Abstract
Repetitive negative thinking and intolerance of uncertainty are risk and maintenance factors for emotional disorders. Although emerging evidence suggests that intolerance of uncertainty predicts increases in distress through repetitive negative thinking, these relationships have yet to be investigated among veterans. The present study examines if repetitive negative thinking mediates the relationships of intolerance of uncertainty with stress, disordered symptoms and impairment among a mixed clinical sample of veterans. Two hundred and forty-four treatment-seeking veterans with diagnoses of major depressive disorder, panic disorder, or posttraumatic stress disorder completed measures of intolerance of uncertainty, repetitive negative thinking, stress, impairment, depression, panic, and posttraumatic stress prior to receiving treatment. Mediation models revealed indirect effects of intolerance of uncertainty through repetitive negative thinking on stress and impairment in the full sample, and on disordered symptoms in subsamples with major depressive disorder and posttraumatic stress disorder. Conversely, intolerance of uncertainty did not have direct or indirect effects on disordered symptoms in a panic disorder subsample. Findings suggest that repetitive negative thinking and intolerance of uncertainty uniquely contribute to stress, impairment, and disordered symptoms, but repetitive negative thinking, may, in part, drive intolerance of uncertainty’s contribution to emotional disorders. Interventions for repetitive negative thinking might improve the efficacy of existing transdiagnostic treatment protocols. Cross-sectional data is a limitation of the present study. Prospective designs in civilian samples can better establish the temporality of these relationships and if they are generalizable to the larger population.
Keywords: repetitive negative thinking, uncertainty, emotional disorders, distress, impairment
Clinical research has increasingly focused on identifying psychological processes that contribute to a range of mental health problems or transdiagnostic factors (Eaton et al., 2015; Lynch et al., 2021). Repetitive negative thinking (RNT) and intolerance of uncertainty (IU) are highly related cognitive factors that increase risk for and maintain emotional disorders (de Jong-Meyer et al., 2009; Mahoney & McEvoy, 2012b; Topper et al., 2010). Yet, the nature of their relationship and their respective roles in psychopathology remain unclear, particularly among veterans. The present study examines if repetitive negative thinking mediates the relationships of intolerance of uncertainty with stress, impairment, and disordered symptoms in a sample of veterans with emotional disorders.
Repetitive negative thinking (RNT) describes recurrent, intrusive, and difficult-to-control negative cognitions. One form of RNT, worry, concerns future outcomes, and is associated with increased depressive, anxiety, and posttraumatic stress symptoms (Tull et al., 2011; Vîslă et al., 2022). Worry was first studied in the context of generalized anxiety disorder (GAD); however, individuals with depressive, anxiety, and trauma- and stressor-related disorders report greater worry than healthy controls and individuals with other mental health problems (Arditte-Hall et al., 2019; Bakhshian et al., 2013; Olatunji et al., 2010). While worry is more frequent and severe in individuals with GAD, it is increasingly viewed as a cognitive process that may perpetuate other emotional disorders (Vîslă et al., 2022).
Rumination, another well-studied form of RNT, focuses more on the past (Papageorgiou & Wells, 1999). Rumination describes repeatedly and passively thinking about the causes and consequences of distressing symptoms (Nolen-Hoeksema, 1991). Rumination was initially studied in reference to major depressive disorder (MDD) and predicts the onset and worsening of depression symptoms (Nolen-Hoeksema, 2000). Rumination is more frequent and severe in individuals with MDD relative to healthy controls and individuals with other disorders (Olatunji et al., 2013). Yet, rumination is not exclusive to MDD. Rumination also predicts increases in anxiety and posttraumatic stress symptoms (McLaughlin & Nolen-Hoeksema, 2011), and individuals with emotional disorders report higher levels of rumination relative to healthy controls (Olatunji et al., 2013). Rumination may be especially relevant to posttraumatic stress disorder (PTSD), given its emphasis on a past traumatic event, and evidence shows that individuals with PTSD report higher levels of rumination compared to non-trauma- and trauma-exposed individuals without PTSD (Moulds et al., 2020). Rumination might be particularly detrimental to veterans. Relative to civilians, rumination is more predictive of posttraumatic stress symptoms and suicidality in veterans (Hetelekides et al., 2022).
