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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptHHS Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
 
Biol Psychiatry. Author manuscript; available in PMC 2010 April 15.
Published in final edited form as:
PMCID: PMC2678684
NIHMSID: NIHMS107039

Impaired Prefrontal Cortical Function and Disrupted Adaptive Cognitive Control in Methamphetamine Abusers: An fMRI Study

Abstract

Background

Methamphetamine (MA) abuse is associated with neurotoxicity to frontostriatal brain regions with concomitant deleterious effects on cognitive processes. Deficits in behavioral control are thought to be one contributing factor to the sustainment of addictive behaviors in chronic MA abuse.

Methods

In order to examine patterns of behavioral control relevant to addiction, we employed a fast-event related fMRI design to examine trial to trial reaction time (RT) adjustments in 12 chronic MA abusers who met DSM-IV criteria for MA dependence and 16 non-substance abusing controls. A variant of the Stroop task was employed to contrast the groups on error rates, RT Stroop conflict effect and the level of trial-to-trial adjustments seen after incongruent trials.

Results

The MA abusers exhibited reduced RT adjustments along with reduced activation in the right prefrontal cortex compared to controls on conditions that measured the ability to use exposure to conflict situations (i.e., conflict trials) to regulate behavior. MA abusers did not differ from controls on accuracy rates or within-trial Stroop conflict effects.

Conclusions

The observed deficits in trial to trial RT adjustments suggest that the ability to adapt a behavioral response based on prior experience may be compromised in MA abusers. Such adjustments are critical to everyday functioning and deficits in modifying behavior based on prior events may reflect a key deficit that contributes to maladaptive drug seeking behavior.

Keywords: Methamphetamine, prefrontal, attention, fMRI, imaging

Introduction

In the past decade the use of the stimulant methamphetamine (MA) has increased in the general population, with worldwide abuse of amphetamines surpassing that of cocaine and opiates combined (1). There is an established literature in both animals (2) and humans (3) that documents damage to regions following MA abuse within neural pathways that are integral to addiction (4, 5). Proton MR spectroscopy (MRS) (68) and positron emission tomography (PET) imaging studies (9, 10) suggest that fronto-cingulate regions of the brain are affected by MA abuse. Consistent with abnormalities in brain structure and function, cognitive impairments have also been observed in MA abusers on tasks that require the suppression of task irrelevant information (8, 11), decision-making (12, 13), and working memory (14). Any combination of the cognitive impairments described above may contribute and promote maintenance of the maladaptive actions associated with drug-seeking behavior (15).

Study Rationale

Neurobiological models of addiction propose that ventral brain regions (i.e., orbital frontal cortex and nucleus accumbens) contribute to the impulse to seek drugs, whereas the recruitment of fronto-cingulate regions may be critical to control those prepotent impulses (5). In the context of addiction, cognitive control can be interpreted as the inhibition of a prepotent response (e.g., habitual drug use) in order to carry out behaviors associated with long-term rewards and positive outcomes (e.g., abstaining from drug use). In order to selectively examine the neural substrates of cognitive control relevant to addiction, we conducted a fast-event related fMRI study in which we examined trial to trial reaction time (RT) adjustments using a variant of the single-trial Stroop task in 12 chronic MA abusers and 16 controls. This version of the Stroop task creates conditions in which performance (RT and accuracy) reflects the ability to recognize and resolve conflict at the time of selection (i.e., within a trial), as well as trial sequences in which performance is influenced by the ability to use exposure to conflict situations (i.e., conflict trials) to regulate behavior (i.e., trial to trial adjustments) (16). Since previous imaging studies have shown that this variant of the Stroop task elicits activity in both the Anterior Cingulate Cortex (ACC) and PreFrontal Cortex (PFC) (1618), these brain regions were the focus of our fMRI imaging analysis. Given the association between PFC activity and cognitive control processes relevant to addiction we hypothesized that the MA abusers would show abnormal patterns of trial to trial adjustments (i.e., conflict adaptation) associated with reduced PFC activity.

Methods

Subjects

Two groups were studied: 12 MA abusing subjects and 16 age-matched non-substance abusing control subjects. The MA abusers met DSM-IV criteria for lifetime methamphetamine dependence determined from the Structured Clinical Interview (SCID) (19) but were currently drug abstinent a minimum of 3 weeks. See Table 1.

Table 1
Demographic and clinical characteristics of 12 methamphetamine (MA) abusers and 16 control subjects.

Procedure

A single-trial Stroop task was administered during the scanning session that employed both Incongruent (conflict) and Congruent (non-conflict) trials (see Supplemental Material for detailed task description). Behavioral analyses contrasted the groups on mean error rates, RT Stroop conflict effect (Conflict minus non-conflict), and the level of trial-to-trial adjustments seen after conflict trials. Analysis of variance procedures (ANOVA) for repeated measures were used to analyze the data in a 2 × 2 mixed ANOVA with group as a between subjects factor (patients vs controls) and wordtype (incongruent vs congruent) as within subjects variables. Incorrect responses were not included within the analysis of variance for RT. Analyses were carried out to examine trial to trial adjustments to conflict-conflict (iI) compared to non-conflict-conflict (cI) sequences.

