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. Author manuscript; available in PMC: 2014 Dec 1.
Published in final edited form as: Drug Alcohol Depend. 2013 Jul 26;133(2):324–329. doi: 10.1016/j.drugalcdep.2013.06.015

Anxiety and Depressive Symptoms and Affective Patterns of Tobacco Withdrawal

Adam M Leventhal 1,2, Katherine J Ameringer 1, Elly Osborn 3, Michael J Zvolensky 4,5, Kirsten J Langdon 6
PMCID: PMC4049140  NIHMSID: NIHMS510496  PMID: 23896304

Abstract

Background

The complex concordance and discordance across and within anxiety and depressive symptoms complicates understanding of the relation between emotional symptoms and manifestations of tobacco withdrawal. The goal of this study was to parse the broad variation in anxiety and depressive symptoms into conceptually discrete components and explore their relative predictive influence on affective patterns of acute tobacco withdrawal.

Methods

We employed a within-participant experimentally-manipulated tobacco abstinence design involving: (i) a baseline visit at which past-week depression and anxiety symptoms were assessed; and (ii) two counterbalanced experimental visits—one after ad lib smoking and one after 16-hours of tobacco abstinence—at which state affect was assessed. Participants were community-dwelling adults (N=187) smoking 10+ cig/day for at least two years without an active mood disorder.

Results

Anxiety-related general distress symptoms (e.g., tension, nervousness) predicted greater abstinence-induced increases in various negative affective states but not changes in positive affect (βs .17 – .33). Depression-related general distress symptoms (e.g., sadness, worthlessness) predicted greater abstinence-induced increases in acute depressed affect only (βs .24 – .25). Anhedonic symptoms (e.g., diminished interest, lack of pleasure) predicted larger abstinence-induced decreases in acute positive affect only (βs .17 – .20). Anxious Arousal symptoms (e.g., shakiness, heart racing) predicted larger abstinence-induced increases in fatigue and depressive affect (βs .15 – .24).

Conclusion

Different components of anxiety and depressive symptoms are associated with unique affective patterns of acute tobacco withdrawal. These results provide insight into the affective mechanisms underlying tobacco dependence and could inform smoking cessation treatment approaches tailored to individuals with emotional distress.

Keywords: Depression, Anxiety, Smoking, Nicotine Withdrawal, Tobacco Abstinence

1. INTRODUCTION

One hypothesis to explain the association between emotional distress and tobacco dependence is that individuals with elevated anxiety or depressive symptoms experience more severe tobacco withdrawal symptoms when abstaining from smoking. Tobacco withdrawal symptoms, which span various undesirable affective, cognitive, and somatic features (Hughes, 2007), may provoke compulsive motivation to smoke to modulate such symptoms (Baker et al., 2004). Hence, tobacco withdrawal may underlie maintenance of smoking due to motivation to delimit or otherwise offset withdrawal that occurs during brief periods of abstinence (e.g., overnight, tobacco use restrictions). Tobacco withdrawal also could increase risk of relapse following a cessation attempt (Piper et al., 2011). Accordingly, elucidating the relation of anxiety and depressive symptoms to tobacco withdrawal could provide unique insight into the affective mechanisms underlying tobacco dependence and inform specialized smoking cessation treatment approaches tailored to individuals with emotional distress. Given that subclinical levels of emotional symptoms among those without an active mood disorder predict smoking cessation failure (Leventhal et al., 2008), understanding how emotional symptoms relate to tobacco withdrawal among non-psychiatric community-dwelling populations is clinically important.

Some prior work has found that smokers with elevated depressive and anxiety symptoms experience more severe withdrawal symptoms (e.g., Breslau et al., 1992; Johnson et al., 2012; Langdon et al., 2013; Leventhal et al., 2008; Piper et al., 2010; Pomerleau et al., 2000; Weinberger et al., 2010; Xian et al., 2005; Zvolensky et al., 2008), even among those without an active mood disorder (Leventhal et al., 2008). Nevertheless, critical gaps remain in this literature. Most notably, extant tobacco withdrawal research has mainly explored the effects of depression and anxiety symptoms using standard syndrome based indices (e.g., DSM-IV diagnoses or composite symptom indexes). This approach overlooks the complex concordance and discordance across and within anxiety and depressive syndromes. Anxiety and depressive symptoms are difficult to differentiate empirically due to their high rates of co-occurrence (Clark and Watson, 1991; Watson et al., 1995). Moreover, there is considerable symptomatic heterogeneity within depressive (Shafer, 2006) and anxiety (Ree et al., 2008) conditions. To address these barriers, Clark and Watson (1991) put forth a tripartite model of anxiety and depression which proposes that the heterogeneity in emotional symptoms can be parsimoniously explained by three distinct constructs. General Distress, a nonspecific factor that is indicative of negative emotions, includes symptoms such as sadness, irritability, worry, and concentration problems, cuts across both anxiety and depression and accounts for a considerable portion of anxiety-depression symptom overlap. Anxious Arousal, a specific factor for anxiety indicative of tension and autonomic arousal, includes panic-like symptoms and is putatively distinct from depression. Anhedonia, a specific factor for depression indicative of reduced interest/motivation, pleasure, and positive affect, and is putatively distinct from anxiety. Hence, the tripartite model could be leveraged to elucidate the relation of anxiety and depressive symptoms to tobacco withdrawal.

