Abstract
Purpose of Review
Alcohol and Addiction Research Domain Criteria (AARDoC) is a transdiagnostic, circuits-based framework for studying addictive behaviors. We examined parallels in individual differences that might increase susceptibility to FA and other addictive disorders using the following units of analysis in AARDoC domains: craving, relative reinforcing value of food and attention bias in the incentive salience domain; decisional impulsivity (delay discounting) and inhibitory control (Go-No-Go, Conner’s Continuous Performance Test, and the flanker task) in the executive function domain; and emotion dysregulation and negative urgency in the negative emotionality domain.
Recent Findings
There are a number of parallels between FA and other addictions in the incentive salience and negative emotionality domains, but somewhat divergent findings in the executive function domain. Trauma appears to be an important environmental stressor in maintenance of FA.
Summary
AARDoC may be a useful organizing framework for studying addictions, including FA. Future studies should incorporate other units of analysis to better characterize FA.
Similar content being viewed by others
Avoid common mistakes on your manuscript.
Introduction
Over the past decade, the addictive nature of ultra-processed foods has been studied using the Yale Food Addiction Scale [1, 2]—a validated measure that has become standard for assessing the presence and severity of food addiction (FA). Ultra-processed foods have been defined as foods with five or more ingredients that include substances not commonly used in culinary preparations [3]. These foods are proposed to have the most addictive potential due to their pharmacokinetic properties, similar to the properties of drugs of abuse (e.g., rapid rate of absorption) [4]. While FA has been a useful research construct in understanding maladaptive eating patterns contributing to obesity, it is not a diagnosis recognized in the DSM-5 [5] nor are there any empirically supported treatment protocols specifically to address FA. However, given the advent of transdiagnostic approaches to psychological interventions, it may be more important to focus on tailoring interventions to specific characteristics of FA (some of which overlap with symptoms of eating disorders) than to the diagnosis itself. Such approaches may facilitate the development of more personalized interventions that are, nevertheless, grounded in empirical findings. We propose using elements from the Research Domain Criteria (RDoC) framework [6], and, more specifically, from the Alcohol and Addiction Research Domain Criteria (AARDoC) model [7, 8], to briefly review the current state of knowledge on the neurobiologically based individual differences underlying FA and other addictive disorders, and to assess the similarities and differences in those characteristics between FA and other addictive disorders. Based on these findings, we also outline directions for future research.
The RDoC framework was proposed by the National Institutes of Mental Health [9] as an alternative to diagnosis-based approaches to characterizing psychopathology. RDoC proposes several empirically based domains subsuming various constructs that can be measured using “units of analysis” at different levels (e.g., behavioral, circuit-level, genetic). The RDoC approach is geared toward discerning the mechanisms of psychopathology based on the current neurobiological findings (https://www.nimh.nih.gov/research/research-funded-by-nimh/rdoc). The five RDoC domains include: negative valence, positive valence, cognitive systems, systems for social processes, and arousal/modulatory systems [9]. In the alcohol field, an addiction-specific RDoC model and assessment framework have been proposed as deeming further study [7, 10]. The AARDoC model [7] focuses on three domains of risk factors for addiction: incentive salience (the equivalent of positive valence), executive function (the equivalent of cognitive systems), and negative emotionality (the equivalent of negative valence). These domains are based on neurobiological models of addiction that emphasize the dysfunction of the reward and stress systems in addiction, and correspond to distinct phases of the “addiction cycle”: incentive salience to the binge/intoxication phase, negative emotionality to the withdrawal/negative affect phase, and executive function to the preoccupation/anticipation phase [11, 12]. The AARDoC model also acknowledges the influence of environmental factors, such as stress exposure. Kwako and others [10] have proposed a battery of assessments falling under the three AARDoC domains (see Table 2 in [10], as a starting point for circuits-based assessment of addictions as disorders of impulsivity and compulsivity.
In this article, we will “try on” the AARDoC framework to the construct of FA in order to examine the parallels and potential differences between processes present in FA and alcohol use disorder. We have identified several units of analysis to review in the context of FA within the AARDoC domains (see Table 1). Therefore, we will use the AARDoC framework to examine individual differences in neurobiologically based mechanisms underlying FA and other addictive disorders (using most recent findings on FA), while also acknowledging that we will not review all units of analysis (partially because not all of them have been used in the context of FA, and partially because we wanted to focus on the most salient ones). We will also discuss how these domains may interact with the environmental factor of trauma.
Incentive Salience
Background
Incentive sensitization models have been adapted to the eating dysregulation field from addiction studies [13], and they posit that cues of the addictive substance capture attention and trigger food cravings more readily if they carry a heightened incentive value. Incentive salience refers to a learning process in which previously neutral cues become imbued with meaning (i.e., salience), making them “wanted”. There is extensive evidence indicating not just heightened incentive salience in individuals with alcohol use disorders but also associations between indicators of incentive salience (e.g., craving) and worse outcomes [13,14,15]. Incentive salience has been studied to a lesser degree in FA. In this review, we will concentrate on subjectively reported craving, relative reinforcing value of food, and attention bias to food as units of analysis for the incentive salience domain.
Craving
Much of the support for FA highlights the fact that there are many similarities between cravings (i.e., a very strong or overwhelming desire) to consume food and cravings to use substances of abuse. Craving is thought to be a hallmark feature of addiction and was added as a diagnostic symptom of alcohol and substance use disorders in DSM-5 [5]. It is believed to play an important role in substance use and relapse after a period of abstinence, with individuals who experience greater cravings also being at higher risk of relapsing [16]. Many have theorized that addictive substances contribute to neuroadaptations in the reward system—hijack the brain’s natural reward system, so to speak—and that food cravings operate similarly to cravings that occur in addiction to psychoactive substances [17,18,19,20]. On the behavioral level, craving represents associative learning: external (environmental) and internal (emotional, cognitive) stimuli paired with consumption repeatedly acquire motivational characteristics, which can lead to both a strong desire to use, i.e., craving [13].
When considering FA, individuals who self-identify as “chocolate addicts” experience more craving and negative affect when presented with chocolate cues relative to control participants [21]. Meeting the FA status on the YFAS is also associated with higher food craving [22, 23]. Interestingly, although individuals with FA experience more food cravings, they do not expect to achieve positive reinforcement from eating [24]. Craving is also a mediator between genetic vulnerability toward food reward sensitivity (expressed by the multilocus genetic profile score [MLGP]) and FA [25]. Reward sensitivity refers to an individual’s tendency to seek highly rewarding things (e.g., experiences, foods, substances) [26]. In the context of FA, individuals with higher reward sensitivity may be more sensitive to the rewarding properties of food, particularly highly palatable and highly caloric ones. Indeed, symptoms of FA correlate with anticipated food reward based on activation in the brain’s reward circuits [27]. Accordingly, in FA, just as in substance use disorders, craving for the reinforcing aspects of high-calorie foods and substances, respectively, are important factors in seeking out a substance and motivating consumption, contributing to an individual’s progression from an inherent biological susceptibility toward rewards to compulsive food seeking characteristic of addictive behaviors. Thus, craving is an individual difference that may increase susceptibility to negative outcomes related to FA as it does in other addictive behaviors. Therefore, it may be a useful unit of analysis, particularly when considering treatment outcomes in FA.
