based on the scores obtained through the posttask rating questionnaires (level confidence and enjoyment associated to each game). Specifically, (i) “betting” events were weighted according to the level of confidence (– 3 = not at all, – 1 = very little, 1 = somewhat, 3 = to a great extent), and (ii) “watching” events were weighted according to the level of enjoyment (– 3 = not at all, – 1 = very little, 1 = somewhat, 3 = to a great extent). For each participant, we computed the following parametric contrast images: (i) confidence about “betting” trials and (ii) enjoyment about “watching” trials. These were then input into a random-effect model for group analysis using nonparametric permutation analyses (FSL Randomize with 10,000 random permutations of the data), with a height threshold of z > 3.1 and a cluster probability of p < .05, FWE corrected for multiple comparisons across the whole brain.
Insula-centered functional connectivity analyses
Psycho-physiological interaction (PPI) analyses were performed on the “betting cues versus watching cues” contrasts, as well as on the parametric contrasts (i.e., level of confidence for the “betting” trials, level of enjoyment for the “watching” trials). We created an insular seed regressor by computing individual average time series within a 10-mm sphere surrounding the individual subject’s peaks within the functional mask of right anterior insula (x = 34, y = 20, z = – 4; see also Fig. 2 and Table 1). The locations of the peak voxels were based on the “betting cues minus watching cues” contrast.
The insular seed mask was first transformed into individual space using FLIRT. Next, the time course of each seed was extracted. For each participant, a first-level PPI model was set up using FSL, including the following user-specified regressors: (1) the time course of the seed region, (2) four regressor codings for the task contrasts, and (3) the four regressor coding interaction terms—that is, the multiplication of time course and each of the task contrasts. The single-subject contrast images for each of these nine regressors were created. Each participant’s PPI contrast image for the interaction regressor was then centered into a second-level random-effect analysis to test for group effects using nonparametric permutation analyses (FSL Randomize with 10,000 random permutations of the data), with a height threshold of z > 3.1 and a cluster probability of p < .05, FWE corrected for multiple comparisons across the whole brain.
Brain activation when viewing cues available for betting versus cues available for watching
Figure 2A and Table 1 show the brain regions in which activation increased for the “betting cues minus watching cues” contrast. This analysis revealed significant activation in the right hippocampus, frontal orbital cortex, anterior insula, medial frontal gyrus, and caudate nucleus. For the “watching cues minus betting cues” contrast (Fig. 2B), significant activation was observed in the left superior gyrus (voxel cluster size = 328, peak = – 68, – 36, 14), extending into the left supramarginal gyrus (peak = – 62, – 46, 26) and the lateral occipital cortex (peak = – 68, – 36, 14).
Brain activation in function of parametric increases
Figure 3A and Table 2 show brain activation increases for the parametric contrast on the level of confidence toward “betting” trials. This analysis revealed clusters of activation in bilateral superior frontal gyrus (BA8), the anterior aspect of right middle frontal gyrus (BA10) or frontal pole, paracingulate gyrus and medial frontal gyrus (BA6), left inferior frontal gyrus, bilateral anterior insula, bilateral hippocampus, bilateral caudate, and lateral occipital cortex.
Figure 3B and Table 2 show brain activation increases for the parametric contrast on the level of enjoyment toward “watching” trials. This analysis revealed clusters of activation in bilateral inferior frontal gyrus, middle frontal gyrus, left frontal orbital cortex, left anterior insula, bilateral caudate nucleus, and lateral occipital cortex.
No significant activation was observed when comparing the level of confidence for the “betting” trials and the level of enjoyment for the “watching” trials (with a height threshold of z > 3.1 and a cluster probability of p < .05, FWE corrected for multiple comparisons across the whole brain).
Insula-centered functional connectivity
Betting cues versus watching cues
For the “betting cues minus watching cues” contrast (see Fig. 4), the analyses identified positive PPI between the anterior insular seed, the right parahippocampal gyrus (voxel cluster size = 570, peak = 8, – 34, – 8; z > 3.72), and the lateral occipital cortex (voxel cluster size = 433, peak = – 34, – 88, – 8, z > 3.72). No significant PPI was found for the “watching cues minus betting cues” contrast.
No significant PPI was found for the parametric contrasts, either with the level of confidence in “betting” trials or the level of enjoyment in “watching” trials (using a threshold of either z > 3.1 or z > 2.3, respectively).