Another factor that complicates understanding of the relation of anxiety and depressive symptoms to tobacco withdrawal is the methodology frequently employed to study such processes. Retrospective designs which ask participants to report on withdrawal symptoms experienced during a past episode of abstinence are subject to recall bias (Shiffman et al., 1997). As one example, smokers may involuntarily overestimate their mood severity during a prior period of abstinence if they are currently in a poor mood state, which can spuriously inflate relations between emotional symptoms and tobacco withdrawal. In prospective designs of active quitters, many relapse back to smoking. Investigations that do not account for people who relapse are subject to confounding by nonabstinent status. Studies have addressed this problem by analyzing the subset of abstainers (e.g., Leventhal et al., 2008; Zvolensky et al., 2008); yet, this approach increases risk of selection bias, as those who relapse and are excluded from analyses may be the most dependent smokers.

The experimentally-manipulated tobacco abstinence paradigm is less susceptible to limitations that affect these other methods because it: (a) utilizes prospective measurement of withdrawal while abstinence is occurring; (b) includes ad lib smoking control conditions, which permits study of abstinence-induced changes from “baseline;” and (c) reduces selection biases due to failure to maintain abstinence given the high rates of abstinence compliance with this method (Gilbert et al., 1999). Tobacco withdrawal severity during experimentally-induced abstinence predicts withdrawal in a subsequent naturalistic self-initiated quit attempt (al'Absi et al., 2005), suggesting that findings from research employing this design may generalize outside the laboratory.

In this study of community smokers without an active mood disorder, we applied the tripartite model of anxiety and depression to investigate the disparate predictive effects of general distress, anxious arousal, and anhedonia symptoms on abstinence-induced expressions of tobacco withdrawal. We focused on affective manifestations of withdrawal because: (a) these symptoms may be more important determinants of smoking motivation in comparison to other symptoms (e.g., hunger; McCarthy et al., 2006); and (b) anxiety and depression may modulate the affective features of withdrawal more strongly than its other components. We suspect that individuals with anxiety and depressive symptoms are motivated to smoke, in part, because tobacco may briefly and temporarily offset their specific emotional symptoms. When they abstain from tobacco, their specific affective symptoms may become exacerbated by acute tobacco withdrawal in the short-term. Accordingly, we hypothesize pathognomonically consistent linkages between the tripartite constructs and particular affective patterns of withdrawal. We expect general distress symptoms to predict withdrawal in a non-specific manner, associating with greater abstinence-induced increases in all aversive affective states. We expect anxious arousal and anhedonia to predict withdrawal patterns in a feature-specific manner, such that anxious arousal will associate only with abstinence-induced increases in anxiety whereas anhedonia will associate with only abstinence-induced decreases in positive affect. Elucidating which facets of anxiety and depressive symptoms give rise to certain affective changes during tobacco withdrawal may inform: (1) clinical use of emotional symptom measures to identify patients at high risk for experiencing elevated state affective disturbance during a quit attempt; and (2) tailored cessation treatment strategies that can be designed to offset the specific withdrawal symptoms that are especially prominent given a patient’s particular precessation emotional symptom profile.

2. METHOD

2.1 Participants

Participants were community residents recruited via public announcements of opportunities to participate in a study on personality and smoking. Inclusion criteria were: (a) ≥ 18 years old; (b) report regular cigarette smoking for ≥ 2 years; (c) report currently smoking ≥ 10 cig/day; and (d) and fluent in English. Exclusion criteria were: (a) current DSM-IV dependence on substances other than nicotine; (b) current DSM-IV mood disorder or psychotic symptoms or use of psychiatric medications; (c) breath carbon monoxide (CO) levels < 10ppm at intake; (d) use of non-cigarette tobacco or nicotine products; and (e) currently pregnant. Participants were compensated $200 after completing the study. In total, 326 participants enrolled in the study after passing a phone screen. Of these, 104 individuals were ineligible due to low CO (n=64), current psychiatric disorder (n=23), other criteria (n=18). Of the eligible participants, 33 dropped out after study entry (there were no significant differences in drop out versus completers on anxiety and depressive symptoms) and 2 twice failed to meet abstinence criteria at the abstinent session (see below), leaving a final sample of 187. The University of Southern California Internal Review Board approved the protocol. The sample in the current study (n = 187) partially overlaps with a prior publication (n = 75; Leventhal et al., 2012). The prior study did not analyze any predictors or outcomes overlapping with the predictors and outcomes reported in the current submission.