Relative Reinforcing Value of Food
People are willing to work for reinforcers that they want up to a certain point. Determining how far someone will go before they decide the reinforcer is not worth the effort demonstrates the reinforcing value of that item. Relative reinforcing value compares two available reinforcers (e.g., two types of food or food and an alternate reinforcer) [28]. Food reinforcement can also be measured using demand curves that demonstrate how much of a reinforcer they would purchase as a function of its price [29]. The demand curves are generated based on purchase tasks, and several indices of demand are produced to evaluate food reinforcement. Higher demand for addictive substances is associated with increased use of that substance and greater problem severity [30, 31]. Similarly, finding food highly reinforcing is associated with higher body mass index (BMI) [32, 33]. Relative to those who do not meet FA criteria, individuals with FA report greater reinforcement value based on nearly all demand indices for sweet and salty snacks [34]. Dopamine receptor gene (DRD2) and its relationship to addictive behavior such as opioid use disorder have also been studied in the context of addiction [35], and one recent study demonstrated that while FA was not associated with the DRD2 polymorphism, women with obesity who were carriers of a particular allele had higher snack food reinforcement relative to non-carriers [36]. Another study that assessed FA and reward-related eating found that while FA was not associated with diet quality during pregnancy or postpartum, greater reward-related eating was associated with reduced diet quality during pregnancy [37]. Therefore, relative reinforcing value of food should be examined more systematically as a promising unit for analysis of FA symptoms.
Attention Bias to Food
Attention bias is the tendency to attend selectively to stimuli that have acquired salience or meaning [38], and a process that has been shown to contribute to substance misuse [39, 40]. There is also evidence that attention bias to food is stronger in individuals with binge eating behaviors compared to those without [41]. Even though binge eating and FA often co-occur [42], there are only two studies to date that examined attention bias in FA [43, 44], and only one of these used the YFAS to assess the presence of FA [43]. In the first study, women with and without FA underwent both, a neutral and a sad mood induction prior to the attention bias task, and their reactions on the task were measured using eye-tracking. The study found that before the mood induction, participants with FA attended to food images significantly more than those without FA and that they had difficulty with disengaging from images of unhealthy foods, compared to those without FA (but that unhealthy food images initially captured the attention of both groups equally). This may suggest a general hypervigilance to food cues in the FA group, coupled with difficulties with redirecting attention away from the unhealthy food cues. Following the sad mood induction, participants with FA increased their sustained attention to unhealthy foods and decreased their sustained attention to healthy foods, suggesting an emotion regulation function of unhealthy foods in that group. For participants without FA, sad mood induction had no significant effect on sustained attention to healthy or unhealthy food cues. This suggests that individuals without FA may primarily regulate their emotions with ways other than food. In another study, no effect of FA diagnosis was found on attention bias to pictures of chocolate, such that participants in the control condition had similar reaction times to individuals with FA [44]. However, in that study, participants self-identified their FA and the YFAS was not used to verify FA status. Given all findings in the attention bias literature, it appears premature to draw conclusions regarding increased attention bias to food in individuals with FA. More studies are warranted using attention bias paradigms due to their potential to measure incentive salience using non-self-report measures.
Executive Function
Background
Executive function can be measured in several ways and includes cognitive control and decision making, key facets of self-regulation (i.e., self-control) [45]. Impulsivity and self-regulation, which typically refer to one’s capacity to regulate their impulses and desires, have shown strong associations with addictive disorders and behavior [46,47,48]. Executive function has been investigated in the context of FA as well. For instance, among recommended treatment strategies for FA is targeting four core features: craving, impulsivity, compulsivity, and motivation,this includes the recommendation to target impulsivity as a personality trait [49]. As impulsivity has several facets, including the trait-based personality facet (covered in Sect. 4.3.), we will concentrate on decisional (delay discounting) and behavioral (difficulties in inhibitory control) impulsivity [50] as manifestations of executive dysfunction.
Delay Discounting
One area of executive dysfunction is impulsive choice. This reflects a tendency to make impulsive choices that do not support one’s long-term interests. This type of difficulty with self-control is known as discounting of delayed rewards (i.e., one’s tendency to choose less valuable rewards that are available now over more valuable rewards that could be received after a delay [51]. If an individual decides to select a smaller reward on the basis of its immediate receipt, forgoing a larger reward that would have been available later, this is thought to demonstrate difficulties with decision making and behavioral control. A small number of studies have examined the relationship between FA and executive dysfunction using measures of impulsive choice. These studies have generally suggested a small relationship between delay discounting and FA [22, 52,53,54,55]. In addition, a recent meta-analysis suggested aggregate correlations between FA and steeper discounting were significant but small in magnitude (r = 0.12) [56]. This is in contrast to a meta-analysis that concluded a robust association between delayed reward discounting across many addictive substances [46]. As relatively few studies have been conducted regarding impulsive choice and FA, more research is needed to determine whether delay discounting may be a transdiagnostic unit of analysis for FA symptomatology.
Inhibitory Control
Another area of executive dysfunction is inhibitory control. This refers to the ability to inhibit impulse choices when needed. The inability to inhibit specific behaviors, including the use of a substance itself, is considered a key component in both addictions to alcohol/substances as well as in behavioral addictions (e.g., video games, the internet) with abnormalities in the prefrontal cortex thought to play a role in the loss of behavioral control that often occurs [57]. This form of impulsivity, often thought of in the context of “inhibition” and “disinhibition,” relates to active and willful processes of cognitive control during which the prefrontal cortex must enact control over a particular response [58]. Several studies have measured cognitive control and impulsive action using tasks such as a Go/No-Go task [59]. While considerable variation between task stimuli exists, the general premise in this type of task is to press a button for certain stimulus but inhibit pressing for others. Failing to react (i.e., press the button) at the target stimulus (i.e., an omission error) is thought to reflect inattention, whereas failing to inhibit pressing the button when the indicated stimulus is shown (i.e., a commission error) is thought to reflect difficulty with inhibitory control. These studies have generally failed to find a relationship between FA and inhibitory control/failed inhibition [53, 55, 60,61,62,63]. Another similar task, The Conners’ Continuous Performance Task [64], similarly requires pressing a key when a stimulus is present and inhibiting pressing when absent. One study comparing individuals with obesity with and without FA failed to find differences between the groups on commission errors when using this task [65]. Another inhibitory control task, the Eriksen flanker task [66], requires individuals to press a key with their left index finger and if the central letter in a series of letters presented is one letter (e.g., “S”) and with their right index finger if it is a different letter (e.g., “H”). On this task, individuals with FA were found to make more errors overall in one research study [67]. Past research of individuals with addictive disorders has shown the individuals who smoke cigarettes made more errors on incongruent tasks than individuals who did not smoke cigarettes [66]. Thus, the preponderance of available evidence to date does not suggest that individuals with FA show similar deficits on tasks of inhibitory control as is seen in other addictions.
