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ORIGINAL RESEARCH article

Front. Psychiatry, 10 August 2022
Sec. Anxiety and Stress Disorders
This article is part of the Research Topic Recent Advances in Understanding Tourette Syndrome, Tic Disorders and Functional Tics View all 13 articles

Urge intolerance predicts tic severity and impairment among adults with Tourette syndrome and chronic tic disorders

  • 1Division of Child and Adolescent Psychiatry, Department of Psychiatry and Behavioral Sciences, Center for OCD, Anxiety, and Related Disorders for Children (COACH), Johns Hopkins University School of Medicine, Baltimore, MD, United States
  • 2Department of Psychology, Texas State University, San Marcos, TX, United States
  • 3Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA, United States
  • 4Division of Child and Adolescent Psychiatry, UCLA Semel Institute for Neuroscience and Human Behavior, Los Angeles, CA, United States
  • 5Department of Psychology, Behavior Therapy and Research Lab, Marquette University, Milwaukee, WI, United States
  • 6Department of Psychology, Choices Youth Psychopathology Lab, Suffolk University, Boston, MA, United States
  • 7Department of Psychiatry, Weill-Cornell Medicine, New York, NY, United States
  • 8Department of Psychiatry and Behavioral Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL, United States

Background: Individuals with Tourette Syndrome and Persistent Tic Disorders (collectively TS) often experience premonitory urges—aversive physical sensations that precede tics and are temporarily relieved by tic expression. The relationship between tics and premonitory urges plays a key role in the neurobehavioral treatment model of TS, which underlies first-line treatments such as the Comprehensive Behavioral Intervention for Tics (CBIT). Despite the efficacy of CBIT and related behavioral therapies, less than 40% of adults with TS respond to these treatments. Further examination of the relationship between premonitory urges, tic severity, and tic impairment can provide new insights into therapeutic targets to optimize behavioral treatment outcomes. This study examined whether urge intolerance—difficulty tolerating premonitory urges—predicted tic severity and tic-related impairment among adults with TS.

Methods: Participants were 80 adults with TS. Assessments characterized premonitory urge, distress tolerance, tic severity, and tic impairment. We used structural equation modeling (SEM) to examine the construct of urge intolerance—comprised of premonitory urge ratings and distress tolerance ratings. We first evaluated a measurement model of urge intolerance through bifactor modeling, including tests of the incremental value of subfactors that reflect premonitory urge severity and distress tolerance within the model. We then evaluated a structural model where we predicted clinician-rated tic severity and tic impairment by the latent variable of urge intolerance established in our measurement model.

Results: Analyses supported a bifactor measurement model of urge intolerance among adults with TS. Consistent with theoretical models, higher levels of urge intolerance predicted greater levels of clinician-rated tic severity and tic impairment.

Conclusion: This investigation supports the construct of urge intolerance among adults with TS and distinguishes it from subcomponents of urge severity and distress tolerance. Given its predictive relationship with tic severity and tic impairment, urge intolerance represents a promising treatment target to improve therapeutic outcomes in adults with TS.

Introduction

Tourette Syndrome and other persistent tic disorders (collectively referred to as TS) are neuropsychiatric conditions characterized by the recurrence of sudden, involuntary motor and vocal tics. Prevalence estimates suggest that TS affects ≈ 1% of youth, and symptoms often persist into adulthood for many patients (1–3). In addition to tics, individuals with TS often experience a variety of comorbid psychiatric conditions [e.g., attention deficit hyperactivity disorder (ADHD), obsessive-compulsive disorder (OCD), anxiety disorders, depressive disorders] and co-occurring challenges with affect and behavioral regulation (e.g., suicidality, affect lability) (4–8). Tics, accompanying premonitory urges, and co-occurring psychiatric conditions contribute to significant impairment for individuals with TS across the lifespan (9–15). Behavioral therapies—such as habit reversal training (HRT), the Comprehensive Behavioral Intervention for Tics (CBIT), and Exposure with Response Prevention (ERP)—have emerged as first-line interventions for individuals with TS (16–18). For individuals who exhibit a positive response to behavioral treatments, therapeutic gains are maintained for over 6 months (19, 20) and can have lasting benefits for up to 11 years (21). Despite the benefit of behavioral treatments for some adults with TS, less than 40% respond to this treatment approach (22). Thus, there is a critical need to understand factors that influence treatment response to evidence-based behavioral therapies in this age group, which can ultimately lead to the identification of novel therapeutic targets that optimize treatment outcomes (23, 24).

Behavior therapy for TS is grounded within a neurobehavioral model of tics. While this model acknowledges neurobiological contributors (e.g., neurotransmitters, brain circuitry, genetics), it suggests that tic expression is influenced by external (e.g., environmental context) and internal factors (e.g., premonitory urge, affective states) (25, 26). These internal and external factors serve as primary targets of intervention in behavior therapy (25). For instance, premonitory urges serve as antecedents to tics and are alleviated by tic expression, which in turn create a negative reinforcement cycle thought to maintain tic expression (27). In behavior therapy, individuals with TS learn to build awareness to tics and associated antecedents (e.g., urges) and implement competing responses to inhibit tics contingent upon antecedents (25, 26). Consequently, greater distress tolerance of premonitory urges would likely allow individuals to effectively implement competing responses even during intense premonitory urges, and therefore be associated with better behavioral therapy outcomes (e.g., reductions in tic severity and tic impairment). To date, the inability to tolerate premonitory urges (i.e., urge intolerance) has received limited investigation (28). Although the precise mechanisms underlying behavioral therapies are not fully explicated (26), urge intolerance represents an important construct that warrants further investigation.