Imaging

Functional MRI data were collected on a 3T Siemens TRIO scanner (see Supplemental Material for scanning parameters and image preprocessing details). Analyses were preformed using a General Linear Model (GLM) as implemented in SPM5. In a first-level analysis, individual subject GLMs were built and fitted to each subject’s functional data. The statistical models included regressors coding for 7 covariates (cC, iC, iI, cI, Errors, Post-Errors and Non-Responses). Parameter estimates obtained from this first level analysis were used to compute maps of the contrasts of interest for effects of conflict and trial-to-trial effects (I-C for RT conflict, and iI-cI for trial to trial RT adjustments). Maps of the contrasts of interest for effects of error conflict were also computed. Hypotheses put forth within this proposal regarding activity in specific regions of interest (ROIs) including ACC and PFC were tested in a second level random-effects analysis of these contrast maps. The volume of search was restricted to areas for which we had specific hypotheses by using an explicit mask of lateral and medial prefrontal cortical areas. The mask was built using the AAL atlas in the SPM5 toolbox (see supplemental material for details). Clusters of active voxels reported were corrected for multiple comparisons at a set level of p < 0.05 (20).

Results

Behavioral Data

Reaction Time Analyses

Analyses revealed main effects of Stroop wordtype [F (1, 26) = 65.09, p< .001] as well as an interaction between group, trial to trial adjustment and wordtype [F (1, 26) =4.04, p = .05]. Analyses revealed that the trial to trial adjustment RT effect (cI-iI) differed significantly between the MA abusers and controls [F (1, 26) = 6.54; p =.04, bonferroni corrected for multiple comparisons). While the controls showed an RT advantage (13 msec benefit) to conflict trials that were preceded by conflict trials (iI) the MA abusers showed no advantage and were actually slower (21 msec cost). Virtually identical results were obtained when the trials that included exact stimulus repetitions (color and word) were included (p=.04). These group differences in Stroop endured with age, education, NART scores as covariates. No group differences were observed on within-trial Stroop conflict effects (F < 1).

Error Analyses

Analyses revealed a main effect of wordtype [F (1,26) = 18.97, p =. 0001] with both groups making significantly more errors in the incongruent condition (7%) than in the congruent condition (4%). No other effects were significant. There was no evidence of a speed-accuracy trade-off for both groups (MA abusers; r=.264; p =.41, controls: r=.287; p =.28].

Imaging Results

We first examined whether activity within the ACC and PFC was associated with within-trial conflict monitoring (I-C) and trial-to-trial adjustments (iI-cI). Using ANOVA procedures with subject as a random variable, significant activation to conflict contrasts (I-C) was observed in the ACC in both groups with no differences observed between groups. In contrast, when we examined the pattern of activation for the trial to trial RT adjustments we found that controls exhibited increased PFC activity, most notably in BA6 on iI sequences compared to the cI sequences. In contrast the MA abusers showed little or no activation within the PFC region. (See Figure 1). We then ran a second-level random-effects analysis to explore group differences across the contrasts of interest. Between group differences emerged in activation in the right middle gyrus centered in Brodmann’s area 6. (p < .05, corrected) (See figure 2). This region showed lower levels of activation in the MA abusers after iI trial sequences relative to cI trial sequences. Table 3 summarizes the data for frontal regions with significantly different activation between the MA abusers and controls.

Figure 1
Regions of Increased Activation Associated with Trial to Trial Adjustments (iI– cI) in Methamphetamine Abusers and Controls
Figure 2
DLPFC region showing increased activity related to trial to trial adjustments (iI-cI) in control subjects relative to methamphetamine (MA) abusers. 2a) Graph of the average coefficients for the iI-cI statistical contrast in the two groups, averaged within ...
Table 3
Brain regions with significant group differences associated with trial to trial adjustments in 12 methamphetamine (MA) abusers and 16 control subjects.

Conclusion

Reduced right PFC activation, most notably in the right mid-frontal cortex (BA6), was observed in MA abusers compared to non-substance abusing controls when contrasting conditions that measured how prior exposure to conflict modulated subsequent behavior. In contrast, no significant group differences were observed in conflict related activation in the ACC (17, 18, 21). These data provide preliminary evidence that MA abuse is associated with deficits in behavioral regulation associated with abnormal PFC activation and to the best of our knowledge constitute the first published data of abnormal trial to trial adjustments in MA abusers. Given that frontally-mediated behavioral regulation assists with maintenance of goal-directed behavior, it is not surprising that the pattern of deficits in the MA abusers involve reduced activation in frontal regions.

These data cannot speak to the acute effects of MA use as our subjects were MA abstinent at the time of study nor can the findings rule out pre-existing vulnerabilities that could have predated the MA abuse. One limitation of the current study is that no significant correlations were observed between trial to trial behavioral RTs and beta coefficients within the PFC, thus future studies in larger groups of MA abusers are needed to confirm brain-behavior relationships. Studies that include at risk populations are needed to determine how deficits in conflict adaptation and abnormal behavioral control may contribute to the development and sustainment of addictive behaviors. Functional imaging techniques, such as those employed in the current study, are powerful tools to probe these questions and to test the validity of neurobiological models as they apply to human addiction (5).

Table 2
Behavioral results from 12 methamphetamine (MA) abusers and 16 control subjects.

Supplementary Material

Acknowledgments

We would like to thank Jerry Sonico for his support and technical assistance with MR data collection. We are also very appreciative of the support of Thomas E. Nordahl, MD, PhD.

Footnotes

Disclosure/Conflict of Interest

The authors declare that this work was funded by NIDA grant DA16293-01 to RS. The authors report no biomedical financial interests or potential conflicts of interest.

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