Negative Emotionality
Background
The AARDoC domain of negative emotionality has been proposed to represent the withdrawal/negative affect phase of the “addiction cycle” [7]. This constitutes the presence of physiological or psychological symptoms in response to substance deprivation or in order to relieve these symptoms [5]. Negative affect regulation is one of the main processes proposed to contribute to the transition from casual to compulsive substance use. The opponent-process theories hypothesize that substances of abuse at first activate the neurocircuitry associated with reward, thus producing the feelings of “high”, contentment, and well-being [12]. To downregulate the reward neurocircuitry, the opponent process involving the stress neurocircuitry follows, contributing to increases in negative affect, vigilance, and tension [68]. The negative reinforcement theory of addiction proposes that in addition to the withdrawal state eliciting negative affect coupled with craving, negative affective states (e.g., disappointment, anxiety, frustration) also become conditioned cues eliciting urges to use the substance [69]. In fact, this theory was reformulated into the affective processing theory of negative reinforcement, proposing that negative affect is the main motivational factor contributing to drug-seeking behavior [70]. With repeated use of a substance, individuals detect a negative affective state (conditioned stimulus) automatically (i.e., outside of awareness) and identify craving (conditioned response) that has been coupled with it but not necessarily the affective state [70]. Craving seems uncontrollable because it seemingly “comes out of nowhere.” Therefore, in this model, negative affect, and not physical withdrawal, is seen as the motivational core of substance misuse [71].
Emotion Dysregulation
In the alcohol use disorders field, the affect regulation model has been extensively supported with data [72,73,74], using various units of analysis. While there is evidence of affective processing theory in binge eating, both in experimental and ecological momentary assessment studies [75, 76], the evidence of this process strictly in FA has been studied to a lesser extent. However, there are numerous studies indicating an association between negative emotionality and food addiction. Therefore, we will review studies that utilized self-report measures of negative emotionality, including symptoms of anxiety, depression, and stress.
DASS-21 is a transdiagnostic self-report measure of negative emotionality [77], measuring levels of depression, anxiety, and stress. In a large Australian sample, high levels of depression measured by DASS-21 were associated with greater odds of having severe FA [78]. In a sample of individuals with type 2 diabetes mellitus, the level of depression, anxiety, and stress reported on DASS-21 increased with the severity of food addiction [79]. More broadly, a meta-analysis of comorbidity between FA and mental health disorders found significant correlations between FA and depression as well as FA and anxiety [80]. Among individuals seeking addictive eating treatment, those with higher DASS-21 scores were less likely to engage in treatment [81]. Overall, there is considerable evidence for the association between FA symptom severity and the severity of negative emotionality, although it is impossible to discern the temporal occurrence of these constructs as they relate to each other.
Negative Urgency
Several studies have examined self-reported impulsivity on the trait level. One measure commonly used for this is the UPPS Impulsive Behavior Scale (UPPS; [82]) that generates subscales including urgency (positive and negative), sensation seeking, lack of premeditation, and lack of perseverance [83, 84]. In the AUD literature, there is extensive evidence that increased level of urgency, and negative urgency in particular (i.e., a tendency to act rashly when experiencing negative emotions), are associated with problematic drinking and AUD symptoms [47, 85]. Research has suggested that negative urgency can impact problematic substance use for a variety of substances [86]. Similarly, across numerous studies, negative urgency has been shown to have a relationship with FA [54, 55, 63, 87,88,89,90,91]. Related, in one study of FA, negative urgency, emotional eating, and FA associations contributed to reduced quality of life [90]. Taken together, negative urgency appears strongly associated with FA, both directly and indirectly, consistent with findings in substance use disorders. Therefore, it may be a useful unit of analysis of the negative emotionality (negative valence) domain.
Interactions of Negative Emotionality Domain with Other Domains
It is important to recognize ways in which domains may interact with one another. Some examples include findings that negative affect increases incentive salience of high-calorie foods in individuals with FA [43] or that craving is not associated with anticipation of reward in individuals with FA [24], potentially reflecting the transition to compulsive food seeking marked by motivation to decrease negative affect [70]. In fact, some [71] have suggested that reactivity to food cues associated with increased activation in the amygdala is an important element of compulsive food intake and evidence for the opponent-process theory, whereby consumption becomes a strategy to regulate negative emotions. Such negative emotional states in turn may contribute to impulsive food-seeking behavior.
Stress and Trauma as Environmental Factors
In addition to aversive emotional states, stressful events in the environment (e.g., adverse childhood events, traumatic experiences) may promote behaviors consistent with food addiction and contribute to neural adaptations in the stress-reward neurocircuitry that might increase susceptibility to FA in some individuals. The link between trauma and alcohol/substance use disorders has been extensively documented [92, 93]. Emerging body of literature is finding similar links between trauma and FA. A cross-sectional retrospective study found a positive relationship between childhood abuse (physical and sexual) and FA symptoms in women [94], and exposure to trauma earlier in life is associated with more FA symptoms [95]. Among Black women with type 2 diabetes, women with FA reported higher severity of childhood trauma and had higher insulin resistance [96]. FA also mediated the relationship between severity of childhood trauma and insulin resistance in that sample [96]. Exposure to at least one traumatic event and lifetime presence of at least one posttraumatic stress disorder (PTSD) symptom have been associated with higher prevalence of FA symptoms [95, 97]. In primarily male veteran samples, current and lifetime diagnoses of PTSD were associated with FA symptoms [98, 99]. In a clinical sample of men and women veterans, those with FA (18% of the overall sample) reported higher severity of PTSD and depression [100]. Overall, recent findings consistently indicate an overlap between experience of trauma and food addiction symptoms and suggest that men are as susceptible to FA in trauma-exposed samples as women (e.g., [98,99,100].