The construct of urge intolerance is comprised of two central features: premonitory urge severity and distress tolerance. At present, no rating scales have been designed to specifically measure individuals' intolerance of urge sensations. In the absence of specific rating scales, existing validated rating scales (i.e., Premonitory Urge for Tics Scale [PUTS], Distress Tolerance Scale [DTS]) can be combined to understand this clinically-relevant construct. Indeed, prior work has started to explore urge intolerance (a latent variable derived from combined PUTS and DTS ratings) among youth with TS, and found that greater levels of urge intolerance predicted greater levels of parent- and child-reported functional impairment (28). However, further research is essential to understand the construct of urge intolerance across the lifespan, which may potentially explain the different rates of treatment response to behavior therapy between youth and adults.

Accordingly, this study investigated urge intolerance in adults with TS. First, structural equation modeling was used to build and test models of urge intolerance using validated rating scales. We hypothesized that a bifactor model of the latent construct of urge intolerance, comprised of urge severity and distress tolerance, would demonstrate good model fit. Second, the relationship between the latent construct urge intolerance and clinician-rated tic severity and tic impairment on the Yale Global Tic Severity Scale (YGTSS) was examined. We anticipated that greater levels of urge intolerance would predict greater levels of clinician-rated tic severity and tic impairment among adults with TS.

Method

Participants

The present sample included 80 adults with TS who participated in a 11.17-year (SD = 1.25) long-term follow-up assessment for a randomized clinical trial of behavior therapy for tics in youth with TS (21, 29). Participants needed to be enrolled in the original clinical trial of behavior therapy to participate in this long-term follow-up assessment. There were no significant differences on demographic and clinical characteristics between participants who completed the long-term follow-up assessment, those who declined to participate in the long-term follow-up assessment, and those who were lost to follow-up [see Espil et al. (21) for further details].

Participants were 23 years of age on average (M = 22.87, SD = 2.70), predominantly male (n = 60, 75%), and mostly Caucasian (n = 69, 86%). Most participants met criteria for a diagnosis of Tourette's disorder (n = 74, 92%), while other participants met criteria for a current diagnosis of chronic motor tic disorder (n = 6, 8%). Common co-occurring conditions among participants included: anxiety disorders (n = 18, 23%), ADHD (n = 11, 14%), and OCD (n = 7, 9%). Less than one-third of participants (n = 8, 29%) were taking medication for tic management (e.g., antipsychotic or alpha-2 adrenergic agonist medication).

Measures

Yale global tic severity scale (YGTSS) (30). The YGTSS is a clinician-administered assessment that measures tic severity in the past week across five domains: number, frequency, intensity, complexity, and interference domains (30). Item ratings are summed for motor and vocal tics to produce a Total Tic Severity score (range: 0–50). Clinicians also record a global rating for tic-related impairment in the past week (range: 0–50). The YGTSS has shown good reliability and validity across studies (30–32).

Premonitory urge for tics scale (PUTS) (33). The PUTS is a 9-item self-report questionnaire that measures premonitory urge phenomena (33). Items inquire about the frequency and discomfort associated with premonitory urges, and are rated on a 4-point scale. Items are summed to produce a total score (range: 0–36), with higher scores indicative of greater levels of premonitory urge severity. The PUTS has good internal consistency and external validity across individuals with TS (34, 35).

Distress tolerance scale (DTS) (36). The DTS is a 15-item self-report questionnaire that assesses an individual's ability to tolerate distress (36). Items are rated on a 5-point scale, and are summed to yield a total score (range: 15–75). Higher total score values indicate less distress tolerance. The DTS has demonstrated good convergent and divergent validity (36).

Procedures

All procedures followed ethical standards for human subject research and were approved by local institutional review boards (IRBs). Participants from the original clinical trial were contacted to participate in a long-term follow-up assessment (21, 29). Eighty participants (i.e., 63.4% of the original sample) were interviewed in-person or via Skype by trained raters to ascertain clinical history and psychiatric diagnoses on the Mini-International Neuropsychiatric Interview (37). Next, clinician-administered assessments were completed to characterize current tic severity (YGTSS). Finally, participants completed self-report measures of premonitory urges (PUTS) and distress tolerance (DTS). Please see Espil et al. (21) for further details.

Analytic plan

Descriptive statistics and correlations characterized the sample and associations between relevant clinical constructs. Structural equation modeling (SEM) in Mplus examined the construct of urge intolerance using items from the PUTS and DTS (38). SEM is ideal for investigating latent theoretical constructs that cannot yet be directly measured or observed (39). Additionally, SEM allows for the further exploration of relationships between a latent construct and other observed characteristics.