2.2 Procedure

Following a baseline visit, participants attended two experimental visits (one abstinent and one nonabstinent; order counterbalanced) that began at 12pm. For abstinent visits, participants were instructed not to smoke after 8pm the day before. For nonabstinent visits, they were instructed to smoke normally. The procedures were identical except that at the beginning of the nonabstinent visit and prior to CO assessment participants smoked a cigarette of their preferred brand in the laboratory to standardize recency of smoking. The abstinent session began with CO measurement. Following prior research and recommendations that a CO ≥ 10ppm indicates recent smoking (Leventhal et al., 2010; SRNT, 2002), participants with a CO ≥ 10ppm at their abstinent session could return later that week for a second attempt to complete their abstinent session (n = 13). Those with CO ≥ 10ppm on their second attempt were discontinued (n = 2). Subsequently, participants completed measures of affect, nicotine withdrawal, and smoking urge.

2.3 Baseline Visit Measures

Structured Clinical Interview for DSM-IV Non Patient Edition (First et al., 2002)

Mood disorder, psychotic screen, and substance use disorder modules were used to assess psychiatric eligibility.

Fagerström Test of Nicotine Dependence (FTND; Heatherton et al., 1991)

The FTND is a well-validated six-item measure of nicotine dependence severity.

Mood and Anxiety Symptom Questionnaire – Short Form (MASQ; Clark and Watson, 1991)

The MASQ is a 62-item self-report measure of emotional symptoms based upon the tripartite model of anxiety and depression. Participants rate how much they experienced each symptom in the previous week (1=not at all; 5=extremely). The MASQ contains four symptom scales: (a) Anxious Arousal, which assesses somatic tension and arousal (17 items; e.g., “was trembling or shaking,” “felt dizzy or lightheaded”) specific to anxiety; (b) Anhedonic Depression, which assesses low interest, pleasure, and positive affect (22 items; e.g., “felt like there wasn't anything interesting or fun to do,” “felt like nothing was very enjoyable”), specific to depression; (c) General Distress-Anxiety, which assesses anxious/tense mood and other nonspecific anxiety symptoms (11 items; e.g., “felt nervous,” “felt uneasy”); and (d) General Distress-Depression, which assesses depressed/sad mood other nonspecific depressive symptoms (12 items; e.g., “felt sad,” “felt like a failure”). Factor analyses of the MASQ have yielded three-factor solutions that correspond to the instrument’s conceptually derived subscales and show that the Anxious Arousal and Anhedonic Depression subscales differentiated anxiety and depression better than the General Distress subscales (Watson et al., 1995). Though considered to be the part of a common overarching construct, the depression- and anxiety-related general distress scales are separated to provide different measures that correspond to traditional anxiety and depression diagnostic distinctions. Further, the MASQ-Anhedonic depression has exhibited good covergent validity with measures of loss of pleasure in non-clinical participants (Gilbert et al., 2002).

2.4 Measures on Experimental Visits

2.4.1 Manipulation Checks

We administered: (1) a breath CO assessment; (2) an 11-item variant of the Minnesota Nicotine Withdrawal Scale (MNWS; Hughes and Hatsukami, 1986), which assesses withdrawal symptoms experienced “so far today” on 6-point scales and produces a mean composite scale (0 – 5 range; Leventhal et al., 2010); and (3) the Brief Questionnaire of Smoking Urges (QSU; Cox et al., 2001), which measures urge to smoke “right now” and includes a total scale based on the average score per item (rage 0 – 5).

2.4.2 The Profile of Mood States (POMS; McNair et al., 1971)

The POMS is a multidimensional affect scale, which served as the primary outcome. This study used a 72-item version in which participants rated affect adjectives based on how they were feeling “right now” (0-not at all; 4-extremely). The POMS yields several aversive affect scales, such as Anger (e.g., “angry,” “grouchy”), Anxiety (e.g., “shaky,” “panicky”), Confusion (e.g., “confused,” “forgetful”), Depression (e.g., “sad,” “hopeless”), and Fatigue (e.g., “worn out,” “fatigued”). The POMS also yields positive affective subscales, including Elation (e.g., “happy,” “satisfied”) and Vigor (e.g., “energetic,” “cheerful”). Each subscale score is computed as a mean score per item.

2.5 Data Analysis

For preliminary analyses, we calculated descriptive statistics, intercorrelations, and Cronbach’s alpha coefficients for each MASQ scale. To test the main effects of abstinence on experimental session measures, we calculated abstinence-induced change scores (Abstinent – Nonabstinent) for each outcome and then conducted single sample t-tests to test for significant departure from zero, which is equivalent to conducting a paired t-test with the raw data.

The primary analyses used linear regression models, in which a single MASQ scale served as a predictor and the abstinence-induced change score for each POMS scale served as the outcome. Separate models were calculated for each MASQ scale predictor and each POMS outcome. We considered combined models in which all MASQ scales were entered as simultaneous predictors; however, there was a high degree of intercorrelation among some MASQ scales (see Table 1), which precluded such analyses because of multicollinearity concerns. To control for baseline state affect, the corresponding nonabstinent outcome measure was included as a covariate in each model. Each model was recalculated after controlling for age, gender, and FTND score because age was significantly associated with MASQ-General Distress Anxiety and both gender and FTND were significantly associated with abstinence-induced changes in several outcomes. Additional post-hoc analyses in which the raw data for the abstinent score served as the dependent variable and the non-abstinent score was included as the covariate yielded equivalent results to those reported in the body of the article that relied on change scores.