It has been proposed that changes in the neuroendocrine system that develop as a result of traumatic experiences in some individuals are a vulnerability factor to experiencing negative metabolic outcomes [101]. As with alcohol or other psychoactive substances, palatable food’s soothing properties [102, 103] may serve as an emotion regulation (via negative reinforcement) strategy among trauma survivors trying to avoid trauma-related emotions, thoughts, and memories [104]. Over time, using food in such a manner becomes a habit consistent with the opponent-process theory [71] whereby negative affective states and PTSD symptoms become cues to seek highly palatable food. Overall, more research is needed on the mechanism by which trauma and PTSD symptoms operate in FA, as it may be a promising direction in treatment of certain subgroup of individuals with FA.
Conclusions
We used selected elements of the Alcohol and Addiction Research Domain Criteria to examine the similarities and differences in the individual characteristics of FA and other addictive disorders. Given that FA is not a DSM-5 diagnosis and that it remains a controversial construct [105, 106], the RDoC framework seems particularly useful and suited for further investigation of FA. While clinical studies have historically studied participants who meet certain diagnostic criteria (often with exclusion of comorbid conditions), the AARDoC approach allows for greater heterogeneity in recruited samples, while the units of analysis allow for multidimensional characterization of the studied construct.
Based on the literature in this narrative review, several transdiagnostic units of analysis appear to be particularly useful in either distinguishing those with FA from those without FA, or appear to be important moderators of processes present in food-seeking behavior. Within the incentive salience domain, self-reported craving may be an expression of sensitivity to reward. As such, it may be particularly useful to include in treatment outcome studies as a unit of analysis predicting outcomes in treatment and by extension, be a treatment target for those who report elevated levels of food craving. Relative reinforcing value of food also appears to be a promising unit of analysis, with the few studies that used it in the context of FA, indicating that on average it is associated with FA symptoms. Attention bias to food should be investigated further as the number of studies is too small to draw conclusions. It appears that investigating the interaction between attentional processes and emotional states may be useful in identifying the mechanisms by which exposure to highly palatable foods leads to consumption. Within the executive dysfunction domain, FA appears to be divergent from many other addictive disorders—while there are statistically significant associations between delay discounting and FA, they are generally small. Individuals with FA also do not appear to differ from controls on measures of inhibitory control. It is possible that the relationship between executive dysfunction and FA is more nuanced and moderated by third variables. It is also possible that the anticipation/preoccupation phase of the addictive cycle in FA is not best represented by measures of decisional and behavioral impulsivity. In the negative emotionality domain, there are strong parallels between FA and other addictive disorders, generally indicating an association between severity of FA and severity of different units of analysis of negative emotionality.
Limitations and strengths
This was not a systematic review and the AARDoC approach was grounded in the most used paradigms in the FA field (thus it was not exhaustive). No quantitative meta-analysis was performed; therefore, empirically based conclusions are more difficult to put forth. Moreover, the AARDoC framework is a recent model and it has not been validated in the addiction field; therefore, it is possible that with more research, that conceptualization of this organizing framework will evolve. However, one of the strengths of the RDoC approach is the transdiagnostic nature of the units of analysis (in most instances) allowing for a characterization of the spectrum of a population. Another strength of this review is incorporating the role of trauma (as an environmental factor) into the framework (as environmental factors were a peripheral part of the AARDoC framework; see Witkiewitz, 2019 for a graphic). It appears that there are several parallels between substance use and FA in the relationship between their severity and trauma exposure.
Future Directions
Considering that the RDoC and AARDoC frameworks may be a helpful organizing principle for future considerations of FA as a clinical construct, future studies should consider incorporating other units of analysis within the RDoC framework. Few studies have considered physiological correlates of FA compared to individuals without FA (such as heart rate variability or skin conductance) and these may offer additional information based on objective measurement in the Arousal domain (subsumed under RDoC, but not AARDoC; [9]. It may also be informative to study the interaction between different domains. For instance, findings in other addictions as well as in binge eating indicate that individuals with high incentive salience combined with high delay discounting, a combination termed reinforcement pathology [107, 108], tend to have the worst outcomes—therefore, it would be important to test that interaction in individuals with FA as it may be a predictor of treatment success. As the RDoC framework’s premise is to identify subtypes of different presentations and pursue precision medicine, it may be useful to generate profiles of individuals based on units of analysis in different domain using person-centered approaches. For example, given the strong link between trauma exposure and FA, it would be helpful to understand whether there is a trauma-exposed subtype of FA and whether such subtype is associated with specific units of analysis in the RDoC framework. Longitudinal studies would also be of use, to ascertain the causality of the reported associations. Overall, the AARDoC framework should be further investigated and validated in the addiction field, including as it applies to FA.
References
Gearhardt AN, Corbin WR, Brownell KD. Food addiction: an examination of the diagnostic criteria for dependence. J Addict Med. 2009;3(1):1.
Gearhardt, Ashley N, Corbin WR, Brownell KD. Development of the Yale Food Addiction Scale Version 2.0. Psychol Addict Behav. 2016;30(1), 113–121. https://doi.org/10.1037/adb0000136
Gibney MJ. Ultra-Processed Foods: Definitions and Policy Issues. Curr Dev Nutr. 2018;3:1–7. https://academic.oup.com/cdn/.
Schulte EM, Avena NM, Gearhardt AN. Which foods may be addictive? The roles of processing, fat content, and glycemic load. PLoS One, 2015;10(2). https://doi.org/10.1371/journal.pone.0117959
American Psychiatric Association. The Diagnostic and Statistical Manual of Mental Disorders: DSM 5. Am Psychiatr Publ. 2013.
Cuthbert BN. The RDoC framework: facilitating transition from ICD/DSM to dimensional approaches that integrate neuroscience and psychopathology. World Psychiatry. 2014;13(1):28–35. https://doi.org/10.1002/wps.20087.
Litten RZ, Ryan ML, Falk DE, Reilly M, Fertig JB, Koob GF. Heterogeneity of alcohol use disorder: understanding mechanisms to advance personalized treatment. Alcohol Clin Exp Res. 2015;39(4):579–84. https://doi.org/10.1111/ACER.12669.
Witkiewitz K, Litten RZ, Leggio L. Advances in the science and treatment of alcohol use disorder. Sci Adv. 2019;5(9). https://doi.org/10.1126/SCIADV.AAX4043/ASSET/D9BBBFA4-87BD-48D6-B3D0-569E1F4D7AF4/ASSETS/GRAPHIC/AAX4043-F1.JPEG
Cuthbert BN, Insel TR. Toward the future of psychiatric diagnosis: the seven pillars of RDoC. BMC Med. 2013;11(1):126. https://doi.org/10.1186/1741-7015-11-126.
Kwako LE, Momenan R, Litten RZ, Koob GF, Goldman D. Addictions Neuroclinical Assessment: A Neuroscience-Based Framework for Addictive Disorders. Biol Psychiat. 2016;80(3):179–89. https://doi.org/10.1016/J.BIOPSYCH.2015.10.024.