A bifactor structural model was selected to measure the latent construct of urge intolerance. A bifactor approach specifies that the covariance among a set of items can be accounted for by a single, general factor that captures the common variance among all items in the set, while also allowing for subfactors to explain item subgroups (40). A bifactor model approach is recommended when there is a strong justification for capturing a superordinate construct along with distinct subordinate constructs. The bifactor model confers several statistical advantages. In addition to better specifying the model (i.e., delineating general and specific subfactors within a single model), this approach allows for simultaneous evaluation of item loading on both the general factor (i.e., urge intolerance) and unique subfactors (PUTS, DTS) (41). In order to evaluate the fit of the hypothesized bifactor model of urge intolerance with its corresponding urge and distress tolerance subfactors, the incremental value of including distinct subfactors of premonitory urge severity and distress tolerance within the model was examined. To evaluate the incremental value of each component of the model, nested models were compared through adjusted likelihood ratio tests (42). In the first step, we evaluated model fit for a full bifactor model, comprised of the PUTS and DTS items loading onto the general urge intolerance factor, as well as their respective urge severity and distress tolerance subfactors. In the second step, a constrained version of the bifactor model was evaluated, with the general latent factor urge intolerance fixed at 0, and the PUTS and DTS items freely loading onto their respective subfactors of urge severity and distress tolerance. In the third step, the bifactor model with urge severity subfactor was examined, with the distress tolerance subfactor fixed at 0. Finally, in the fourth step, the bifactor model with the distress tolerance subfactor was examined, with the urge severity subfactor fixed at 0.

Finally, after establishing a bifactor measurement model of urge intolerance, we examined a structural model where we predicted clinician-rated tic severity and tic impairment by the latent variable urge intolerance among adults with TS.

Models were estimated using weighted least squares mean and variance adjusted (WLSMV) estimation. Model fit was examined using the Comparative Fit Index (CFI), the Standardized Root Mean Square Residual (SRMR), and the Root Mean Square Error of Approximation (RMSEA). Following the precedent established by Hu and Bentler (43), acceptable model fit was defined by CFI values ≥0.95, SRMR values ≤0.08, and RMSEA values ≤0.06. Standardized path coefficients (β) for paths are reported for all models.

Results

Characteristics and clinical correlates

Adult participants exhibited a moderate level of tic severity (M = 16.22, SD = 9.54) and impairment (M = 10.00, SD = 10.77) (44). Participants reported experiencing premonitory urge severity (M = 21.01, SD = 7.25) that is comparable with other samples of adults with TS (34). Finally, adults reported moderate levels of distress tolerance (M = 37.46, SD = 11.41).

There was a moderate relationship between premonitory urge severity and distress tolerance (r = 0.39, p = 0.001), such that participants who endorsed greater levels of premonitory urges reported lower levels of distress tolerance. Premonitory urges exhibited moderate correlations with clinician-rated tic severity (r = 0.37, p = 0.002) and tic impairment (r = 0.43, p < 0.001), such that greater levels of premonitory urges were associated with greater levels of tic severity and impairment. Similarly, distress tolerance was moderately correlated with clinician-rated tic severity (r = 0.39, p = 0.001) and tic impairment (r = 0.39, p = 0.001), such that greater levels of tic severity and impairment were associated with lower levels of distress tolerance. Participants' age and sex were not significantly correlated with premonitory urge and distress tolerance ratings. However, participant age exhibited a small association with clinician-rated tic severity (r = 0.26, p = 0.020) and impairment (r = 0.29, p = 0.009), such that greater tic severity and impairment was associated with older participant age. Collectively, these findings highlight the modest positive relationships between premonitory urge severity, distress tolerance, tic severity, and tic impairment among adults with TS.

Evaluating bifactor model of urge intolerance

Step 1: General urge intolerance factor, urge severity and distress tolerance subfactors

First, we evaluated the least constrained model (Figure 1)—with all PUTS and DTS items loading onto the general latent factor, urge intolerance, and each items' respective subfactor, urge severity and distress tolerance. Model fit indices were acceptable (CFI = 0.95, RMSEA = 0.08 [90% CI = 0.06–0.09], SRMR = 0.08). Table 1 provides item loadings for the model. As shown in Table 1, the majority of PUTS and DTS scale items loaded onto the general factor of urge intolerance.

FIGURE 1
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Figure 1. Final bifactor model of urge intolerance, with urge severity and distress tolerance subfactors. Black lines indicate significant standardized item loadings, while gray lines indicate non-significant standardized item loadings.

TABLE 1
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Table 1. Final retained bifactor model of urge intolerance with premonitory urge and distress tolerance subfactors.

Step 2: Urge severity and distress tolerance subfactors, general urge intolerance factor fixed at 0

Next, we evaluated whether the exclusion of the general factor of urge intolerance improved the overall model fit. Here, the general factor of urge intolerance was constrained to 0. All items of the PUTS and DTS were exclusively allowed to load onto their respective subfactors of urge severity and distress tolerance. Relative to the full model, model fit statistics deteriorated (CFI = 0.86, RMSEA = 0.12 [90% CI = 0.10–0.13], SRMR = 0.17). Chi-square results indicated that the constrained model (model 2) fit significantly worse than the full model (model 1), χ2(24) = 111.94, p < 0.001. Stated differently, the full, unconstrained model (with the general urge intolerance factor and the premonitory urge and distress tolerance subfactors) demonstrated significantly better model fit than the partially constrained model with the general urge intolerance factor constrained to 0.