While most findings specifically focus on worry and rumination, researchers increasingly recognize their considerable overlap and question how much they are meaningfully different (McEvoy et al., 2010; Topper et al., 2010). Consequently, RNT was recently introduced as a broad transdiagnostic cognitive process to subsume worry, rumination, and other maladaptive thinking patterns. Measures of RNT (e.g., Ehring et al., 2011; McEvoy et al., 2010) do not explicitly refer to “worry” or “rumination,” nor do they specify whether negative thoughts concern future or past issues or situations. Rather, items capture the tendency to experience negative thoughts as intrusive (“Thoughts intrude into my mind”), recurring (“I keep thinking about the same issue all the time;” Ehring et al., 2011) and uncontrollable (“Once I start thinking about the situation, I can’t stop;” McEvoy et al., 2010). RNT measures exhibit strong relationships with established measures of worry and rumination and are just as predictive of emotional disorder symptom severity (Ehring et al., 2011; McEvoy et al., 2010). Further, evidence demonstrates that RNT can be effectively targeted to treat emotional disorders (Akbari et al., 2015). However, to effectively target RNT, it is critical to understand what prompts individuals to engage in it in the first place.
Individuals may engage in RNT about an issue or situation that is uncertain. That is, they may be high in IU, or the tendency to perceive ambiguity as harmful and experience discomfort when encountering uncertain stimuli (Dugas et al., 1997). IU was introduced to contextualize GAD’s hallmark symptom, excessive and uncontrollable worry. The Intolerance of Uncertainty Model (IUM) theorizes that individuals with GAD find uncertain situations particularly threatening and cope with the associated distress they feel by considering a range of future adverse outcomes (Dugas et al., 1995). That is, they worry to increase their sense of certainty and control when facing ambiguity (Freeston et al., 1994).
In line with IUM, findings support that IU predicts GAD onset, GAD symptom severity, and worry (Dugas et al., 1997; Gentes & Ruscio, 2011; Ladoucer et al., 1997). However, IU is not unique to GAD and worry. Evidence demonstrates that IU is a risk and maintenance factor for other disorders characterized by RNT (Mahoney & McEvoy, 2012b), including MDD, anxiety disorders, and PTSD (Carleton et al., 2012; Hunt et al., 2022; McEvoy et al., 2019; White & Gumley, 2009). Accumulating findings show that IU predicts rumination (e.g., de Jong-Meyer et al., 2009; Liao & Wei, 2011; Yook et al., 2010) and other forms of RNT such as catastrophizing and post-event processing (Rondung et al., 2019; Shikatani et al., 2016).
Although a growing body of literature supports IU’s relationship with RNT, the directionality and nature of their relationship are less studied. IU is expected to precede engagement in RNT (Dugas et al., 2004; Bredemeier & Berenbaum, 2008), and multiple studies support this theory. Measurement models show that IU connects more distal, higher-order factors like neuroticism to worry and rumination (e.g., Clarke & Kiropoulos, 2021; McEvoy & Mahoney, 2012, 2013), and IU mediates the relationship between retrospective reports of anxious parenting and worry (Zlomke & Young, 2009). These findings suggest IU drives the development of RNT. Still, another study found that IU and worry exhibit a reciprocal relationship over time in adolescents (Dugas et al., 2012).
Specific forms of RNT have been evaluated as mediators between IU and symptoms in non-clinical and clinical samples. Cross-sectionally and longitudinally, Huang et al. (2019) found that worry mediated the relationships of IU with anxiety and depression, and Yao et al. (2022) found that rumination mediated the relationship between IU and depression among community participants. Yook and colleagues (2010) found that worry partially mediated the relationship between IU and anxiety and fully mediated the relationship between IU and depression in a small sample of individuals with MDD and/or GAD. RNT may explain why IU predicts symptoms of depression and anxiety.
While multiple findings suggest IU may influence emotional disorders through worry and rumination, no studies have evaluated the indirect effect of IU through RNT on symptoms in a clinical sample of veterans. As veterans exhibit higher rates of emotional disorders (Black et al., 2004; Kessler et al., 2005) and are more likely to experience resulting problems (i.e., homelessness, suicidality; Olenick et al., 2015) relative to civilians, they could benefit from treatments informed by an improved understanding of transdiagnostic factors that contribute to anxiety, depressive and related disorders.
The present investigation addresses gaps in the literature by exploring RNT as a mediator between IU and psychopathological outcomes in a mixed clinical sample of treatment-seeking veterans with emotional disorders. The indirect effects of IU through RNT on 1) stress and 2) impairment will be tested in a full sample of participants with primary emotional disorder diagnoses, while the indirect effects of IU through RNT will be tested on 3) depressive symptoms in a subsample of participants with MDD; 4) panic symptoms in a subsample of participants with panic disorder; and 5) posttraumatic stress symptoms in a subsample of participants with PTSD. RNT is expected to partially mediate the relationships of IU with stress and impairment in the full sample and partially mediate the relationships of IU with specific symptoms in the MDD, panic disorder, and PTSD subsamples.