Koob GF. Alcoholism: allostasis and beyond. Alcohol Clin Exp Res. 2003;27(2):232–43. https://doi.org/10.1097/01.ALC.0000057122.36127.C2.
Koob GF, Volkow ND. Neurobiology of addiction: a neurocircuitry analysis. The Lancet Psychiatry. 2016;3(8):760–73. https://doi.org/10.1016/S2215-0366(16)00104-8.
Robinson TE, Berridge KC. The neural basis of drug craving: An incentive-sensitization theory of addiction. Brain Res Rev 1993;18(3)247–291. Elsevier. https://doi.org/10.1016/0165-0173(93)90013-P
MacKillop J, Monti PM. Advances in the scientific study of craving for alcohol and tobacco. In P. M. Miller & D. Kavanagh (Eds.), Translation of addictions science into practice. 2007;189–209. Elsevier Science. http://proxy-remote.galib.uga.edu/login?url=http://search.ebscohost.com/login.aspx?direct=true&db=psyh&AN=2007-04711-010&site=ehost-live
Robinson TE, Berridge KC. The psychology and neurobiology of addiction: an incentive-sensitization view. Addiction. 2000;95(8s2)91–117. https://doi.org/10.1046/j.1360-0443.95.8s2.19.x
Weiss F. Neurobiology of craving, conditioned reward and relapse. Curr Opin Pharmacol. 2005;5(1):9–19. https://doi.org/10.1016/J.COPH.2004.11.001.
Volkow ND, Wang G-J, Tomasi D, Baler RD. Obesity and addiction: neurobiological overlaps. Obes Rev. 2013;14(1):2–18. https://doi.org/10.1111/j.1467-789X.2012.01031.x.
Volkow ND, Wang GJ, Tomasi D, Baler RD. The addictive dimensionality of obesity. In Biol Psychiatry. 2013;73(9)811–818. https://doi.org/10.1016/j.biopsych.2012.12.020
Volkow ND, Wise RA. How can drug addiction help us understand obesity? Nat Neurosci. 2005;8(5):555–60. https://doi.org/10.1038/nn1452.
Wise RA. Neurobiology of addiction. Curr Opin Neurobiol. 1996;6(2):243–51. https://doi.org/10.1016/S0959-4388(96)80079-1.
Tuomisto T, Hetherington MM, Morris M-F, Tuomisto MT, Turjanmaa V, Lappalainen R. Psychological and Physiological Characteristics of Sweet Food “‘Addiction.’” Int J Eat Disord. 1999;25:169–75. https://doi.org/10.1002/(SICI)1098-108X(199903)25:2.
Davis C, Curtis C, Levitan RD, Carter JC, Kaplan AS, Kennedy JL. Evidence that “food addiction” is a valid phenotype of obesity. Appetite. 2011;57(3):711–7. https://doi.org/10.1016/j.appet.2011.08.017.
Eichen DM, Lent MR, Goldbacher E, Foster GD. Exploration of “Food Addiction” in overweight and obese treatment-seeking adults. Appetite. 2013;67:22–4. https://doi.org/10.1016/j.appet.2013.03.008.
Meule A, Kübler A. Food cravings in food addiction: The distinct role of positive reinforcement. Eat Behav. 2012;13(3):252–5. https://doi.org/10.1016/J.EATBEH.2012.02.001.
Loxton NJ, Tipman RJ. Reward sensitivity and food addiction in women. Appetite. 2017;115:28–35. https://doi.org/10.1016/J.APPET.2016.10.022.
Grey JA, McNaughton N. The neuropsychology of anxiety: An enquiry into the functions of the septo-hippocampal system 2000(2nd ed.). Oxford University Press.
Gearhardt AN, Yokum S, Orr PT, Stice E, Corbin WR, Brownell KD. Neural correlates of food addiction. Arch Gen Psychiatry. 2011;68(8):808–16. https://doi.org/10.1001/archgenpsychiatry.2011.32.
Epstein LH, Leddy JJ, Temple JL, Faith MS. Food reinforcement and eating: A multilevel analysis. Psychol Bull. 2007;133(5):884–906. https://doi.org/10.1037/0033-2909.133.5.884.
Jacobs EA, Bickel WK. Modeling drug consumption in the clinic using simulation procedures: Demand for heroin and cigarettes in opioid-dependent outpatients. Exp Clin Psychopharmacol. 1999;7(4):412–26. https://doi.org/10.1037/1064-1297.7.4.412.
Mackillop J, Few LR, Murphy JG, Wier LM, Acker J, Murphy C, Stojek M, Carrigan M, Chaloupka F. High-resolution behavioral economic analysis of cigarette demand to inform tax policy. Addiction. 2012;107(12). https://doi.org/10.1111/j.1360-0443.2012.03991.x
Sumnall HR, Tyler E, Wagstaff GF, Cole JC. A behavioural economic analysis of alcohol, amphetamine, cocaine and ecstasy purchases by polysubstance misusers. Drug Alcohol Depend. 2004;76(1):93–9. https://doi.org/10.1016/J.DRUGALCDEP.2004.04.006.
Best JR, Theim KR, Gredysa DM, Stein RI, Welch RR, Saelens BE, Perri MG, Schechtman KB, Epstein LH, Wilfley DE. Behavioral economic predictors of overweight children’s weight loss. J Consult Clin Psychol. 2012;80(6):1086–96. https://doi.org/10.1037/a0029827.
Epstein LH, Dearing KK, Roba LG. A questionnaire approach to measuring the relative reinforcing efficacy of snack foods. Eat Behav. 2010;11(2):67–73. https://doi.org/10.1016/j.eatbeh.2009.09.006.
Wenzel KR, Weinstock J, McGrath AB. The Clinical Significance of Food Addiction. J Addict Med. 2020;14(5):e153–9. https://doi.org/10.1097/ADM.0000000000000626.
Clarke TK, Weiss ARD, Ferarro TN, Kampman KM, Dackis CA, Pettinati HM, O’brien, C. P., Oslin, D. W., Lohoff, F. W., & Berrettini, W. H. The Dopamine Receptor D2 (DRD2) SNP rs1076560 is Associated with Opioid Addiction. Ann Hum Genet. 2014;78(1):33–9. https://doi.org/10.1111/AHG.12046.
Obregón AM, Oyarce K, García-Robles MA, Valladares M, Pettinelli P, Goldfield GS. Association of the dopamine D2 receptor rs1800497 polymorphism with food addiction, food reinforcement, and eating behavior in Chilean adults. Eat Weight Disord. 2022;27(1):215–24. https://doi.org/10.1007/S40519-021-01136-1/TABLES/6.