Step 3: General urge intolerance factor, urge severity subfactor (distress tolerance fixed at 0)

Next, we evaluated whether the exclusion of the subfactor of distress tolerance improved the overall model fit. Here, the subconstruct of distress tolerance was constrained to 0. Essentially, items on the DTS were only allowed to load onto the general subfactor urge intolerance. Relative to the unconstrained model (model 1), model fit indices deteriorated (CFI = 0.93, RMSEA = 0.09 [90% CI = 0.07–0.10], SRMR = 0.09). Chi-square results indicated that the partially constrained model (model 3) fit significantly worse than the full saturated model (model 1), χ2(15) = 54.05, p < 0.001. Stated differently, the saturated model (with the general urge intolerance factor and both distress tolerance and premonitory urge subfactors) demonstrated significantly better model fit than the partially constrained model with the distress tolerance subfactor constrained to 0.

Step 4: General urge intolerance factor, distress tolerance subfactor (urge severity fixed at 0)

Following this, we evaluated whether the exclusion of the subfactor of urge severity improved the overall model fit. Here, the subconstruct of urge severity was constrained to 0. Essentially, items on the PUTS were only allowed to load onto the general subfactor urge intolerance. Relative to the unconstrained model (model 1), model fit indices deteriorated (CFI = 0.92, RMSEA = 0.09 [90% CI = 0.07–0.11], SRMR = 0.09). Chi-square results indicated that the partially constrained model (model 4) fit significantly worse than the full saturated model (model 1), χ2(9) = 25.60, p < 0.01. Stated differently, the saturated model (with the general urge intolerance factor and both distress tolerance and premonitory urge subfactors) demonstrated significantly better model fit than the partially constrained model with the urge severity subfactor constrained to 0.

Final model

Collectively, these findings suggest that the full bifactor model of urge intolerance (Figure 1), which includes the general urge intolerance factor as well as its premonitory urge and distress tolerance subfactors, is the optimal fit. Consequently, the full bifactor model was used for subsequent analyses.

Urge intolerance, urge severity, and distress tolerance as predictors of TS severity and impairment

Figure 2 illustrates the relationship between the latent construct of urge intolerance, its subfactors premonitory urge severity and distress tolerance, and clinician-rated tic severity and impairment. Table 2 presents standardized path coefficients in the model. Model fit indices were acceptable (CFI = 0.95, RMSEA = 0.07 [90% CI = 0.05–0.08], SRMR = 0.08). Urge intolerance predicted tic severity (β = 0.35, p = 0.001) and impairment (β = 0.32, p = 0.005). Specifically, greater levels of urge intolerance predicted higher levels of tic severity and impairment.

FIGURE 2
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Figure 2. Final bifactor model of urge intolerance, with urge severity and distress tolerance subfactors, predicts YGTSS tic severity and tic impairment. Black lines indicate significant standardized item loadings, while gray lines indicate non-significant standardized item loadings.

TABLE 2
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Table 2. Standardized path coefficients for bifactor model of urge intolerance, with premonitory urge and distress tolerance subfactors, predicting YGTSS tic severity and tic impairment.

Discussion

This study examined urge intolerance in adults with TS—a latent construct that encapsulates the ability to tolerate aversive premonitory urges. The bifactor model of the latent construct of urge intolerance was found to be the optimal fit and consisted of a general urge intolerance factor, as well as both premonitory urge and distress tolerance subfactors. In this model, greater levels of urge severity (higher scores on the PUTS) and lower levels of distress tolerance (higher scores on the DTS) contributed to greater levels of urge intolerance (greater difficulty tolerating premonitory urge sensations). Consistent with theorized models, urge intolerance predicted clinician-rated tic severity and tic impairment. Although mixed evidence has been found for the relationship between premonitory urges and tic severity, these findings suggest that the influence of distress tolerance may partly explain the variable relationships premonitory urges and tic severity.

Based on these findings, there are at least two key implications for the field of TS. In regard to the assessment of TS, it is important for clinicians to consider and characterize urge intolerance when conducting evaluations of patients with TS. While this study leveraged existing validated rating scales and used SEM models, there is a need for the development of a standardized rating scale of urge intolerance for individuals with TS. This rating scale could blend items from both the PUTS and DTS, and potentially incorporate other related somatosensory sensations that may be interpreted as urges (e.g., “not just right” sensations). In addition to convergent validity with the PUTS, DTS, and tic severity scales, convergence with objective measures such as tic suppression tasks could also be informative. While empirical testing and validation of such a rating scale would take time, such a standardized scale would allow for a reliable and efficient approach to assess this potentially clinically meaningful construct.