Methods
Participants
The current study includes participants (175 males and 69 females) enrolled in larger ongoing randomized controlled trials. Participants presented to a Southeastern Veteran Affairs Healthcare System (VAHCS) for treatment and agreed to enroll in a study of evidence-based psychotherapy for emotional disorders. To be eligible, participants needed to 1) demonstrate competence to complete study consent and procedures, 2) meet diagnostic criteria for a primary emotional disorder of MDD, PTSD, or panic disorder in the 5th edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM-5; American Psychiatric Association, 2013), and 3) be 18 to 80 years old. Participants were not eligible to participate if they had 1) recently (≤ 2 months) been hospitalized or made a suicide attempt; 2) an acute, severe illness or medical condition that would impede study procedures; or 3) a psychotic, personality, bipolar, or substance use disorder diagnosis. Two-hundred fifty-seven participants were eligible and included in the study.
Participants ranged in age from 20 to 80 years old (M = 45.91; SD = 13.97), and their racial and ethnic makeup was consistent with that of the Southeastern United States (55.3% White, 36.1% Black, 7% Hispanic/Latino, 0.8% Native American, 0.4% Asian American, and 0.4% Other). Approximately half of participants were employed (52.3%). Participants varied in educational attainment (0.4% did not graduate high school, 13.7% completed high school, 46.1% finished some college or earned a 2-year degree, 39.8% earned a college degree or more) and income (37.8% $0–40K, 40.4% $40–80K, 21.71% >$80K). Primary diagnoses included MDD (n = 108), panic disorder (n = 51), and PTSD (n = 85), and 75% of participants met criteria for at least one comorbid diagnosis. Given symptom-specific outcomes of interest, participants with comorbid MDD, panic disorder, and PTSD were included in disorder subsamples. The present study included a full sample (N= 244) and three subsamples (MDD = 190; panic disorder = 65; PTSD = 140).
Procedures
The local VAHCS Research and Development Committee and the affiliated university’s institutional review board approved all study procedures. At baseline, participants completed informed consent documents and self-report measures, and underwent a diagnostic interview conducted by trained clinician interviewers.
Measures
Anxiety Disorders Interview Schedule-5
The Anxiety Disorders Interview Schedule-5 (ADIS-5; Brown, 2014) is a semi-structured interview designed to diagnose anxiety, mood, obsessive-compulsive, trauma, and related disorders using DSM-5 diagnostic criteria. A diagnosis of PTSD requires endorsement of exposure to and symptoms in response to a criterion A traumatic event, defined in DSM-5 as experiencing or witnessing events associated with death, serious injury or sexual violence. ADIS-5 is a valid diagnostic interview for emotional disorders and exhibits excellent interrater reliability (Brown, 2014). As data collection is ongoing, interrater reliability has yet to be available for this dataset. In past studies from the same research group (Gros & Allan, 2019), independent raters scored 20% of interviews, and findings demonstrated excellent interrater agreement.
Intolerance of Uncertainty Scale-12
The Intolerance of Uncertainty Scale-12 (IUS-12; Carleton et al., 2007). The IUS-12 is a 12-item self-report measure of the tendency to perceive the potential of negative outcomes as threatening. Respondents rate how characteristic items are of them in general on a 5-point Likert scale from 1 (not at all characteristic of me) to 5 (entirely characteristic of me). Item ratings are summed for a total score, with higher scores indicating greater intolerance of uncertainty (score range: 12–60). The IUS-12 exhibits strong relationships with a range of anxiety disorder symptoms (Carleton et al., 2007), and its longer predecessor, the intolerance of uncertainty scale (IUS), demonstrates good test-retest reliability after five weeks (r = .74) and accounts for additional variance in anxiety symptoms beyond neuroticism (Freeston et al., 1994). The IUS-12 demonstrated excellent internal consistency in the current investigation (α = 0.92).
Perseverative Thinking Questionnaire
The Perseverative Thinking Questionnaire (PTQ; Ehring et al., 2011) is a 15-item self-report measure of repetitive negative thinking. PTQ items are rated on a 5-point Likert scale from 0 (never) to 4 (almost always) based on how typical they are of a person’s reactions to stressors. Item responses are summed to produce a PTQ total score, with higher scores suggesting higher levels of repetitive negative thinking (score range: 0–75). The PTQ correlates strongly with worry and rumination measures, demonstrating satisfactory test-retest reliability after four weeks (r = .69; Ehring et al., 2011). In this study, the PTQ exhibited excellent internal consistency (α = 0.96).