Assessment of possible moderators
When each of the variables was entered in the GLM as a covariate, we found no significant effect of sports betting frequency, problem gambling severity, or alcohol use severity. We also observed no significant correlation (Spearman’s rho) between these scores and the parameter estimate values extracted from the significant clusters of activation obtained with each specific contrast (including the brain connectivity analyses).
The aim of this study was to examine how gambling availability impacts on the neural response during sports cue exposure. We used a paradigm in which participants (all football fans) viewed cues depicting games from European professional football leagues. Each of the cues represented games that were going to occur shortly after the scanning session. In the “betting” condition, the cues were available to bet on at the end of the block, whereas at the end of the block in the “watching” condition, participants chose the game they would prefer to watch.
When contrasting “betting” cues against “watching” cues, we observed significant activations in the right middle frontal gyrus and right frontal orbital cortex. These regions are usually activated during tasks that engage emotion regulation, executive, and inhibitory control processes (e.g., Kober et al., 2010). We also observed significant whole-brain activations in the caudate nucleus and anterior insula. Accordingly, activations within the caudate nucleus have been reported during reward anticipation while gambling (Limbrick-Oldfield et al., 2017; van Holst, Veltman, Büchel, van den Brink, and Goudriaan, 2012b). Our present findings are also consistent with previous studies showing that the anterior insula is involved during the processing of gambling (Goudriaan et al., 2010) and complex emotional cues (Deen, Pitskel, N. B., & Pelphrey, 2011). More specifically, we observed that the anterior insula is more strongly activated when individuals are viewing a sports event that is associated with a betting prospect. This result is in line with a theoretical account advancing that the anterior insula plays a key role in developing and updating motivational states with specific associated actions (Wager & Barrett, 2004), and most likely provides information necessary for goal-directed behavior (Droutman et al. 2015a, b; Nelson et al., 2010). Interestingly, we observed significant supramarginal gyrus activation when contrasting “watching” cues against “betting” cues. Since this brain area is involved in heightened visual processing (Makino, Yokosawa, Takeda, & Kumada, 2004; Roland & Gulyás 1995; Servos, Osu, Santi, & Kawato, 2002) and recognition of familiar objects (Sugiura, Shah, Zilles, & Fink, 2005) and memories (Yonelinas, Otten, Shaw, & Rugg, 2005), the present results suggest that reflecting on a game to “watch” (when exposed to the teams’ names and logos) might have required a higher level of semantic–visual processing than reflecting on which game to bet on.
Parametric contrasts were also undertaken to examine how brain activation was modulated by participants’ level of confidence in their chosen team for each of the “betting” trials, or by the degree of watching enjoyment for each cue presented during the “watching” trials. We observed patterns of activations that, taken together, should offer a representative brain map of activations showing how the neural response is modulated by participants’ level of interest toward a sporting event (i.e., on either confidence or enjoyment). Specifically, for these two parametric contrasts, we observed significant clusters of activations that have previously been reported in experimental tasks that engaged (1) emotion regulation and cognitive control (superior, middle, medial prefrontal cortices, and paracingulate gyrus; Everitt & Robbins, 2005; Koob & Le Moal, 2001; Lebreton, Abitbol, Daunizeau, & Pessiglione, 2015; Volkow, Fowler, & Wang, 2003), (2) feelings of desire, reward anticipation, or urge (anterior insula and caudate nucleus; Naqvi & Bechara, 2009; Paulus & Stewart, 2014; Verdejo-Garcia, Clark, & Dunn, 2012), and (3) the processing of visual information (the lateral occipital cortex).