Nansel TR, Lipsky LM, Faith M, Liu A, Siega-Riz AM. The accelerator, the brake, and the terrain: associations of reward-related eating, self-regulation, and the home food environment with diet quality during pregnancy and postpartum in the pregnancy eating attributes study (PEAS) cohort. Int J Behav Nutr Phys Act. 2020;17(1):1–11. https://doi.org/10.1186/S12966-020-01047-X/FIGURES/2.
Cisler JM, Koster EHW. Mechanisms of attentional biases towards threat in anxiety disorders: An integrative review. Clin Psychol Rev. 2010;30(2):203–16. https://doi.org/10.1016/J.CPR.2009.11.003.
Field M, Cox WM. Attentional bias in addictive behaviors: A review of its development, causes, and consequences. Drug Alcohol Depend. 2008;97(1):1–20. https://doi.org/10.1016/j.drugalcdep.2008.03.030.
Franken IHA. Drug craving and addiction: integrating psychological and neuropsychopharmacological approaches. Prog Neuropsychopharmacol Biol Psychiatry. 2003;27(4):563–79. https://doi.org/10.1016/S0278-5846(03)00081-2.
Stojek M, Shank LM, Vannucci A, Bongiorno DM, Nelson EE, Waters AJ, Engel SG, Boutelle KN, Pine DS, Yanovski JA, Tanofsky-Kraff M. A systematic review of attentional biases in disorders involving binge eating. Appetite. 2018;123. https://doi.org/10.1016/j.appet.2018.01.019
Gearhardt AN, White MA, Masheb RM, Grilo CM. An examination of food addiction in a racially diverse sample of obese patients with binge eating disorder in primary care settings. Compr Psychiatry. 2013;54(5):500–5. https://doi.org/10.1016/j.comppsych.2012.12.009.
Frayn M, Sears CR, von Ranson KM. A sad mood increases attention to unhealthy food images in women with food addiction. Appetite. 2016;100:55–63. https://doi.org/10.1016/J.APPET.2016.02.008.
Ruddock HK, Field M, Jones A, Hardman CA. State and trait influences on attentional bias to food-cues: The role of hunger, expectancy, and self-perceived food addiction. Appetite. 2018;131:139–47. https://doi.org/10.1016/J.APPET.2018.08.038.
Nigg JT. Annual Research Review: On the relations among self-regulation, self-control, executive functioning, effortful control, cognitive control, impulsivity, risk-taking, and inhibition for developmental psychopathology. J Child Psychol Psychiatry. 2017;58(4):361–83. https://doi.org/10.1111/JCPP.12675.
Amlung M, Vedelago L, Acker J, Balodis I, MacKillop J. Steep delay discounting and addictive behavior: a meta-analysis of continuous associations. Addiction. 2017;112(1):51–62. https://doi.org/10.1111/ADD.13535.
Coskunpinar A, Cyders MA. Impulsivity and substance-related attentional bias: A meta-analytic review. Drug Alcohol Depend. 2013;133(1):1–14. https://doi.org/10.1016/J.DRUGALCDEP.2013.05.008.
Stanford MS, Mathias CW, Dougherty DM, Lake SL, Anderson NE, Patton JH. Fifty years of the Barratt Impulsiveness Scale: An update and review. Personality Individ Differ. 2009;47(5):385–95. https://doi.org/10.1016/J.PAID.2009.04.008.
Vella SLC, Pai NB. A narrative review of potential treatment strategies for food addiction. Eating and Weight Disorders - Studies on Anorexia, Bulimia and Obesity 2017. 2017;22:3, 22(3), 387–393. https://doi.org/10.1007/S40519-017-0400-2
de Wit H. Impulsivity as a determinant and consequence of drug use: a review of underlying processes. Addict Biol. 2009;14(1):22–31. https://doi.org/10.1111/j.1369-1600.2008.00129.x.
Ainslie G. Specious reward: A behavioral theory of impulsiveness and impulse control. Psychol Bull. 1975;82(4):463–96.
Kekic M, McClelland J, Bartholdy S, Chamali R, Campbell IC, Schmidt U. Bad Things Come to Those Who Do Not Wait: Temporal Discounting Is Associated With Compulsive Overeating, Eating Disorder Psychopathology and Food Addiction. Front Psych. 2020;10:978. https://doi.org/10.3389/FPSYT.2019.00978/BIBTEX.
Minhas M, Murphy CM, Balodis IM, Acuff SF, Buscemi J, Murphy JG, MacKillop J. Multidimensional elements of impulsivity as shared and unique risk factors for food addiction and alcohol misuse. Appetite. 2021;159: 105052. https://doi.org/10.1016/J.APPET.2020.105052.
Peng-Li D, Sørensen TA, Li Y, He Q. Systematically lower structural brain connectivity in individuals with elevated food addiction symptoms. Appetite. 2020;155: 104850. https://doi.org/10.1016/J.APPET.2020.104850.
VanderBroek-Stice L, Stojek MK, Beach SRH, vanDellen MR, MacKillop J. Multidimensional assessment of impulsivity in relation to obesity and food addiction. Appetite. 2017;112. https://doi.org/10.1016/j.appet.2017.01.009
Weinsztok S, Brassard S, Balodis I, Martin LE, Amlung M. Delay Discounting in Established and Proposed Behavioral Addictions: A Systematic Review and Meta-Analysis. Front Behav Neurosci. 2021;15. https://doi.org/10.3389/FNBEH.2021.786358/FULL
Luijten M, Machielsen MWJ, Veltman DJ, Hester R, de Haan L, Franken IHA. Systematic review of ERP and fMRI studies investigating inhibitory control and error processing in people with substance dependence and behavioural addictions. J Psychiatry Neurosci. 2014;39(3):149–69. https://doi.org/10.1503/JPN.130052.
Aron AR. The neural basis of inhibition in cognitive control. Neuroscientist. 2007;13(3):214–28. https://doi.org/10.1177/1073858407299288.
Kiehl KA, Liddle PF, Hopfinger JB. Error processing and the rostral anterior cingulate: An event-related fMRI study. Psychophysiology. 2000;37(2):216–23. https://doi.org/10.1111/1469-8986.3720216.
Blume M, Schmidt R, Hilbert A. Executive Functioning in Obesity, Food Addiction, and Binge-Eating Disorder. Nutrients 2019. 2018;11(1):54. https://doi.org/10.3390/NU11010054
Hsu JS, Wang PW, Ko CH, Hsieh TJ, Chen CY, Yen JY. Altered brain correlates of response inhibition and error processing in females with obesity and sweet food addiction: A functional magnetic imaging study. Obes Res Clin Pract. 2017;11(6):677–86. https://doi.org/10.1016/J.ORCP.2017.04.011.