Patient Health Questionnaire-9
The Patient Health Questionnaire-9 (PHQ-9; Kroenke, 2001) is a 9-item self-report measure of depressive symptoms. Items are rated on a 4-point Likert scale from 0 (not at all) to 3 (nearly every day) based on how bothersome symptoms have been in the preceding two weeks. Item responses are added to produce a total score, with higher scores reflecting greater symptom severity (score range: 0–27). The PHQ-9 predicts functional impairment and exhibits strong test-retest reliability after two days (r = .84; Kroenke, 2001). In the present study, the PHQ-9 demonstrated good internal consistency (α = 0.86).
Albany Panic and Phobia Questionnaire-Interoceptive Subscale
The Albany Panic and Phobia Questionnaire-Interoceptive Subscale (APPQ-I; Rapee et al., 1994) is a self-report measure of fear of specific activities, and the 8-item interoceptive subscale assesses fear of activities that induce physiological sensations characteristic of panic. APPQ items are rated on a 9-point Likert scale from 0 (no fear) to 8 (extreme fear) based on how much fear a person would expect to experience in the upcoming week if they engaged in an activity. Item ratings are summed to produce an APPQ-I subscale score, with higher scores suggesting greater fear of interoceptive symptom-inducing activities (score range: 0–64; Rapee et al., 1994). The APPQ-I is strongly associated with the anxiety sensitivity index, particularly the physical concerns relative to the social concerns subscales (Brown et al., 2005). The APPQ-I demonstrated good internal consistency in the current study (α = 0.86). As interoceptive fear is considered a core feature of panic disorder (Taylor et al., 2007), the APPQ-I was used as a proxy measure of panic symptoms.
PTSD Checklist-5 for DSM-5
The PTSD Checklist-5 for DSM-5 (PCL-5; Weathers et al., 2013) is a 20-item self-report measure of PTSD symptoms. Items are rated on a 5-point Likert scale from 0 (not at all) to 4 (extremely) based on how bothersome a symptom has been in the past month. Items are summed to produce a total PCL-5 score, with higher scores indicating higher symptom severity (range 0–80). The PCL-5 exhibits strong relationships with other measures of PTSD, weak relationships with measures of antisocial personality disorder and mania, and good test-retest reliability over one week (r = .82; Blevins et al., 2015). The PCL-5 exhibited excellent internal consistency in this study (α = 0.93).
Depression Anxiety Stress Scales-21-Stress Scale
The 7-item stress scale (DASS-21-S) in the Depression Anxiety Stress Scales-21 (DASS-21; Lovibond & Lovibond, 1995) is designed to assess tension and agitation. The DASS-21-S was employed in the present study as it assesses common, rather than unique, characteristics of depression and anxiety (Antony et al., 1998). Items are rated on a 4-point Likert scale from 0 (Did not apply to me at all) to 3 (Applied to me very much or most of the time) based on the degree to which a person experienced symptoms over the preceding week. Item responses are summed to create a total score, with higher scores indicating greater stress (range 0–21). The DASS-21-S is moderately associated with measures of anxiety and depression (Lovibond & Lovibond, 1995). In the present investigation, the DASS-21-S demonstrated good internal consistency (α = 0.88).
Illness Intrusiveness Ratings Scale
The Illness Intrusiveness Ratings Scale (IIRS; Devins, 2010) measures the extent to which illness or treatment interferes with different domains of functioning. Respondents rate 13 items on a 7-point Likert scale from 1 (not very much) to 7 (very much) about how much their illness and treatment currently interfere with their functioning in different domains. Item ratings are summed to produce a total score, with higher scores suggesting greater functional impairment (range: 7–91). The IIRS is associated with different levels of care and symptom severity among patients with different illnesses and demonstrates good to excellent test-retest reliability over 3–18 months (r = .79-.85). The IIRS exhibited excellent internal consistency in this investigation (α = 0.91).
Statistical analysis
All data were inspected for item-level missing values. Thirteen participants in the sample, thirteen participants in the MDD subsample, three in the panic disorder subsample, and twelve in the PTSD subsample had significant item-level missing data (>10%) on outcome measures and were excluded from analyses. The remaining full sample and subsamples contained <1% item-level missing data. Item-level missing values were replaced using within-scale mean substitution for remaining participants with minimal missing data.
IBM SPSS Statistics (Version 19) was used to conduct initial correlations between 4 variables in the full sample (IU, RNT, stress, and functional impairment) and the three variables in each subsample (IU and RNT with depressive, panic, and PTSD symptoms), generating 15 correlations total. A p-value less than .05 was deemed statistically significant; however, due to multiple comparisons, a Bonferroni correction was used (.05/15 = .003).