PPI analyses were conducted using the right anterior insula as a seed. For the “betting trials minus watching trials” contrast, the PPI analyses highlighted significant positive couplings between the right anterior insula, parahippocampal gyrus, lingual gyrus, lateral occipital cortex, and occipital pole. One interpretation of these PPI results is that the exposure to “betting” trials elicited increased insular cortex coupling, as compared to the context of “watching” trials (i.e., a context-specific modulation of effective connectivity; Friston et al., 1997; see also Di, Huang, & Biswal, 2017; McLaren, Ries, Xu, & Johnson, 2012; D. V. Smith, Gseir, Speer, & Delgado, 2016). Another interpretation is that the insula modulated the parahippocampal, lingual, and occipital gyri’s responses to “betting” trials, as compared to the context of “watching” trials (i.e., a modulation of stimulus-specific responses; Friston et al., 1997; see also Di et al., 2017; McLaren et al., 2012; D. V. Smith et al., 2016). Interestingly, comparable insula-centered PPI with the parahippocampal and occipital gyri has been highlighted in the literature during tasks featuring emotional stimuli and face recognition (Dalgleish et al., 2017; Denny et al., 2014). Hence, the PPI patterns observed in the present study might reflect a higher engagement of stimulus recognition and perceptual saliency processes for the football game stimuli that were associated with a gambling opportunity, as compared to those that were not (i.e., the “watching” condition of the cue exposure task). Importantly, the parametric contrasts did not lead to significant PPI activation. This suggests that the pattern of insula-centered PPI was significantly modulated by the type of condition (“betting” vs. “watching”), but not by the reported levels of winning confidence and enjoyment associated with the betting and “watching” conditions, respectively.
In the present study, the exposure to stimuli during the “watching” and “betting” conditions did not simply involve watching cues (as it would in a pure test of cue reactivity; Jasinska et al., 2014), but also decision-making (i.e., reflecting on whether to select the game for betting or watching). This procedure was adopted in order to mimic the current offer of sports betting, which is highly accessible (e.g., betting is available simply by using a smartphone app) and also features a ubiquity of cues (e.g., advertisements) reminding you of this fact. Nevertheless, one limitation of this study is that the decision demands might have differed between the betting and watching trials of the cue exposure task. More specifically, exposure to betting trials was associated with the prospect of winning money, whereas exposure to the watching trials was not associated with any reward. Therefore, in the present study, deciding which game to bet on might have been more likely to elicit stronger activation of neural valuation and instrumental choice circuits than was deciding which game to watch. One possible direction for future studies could be to associate the exposure to watching trials with a concrete incentive, such as Internet or television access that would allow the participant to view the games he or she selected for watching. Another option would be to compare a condition associated with money (e.g., the “betting” condition from the present study) to a condition that was similar but did not involve monetary reward (e.g., participants might just have to select the team with the highest chance to win the game). This procedure would allow us to further advance our understanding on how sports betting impacts on the experience of watching sports. It would be also interesting to contrast different types of “betting” conditions (i.e., to include only “betting” trials within the cue exposure task). For instance, previous neuroimaging studies have shown that insular cortex activity is triggered by “frustration,” such as when individuals are being denied (or “blocked”) gambling opportunities (Weiss, Sullivan, & Tull, 2015; Xue, Lu, Levin, & Bechara, 2010; Yu, Mobbs, Seymour, Rowe, & Calder, 2014; see also Bierzynska et al., 2016). Through this procedure, we would also expect to obtain higher insula-centered connectivity for the “blocked” trials (as compared to trials available for betting), especially with the amygdala, which is a brain structure that has been implicated in the processing of frustration (Yu et al. 2014).
Another caveat of this study is that our sample was essentially constituted of male participants, which hampers generalization of the present results to the population of female football fans. It will also certainly be important to extend this research to a sample of individual with problem sports-bettors in which both extreme ends of the spectrum of gambling dependence will be well represented. Specifically, the results from the present study could be used as functional masks by future studies when assessing group activation differences in predefined regions of interest. This should be especially helpful for increasing the statistical power of studies that involve specific types of populations—that is, those that are difficult to recruit, usually resulting in small samples.
In summary, the present study extends previous neuroimaging work on reward availability by highlighting how the prospect of a gambling-related choice impacts on brain activations and on insula-centered functional connectivity. Specifically, the results from the present study demonstrate that sports betting cues trigger neural networks commonly observed in brain research on cognition and emotion. In addition, functional connectivity analyses further confirmed that the insula is a region that serves as a key hub for interactions among the brain networks involved in the processing of salient and motivational cues. Further research should build on the present findings in order to further examine how the high availability of ready-to-consume rewards in today’s environments exploits human hedonic tendencies.
This work was supported by the Belgian National Fund for Scientific Research (FNRS; Chargé de Recherche Grant). The authors thank Kristof De Mey for his help in recruiting participants and Pieter Vandemaele for his help in building the fMRI protocol. The experimental task code is available at github: https://github.com/dbrevers/sports_betting_study. The raw data are available at openneuro.org: https://openneuro.org/datasets/ds001247/versions/00001. The unthresholded statistical maps are available at Neurovault.org: https://neurovault.org/collections/3517/.