Meule A, Lutz A, Vögele C, Kübler A. Women with elevated food addiction symptoms show accelerated reactions, but no impaired inhibitory control, in response to pictures of high-calorie food-cues. Eat Behav. 2012;13(4):423–8. https://doi.org/10.1016/J.EATBEH.2012.08.001.
Minhas M, Murphy CM, Balodis IM, Samokhvalov AV, MacKillop J. Food addiction in a large community sample of Canadian adults: prevalence and relationship with obesity, body composition, quality of life and impulsivity. Addiction. 2021;116(10):2870–9. https://doi.org/10.1111/ADD.15446.
Conners CK. Conners’ Continuous Performance Test II Users’ Manual. Multi Health Systems. 2000.
Steward T, Mestre-Bach G, Vintró-Alcaraz C, Lozano-Madrid M, Agüera Z, Fernández-Formoso JA, Granero R, Jiménez-Murcia S, Vilarrasa N, García-Ruiz-de-Gordejuela A, Veciana de las Heras M, Custal N, Virgili N, López-Urdiales R, Gearhardt AN, Menchón JM, Soriano-Mas C, Fernández-Aranda F. Food addiction and impaired executive functions in women with obesity. Eur Eat Disord Rev. 2018;26(6):574–84. https://doi.org/10.1002/ERV.2636.
Franken IHA, van Strien JW, Kuijpers I. Evidence for a deficit in the salience attribution to errors in smokers. Drug Alcohol Depend. 2010;106(2–3):181–5. https://doi.org/10.1016/J.DRUGALCDEP.2009.08.014.
Franken IHA, Nijs IMT, Toes A, van der Veen FM. Food addiction is associated with impaired performance monitoring. Biol Psychol. 2018;131:49–53. https://doi.org/10.1016/J.BIOPSYCHO.2016.07.005.
Koob GF, Bloom FE. Cellular and Molecular Mechanisms of Drug Dependence. Science. 1988;242(4879):715–23. https://doi.org/10.1126/SCIENCE.2903550.
Sherman JE, Morse E, Baker TB. Urges/craving to smoke: Preliminary results from withdrawing and continuing smokers. Adv Behav Res Ther. 1986;8(4):253–69. https://doi.org/10.1016/0146-6402(86)90008-1.
Baker TB, Piper ME, McCarthy DE, Majeskie MR, Fiore MC. Addiction Motivation Reformulated: An Affective Processing Model of Negative Reinforcement. Psychol Rev. 2004;111(1):33–51. https://doi.org/10.1037/0033-295X.111.1.33.
Zorrilla EP, Koob GF. The dark side of compulsive eating and food addiction. In P. Cottone, V. Sabino, C. F. Moore, & G. F. Koob (Eds.), Compulsive Eating Behavior and Food Addiction: Emerging Pathological Constructs. 2019;115–192. Academic Press. https://doi.org/10.1016/B978-0-12-816207-1.00006-8
George O, Koob GF, Vendruscolo LF. Negative reinforcement via motivational withdrawal is the driving force behind the transition to addiction. Psychopharmacology 2014. 2014;231:19, 231(19), 3911–3917. https://doi.org/10.1007/S00213-014-3623-1
Koob GF, Buck CL, Cohen A, Edwards S, Park PE, Schlosburg JE, Schmeichel B, Vendruscolo LF, Wade CL, Whitfield TW, George O. Addiction as a stress surfeit disorder. Neuropharmacology. 2014;76(PART B), 370–382. https://doi.org/10.1016/J.NEUROPHARM.2013.05.024
Sinha R. The role of stress in addiction relapse. Curr Psychiatry Rep. 2007;9:388–95.
Naish KR, Laliberte M, Mackillop J, Balodis IM, Joseph’, S., Hamilton, H., & Hamilton, C. Systematic review of the effects of acute stress in binge eating disorder. Eur J Neurosci. 2019;50(3):2415–29. https://doi.org/10.1111/EJN.14110.
Schaefer LM, Smith KE, Anderson LM, Cao L, Crosby RD, Engel SG, Crow SJ, Peterson CB, Wonderlich SA. The Role of Affect in the Maintenance of Binge-Eating Disorder: Evidence From an Ecological Momentary Assessment Study. J Abnorm Psychol. 2020. https://doi.org/10.1037/ABN0000517.
Henry JD, Crawford JR. The short-form version of the Depression Anxiety Stress Scales (DASS-21): Construct validity and normative data in a large non-clinical sample. Br J Clin Psychol. 2005;44(2):227–39. https://doi.org/10.1348/014466505X29657.
Burrows T, Hides L, Brown R, Dayas CV, Kay-Lambkin F. Differences in Dietary Preferences, Personality and Mental Health in Australian Adults with and without Food Addiction. Nutrients 2017. 2017;9(3):285. https://doi.org/10.3390/NU9030285
Raymond KL, Kannis-Dymand L, Lovell GP. A graduated food addiction classifications approach significantly differentiates depression, anxiety and stress among people with type 2 diabetes. Diabetes Res Clin Pract. 2017;132:95–101. https://doi.org/10.1016/J.DIABRES.2017.07.028.
Burrows, T, Kay-Lambkin, F., Pursey, K., Skinner, J., & Dayas, C. (2018). Food addiction and associations with mental health symptoms: a systematic review with meta-analysis. In Journal of Human Nutrition and Dietetics (Vol. 31, Issue 4, pp. 544–572). Blackwell Publishing Ltd. https://doi.org/10.1111/jhn.12532
Pursey KM, Collins R, Skinner J, Burrows TL. Characteristics of individuals seeking addictive eating treatment. Eat Weight Disord. 2021;26(8):2779–86. https://doi.org/10.1007/S40519-021-01147-Y/TABLES/2.
Whiteside SP, Lynam DR, Miller JD, Reynolds SK. Validation of the UPPS impulsive behavior scale: A four-factor model of impulsivity. Eur J Pers. 2005;19:559–74.
Lynam D, Smith GT, Whiteside SA, Cyders MA. The UPPS-P: Assessing five personality pathways to impulsive behavior. 2006.
Cyders MA, Smith GT. Mood-based rash action and its components: Positive and negative urgency. Personality Individ Differ. 2007;43:839–50.
McCarty KN, Morris DH, Hatz LE, McCarthy DM. Differential Associations of UPPS-P Impulsivity Traits With Alcohol Problems. J Studies Alcoh Drugs. 2017;78(4):617–622. https://doi.org/10.15288/JSAD.2017.78.617
Kaiser AJ, Milich R, Lynam DR, Charnigo RJ. Negative Urgency, Distress Tolerance, and substance abuse among college students. Addict Behav. 2012;37(10):1075–83. https://doi.org/10.1016/J.ADDBEH.2012.04.017.