To determine if RNT mediated the relationship between IU and outcomes, bootstrap mediation analyses through the SPSS Process macro were conducted. Since bootstrap mediation is nonparametric and does not assume normality on the sampling distribution of the indirect effect, it is considered more robust for mediation analyses than Sobel’s test (Preacher & Hayes, 2004, 2008). The present analyses used 5000 bootstrap samples to estimate indirect effects, which were considered statistically significant if the 95% bias-corrected confidence intervals did not include zero (Preacher & Hayes, 2004, 2008). Per Wen and Fan’s (2015) recommendation, indirect and direct effects ratios were reported as effect sizes for consistent mediation paths in addition to the ratio of indirect and total effects. For inconsistent mediation, as the ratio of indirect and direct effects is not considered an appropriate effect size (Wen & Fan, 2015), the standardized, which is considered directly interpretable, was reported (Preacher & Kelly, 2011).
Results
Correlations
Pearson correlations, mean scores, and standard deviations for each of the four variables in the full sample and each of the three variables in the three subsamples are presented in Table 1, respectively. IU, RNT, stress, and functional impairment exhibited medium to large relationships with one another in the full sample (rs = .42-.61). MDD and PTSD subsample relationships among IU, RNT, depressive, and PTSD symptoms ranged from medium to large (rs = .42-.64). Although PTQ moderately correlated with panic symptoms in the panic disorder subsample, the relationship between IU and panic symptoms was not significant. Further, after Bonferroni correction for multiple comparisons (p < 0.05/15 = 0.003), relationships among variables remained significant in the full sample and MDD and PTSD subsamples, but PTQ no longer correlated with symptoms in the panic disorder subsample.
Table 1.
Means, standard deviations (SDs) and correlations of measures in full sample and subsamples
| Full sample (N = 244) | ||||||
|---|---|---|---|---|---|---|
| Measure | M | SD | 1 | 2 | 3 | 4 |
|
| ||||||
| 1 IUS-12 | 39.15 | 11.00 | 1 | 0.61** | 0.60** | 0.43** |
| 2 PTQ | 37.12 | 13.59 | 1 | 0.55** | 0.54** | |
| 3 DASS-21-S | 12.06 | 5.34 | 1 | 0.60** | ||
| 4 IIRS | 62.49 | 17.10 | 1 | |||
|
| ||||||
| MDD subsample (n = 190) | ||||||
|
| ||||||
| Measure | M | SD | 1 | 2 | 3 | |
|
| ||||||
| 1 IUS-12 | 39.52 | 10.84 | 1 | 0.63** | 0.42** | |
| 2 PTQ | 38.19 | 13.28 | 1 | 0.48** | ||
| 3 PHQ-9 | 18.06 | 5.23 | 1 | |||
|
| ||||||
| Panic disorder subsample (n = 65) | ||||||
|
| ||||||
| Measure | M | SD | 1 | 2 | 3 | |
| 1 IUS-12 | 41.18 | 12.12 | 1 | 0.66** | 0.13 | |
| 2 PTQ | 38.98 | 14.16 | 1 | 0.32* | ||
| 3 APPQ-I | 16.12 | 12.07 | 1 | |||
|
| ||||||
| PTSD subsample (n = 140) | ||||||
|
| ||||||
| Measure | M | SD | 1 | 2 | 3 | |
|
| ||||||
| 1 IUS-12 | 39.97 | 10.44 | 1 | 0.63** | 0.56** | |
| 2 PTQ | 38.25 | 13.50 | 1 | 0.64** | ||
| 3 PCL-5 | 50.52 | 14.61 | 1 | |||
IUS-12 = Intolerance of Uncertainty Scale; PTQ = Perseverative Thinking Questionnaire; DASS-21-S = Depression Anxiety and Stress Scales Stress Scale; IIRS = Illness Intrusiveness Rating Scale; PHQ-9 = Patient Health Questionnaire; APPQ-I = Albany Panic and Phobia Questionnaire Interoceptive Subscale; PCL-5 = PTSD Checklist for DSM-5.
Notes:
p < .05;
p < 0.001
Correlations at *p < .05 did not survive the Bonferroni correction for multiple comparisons
Mediation effects of RNT on the relationships of IU with stress and functional impairment in full sample
Results are presented in Table 2. Separate mediation analyses were conducted with stress and impairment as outcomes. The total effect of IU on stress was significant. When RNT was included the analysis, the strength of the of IU’s relationship with stress was reduced. IU demonstrated an indirect effect on stress through RNT.
Table 2.