Addicott, M. A., Sweitzer, M. M., Froeliger, B., Rose, J. E., & McClernon, F. J. (2015). Increased functional connectivity in an insula-based network is associated with improved smoking cessation outcomes. Neuropsychopharmacology, 40, 2648–2656. https://doi.org/10.1038/npp.2015.114
Andersson, J. L. R., Jenkinson, M., & Smith, S. (2007a). Non-linear optimisation (FMRIB Technical Report TR07JA1). Oxford, UK: FMRIB Analysis Group. Retrieved from www.fmrib.ox.ac.uk/datasets/techrep
Andersson, J. L. R., Jenkinson, M., & Smith, S. (2007b). Non-linear registration, aka spatial normalisation (FMRIB Technical Report TR07JA2). Oxford, UK: FMRIB Analysis Group. Retrieved from www.fmrib.ox.ac.uk/datasets/techrep
Bechara, A. (2005). Decision making, impulse control and loss of willpower to resist drugs: A neurocognitive perspective. Nature Neuroscience, 8, 1458–1463. https://doi.org/10.1038/nn1584
Bickel, W. K., Miller, M. L., Yi, R., Kowal, B. P., Lindquist, D. M., & Pitcock, J. A. (2007). Behavioral and neuroeconomics of drug addiction: Competing neural systems and temporal discounting processes. Drug and Alcohol Dependence, 90, S85–S91. https://doi.org/10.1016/j.drugalcdep.2006.09.016
Bierzynska, M., Bielecki, M., Marchewka, A., Debowska, W., Duszyk, A., Zajkowski, W., … Kossut, M. (2016). Effect of frustration on brain activation pattern in subjects with different temperament. Frontiers in Psychology, 6, 1989. https://doi.org/10.3389/fpsyg.2015.01989
Blechert, J., Klackl, J., Miedl, S. F., & Wilhelm, F. H. (2016). To eat or not to eat: Effects of food availability on reward system activity during food picture viewing. Appetite, 99, 254–261. https://doi.org/10.1016/j.appet.2016.01.006
Brevers, D., Bechara, A., Kilts, C. D., Antoniali, V., Bruylant, P., Verbanck P., ... Noël, X. (2017). Competing motivations: Proactive response inhibition toward addiction-related stimuli in quitting-motivated individuals. Journal of Gambling Studies. Advance online publication. https://doi.org/10.1007/s10899-017-9722-2
Burke, C. J., & Tobler, P. N. (2011). Reward skewness coding in the insula independent of probability and loss. Journal of Neurophysiology, 106, 2415–2422. https://doi.org/10.1152/jn.00471.2011
Chang, L. J., Yarkoni, T., Khaw, M. W., & Sanfey, A. G. (2013). Decoding the role of the insula in human cognition: Functional parcellation and large-scale reverse inference. Cerebral Cortex, 23, 739–749. https://doi.org/10.1093/cercor/bhs065
Craig, A. D. B. (2009). How do you feel—now? The anterior insula and human awareness. Nature Reviews Neuroscience, 10, 59–70. https://doi.org/10.1038/nrn2555
Crockford, D. N., Goodyear, B., Edwards, J., Quickfall, J., & el-Guebaly, N. (2005). Cue-induced brain activity in pathological gamblers. Biological Psychiatry, 58, 787–795. https://doi.org/10.1016/j.biopsych.2005.04.037
Dalgleish, T., Walsh, N. D., Mobbs, D., Schweizer, S., van Harmelen, A.-L., Dunn, B.,… Stretton, J. (2017). Social pain and social gain in the adolescent brain: A common neural circuitry underlying both positive and negative social evaluation. Scientific Reports, 7, 42010. https://doi.org/10.1038/srep42010
Deen, B., Pitskel, N. B., & Pelphrey, K. A. (2011). Three systems of insular functional connectivity identified with cluster analysis. Cerebral Cortex, 21, 1498–1506. https://doi.org/10.1093/cercor/bhq186
Denny, B. T., Fan, J., Liu, X., Guerreri, S., Mayson, S. J., Rimsky, L., … Koenigsberg, H. W. (2014). Insulaamygdala functional connectivity is correlated with habituation to repeated negative images. Social Cognitive and Affective Neuroscience, 9(11), 1660–1667. https://doi.org/10.1093/scan/nst160
Di, X., Huang, J., & Biswal, B. B. (2017). Task modulated brain connectivity of the amygdala: A meta-analysis of psychophysiological interactions. Brain Structure and Function, 222, 619–634. https://doi.org/10.1007/s00429-016-1239-4