In regard to the behavioral treatment of TS, it is important to consider that urge intolerance was found to predict both tic severity and tic impairment. This suggests that urge intolerance may serve as a novel treatment target to further tic severity reductions among adults with TS. Specifically, CBIT and related behavioral interventions build attention to premonitory urges (i.e., awareness training) and implement behavioral strategies to inhibit tics until premonitory urges are manageable (i.e., competing response training) (16–18). Thus, individuals who have greater difficulty tolerating distressing premonitory urges may have difficulty effectively implementing competing responses in the context of intense premonitory urges. While this possibility requires further empirical investigation, two potential therapeutic strategies exist that could be used to target and improve urge tolerance (i.e., reduce urge intolerance) among individuals with TS to help optimally implement behavioral treatment strategies. One set of skills focuses on mindfulness-based interventions. Gev et al. (45) found that youth with TS experienced reduced levels of tic frequency, distress, and premonitory urges when implementing acceptance-based strategies to address urge phenomena relative to tic suppression strategies. Similarly, Reese and colleagues found that adolescents and adults with TS exhibited improvements in tic severity and functional impairment following a mindfulness-based stress reduction (MBSR) intervention for tics (46, 47). The second set of potential therapeutic strategies focuses on providing distress tolerance skills, which are commonly taught in Dialectical Behavioral Therapy (DBT). This includes training individuals to bring mindful awareness to distressing emotions, physical sensations, and situations and equips them with coping strategies to manage these challenges (48). DBT skills training has been shown to increase distress tolerance capabilities across clinical and non-clinical populations (49, 50). Although future research is essential to determine whether these therapeutic strategies would enhance distress tolerance to premonitory urges (i.e., urge tolerance), such enhancements would have clear implications for reducing tic severity and tic impairment. As urge intolerance is related to TS outcomes for both youth and adults (e.g., tic severity, tic-related impairment) (28), it represents a novel and important therapeutic target. Further research is needed to explore the associations among distress tolerance, urge intolerance, and health-related quality of life among individuals with TS (51). Future work should test treatment strategies that target and improve urge intolerance—particularly during childhood—which may improve patients' clinical trajectories across the lifespan.

Despite the strengths of the present investigation, some limitations exist. First, our bifactor model of the latent construct of urge intolerance was based on subjective, self-report measures (i.e., PUTS, DTS). While these measures are commonly used and facilitate generalizability to other TS studies, they are both self-report ratings. Future research should include a multi-modal assessment of urge intolerance. Alongside self-report ratings, this examination could include clinician-administered measures of premonitory urges (I-PUTS), and standardized tic suppression tasks. This could provide further insights into the relationship between premonitory urges, urge intolerance, and tic severity. It is also important to acknowledge that while many of the instruments utilized in this investigation (i.e., YGTSS, PUTS) have been extensively validated within this clinical population, the DTS has received limited psychometric evaluation in work with adults with TS. Future research is needed to establish the reliability and validity of the DTS within this clinical population. Second, the sample size in the present study was relatively modest for SEM analyses. Despite this, we were able to validate the bifactor model of urge intolerance and identify significant pathways between urge intolerance and TS clinical scales. Finally, the present sample was drawn from a long-term follow-up assessment of a clinical trial for youth with TS. While the sample clinical characteristics are comparable to other samples of adults with TS, future studies should seek to replicate and expand upon findings in both treatment-seeking and non-treatment seeking samples of adults with TS.

In summary, this study provides further evidence for the construct of urge intolerance among patients with TS. Findings highlight the importance of urge intolerance in relation to tic severity and impairment. While behavioral therapies like CBIT remain the front-line treatment for youth and adults with TS (16, 22, 29, 52), patients who do not fully respond to behavioral therapies for tics may benefit from additional therapeutic strategies that target urge intolerance. This could include mindfulness-based interventions and/or distress tolerance skills to enable patients to tolerate distressing premonitory urge sensations. For youngsters with TS, developmentally tailored strategies could be taught alongside CBIT to help youth better tolerate distressing premonitory urges. In turn, youth would be able to optimally implement behavioral strategies (i.e., competing responses) to inhibit tic expression and response to behavioral therapy. This is important because youth who exhibit a treatment response to CBIT in childhood continue to experience therapeutic improvement 11 years later (21) which may be accompanied by other therapeutic benefits as well. Meanwhile for adults with TS, the utilization of strategies targeting urge intolerance could help improve the implementation of behavioral strategies (i.e., competing responses) in the context of treatment. This could lead to greater treatment response rates among those receiving behavior therapy for TS. Ultimately, this line of research holds the potential to provide new insights into the mechanisms underlying tic severity reductions and improve therapeutic outcomes for patients with TS. However, future research is needed to replicate and extend these findings and explore them within the context of treatment.

Data availability statement

Generated datasets are not available at this time due to forthcoming manuscripts. However, we intend to make the datasets available to qualified investigators upon request once all articles are finalized. Requests to access the datasets should be directed to JM, amZtY2d1aXJlJiN4MDAwNDA7amhtaS5lZHU=.

Ethics statement

The studies involving human participants were reviewed and approved by respective institutions, including UCLA Semel Institute for Neuroscience and Human Behavior, Marquette University, and Weill-Cornell Medicine. The patients/participants provided their written informed consent to participate in this study.

Author contributions

KR contributed to the conceptualization, methodology, formal analysis, validation, and writing–original draft. AD, ER, DW, and JP all contributed to the conceptualization, methodology, formal analysis, and writing–review and editing. JM contributed to the conceptualization, methodology, validation, supervision, and writing–review and editing. All other study authors contributed to the data curation, and/or writing–review and editing. All authors contributed to the article and approved the submitted version.