Table 1.

Descriptive Statistics, Internal Consistency and Intercorrelations for Anxiety and Depressive Symptom Scales

Intercorrelations

MASQ Scale M(SD) 1. 2. 3. 4.
1. Anxious Arousal 20.78 (5.85) (.88)
2. General Distress-Anxiety 14.54 (4.93) .85 (.86)
3. Anhedonic Depression 52.26 (14.24) .34 .35 (.90)
4. General Distress-Depression 17.16 (6.52) .70 .78 .46 (.91)

Note. N = 187. MASQ = Mood and Anxiety Symptoms Questionnaire—Short Form. Values in parentheses represent Cronbach αs for the respective MASQ scale. All intercorrelations significant at p < .0001.

Variables with non-normal distributions were transformed to approximate normality when appropriate. Results are reported as standardized regression coefficients (βs) and significance was set at p < .05 (two-tailed). We also report Benjamini-Hochberg corrected significance determinations (Keselman et al., 2002) to allow the reader to interpret the findings with respect to a more conservative type-I error protection due to multiple tests.

3. RESULTS

3.1 Preliminary analyses

3.1.1 Sample Characteristics

Participants were on average 43.7 (SD=10.3) years of age, 67% male, smoked 19.3 (SD=5.3) cig/day, began smoking at age 16.7 (SD=6.6), and had an FTND score of 5.3 (SD=2.0) indicating medium level of nicotine dependence on average. The ethnic distribution was 55% African American, 36% Caucasian, and 9% other, with 15% self-identifying as Hispanic.

3.1.2 Anxiety and Depressive Symptoms

Each MASQ scale exhibited strong internal consistency (Table 1). On average, there was a low severity of anxiety and depressive symptoms and high between-participant variability, similar to those reported in prior general community samples (Gilbert et al., 2002). The proportion who surpassed clinical cutoffs for anxious arousal was 6%, anxiety-related general distress (10%), depression-related general distress (17%), and anhedonic depression (52%), based on cutpoints yielded from prior work (Schulte-van Maaren et al., 2012). There was a high degree of convergence between the two General Distress scales and comparatively lower correlations (and higher discriminant validity) of Anhedonic Depression to the other MASQ scales. Anxious Arousal exhibited sizeable correlations with the two General Distress scales, which is inconsistent with intended discrimination between this scale and non-specific distress.

3.1.3 Main Effects of Abstinence

Abstinence had a significant effect on each POMS scale, except Fatigue, as well as all of the manipulation check measures (Table 2).

Table 2.

Main Effects of Abstinence on Affect States and Other Measures

M(SD)
Nonabstinent
M(SD)
Abstinent
M(SD)
Abstinent-
Nonabstinent
Cohen’s da
POMS Scales
  Anger 0.40 (0.66) 0.68 (0.82) 0.28 (0.78) 0.36†
  Anxiety 0.73 (0.74) 1.21 (0.96) 0.48 (0.92) 0.52†
  Confusion 0.80 (0.68) 0.96 (0.78) 0.16 (0.79) 0.20**
  Depression 0.43 (0.64) 0.53 (0.69) 0.10 (0.64) 0.16*
  Elation 1.95 (0.89) 1.45 (0.83) −0.50 (0.82) −0.61†
  Fatigue 0.85 (0.91) 0.87 (0.92) 0.01 (0.64) 0.02
  Vigor 2.24 (1.01) 1.80 (0.97) −0.44 (0.82) −0.54†
Manipulation Check measures
  CO ppm 28.25 (13.79) 5.54 (2.10) −25.08 (12.07) −2.08†
  MNWS 1.07 (1.00) 1.94 (1.12) 0.88 (1.07) 0.82†
  QSU 0.96 (1.11) 3.34 (1.07) 2.39 (1.25) 1.91†

Note. N = 187.

a

Effect sizes (Cohen’s d) and p-values for single sample t-tests of abstinent-nonabstinent change score for significant departure from zero;

MNWS = Minnesota Nicotine Withdrawal Scale; CO = Carbon Monoxide; POMS = Profile of Mood States; MNWS = Minnesota Nicotine Withdrawal Scale. QSU = Brief Questionnaire of Smoking Urges.

*

p<.05;

**

p<.01;

***

p<.001;

†

p<.0001

3.2 Primary Analysis

Analyses examining MASQ subscales as predictors of abstinence-induced changes in POMS scales after adjusting for non-abstinent POMS scores are presented in Table 3. Anxious Arousal significantly predicted abstinence-induced increases on the POMS Depression and Fatigue Scales. General Distress-Anxiety significantly predicted abstinence-induced increases in each aversive affect state (Anger, Anxiety, Confusion, Depression, and Fatigue) and did not predict the two positive affect measures (Vigor and Elation). General Distress-Depression significantly predicted abstinence-induced increases in POMS Depression only. Anhedonic Depression predicted abstinence-induced decreases in the two positive affect scales (Vigor and Elation). Each of these findings remained statistically significant after controlling for demographics and nicotine dependence, yet only some remained significant after applying a type-I error correction (Table 3). Additional post-hoc analyses in which the raw data for the abstinent score served as the dependent variable and the non-abstinent score was included as the covariate yielded equivalent results to those reported in the body of the article that relied on change scores.