Droutman, V., Bechara, A., & Read, S. J. (2015a). Roles of the different sub-regions of the insular cortex in various phases of the decision-making process. Frontiers in Behavioral Neuroscience, 9, 309. https://doi.org/10.3389/fnbeh.2015.00309
Droutman, V., Read, S. J., & Bechara, A. (2015b). Revisiting the role of the insula in addiction. Trends in Cognitive Sciences, 19, 414–420. https://doi.org/10.1016/j.tics.2015.05.005
Dwyer, B., Shapiro, S. L., & Drayer, J. (2017). Daily fantasy football and self-reported problem behavior in the United States. Journal of Gambling Studies. Advance online publication. https://doi.org/10.1007/s10899-017-9720-4
Dwyer, B., & Weiner, J. (2018). Daily grind: A comparison of causality orientations, emotions, and fantasy sport participation. Journal of Gambling Studies, 34, 1–20. https://doi.org/10.1007/s10899-017-9684-4
Everitt, B. J., & Robbins, T. W. (2005). Neural systems of reinforcement for drug addiction: From actions to habits to compulsion. Nature Neuroscience, 8, 1481–1489. https://doi.org/10.1038/nn1579
Ferris, J., & Wynne, H. (2001). The Canadian Problem Gambling Index: Final report. Ottawa, ON: Canadian Centre on Substance Abuse.
Friston, K. J., Buechel, C., Fink, G. R., Morris, J., Rolls, E., & Dolan, R. J. (1997). Psychophysiological and modulatory interactions in neuroimaging. NeuroImage, 6, 218–229. https://doi.org/10.1006/nimg.1997.0291
Goudriaan, A. E., de Ruiter, M. B., van den Brink, W., Oosterlaan, J., & Veltman, D. J. (2010). Brain activation patterns associated with cue reactivity and craving in abstinent problem gamblers, heavy smokers and healthy controls: An fMRI study. Addiction Biology, 15, 491–503. https://doi.org/10.1111/j.1369-1600.2010.00242.x
Grosenick, L., Greer, S., & Knutson, B. (2008). Interpretable classifiers for FMRI improve prediction of purchases. IEEE Transactions on Neural Systems and Rehabilitation Engineering, 16, 539–548. https://doi.org/10.1109/TNSRE.2008.926701
Hayashi, T., Ko, J. H., Strafella, A. P., & Dagher, A. (2013). Dorsolateral prefrontal and orbitofrontal cortex interactions during self-control of cigarette craving. Proceedings of the National Academy of Sciences, 110, 4422–4427. https://doi.org/10.1073/pnas.1212185110
Hing, N., Li, E., Vitartas, P., & Russell, A. M. T. (2017a). On the spur of the moment: Intrinsic predictors of impulse sports betting. Journal of Gambling Studies. Advance online publication. https://doi.org/10.1007/s10899-017-9719-x
Hing, N., Russell, A. M., & Browne, M. (2017b). Risk factors for gambling problems on online electronic gaming machines, race betting and sports betting. Frontiers in Psychology, 8, 779. https://doi.org/10.3389/fpsyg.2017.00779
Hing, N., Russell, A. M. T., Lamont, M., & Vitartas, P. (2017c). Bet anywhere, anytime: An analysis of Internet sports bettors’ responses to gambling promotions during sports broadcasts by problem gambling severity. Journal of Gambling Studies, 33, 1051–1065. https://doi.org/10.1007/s10899-017-9671-9
James, R. J. E., O’Malley, C., & Tunney, R. J. (2016). Understanding the psychology of mobile gambling: A behavioural synthesis. British Journal of Psychology, 108, 608–625. https://doi.org/10.1111/bjop.12226
Janes, A. C., Pizzagalli, D. A., Richardt, S., Frederick, B. D., Chuzi, S., Pachas, G., … Kaufman, M. J. (2010). Brain reactivity to smoking cues prior to smoking cessation predicts ability to maintain tobacco abstinence. Biological Psychiatry, 67, 722–729. https://doi.org/10.1016/j.biopsych.2009.12.034
Jasinska, A. J., Stein, E. A., Kaiser, J., Naumer, M. J., & Yalachkov, Y. (2014). Factors modulating neural reactivity to drug cues in addiction: A survey of human neuroimaging studies. Neuroscience & Biobehavioral Reviews, 38, 1–16. https://doi.org/10.1016/j.neubiorev.2013.10.013
Jenkinson, M. (2004). Improving the registration of B0-disorted EPI images using calculated cost function weights. Paper presented at Tenth International Conference on Functional Mapping of the Human Brain, Budapest, Hungary.