Funding

This study was funded by the Tourette Association of America Research Grants Award (JP, Walkup, Woods, & Specht) and the Tourette Association of America Young Investigator Award (KR).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. Scahill L, Specht M, Page C. The prevalence of tic disorders and clinical characteristics in children. J Obsessive-Compuls Relat Disord. (2014) 3:394–400. doi: 10.1016/j.jocrd.2014.06.002

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Scharf JM, Miller LL, Gauvin CA, Alabiso J, Mathews CA, Ben-Shlomo Y. Population prevalence of Tourette syndrome: a systematic review and meta-analysis. Mov Disord. (2015) 30:221–8. doi: 10.1002/mds.26089

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Leckman JF, King RA, Bloch MH. Clinical features of Tourette syndrome and tic disorders. J Obsessive-Compuls Relat Disord. (2014) 3:372–9. doi: 10.1016/j.jocrd.2014.03.004

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Freeman RD, Fast DK, Burd L, Kerbeshian J, Robertson MM, Sandor P. An international perspective on Tourette syndrome: selected findings from 3,500 individuals in 22 countries. Dev Med Child Neurol. (2000) 42:436–47. doi: 10.1017/S0012162200000839

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Specht MW, Woods DW, Piacentini J, Scahill L, Wilhelm S, Peterson AL, et al. Clinical characteristics of children and adolescents with a primary tic disorder. J Dev Phys Disabil. (2011) 23:15–31. doi: 10.1007/s10882-010-9223-z

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Ramsey KA, Essoe JKY, Storch EA, Lewin AB, Murphy TK, McGuire JF. The role of affect lability on tic severity and impairment in youth with Tourette's disorder. J Obsessive-Compuls Relat Disord. (2020) 27:100578. doi: 10.1016/j.jocrd.2020.100578

CrossRef Full Text | Google Scholar

7. Storch EA, Hanks CE, Mink JW, McGuire JF, Adams HR, Augustine EF, et al. Suicidal thoughts and behaviors in children and adolescents with chronic tic disorders. Depress Anxiety. (2015) 32:744–53. doi: 10.1002/da.22357

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Johnco C, McGuire JF, McBride NM, Murphy TK, Lewin AB, Storch EA. Suicidal ideation in youth with tic disorders. J Affect Disord. (2016) 200:204–11. doi: 10.1016/j.jad.2016.04.027

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Conelea CA, Woods DW, Zinner SH, Budman CL, Murphy TK, Scahill LD, et al. The impact of Tourette syndrome in adults: results from the Tourette syndrome impact survey. Community Ment Health J. (2013) 49:110–20. doi: 10.1007/s10597-011-9465-y

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Storch EA, Merlo LJ, Lack C, Milsom VA, Geffken GR, Goodman WK, et al. Quality of life in youth with Tourette's syndrome and chronic tic disorder. J Clin Child Adolesc Psychol. (2007) 36:217–27. doi: 10.1080/15374410701279545

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Ricketts EJ, Montalbano GE, Burgess HJ, McMakin DL, Coles ME, Piacentini J, et al. Sleep and chronotype in adults with persistent tic disorders. J Clin Psychol. (2022) 78:1516–39. doi: 10.1002/jclp.23323

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Hanks CE, McGuire JF, Lewin AB, Storch EA, Murphy TK. Clinical correlates and mediators of self-concept in youth with chronic tic disorders. Child Psychiatry Hum Dev. (2016) 47:64–74. doi: 10.1007/s10578-015-0544-0

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Ricketts EJ, Wolicki SB, Danielson ML, Rozenman M, McGuire JF, Piacentini J, et al. Academic, interpersonal, recreational, and family impairment in children with Tourette syndrome and attention-deficit/hyperactivity disorder. Child Psychiatry Hum Dev. (2022) 53:3–15. doi: 10.1007/s10578-020-01111-4

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Storch EA, Johnco C, McGuire JF, Wu MS, McBride NM, Lewin AB, et al. An initial study of family accommodation in children and adolescents with chronic tic disorders. Eur Child Adolesc Psychiatry. (2017) 26:99–109. doi: 10.1007/s00787-016-0879-5

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Conelea CA, Woods DW, Zinner SH, Budman C, Murphy T, Scahill LD, et al. Exploring the impact of chronic tic disorders on youth: results from the Tourette syndrome impact survey. Child Psychiatry Hum Dev. (2011) 42:219–42. doi: 10.1007/s10578-010-0211-4

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Pringsheim T, Okun MS, Müller-Vahl K, Martino D, Jankovic J, Cavanna AE, et al. Practice guideline recommendations summary: treatment of tics in people with Tourette syndrome and chronic tic disorders. Neurology. (2019) 92:896–906. doi: 10.1212/WNL.0000000000007466

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Murphy TK, Lewin AB, Storch EA, Stock S. Practice parameter for the assessment and treatment of children and adolescents with tic disorders. J Am Acad Child Adolesc Psychiatry. (2013) 52:1341–59. doi: 10.1016/j.jaac.2013.09.015

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Andrén P, Jakubovski E, Murphy TL, Woitecki K, Tarnok Z, Zimmerman-Brenner S, et al. European clinical guidelines for Tourette syndrome and other tic disorders-version 20 Part II: psychological interventions. Eur Child Adolesc Psychiatry. (2022) 31:403–23. doi: 10.1007/s00787-021-01845-z

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Woods DW, Piacentini JC, Scahill L, Peterson AL, Wilhelm S, Chang S, et al. Behavior therapy for tics in children: acute and long-term effects on psychiatric and psychosocial functioning. J Child Neurol. (2011) 26:858–65. doi: 10.1177/0883073810397046