Murphy CM, Stojek MK, MacKillop J. Interrelationships among impulsive personality traits, food addiction, and Body Mass Index. Appetite. 2014;73:45–50. https://doi.org/10.1016/j.appet.2013.10.008.
Pivarunas B, Conner BT. Impulsivity and emotion dysregulation as predictors of food addiction. Eat Behav. 2015;19:9–14. https://doi.org/10.1016/j.eatbeh.2015.06.007.
Rodrigue C, Gearhardt AN, Bégin C. Food Addiction in Adolescents: Exploration of psychological symptoms and executive functioning difficulties in a non-clinical sample. Appetite. 2019;141: 104303. https://doi.org/10.1016/J.APPET.2019.05.034.
Rose MH, Nadler EP, Mackey ER. Impulse Control in Negative Mood States, Emotional Eating, and Food Addiction are Associated with Lower Quality of Life in Adolescents with Severe Obesity. J Pediatr Psychol. 2018;43(4):443–51. https://doi.org/10.1093/JPEPSY/JSX127.
Wolz I, Hilker I, Granero R, Jiménez-Murcia S, Gearhardt AN, Dieguez C, Casanueva FF, Crujeiras AB, Menchón JM, Fernández-Aranda F. “Food Addiction” in Patients with Eating Disorders is Associated with Negative Urgency and Difficulties to Focuson Long-Term Goals. Frontiers in Psychology. 2016;7:61. https://doi.org/10.3389/FPSYG.2016.00061/BIBTEX
Brady KT, Back SE. Childhood Trauma, Posttraumatic Stress Disorder, and Alcohol Dependence. Alcohol Res Curr Rev. 2012;34(4):408. /pmc/articles/PMC3860395/
Jacobsen LK, Southwick SM, Kosten TR. Substance use disorders in patients with posttraumatic stress disorder: A review of the literature. Am J Psychiatry. 2001;158(8):1184–90. https://doi.org/10.1176/APPI.AJP.158.8.1184/ASSET/IMAGES/LARGE/J52F1.JPEG.
Mason SM, Flint AJ, Field AE, Austin SB, Rich-Edwards JW. Abuse victimization in childhood or adolescence and risk of food addiction in adult women. Obesity. 2013;21(12):E775–81. https://doi.org/10.1002/oby.20500.
Mason SM, Flint AJ, Roberts AL, Agnew-Blais J, Koenen KC, Rich-Edwards JW. Posttraumatic Stress Disorder Symptoms and Food Addiction in Women by Timing and Type of Trauma Exposure. JAMA Psychiat. 2014. https://doi.org/10.1001/jamapsychiatry.2014.1208.
Stojek MM, Maples-Keller JL, Dixon HD, Umpierrez GE, Gillespie CF, Michopoulos V. Associations of childhood trauma with food addiction and insulin resistance in African-American women with diabetes mellitus. Appetite. 2019;141: 104317. https://doi.org/10.1016/J.APPET.2019.104317.
Hardy R, Fani N, Jovanovic T, Michopoulos V. Food addiction and substance addiction in women: Common clinical characteristics. Appetite. 2018;120:367–73. https://doi.org/10.1016/J.APPET.2017.09.026.
Masheb RM, Ruser CB, Min KM, Bullock AJ, Dorflinger LM. Does food addiction contribute to excess weight among clinic patients seeking weight reduction? Examination of the Modified Yale Food Addiction Survey. Compr Psychiatry. 2018;84:1–6. https://doi.org/10.1016/j.comppsych.2018.03.006.
Mitchell KS, Wolf EJ. PTSD, food addiction, and disordered eating in a sample of primarily older veterans: The mediating role of emotion regulation. Psychiatry Res. 2016;243:23–9. https://doi.org/10.1016/J.PSYCHRES.2016.06.013.
Stojek MM, Lipka J, Maples-Keller JM, Rauch SAM, Black K, Michopoulos V, Rothbaum BO. Investigating Sex Differences in Rates and Correlates of Food Addiction Status in Women and Men with PTSD. Nutrients. 2021;13(6):1840. https://doi.org/10.3390/nu13061840.
Michopoulos V, Vester A, Neigh G. Posttraumatic stress disorder: A metabolic disorder in disguise? Exp Neurol. 2016;284(Pt B):220–9. https://doi.org/10.1016/j.expneurol.2016.05.038.
Avena NM, Rada P, Hoebel BG. Evidence for sugar addiction: behavioral and neurochemical effects of intermittent, excessive sugar intake. Neurosci Biobehav Rev. 2008;32(1):20–39.
Cottone P, Sabino V, Steardo L, Zorrilla EP. Consummatory, anxiety-related and metabolic adaptations in female rats with alternating access to preferred food. Psychoneuroendocrinology. 2009;34(1):38–49. https://doi.org/10.1016/J.PSYNEUEN.2008.08.010.
Brewerton TD. Posttraumatic Stress Disorder and Disordered Eating: Food Addiction as Self-Medication. Journal of Women’s Health. 2011;20(8):1133–4. https://doi.org/10.1089/jwh.2011.3050.
Fletcher PC, Kenny PJ. Food addiction: a valid concept? Neuropsychopharmacology. 2018;43(13):2506–13. https://doi.org/10.1038/s41386-018-0203-9.
Hebebrand J, Gearhardt AN. The concept of “food addiction” helps inform the understanding of overeating and obesity: NO. Am J Clin Nutr. 2021;113(2):268–73. https://doi.org/10.1093/ajcn/nqaa344.
Bickel WK, Johnson MW, Koffarnus MN, MacKillop J, Murphy JG. The behavioral economics of substance use disorders: reinforcement pathologies and their repair. Annu Rev Clin Psychol. 2014;10:641–77. https://doi.org/10.1146/annurev-clinpsy-032813-153724.
Carr KA, Daniel TO, Lin H, Epstein LH. Reinforcement pathology and obesity. Curr Drug Abuse Rev. 2011;4(3):190–6.
Funding
Prof. Monika Stojek receives funding from the National Science Center (Narodowe Centrum Nauki) for project 2021/41/B/HS6/04029 (Relationship between PTSD symptoms, eating behaviors and physical health: Inflammatory, cardiometabolic, and psychophysiological correlates).
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflicts of Interest
The authors do not have existing conflict of interest.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
This article is part of the Topical Collection on Food Addiction
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Stojek, M.M., Murphy, C.M. Examination of Individual Differences in Susceptibility to Food Addiction using Alcohol and Addiction Research Domain Criteria (AARDoC): Recent Findings and Directions for the Future. Curr Addict Rep 9, 334–343 (2022). https://doi.org/10.1007/s40429-022-00433-8
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s40429-022-00433-8