Table 3.

Anxiety and Depressive Symptoms Predicting Abstinence-Induced Changes in Affect

MASQ Predictor

Anxious
Arousal
General Distress-
Anxiety
General Distress-
Depression
Anhedonic
Depression




POMS Outcome β-Unadja β-Adjb β-Unadja β-Adjb β-Unadja β-Adjb β-Unadja β-Adjb
Anger - - .26***c .22**c - - - -
Anxiety - - .25**c .22**c - - - -
Confusion - - .23**c .19* - - - -
Depression .24**c .21**c .33†c .30†c .25***c .24***c - -
Elation - - - - - - −.17* −.17*
Fatigue .15* .15* .17* .18* - - - -
Vigor - - - - - - −.20** −.20**

Note. N=187.

a

Predicting change score in respective outcome variable after controlling only for non-abstinence score

b

Predicting change score in respective outcome variable after controlling for nonabstinent score, gender, age, Fagerström Test of Nicotine Dependence Score.

c

Significant following Benjamini-Hochberg type-I error correction for multiple tests. Only significant findings (p < .05) displayed.

MASQ = Mood and Anxiety Symptoms Questionnaire—Short Form. POMS = Profile of Mood States.

*

p <.05;

**

p < .01;

***

p<.001;

†

p<.0001

4. DISCUSSION

This study found that different domains of anxiety and depressive symptoms predicted different affective profiles during acute tobacco withdrawal. We found pathognomonically-concordant findings for anhedonia, the emotional symptom component putatively specific to depression and distinct from anxiety. Anhedonia was associated with only abstinence-induced reductions in positive affect. Prior research has demonstrated that smokers with lower levels of trait hedonic capacity (i.e., ability to experience pleasure in response to rewarding stimuli) experience greater abstinence-induced reductions in vigor but not abstinence-induced changes on a composite measure of negative affect (Cook et al., 2004). The current results cohere with and uniquely extend past work by: (a) using a symptom-based measure of anhedonia that assesses a broader array of features (i.e., diminished interest/motivation, pleasure, and positive affect); (b) demonstrating consistent effects on an additional positive affect outcome (i.e., elation); and (c) illustrating that anhedonia is not significantly associated with various negative affective expressions of withdrawal. Extant investigations have shown that higher precessation anhedonia, as measured by the MASQ-Anhedonic Depression and other anhedonia scales, redicts greater smoking relapse risk (Cook et al., 2010; Leventhal et al., 2008; Niaura et al., 2001; Zvolensky et al., 2009). These results are consistent with notions that high-anhedonia individuals may smoke in order to briefly and temporarily offset positive affect deficits (Cook et al., 2007), and these deficits may become expressed and exacerbated during acute tobacco withdrawal, which could in turn motivate the resumption of smoking following abstinence.

We hypothesized that both anxiety and depression-based measures of general distress would exhibit non-specific associations with a variety of aversive affect states during abstinence. The anxiety-based measure of general distress showed the predicted pattern, such that it associated with greater abstinence-induced increases across all aversive affect states (i.e., anger, anxiety, depression, confusion, and fatigue). Anxiety-related general distress symptoms are characteristic of generalized anxiety disorder, a syndrome defined by excessive worry, tension, fatigue, concentration problems, and irritability. Prior work illustrates that diagnostic measures of generalized anxiety disorder predict poorer short-term smoking cessation outcomes (Piper et al., 2010). The current findings raise the possibility that anxiety-related general distress symptoms may mark a more severe tobacco dependence phenotype characterized by a tendency to smoke for various negative affective reasons.

The depression-based measure of general distress, however, did not show the non-specific pattern of effects we hypothesized. Depression-related general distress predicted only abstinence-induced increases in state depression. The symptoms in the MASQ-General Distress-Depression scale focus on elements of self-critical and pessimistic cognitions, sadness, and other low-arousal negative affects. We speculate that smokers with these symptoms are disproportionately prone to smoke in order to temporarily alleviate these particular emotional features. Hence, upon acute abstinence, these types of features, which are represented on the POMS-Depression scale (e.g., “sad,” “hopeless,” “unworthy”) may be disproportionately expressed among smokers with depression-related general distress symptoms. It is unclear why, unlike anxiety-related general distress, depression-related general distress was not non-specifically associated with a variety of negative affective states during withdrawal. Depression-related general distress in this sample strongly covaried with anxiety-related general distress (r=.78), which is in line with respective correlations in some past research (rs .69 to .78; Wacker et al., 2009; Watson et al., 1995) and prior psychometric work (Wardenaar et al., 2010). Methodologically, it is possible that the relatively low level of depression in this sample (due to screening out those with current major depression) may have limited the ability to detect certain relations to withdrawal effects, which may only be prominent among the more severely depressed.