PubMed Abstract | CrossRef Full Text | Google Scholar

20. McGuire JF, Ginder N, Ramsey K, Essoe JKY, Ricketts EJ, McCracken JT, et al. Optimizing behavior therapy for youth with Tourette's disorder. Neuropsychopharmacology. (2020) 45:2114–9. doi: 10.1038/s41386-020-0762-4

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Espil FM, Woods DW, Specht MW, Bennett SM, Walkup JT, Ricketts EJ, et al. Long-term outcomes of behavior therapy for youth with Tourette disorder. J Am Acad Child Adolesc Psychiatry. 61:764–71. (2022). doi: 10.1016/j.jaac.2021.08.022

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Wilhelm S, Peterson AL, Piacentini J, Woods DW, Deckersbach T, Sukhodolsky DG, et al. Randomized trial of behavior therapy for adults with Tourette's disorder. Arch Gen Psychiatry. (2012) 69:795–803. doi: 10.1001/archgenpsychiatry.2011.1528

PubMed Abstract | CrossRef Full Text | Google Scholar

23. McGuire JF, Ricketts EJ, Piacentini J, Murphy TK, Storch EA, Lewin AB. Behavior therapy for tic disorders: an evidenced-based review and new directions for treatment research. Curr Dev Disord Rep. (2015) 2:309–17. doi: 10.1007/s40474-015-0063-5

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Ramsey K, McGuire J. Tourette's Disorder. In: Storch EA, Abramowitz JS, McKay D, eds. Complexities in Obsessive Compulsive and Related Disorders: Advances in Conceptualization and Treatment. New York, NY: Oxford University Press (2021). p. 201–30. doi: 10.1093/med-psych/9780190052775.003.0012

CrossRef Full Text | Google Scholar

25. Woods DW, Piacentini JC, Chang SW, Deckersbach T, Ginsburg GS, Peterson AL, et al. Managing Tourette Syndrome: A Behavioral Intervention for Children and Adults (Therapist Guide). New York, NY: Oxford University Press (2008). doi: 10.1093/med:psych/9780195341287.001.0001

CrossRef Full Text | Google Scholar

26. Essoe JKY, Ramsey KA, Singer HS, Grados M, McGuire JF. Mechanisms underlying behavior therapy for tourette's disorder. Curr Dev Disord Rep. (2021) 8:161–74. doi: 10.1007/s40474-021-00225-1

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Leckman JF, Walker DE, Cohen DJ. Premonitory urges in Tourette's syndrome. Am J Psychiatry. (1993) 150:98–102. doi: 10.1176/ajp.150.1.98

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Ramsey KA, Essoe JKY, Storch EA, Lewin AB, Murphy TK, McGuire JF. Urge intolerance and impairment among youth with Tourette's and chronic tic disorders. Child Psychiatry Hum Dev. (2021) 52:761–71. doi: 10.1007/s10578-020-01085-3

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Piacentini J, Woods DW, Scahill L, Wilhelm S, Peterson AL, Chang S, et al. Behavior therapy for children with Tourette disorder: a randomized controlled trial. JAMA. (2010) 303:1929–37. doi: 10.1001/jama.2010.607

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Leckman JF, Riddle MA, Hardin MT, Ort SI, Swartz KL, Stevenson J, et al. The yale global tic severity scale: initial testing of a clinician-rated scale of tic severity. J Am Acad Child Adolesc Psychiatry. (1989) 28:566–73. doi: 10.1097/00004583-198907000-00015

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Storch EA, Murphy TK, Geffken GR, Sajid M, Allen P, Roberti JW, et al. Reliability and validity of the Yale global tic severity scale. Psychol Assess. (2005) 17:486–91. doi: 10.1037/1040-3590.17.4.486

PubMed Abstract | CrossRef Full Text | Google Scholar

32. McGuire JF, Piacentini J, Storch EA, Murphy TK, Ricketts EJ, Woods DW, et al. A multicenter examination and strategic revisions of the Yale global tic severity scale. Neurology. (2018) 90:e1711–9. doi: 10.1212/WNL.0000000000005474

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Woods DW, Piacentini J, Himle MB, Chang S. Premonitory urge for tics scale (PUTS): initial psychometric results and examination of the premonitory urge phenomenon in youths with tic disorders. J Dev Behav Pediatr. (2005) 26:397–403. doi: 10.1097/00004703-200512000-00001

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Reese HE, Scahill L, Peterson AL, Crowe K, Woods DW, Piacentini J, et al. The premonitory urge to tic: measurement, characteristics, and correlates in older adolescents and adults. Behav Ther. (2014) 45:177–86. doi: 10.1016/j.beth.2013.09.002

PubMed Abstract | CrossRef Full Text | Google Scholar

35. McGuire JF, McBride N, Piacentini J, Johnco C, Lewin AB, Murphy TK, et al. The premonitory urge revisited: an individualized premonitory urge for tics scale. J Psychiatr Res. (2016) 83:176–83. doi: 10.1016/j.jpsychires.2016.09.007

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Simons JS, Gaher RM. The distress tolerance scale: development and validation of a self-report measure. Motiv Emot. (2005) 29:83–102. doi: 10.1007/s11031-005-7955-3

CrossRef Full Text | Google Scholar

37. Sheehan DV, Lecrubier Y, Sheehan KH, Amorim P, Janavs J, Weiller E, et al. The Mini-International Neuropsychiatric Interview (MINI): the development and validation of a structured diagnostic psychiatric interview for DSM-IV and ICD-10. J Clin Psychiatry. (1998) 59:22–33. doi: 10.1037/t18597-000

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Muthén LK, Muthén BO. Mplus User's Guide. Eighth Los Angeles, CA: Muthén & Muthén. (1998).