Jenkinson, M., Bannister, P., Brady, M., & Smith, S. (2002). Improved optimization for the robust and accurate linear registration and motion correction of brain images. NeuroImage 17, 825–841. https://doi.org/10.1006/nimg.2002.1132
Jenkinson, M., & Smith, S. (2001). A global optimisation method for robust affine registration of brain images. Medical Image Analysis, 5, 143–156.
Knutson, B., Rick, S., Wimmer, G. E., Prelec, D., & Loewenstein, G. (2007). Neural predictors of purchases. Neuron, 53, 147–156. https://doi.org/10.1016/j.neuron.2006.11.010
Kober, H., Mende-Siedlecki, P., Kross, E. F., Weber, J., Mischel, W., Hart, C. L., & Ochsner, K. N. (2010). Prefrontal-striatal pathway underlies cognitive regulation of craving. Proceedings of the National Academy of Sciences, 107, 14811–14816. https://doi.org/10.1073/pnas.1007779107
Koob, G. F., & Le Moal, M. (2001). Drug addiction, dysregulation of reward, and allostasis. Neuropsychopharmacology, 24, 97–129. https://doi.org/10.1016/S0893-133X(00)00195-0
Lebreton, M., Abitbol, R., Daunizeau, J., & Pessiglione, M. (2015). Automatic integration of confidence in the brain valuation signal. Nature Neuroscience, 18, 1159–1167. https://doi.org/10.1038/nn.4064
Limbrick-Oldfield, E. H., Mick, I., Cocks, R. E., McGonigle, J., Sharman, S. P., Goldstone, A. P.,… Clark, L. (2017). Neural substrates of cue reactivity and craving in gambling disorder. Translational Psychiatry, 7, e992. https://doi.org/10.1038/tp.2016.256
Makino, Y., Yokosawa, K., Takeda, Y., & Kumada, T. (2004). Visual search and memory search engage extensive overlapping cerebral cortices: An fMRI study. NeuroImage, 23, 525–533.
McBride, D., Barrett, S. P., Kelly, J. T., Aw, A., & Dagher, A. (2006). Effects of expectancy and abstinence on the neural response to smoking cues in cigarette smokers: An fMRI study. Neuropsychopharmacology, 31, 2728–2738. https://doi.org/10.1038/sj.npp.1301075
McClure, S. M., & Bickel, W. K. (2014). A dual-systems perspective on addiction: Contributions from neuroimaging and cognitive training. Annals of the New York Academy of Sciences, 1327, 62–78. https://doi.org/10.1111/nyas.12561
McLaren, D. G., Ries, M. L., Xu, G., & Johnson, S. C. (2012). A generalized form of context-dependent psychophysiological interactions (gPPI): A comparison to standard approaches. NeuroImage, 61, 1277–1286. https://doi.org/10.1016/j.neuroimage.2012.03.068
Menon, V., & Uddin, L. Q. (2010). Saliency, switching, attention and control: A network model of insula function. Brain Structure and Function, 214, 655–667. https://doi.org/10.1007/s00429-010-0262-0
Metcalfe, J., & Mischel, W. (1999). A hot/cool-system analysis of delay of gratification: Dynamics of willpower. Psychological Review, 106, 3–19. https://doi.org/10.1037/0033-295X.106.1.3
Naqvi, N. H., & Bechara, A. (2009). The hidden island of addiction: The insula. Trends in Neurosciences, 32, 56–67. https://doi.org/10.1016/j.tins.2008.09.009
Naqvi, N. H., & Bechara, A. (2010). The insula and drug addiction: An interoceptive view of pleasure, urges, and decision-making. Brain Structure and Function, 214, 435–450. https://doi.org/10.1007/s00429-010-0268-7