Anxious arousal, the symptom component putatively specific to anxiety and distinct from depression, did not exhibit pathognomonically-consistent relations with withdrawal symptoms. Anxious arousal predicted greater abstinence-induced changes in depression and fatigue only. Intercorrelations among the MASQ subscales illustrated that anxious arousal did not adequately separate from the measures of general distress, which raises questions about the discriminant validity of this scale in our sample. Perhaps these symptom domains cluster together more strongly in general community samples in which overall symptom levels are low, which could ultimately reduce phenotype differentiation across manifestations of emotional distress, as demonstrated previously in non-clinical samples (Wacker et al., 2009). Thus, these findings should be interpreted with this caveat in mind. Nonetheless, anxious arousal and anhedonic depression were only modestly correlated (r = .34), which is consistent with the primary tenet of the tripartite model that these two constructs reflect “pure” measures of anxiety and depression, respectively (Clark and Watson, 1991), and with correlations between these measures in past samples of smokers (rs = .33 – .40; Gregor et al., 2007; Zvolensky et al., 2009).

Instead of relying on composite measures of negative affect or nicotine withdrawal as outcomes, we utilized outcome measures that differentiated qualitatively distinct subtypes of negative affect states (e.g., anger vs. anxiety) that could be expressed during acute tobacco withdrawal. This approach proved useful as it illustrated that certain domains of anxiety and depression predict qualitatively unique affective withdrawal profiles, which ultimately could advance treatment strategies that target particular affective subtypes. For instance, given that the current results suggest that smokers with depression-related general distress are characterized by a withdrawal profile involving elevated state depression only (and not other forms of negative affect), they may benefit from cessation strategies that specifically target low-arousal depressive emotions and cognitions (e.g., feeling “hopeless” and “unworthy” on POMS Depression scale) as emphasized in cognitive-behavioral depression-based smoking cessation treatments (Brown et al., 2007). Whereas, because smokers with anxiety-related general distress may be characterized by a withdrawal profile involving multiple negative affect elevations, they may benefit from a multi-faceted cessation treatment that targets both high-arousal (i.e., anger and anxiety) and low-arousal (i.e., depression) affective states as emphasized in acceptance and commitment based smoking cessation treatments (Brown et al., 2008).

Regarding study limitations, we excluded individuals who currently were taking psychiatric medications, in an acute mood disorder episode, or substance-dependent to limit the possible effects of psychoactive substances or substance withdrawal on tobacco withdrawal phenomena. Hence, it is unclear if these findings would generalize to individuals on the severe end of psychopathology continuum. Given that prior results indicate that higher levels of emotional psychopathology in those without an active emotional disorder is associated with more severe tobacco dependence and higher relapse risk (Leventhal et al., 2008; Niaura et al., 2001), the current results may nonetheless shed light on the clinical impact of subclinical emotional symptomatology in smokers. There are also limitations to ecological validity, including that this sample of participants did not wish to quit and that abstinence was not self-imposed. We used only one self-report measure of emotional symptomatology. It would be preferable to explore if effects are consistent across clinical ratings and diagnoses, yet we are unaware of any clinical rating tool comparable to the MASQ that yields symptom indexes for each of the tripartite constructs. We confirmed abstinence with only CO and did not conduct a plasma nicotine analysis, which would have been preferable. Finally, when significance correction for multiple comparisons was applied, not all of the findings surpassed the significance threshold, which suggests that some of the findings should be interpreted with caution.

Overall, this study yields several scientific and clinical insights into the relation between emotional symptoms and tobacco dependence. For instance, utilizing standard depressive symptom measures that amalgamate all depressive symptoms into a composite index may obscure addiction-relevant variability among disparate symptomatic expressions of depression. Rather, it may behoove clinicians and researchers to assess anhedonic depressive symptoms, in particular, to identify the subgroup of smokers who experience disproportionate deficiencies in positive affect during tobacco withdrawal. Given that post-quit declines in positive affect increase risk of smoking relapse (Strong et al., 2009, 2011), anhedonic smokers may benefit from smoking cessation treatment strategies that emphasize bolstering positive affect. For instance, behavioral activation is a treatment that aims to teach individuals how to increase access to and mood enhancement from pleasant activities, which has recently shown promise for enhancing smoking cessation outcomes (MacPherson et al., 2010). Perhaps, this treatment may be warranted for anhedonic smokers who experience markedly diminished positive affect during treatment. In addition, measures of anxiety-related general distress symptoms may help to identify smokers who may be particularly prone to experiencing various forms of negative affect upon tobacco abstinence and benefit from cessation treatments focused on negative affect management. For example, behavioral interventions that teach smokers tolerance and acceptance of the affective distress associated with tobacco withdrawal by graduated exposure to abstinence may be useful for smokers with anxiety-related general distress (Brown et al., 2008). Broadly, this work illustrates that applying alternative models of emotional symptomatology rather than relying solely on standard unitary syndrome based models may promote a more refined understanding of the relation between emotional symptoms and tobacco dependence.