Google Scholar

39. Wang J, Wang X. Structural Equation Modeling: Applications Using Mplus. 2nd ed. West Sussex, UK: Wiley. (2019). doi: 10.1002/9781119422730

CrossRef Full Text | Google Scholar

40. Reise SP. The rediscovery of bifactor measurement models. Multivar Behav Res. (2012) 47:667–96. doi: 10.1080/00273171.2012.715555

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Chen FF, Hayes A, Carver CS, Laurenceau JP, Zhang Z. Modeling general and specific variance in multifaceted constructs: a comparison of the bifactor model to other approaches. J Pers. (2012) 80:219–51. doi: 10.1111/j.1467-6494.2011.00739.x

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Satorra A, Bentler PM. Ensuring positiveness of the scaled difference chi-square test statistic. Psychometrika. (2010) 75:243–8. doi: 10.1007/s11336-009-9135-y

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Hu L, Bentler PM. Cutoff criteria for fit indexes in covariance structure analysis: conventional criteria versus new alternatives. Struct Equ Model Multidiscip J. (1999) 6:1–55. doi: 10.1080/10705519909540118

CrossRef Full Text | Google Scholar

44. McGuire JF, Piacentini J, Storch EA, Ricketts EJ, Woods DW, Peterson AL, et al. Defining tic severity and tic impairment in Tourette disorder. J Psychiatr Res. (2021) 133:93–100. doi: 10.1016/j.jpsychires.2020.12.040

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Gev E, Pilowsky-Peleg T, Fennig S, Benaroya-Milshtein N, Woods DW, Piacentini J, et al. Acceptance of premonitory urges and tics. J Obsessive-Compuls Relat Disord. (2016) 10:78–83. doi: 10.1016/j.jocrd.2016.06.001

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Reese HE, Vallejo Z, Rasmussen J, Crowe K, Rosenfield E, Wilhelm S. Mindfulness-based stress reduction for tourette syndrome and chronic tic disorder: a pilot study. J Psychosom Res. (2015) 78:293–8. doi: 10.1016/j.jpsychores.2014.08.001

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Reese HE, Brown WA, Summers BJ, Shin J, Wheeler G, Wilhelm S. Feasibility and acceptability of an online mindfulness-based group intervention for adults with tic disorders. Pilot Feasibility Stud. (2021) 7:82. doi: 10.1186/s40814-021-00818-y

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Linehan MM, Wilks CR. The course and evolution of dialectical behavior therapy. Am J Psychother. (2015) 69:97–110. doi: 10.1176/appi.psychotherapy.2015.69.2.97

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Zeifman RJ, Boritz T, Barnhart R, Labrish C, McMain SF. The independent roles of mindfulness and distress tolerance in treatment outcomes in dialectical behavior therapy skills training. Personal Disord. (2020) 11:181–90. doi: 10.1037/per0000368

PubMed Abstract | CrossRef Full Text | Google Scholar

50. Muhomba M, Chugani CD, Uliaszek AA, Kannan D. Distress tolerance skills for college students: a pilot investigation of a brief DBT group skills training program. J Coll Stud Psychother. (2017) 31:247–56. doi: 10.1080/87568225.2017.1294469

CrossRef Full Text | Google Scholar

51. Cavanna AE, David K, Bandera V, Termine C, Balottin U, Schrag A, et al. Health-related quality of life in gilles de la Tourette syndrome: a decade of research. Behav Neurol. (2013) 27:83–93. doi: 10.1155/2013/732038

PubMed Abstract | CrossRef Full Text | Google Scholar

52. McGuire JF, Piacentini J, Brennan EA, Lewin AB, Murphy TK, Small BJ, et al. A meta-analysis of behavior therapy for Tourette syndrome. J Psychiatr Res. (2014) 50:106–12. doi: 10.1016/j.jpsychires.2013.12.009

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: Tourette Syndrome, premonitory urge, distress tolerance, adults, impairment

Citation: Ramsey KA, De Nadai AS, Espil FM, Ricketts E, Stiede JT, Schild J, Specht MW, Woods DW, Bennet S, Walkup JT, Chang S, Piacentini J and McGuire JF (2022) Urge intolerance predicts tic severity and impairment among adults with Tourette syndrome and chronic tic disorders. Front. Psychiatry 13:929413. doi: 10.3389/fpsyt.2022.929413

Received: 26 April 2022; Accepted: 11 July 2022;
Published: 10 August 2022.

Edited by:

Amanda Ludlow, University of Hertfordshire, United Kingdom

Reviewed by:

A. Cavanna, Birmingham and Solihull Mental Health NHS Foundation Trust, United Kingdom
David Houghton, University of Texas Medical Branch at Galveston, United States
Yukiko Kano, The University of Tokyo, Japan

Copyright © 2022 Ramsey, De Nadai, Espil, Ricketts, Stiede, Schild, Specht, Woods, Bennet, Walkup, Chang, Piacentini and McGuire. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Joseph F. McGuire, amZtY2d1aXJlJiN4MDAwNDA7amhtaS5lZHU=

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