Mediating effects of PTQ of IUS-12 with DASS-21-S and IIRS in full sample
| Full sample (N = 244) | 95% CI |
||||
|---|---|---|---|---|---|
| B | P | LL | UL | ||
|
| |||||
| Between IUS-12 and DASS-21-S | |||||
| Total effect (c) | 0.29 | < .001 | 0.24 | 0.34 | |
| Direct effect (c’) | 0.21 | < .001 | 0.15 | 0.27 | |
| Indirect effect (ab) | 0.09 | 0.05 | 0.13 | ||
| Ratio of indirect to direct effect: | 0.43 | ||||
| Ration of indirect to total effect: | 0.31 | ||||
| Between IUS-12 and IIRS | |||||
| Total effect (c) | 0.66 | < .001 | 0.49 | 0.84 | |
| Direct effect (c’) | 0.24 | 0.02 | 0.03 | 0.45 | |
| Indirect effect (ab) | 0.43 | 0.29 | 0.58 | ||
| Ratio of indirect to direct effect: | 1.79 | ||||
| Ratio of indirect to total effect: | 0.65 | ||||
CI = Confidence Interval; LL = Lower Limit; UL = Upper Limit; IUS-12 = Intolerance of Uncertainty Scale; PTQ = Perseverative Thinking Questionnaire; DASS-21-S = Depression Anxiety and Stress Scales Stress Scale; IIRS = Illness Intrusiveness Rating Scale.
Likewise, the total effect of IU on impairment was significant. After accounting for the contribution of RNT, the direct effect of IU on impairment exceeded the corrected significance threshold, suggesting an indirect effect of IU on impairment through RNT.
Mediation effects of RNT on the relationships between IU and symptoms in subsamples
Results of three subsample analyses are presented in Table 3. IU exhibited a total effect on depressive symptoms in the MDD subsample. Using the Bonferroni corrected threshold (p = .003), the direct effect of IU on depressive symptoms was not significant after RNT was included in the analysis IU, indicating an indirect effect of IU on depressive symptoms through RNT.
Table 3.
Mediating effects of PTQ of IUS-12 with disorder specific symptom measures in subsamples
| MDD subsample (n = 190) | 95% CI |
||||
|---|---|---|---|---|---|
| B | P | LL | UL | ||
|
| |||||
| Between IUS-12 and PHQ-9 | |||||
| Total effect (c) | 0.20 | < .001 | 0.14 | 0.27 | |
| Direct effect (c’) | 0.10 | 0.02 | 0.02 | 0.17 | |
| Indirect effect (ab) | 0.11 | 0.04 | 0.18 | ||
| Ratio of indirect to direct effect: | 1.10 | ||||
| Ratio of indirect to total effect: | 0.55 | ||||
|
| |||||
| Panic disorder subsample (n = 65) | 95% CI |
||||
| B | P | LL | UL | ||
|
| |||||
| Between IUS-12 and APPQ-I | |||||
| Total effect (c) | 0.13 | 0.29 | −0.12 | 0.38 | |
| Direct effect (c’) | −0.13 | 0.41 | −0.45 | 0.18 | |
| Indirect effect (ab) | 0.27 | 0.08 | 0.44 | ||
|
ꞵ |
|||||
| Standardized indirect effect (ab) | 0.27 | 0.08 | 0.44 | ||
|
| |||||
| PTSD subsample (n = 140) | 95% CI |
||||
| B | P | LL | UL | ||
|
| |||||
| Between IUS-12 and PCL-5 | |||||
| Total effect (c) | 0.78 | <.001 | 0.59 | 0.98 | |
| Direct effect (c’) | 0.36 | .002 | 0.13 | 0.59 | |
| Indirect effect (ab) | 0.42 | 0.27 | 0.62 | ||
| Ratio of indirect to direct effect: | 1.17 | ||||
| Ratio of indirect to total effect: | 0.54 | ||||
CI = Confidence Interval; LL = Lower Limit; UL = Upper Limit; IUS-12 = Intolerance of Uncertainty Scale; PTQ = Perseverative Thinking Questionnaire; PHQ-9 = Patient Health Questionnaire; APPQ-I = Albany Panic and Phobia Questionnaire Interoceptive Subscale; PCL-5 = PTSD Checklist for DSM-5.
The total effect of IU on panic symptoms in the panic disorder subsample was not significant. With the Bonferroni corrected threshold (p > .003), RNT did not predict panic symptoms. When RNT was included in the analysis, IU did not exhibit a direct effect on panic symptoms. IU did not demonstrate an indirect effect on panic symptoms through RNT.
IU demonstrated a total effect on posttraumatic stress symptoms in the PTSD subsample. Once RNT was included in the analysis, the direct effect of IU on posttraumatic stress symptoms was significant. IU exhibited an indirect effect on posttraumatic stress symptoms through RNT.