Naqvi, N. H., Gaznick, N., Tranel, D., & Bechara, A. (2014). The insula: A critical neural substrate for craving and drug seeking under conflict and risk. Annals of the New York Academy of Sciences, 1316, 53–70. https://doi.org/10.1111/nyas.12415
Nelson, S. M., Dosenbach, N. U. F., Cohen, A. L., Wheeler, M. E., Schlaggar, B. L., & Petersen, S. E. (2010). Role of the anterior insula in task-level control and focal attention. Brain Structure and Function, 214(5–6), 669–680. https://doi.org/10.1007/s00429-010-0260-2
Noël, X., Brevers, D., & Bechara, A. (2013a). A neurocognitive approach to understanding the neurobiology of addiction. Current Opinion in Neurobiology, 23, 632–638. :https://doi.org/10.1016/j.conb.2013.01.018
Noël, X., Brevers, D., & Bechara, A. (2013b). A triadic neurocognitive approach to addiction for clinical interventions. Frontiers in Psychiatry, 4, 179. https://doi.org/10.3389/fpsyt.2013.00179
Paulus, M. P., & Frank, L. R. (2006). Anterior cingulate activity modulates nonlinear decision weight function of uncertain prospects. NeuroImage, 30, 668–677. https://doi.org/10.1016/j.neuroimage.2005.09.061
Paulus, M. P., & Stewart, J. L. (2014). Interoception and drug addiction. Neuropharmacology, 76(Part B),342–350. https://doi.org/10.1016/j.neuropharm.2013.07.002
Roland, P. E., & Gulyás, B. (1995). Visual memory, visual imagery, and visual recognition of large field patterns by the human brain: Functional anatomy by positron emission tomography. Cerebral Cortex, 5, 79–93. https://doi.org/10.1093/cercor/5.1.79
Saunders, J. B., Aasland, O. G., Babor, T. F., de la Fuente, J. R., & Grant, M. (1993). Development of the Alcohol Use Disorders Identification Test (AUDIT): WHO Collaborative Project on Early Detection of Persons with Harmful Alcohol Consumption—II. Addiction, 88, 791–804.
Servos, P., Osu, R., Santi, A., & Kawato, M. (2002). The neural substrates of biological motion perception: An fMRI study. Cerebral Cortex, 12, 772–782. https://doi.org/10.1093/cercor/12.7.772
Sescousse, G., Barbalat, G., Domenech, P., & Dreher, J.-C. (2013). Imbalance in the sensitivity to different types of rewards in pathological gambling. Brain, 136, 2527–2538. https://doi.org/10.1093/brain/awt126
Shaffer, H. J., LaPlante, D. A., LaBrie, R. A., Kidman, R. C., Donato, A. N., & Stanton, M. V. (2004). Toward a syndrome model of addiction: Multiple expressions, common etiology. Harvard Review of Psychiatry, 12, 367–374. https://doi.org/10.1080/10673220490905705
Smith, B. W., Mitchell, D. G. V., Hardin, M. G., Jazbec, S., Fridberg, D., Blair, R. J. R., & Ernst, M. (2009). Neural substrates of reward magnitude, probability, and risk during a wheel of fortune decision-making task. NeuroImage, 44, 600–609. https://doi.org/10.1016/j.neuroimage.2008.08.016
Smith, D. V., Gseir, M., Speer, M. E., & Delgado, M. R. (2016). Toward a cumulative science of functional integration: A meta-analysis of psychophysiological interactions. Human Brain Mapping, 37, 2904–2917. https://doi.org/10.1002/hbm.23216
Sugiura, M., Shah, N. J., Zilles, K., & Fink, G. R. (2005). Cortical representations of personally familiar objects and places: Functional organization of the human posterior cingulate cortex. Journal of Cognitive Neuroscience, 17, 183–198.
