In summary, previous studies have focused only on the association between persistent drug use and impairment in inhibitory functioning, without focusing on the role of factors such as depression in first-time participants in compulsory drug treatment. Therefore, focusing on patients participating in mandatory drug treatment for the first time, this work explored the role of depression in people with SUD in their inhibitory control through two studies based on the dual-systems model of substance addiction and the susceptibility dual-processing theory of depression, thereby informing comprehensive research and potential treatment targets in the cognitive domain related to substance use disorders.
4. General DiscussionWe used a cross-sectional survey to find that depression negatively predicted cognitive inhibition in patients participating in compulsory drug treatment for the first time. Then, we used the Stroop paradigm to find that cognitive inhibition was worse in high-depression patients compared to low-depression patients. Both studies provided some evidence that depression can predict decreased inhibition in SUD populations. This result suggests a special angle of discussion to address factors associated with impaired inhibitory function in drug addicts and provides new enlightenment for the current field of working memory training for substance addiction.
The effect of depression on cognitive inhibition has been demonstrated in the general population. For example, Colich et al. found that depressed individuals show abnormalities in the prefrontal cortex during inhibition tasks in response to negative stimuli compared to normal individuals, i.e., there is an impairment in inhibitory control [37]. According to cognitive theory, depressed individuals develop a negative cognitive schema based on early traumatic experiences that leads to depressive beliefs wherein they view themselves, the world around them, and their future pessimistically [38]. The schema is activated with a diminished ability to inhibit negative automatic thinking when processing subsequent information, creating a negative cognitive bias in attention, assessment, and other areas [25,39]. A meta-analysis of the Stroop mood study showed that depressed patients were subject to stronger negative stimulus interference effects compared to healthy controls [40,41] and that the interference effects were greater, with higher severity of depressive symptoms [40]. It was confirmed that it is more difficult to inhibit negative stimuli in depressed patients. This effect should also exist in the addicted population.The results of both Study 1 and Study 2 support the hypothesis that depression in people with SUD may exacerbate the degree of impairment in their inhibitory control functions. Specifically, inhibitory control scores were significantly lower in the highly depressed group than in the non-depressed group, conditional on the control age and age of first drug use. The dual-systems model suggests [42] that impulsive behaviors such as drug use arise primarily due to the activation of impulsive systems, which are several automatic emotional responses and behavioral association tendencies derived from long-term experience and learning, activated by specific social situations. This process is automated and requires little involvement of cognitive resources [43]. The inhibition system, on the other hand, functions as a primary reflection of the individual’s self-control or strength of willpower and includes deliberate evaluation and inhibition criteria [44]. This system is relatively slow due to the need for individuals to consciously employ symbol-based representational systems and operating systems. Control systems depend more on control resources and are more proactive [45,46].However, according to the depression susceptibility dual-processing theory, depressed individuals or those with high scores on depression scales engage in negative automatic processing and produce negative automatic ruminative thinking, which diminishes their cognitive resources and impairs the resources allocated to other tasks [26]. Substance use by addicted individuals can alleviate or eliminate states of discomfort or aversion within the body, a behavior that may be reinforced through negative reinforcement processes [47]. Individuals continue to use drugs to alleviate uncomfortable states such as those associated with negative emotional states, tension, arousal, craving, or withdrawal, and these states persist throughout the individual’s withdrawal period [48]. These uncomfortable states also serve as sensitive cues which the addict preferentially processes in response. Processing of these cues also diminishes their cognitive resources and, in turn, impairs resources allocated to other tasks. Thus, in the Stroop task, individuals need to mobilize brain resources to cope with inconsistent information. Insufficient cognitive resources at this point can limit the operation of the control system and make it difficult for individuals to inhibit dominant responses [48]. Thus, subjects in this category show a slower response to color stimuli when the word meaning is inconsistent with the color.Furthermore, the present study examined the role of the type of substance use (methamphetamine and heroin) in the relationship between depression and cognitive inhibition, and no significant interaction was found. This result shows, to some extent, that the different pharmacological effects of the two types of addiction sources do not affect the relationship between depression and cognitive inhibition.
Once severe drug addictive behaviors have developed, there is no definitive treatment available, except for some that can be treated with drug substitution. However, high relapse rates can occur after a drug addict is released from mandatory isolation. For this reason, various disciplines have explored treatment modalities from different perspectives. Neurobiological and psychological studies of drug addiction find that people with SUD are susceptible to impairments in inhibition function [49], which is relevant to the treatment outcome of substance use disorders [50]. Most current research suggests that working memory or executive function training can improve cognitive performance in addicts, but the effects of training and the transfer it produces are inconsistent. Many researchers have attributed this to the site and extent of brain damage and the resulting different cognitive deficits caused by different types of drugs in addicts [51,52], and some have also focused on the differences between pathological states that can be caused by individuals of different genders [53]. However, less attention has been paid to the impact of comorbidities associated with substance addiction, yet people with SUD often suffer from other disorders, creating a state of comorbidity [54]. This study found a strong association between impaired cognitive inhibition and depressive symptoms in people with SUD, suggesting that the impact of patients’ psychiatric comorbidities should be attended to during working memory training treatment for substance addicts. Additionally, this result has important implications for standard screening in the early stages of substance addiction treatment to define the treatment process and treat patients with comorbidities such as addiction and depression.Although we provided a credible predictive result through larger samples and two methods, we still cannot explain causality. In the future, animal experiments can be used to further clarify the causal relationship between depression and the impairment of inhibition function in addicts. We compared the effect of drug type on cognitive depression in Study 2, but the small number of people in the heroin group relative to the methamphetamine group due to sampling limitations makes this result potentially less credible. The number of people in the heroin group could be increased in the future to obtain more reliable results. Since cognitive suppression may depend on the time of discontinuation, we did not consider the time of discontinuation of participants and could focus on this variable in the future. The present study also only discussed the difference in cognitive inhibition between addiction in depressed patients and non-depressed patients and did not discuss the underlying mechanism of depression-induced cognitive inhibition impairment, which needs to be further discussed by incorporating physiological and brain imaging data in the future. Nevertheless, our work contributed to the literature on discovering the negative relationship between depression and cognitive inhibition among addicts. It enlightened the researchers to select more proper solutions for helping the addicts to overcome their mental health problems. Considering that depression would induce impairment of cognitive inhibition, the cognitive and behavioral therapies that need cognitive inhibition might not be the way to go for people with comorbidity of addiction and depression. Other therapies might be more useful, such as motivational interviewing or contingency management.
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