Discussion
The present study aimed to address gaps in the literature by evaluating RNT as a mediator of IU’s relationships with broad and specific symptoms among veterans with a range of emotional disorders. IU exhibited indirect effects on stress and impairment through RNT in the full mixed clinical sample. Similarly, IU exhibited indirect effects on depression and posttraumatic stress through RNT in the MDD and PTSD subsamples. This is consistent with previous studies that suggest IU’s influence over psychopathology is exerted through forms of RNT, like worry and rumination (Huang et al., 2019; Yao et al., 2022; Yook et al., 2010). The present findings are in line with previous studies that indicate IU (Carleton et al., 2012; McEvoy et al., 2019; White & Gumley, 2009) and RNT (Arditte-Hall et al., 2019; Bakhshian et al., 2013; Olatunji et al., 2010) contribute to symptom severity in individuals with MDD and PTSD. Given that these findings extended to stress and impairment in the full mixed clinical sample and specific symptoms in two of the three clinical subsamples, this further supports IU and RNT as transdiagnostic factors.
If IU and RNT uniquely contribute to a range of symptoms, and RNT can partially explain IU’s deleterious effects, this has implications for specific models of emotional disorders. In particular, although IUM was initially conceptualized in reference to GAD (Dugas et al., 1995), it may be extended to MDD and PTSD. Likewise, existing models of MDD and PTSD symptoms may benefit from contextualizing pathological thinking and behavioral patterns with IU to improve our understanding of these disorders. The cognitive model of MDD emphasize negative thoughts about the self, world, and future (Beck, 1967), and the behavioral activation model of MDD emphasize behavioral restriction (Lewinsohn, 1974). IU may enhance or connect cognitive and behavioral models of MDD. Individuals report greater depressive symptoms when they are uncertain about their ability to cope with negative affect and experience positive affect (Thibodeau et al., 2015). This might explain why IU predicts behavioral restriction in individuals with MDD (Mahoney & McEvoy, 2012a). Perhaps individuals with MDD engage in fewer activities because they do not know if activities will make them feel worse and/or not feel better. Likewise, IU may improve conceptualizations of thoughts and behaviors characteristic of PTSD (Brewin & Holmes, 2003). Individuals report increased posttraumatic stress symptoms when they are unclear about the affective consequences of talking or thinking about traumatic events (Mahoney & McEvoy, 2012a). Individuals with PTSD might avoid trauma reminders because they do not know how facing reminders will make them feel (Fetzner et al., 2013).
Findings also have transdiagnostic implications for treatments of emotional disorders. Although existing treatments that explicitly target IU and RNT, including IU therapy, metacognitive therapy, and mindfulness-based therapies, were designed to address GAD and MDD, they may be adapted to other emotional disorders. IU therapy and metacognitive therapy entail interventions to challenge beliefs about the threat of uncertainty and the utility of RNT. Mindfulness-based therapies entail techniques to disengage from the perceived threat of uncertain stimuli and RNT. Multiple randomized clinical trials demonstrate that IU therapy, metacognitive therapy, and mindfulness-based therapies result in significant decreases in IU and RNT (Alimehdi et al., 2016; Hui & Zhihui, 2016; van der Heiden et al., 2012; Zemestani et al., 2021). Alternatively, specific interventions within these treatments (i.e., behavioral experiments, metacognitive restructuring, and mindfulness) may be incorporated into treatments for other emotional disorders.
Even when transdiagnostic interventions do not explicitly target IU and RNT, they appear to produce comparable reductions in IU and RNT, including applied relaxation, cognitive restructuring, exposure, behavioral activation, and problem-solving (Mahoney & McEvoy, 2012c; Monteregee et al., 2020). Findings show transdiagnostic treatments lead to significant decreases in IU and RNT in individuals with anxiety and depressive disorders, and changes in IU and RNT correspond to changes in symptoms (Boswell et al., 2013; Laposa et al., 2017; Talkovsky & Norton, 2016). This may be especially important for veterans who struggle with IU and RNT. IU predicts symptom severity among veterans with emotional disorders (Hunt et al., 2022) and they report smaller reductions in RNT following treatment relative to civilians (Barrera et al., 2015; Hundt et al., 2014). Since veterans are more likely to have comorbid mental health problems (Black et al., 2004; Kessler et al., 2005), they may benefit from transdiagnostic treatments that reduce IU and RNT.