Symmonds, M., Wright, N. D., Bach, D. R., & Dolan, R. J. (2011). Deconstructing risk: Separable encoding of variance and skewness in the brain. NeuroImage, 58, 1139–1149. https://doi.org/10.1016/j.neuroimage.2011.06.087
van Holst, R. J., van Holstein, M., van den Brink, W., Veltman, D. J., & Goudriaan, A. E. (2012a). Response inhibition during cue reactivity in problem gamblers: An fMRI study. PLoS ONE, 7, e30909. https://doi.org/10.1371/journal.pone.0030909
van Holst, R. J., Veltman, D. J., Büchel, C., van den Brink, W., & Goudriaan, A. E. (2012b). Distorted expectancy coding in problem gambling: Is the addictive in the anticipation? Biological Psychiatry, 71, 741–748. https://doi.org/10.1016/j.biopsych.2011.12.030
Verdejo-Garcia, A., Clark, L., & Dunn, B. D. (2012). The role of interoception in addiction: A critical review. Neuroscience & Biobehavioral Reviews, 36, 1857–1869. https://doi.org/10.1016/j.neubiorev.2012.05.007
Volkow, N. D., Fowler, J. S., & Wang, G. J. (2003). The addicted human brain: Insights from imaging studies. Journal of Clinical Investigation, 111, 1444–1451. https://doi.org/10.1172/JCI18533
Wager, T. D., & Barrett, L. F. (2004). From affect to control: Functional specialization of the insula in motivation and regulation. Unpublished paper. Retrieved from www.affective-science.org/pubs/2004/Wager_Edfest_submitted_copy.pdf
Weiss, N. H., Sullivan, T. P., & Tull, M. T. (2015). Explicating the role of emotion dysregulation in risky behaviors: A review and synthesis of the literature with directions for future research and clinical practice. Current Opinion in Psychology, 3, 22–29. https://doi.org/10.1016/j.copsyc.2015.01.013
Wilcox, C. E., Teshiba, T. M., Merideth, F., Ling, J., & Mayer, A. R. (2011). Enhanced cue reactivity and fronto-striatal functional connectivity in cocaine use disorders. Drug and Alcohol Dependence, 115, 137–144. https://doi.org/10.1016/j.drugalcdep.2011.01.009
Wilson, S. J., & Sayette, M. A. (2015). Neuroimaging craving: Urge intensity matters. Addiction, 110, 195–203. https://doi.org/10.1111/add.12676
Wilson, S. J., Sayette, M. A., Delgado, M. R., & Fiez, J. A. (2005). Instructed smoking expectancy modulates cue-elicited neural activity: A preliminary study. Nicotine and Tobacco Research, 7, 637–645. https://doi.org/10.1080/14622200500185520
Wu, C. C., Bossaerts, P., & Knutson, B. (2011). The affective impact of financial skewness on neural activity and choice. PLoS ONE, 6, e16838. https://doi.org/10.1371/journal.pone.0016838
Wu, C. C., Sacchet, M. D., & Knutson, B. (2012). Toward an affective neuroscience account of financial risk taking. Frontiers in Neuroscience, 6, 159. https://doi.org/10.3389/fnins.2012.00159
Xue, G., Lu, Z., Levin, I. P., & Bechara, A. (2010). The impact of prior risk experiences on subsequent risky decision-making: The role of the insula. NeuroImage, 50, 709–716. https://doi.org/10.1016/j.neuroimage.2009.12.097
Yalachkov, Y., Kaiser, J., & Naumer, M. J. (2012). Functional neuroimaging studies in addiction: Multisensory drug stimuli and neural cue reactivity. Neuroscience & Biobehavioral Reviews, 36, 825–835. https://doi.org/10.1016/j.neubiorev.2011.12.004
Yonelinas, A. P., Otten, L. J., Shaw, K. N., & Rugg, M. D. (2005). Separating the brain regions involved in recollection and familiarity in recognition memory. Journal of Neuroscience, 25, 3002–3008. https://doi.org/10.1523/JNEUROSCI.5295-04.2005
Yu, R., Mobbs, D., Seymour, B., Rowe, J. B., & Calder, A. J. (2014). The neural signature of escalating frustration in humans. Cortex, 54, 165–178. https://doi.org/10.1016/j.cortex.2014.02.013
Zelle, S. L., Gates, K. M., Fiez, J. A., Sayette, M. A., & Wilson, S. J. (2017). The first day is always the hardest: Functional connectivity during cue exposure and the ability to resist smoking in the initial hours of a quit attempt. NeuroImage, 151, 24–32. https://doi.org/10.1016/j.neuroimage.2016.03.015
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Brevers, D., Herremans, S.C., He, Q. et al. Facing temptation: The neural correlates of gambling availability during sports picture exposure. Cogn Affect Behav Neurosci 18, 718–729 (2018). https://doi.org/10.3758/s13415-018-0599-z
- Sports betting
- Reward availability
- Functional connectivity
- Insular cortex