Acknowledgements

The authors wish to think Mr. Michael Trujillo and Ms. Jodie Greenberg who were instrumental to collecting the data presented here

Role of Funding Source: This work was supported by NIH grants R01DA026831 and K08DA025041.

Footnotes

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Contributors: All authors significantly contributed to and approved of this manuscript.

Conflict of Interest: All authors declare no conflicts of interest.

REFERENCES

  1. al'Absi M, Hatsukami D, Davis GL. Attenuated adrenocorticotropic responses to psychological stress are associated with early smoking relapse. Psychopharmacol. (Berl.) 2005;181:107–117. doi: 10.1007/s00213-005-2225-3. [DOI] [PubMed] [Google Scholar]
  2. Baker TB, Piper ME, McCarthy DE, Majeskie MR, Fiore MC. Addiction motivation reformulated: an affective processing model of negative reinforcement. Psychol. Rev. 2004;111:33–51. doi: 10.1037/0033-295X.111.1.33. [DOI] [PubMed] [Google Scholar]
  3. Breslau N, Kilbey MM, Andreski P. Nicotine withdrawal symptoms and psychiatric disorders: findings from an epidemiologic study of young adults. Am. J. Psychiatry. 1992;149:464–469. doi: 10.1176/ajp.149.4.464. [DOI] [PubMed] [Google Scholar]
  4. Brown RA, Niaura R, Lloyd-Richardson EE, Strong DR, Kahler CW, Abrantes AM, Abrams D, Miller IW. Bupropion and cognitive-behavioral treatment for depression in smoking cessation. Nicotine Tob. Res. 2007;9:721–730. doi: 10.1080/14622200701416955. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Brown RA, Palm KM, Strong DR, Lejuez CW, Kahler CW, Zvolensky MJ, Hayes SC, Wilson KG, Gifford EV. Distress tolerance treatment for early-lapse smokers: rationale, program description, and preliminary findings. Behav. Modif. 2008;32:302–332. doi: 10.1177/0145445507309024. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Clark LA, Watson D. Tripartite model of anxiety and depression: psychometric evidence and taxonomic implications. J. Abnorm. Psychol. 1991;100:316–336. doi: 10.1037//0021-843x.100.3.316. [DOI] [PubMed] [Google Scholar]
  7. Cook J, Spring B, McChargue D, Doran N. Effects of anhedonia on days to relapse among smokers with a history of depression: a brief report. Nicotine Tob. Research. 2010;12:978–982. doi: 10.1093/ntr/ntq118. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Cook JW, Spring B, McChargue D. Influence of nicotine on positive affect in anhedonic smokers. Psychopharmacol. (Berl.) 2007;192:87–95. doi: 10.1007/s00213-006-0688-5. [DOI] [PubMed] [Google Scholar]
  9. Cook JW, Spring B, McChargue D, Hedeker D. Hedonic capacity, cigarette craving, and diminished positive mood. Nicotine Tob. Res. 2004;6:39–47. doi: 10.1080/14622200310001656849. [DOI] [PubMed] [Google Scholar]
  10. Cox LS, Tiffany ST, Christen AG. Evaluation of the brief questionnaire of smoking urges (QSU-brief) in laboratory and clinical settings. Nicotine Tob. Res. 2001;3:7–16. doi: 10.1080/14622200020032051. [DOI] [PubMed] [Google Scholar]
  11. First MB, Spitzer RL, Gibbon M, Williams JBW. Structured Clinical Interview for DSM-IV-TR Axis I Disorders, Research Version, Non-Patient Edition. (SCID-I/NP) New York: Biometrics Research, New York State Psychiatric Institute; 2002. [Google Scholar]
  12. Gilbert DG, McClernon FJ, Rabinovich NE, Dibb WD, Plath LC, Hiyane S, Jensen RA, Meliska CJ, Estes SL, Gehlbach BA. EEG, physiology, and task-related mood fail to resolve across 31 days of smoking abstinence: relations to depressive traits, nicotine exposure, and dependence. Exp. Clin. Psychopharmacol. 1999;7:427–443. doi: 10.1037//1064-1297.7.4.427. [DOI] [PubMed] [Google Scholar]
  13. Gilbert P, Allan S, Brough S, Melley S, Miles JN. Relationship of anhedonia and anxiety to social rank, defeat and entrapment. J. Affect. Disord. 2002;71:141–151. doi: 10.1016/s0165-0327(01)00392-5. [DOI] [PubMed] [Google Scholar]
  14. Gregor K, Zvolensky MJ, Bernstein A, Marshall EC, Yartz AR. Smoking motives in the prediction of affective vulnerability among young adult daily smokers. Behav. Res. Ther. 2007;45:471–482. doi: 10.1016/j.brat.2006.03.019. [DOI] [PubMed] [Google Scholar]