Neither IU nor RNT predicted symptoms in the panic disorder subsample. This could suggest that IU and RNT may not contribute to panic, which conflicts with previous results (Carleton et al., 2014; Mahoney et al., 2012). Other studies have found that IU and RNT may not contribute or contribute less to panic symptoms relative to symptoms of other emotional disorders (Dugas et al., 2001; McEvoy et al., 2012). Null results might also stem from methodological issues. Evidence suggests that the panic outcome measure in this study (APPQ-INT) may be a suboptimal measure of panic symptoms. The feared activities and situations described in the APPQ-INT may be more relevant to agoraphobia, or physical exertion symptoms of panic more so than other panic symptoms (Brown et al., 2005). Additionally, the present panic analyses may have been underpowered. Due to multiple comparisons, the present study employed a Bonferroni correction, reducing the typical p-value from .05 to .003. Without this correction, RNT exhibited a significant direct effect (p = .01) on panic symptoms in the panic disorder subsample. Further, the panic disorder subsample (n = 65) was substantially smaller than the MDD (n = 189) and PTSD (n = 140) subsamples. Given the generally small to medium effects of IU and RNT on panic in the literature (e.g., Carleton et al., 2014; McEvoy et al., 2012) and the small subsample size, the present secondary data analysis was likely underpowered to detect direct and indirect effects.
Limitations
Implications of present findings are tempered by limitations. First, the relationships were analyzed cross-sectionally, which prevents the establishment of directionality of relationships among IU, RNT, and symptoms. It may be particularly important to establish temporal precedence between IU and RNT, given that previous findings suggest that IU may mediate the relationship of RNT with symptoms (Zlomke & Young, 2009). Second, as previously mentioned, the mediation analysis within the panic subsample may have employed suboptimal measures and was underpowered to detect direct and indirect effects due to the small subsample size. Third, the full mixed clinical sample included individuals with primary MDD, panic disorder, and PTSD diagnoses, which represent a portion of individuals with emotional disorders. Emotional disorders also include other depressive, anxiety, and categories of disorders. Fourth, results from a veteran sample may not apply to civilians with MDD, panic disorder, and PTSD.
To address these limitations, these relationships must be examined prospectively to determine directionality. RNT should also be investigated as a mediator of IU, and symptoms should also be examined in a larger sample of individuals with panic disorder with a broader measure of panic symptoms (e.g., Panic Disorder Severity Scale; Shear et al., 1997). RNT should also be examined as a mediator of IU’s relationships with symptoms in other mental health problems with strong relationships to these constructs, including obsessive-compulsive and related disorders and eating disorders (Brown et al., 2017; Gentes et al., 2011). These relationships should be examined in non-veteran samples to ensure generalizability to the greater clinical population.
Future Directions
Future research could investigate RNT as an explanatory mechanism between different subtypes of IU and symptoms. While situational IU concerns IU regarding scenarios that may be threatening to individuals with different disorders, prospective IU and inhibitory IU represent subdimensions of trait IU. Prospective IU concerns uncertainty around future outcomes, while inhibitory IU concerns difficulty coping with uncertainty (Hong et al., 2015). Analyzing the indirect effects of specific forms of IU on symptoms through RNT may yield a more granular understanding and targeting of IU for specific symptom presentations. For example, if a veteran is higher in prospective IU, they may benefit more from interventions designed to challenge beliefs about uncertainty related to future events and the utility of worry. As RNT partially mediates the relationships between IU and symptoms, other mediators, particularly maladaptive forms of coping, should be studied. Evidence indicates that IU contributes to behavioral avoidance (Flores et al., 2018), another driver of psychopathology in emotional disorders. Researchers may fully explain why IU results in symptoms by identifying other mediators.
Conclusions
The present study is the first exploration of IU’s indirect effects on distress and impairment through RNT in a mixed clinical sample of veterans. RNT may help explain why IU leads to 1) stress and impairment in emotional disorders, 2) depressive symptoms in MDD, and 3) posttraumatic stress symptoms in PTSD. IU and RNT are established transdiagnostic risk and maintenance factors for emotional disorders that are strongly related to one another. The present findings demonstrate how the dynamic between IU and RNT contributes to psychopathology. By improving our understanding of how their relationship contributes to symptoms, IU and RNT can be effectively targeted to reduce distress and impairment for veterans with emotional disorders.
Acknowledgments
This study is supported by the Department of Veterans Affairs Office of Research and Development, RR&D grant# 1I0 1RX002910 and CSR&D grant# I01 CX001846 (PI: Gros). The views expressed in this article are those of the authors and do not necessarily reflect the position or policy of the Department of Veterans Affairs or the United States government.
Footnotes
We have no conflicts to disclose.
Contributor Information
Kerry C. Kelso, Mental Health Service, Durham Veterans Affairs Healthcare System
Daniel F. Gros, Mental Health Service, Ralph H. Johnson Veterans Affairs Healthcare System, and the Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina
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