  15. Heatherton TF, Kozlowski LT, Frecker RC, Fagerstrom KO. The Fagerstrom Test for Nicotine Dependence: a revision of the Fagerstrom Tolerance Questionnaire. Br. J. Addict. 1991;86:1119–1127. doi: 10.1111/j.1360-0443.1991.tb01879.x. [DOI] [PubMed] [Google Scholar]
  16. Hughes JR. Effects of abstinence from tobacco: valid symptoms and time course. Nicotine Tob. Res. 2007;9:315–327. doi: 10.1080/14622200701188919. [DOI] [PubMed] [Google Scholar]
  17. Hughes JR, Hatsukami D. Signs and symptoms of tobacco withdrawal. Arch. Gen. Psychiatry. 1986;43:289–294. doi: 10.1001/archpsyc.1986.01800030107013. [DOI] [PubMed] [Google Scholar]
  18. Johnson KA, Stewart S, Rosenfield D, Steeves D, Zvolensky MJ. Prospective evaluation of the effects of anxiety sensitivity and state anxiety in predicting acute nicotine withdrawal symptoms during smoking cessation. Psychol. Addict. Behav. 2012;26:289–297. doi: 10.1037/a0024133. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Keselman HJ, Cribbie R, Holland B. Controlling the rate of Type I error over a large set of statistical tests. Br. J. Math Stat. Psychol. 2002;55:27–39. doi: 10.1348/000711002159680. [DOI] [PubMed] [Google Scholar]
  20. Langdon KJ, Leventhal AM, Stewart S, Rosenfield D, Steeves D, Zvolensky MJ. Anhedonia and anxiety sensitivity: Prospective relations to nicotine withdrawal symptoms during smoking cessation. J. Stud. Alcohol Drugs. 2013;74:469–478. doi: 10.15288/jsad.2013.74.469. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Leventhal AM, Munafo M, Tidey JW, Sussman S, Monterosso JR, Sun P, Kahler CW. Anhedonia predicts altered processing of happy faces in abstinent cigarette smokers. Psychopharmacol. (Berl.) 2012;222:343–351. doi: 10.1007/s00213-012-2649-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Leventhal AM, Ramsey SE, Brown RA, LaChance HR, Kahler CW. Dimensions of depressive symptoms and smoking cessation. Nicotine Tob. Res. 2008;10:507–517. doi: 10.1080/14622200801901971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Leventhal AM, Waters AJ, Moolchan ET, Heishman SJ, Pickworth WB. A quantitative analysis of subjective, cognitive, and physiological manifestations of the acute tobacco abstinence syndrome. Addict. Behav. 2010;35:1120–1130. doi: 10.1016/j.addbeh.2010.08.007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. MacPherson L, Tull MT, Matusiewicz AK, Rodman S, Strong DR, Kahler CW, Hopko DR, Zvolensky MJ, Brown RA, Lejuez CW. Randomized controlled trial of behavioral activation smoking cessation treatment for smokers with elevated depressive symptoms. J. Consult. Clin. Psychol. 2010;78:55–61. doi: 10.1037/a0017939. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. McCarthy DE, Piasecki TM, Fiore MC, Baker TB. Life before and after quitting smoking: an electronic diary study. J. Abnorm. Psychol. 2006;115:454–466. doi: 10.1037/0021-843X.115.3.454. [DOI] [PubMed] [Google Scholar]
  26. McNair D, Lorr M, Droppleman DL. Profile of Mood States. San Diego: Educational and Industrial Testing Service; 1971. [Google Scholar]
  27. Niaura R, Britt DM, Shadel WG, Goldstein M, Abrams D, Brown R. Symptoms of depression and survival experience among three samples of smokers trying to quit. Psychol. Addict. Behav. 2001;15:13–17. doi: 10.1037/0893-164x.15.1.13. [DOI] [PubMed] [Google Scholar]
  28. Piper ME, Schlam TR, Cook JW, Sheffer MA, Smith SS, Loh WY, Bolt DM, Kim SY, Kaye JT, Hefner KR, Baker TB. Tobacco withdrawal components and their relations with cessation success. Psychopharmacol. (Berl.) 2011;216:569–578. doi: 10.1007/s00213-011-2250-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Piper ME, Smith SS, Schlam TR, Fleming MF, Bittrich AA, Brown JL, Leitzke CJ, Zehner ME, Fiore MC, Baker TB. Psychiatric disorders in smokers seeking treatment for tobacco dependence: relations with tobacco dependence and cessation. J. Consult. Clin. Psychol. 2010;78:13–23. doi: 10.1037/a0018065. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Pomerleau CS, Marks JL, Pomerleau OF. Who gets what symptom? Effects of psychiatric cofactors and nicotine dependence on patterns of smoking withdrawal symptomatology. Nicotine Tob. Res. 2000;2:275–280. doi: 10.1080/14622200050147547. [DOI] [PubMed] [Google Scholar]
  31. Ree MJ, French D, MacLeod C, Locke V. Distinguishing cognitive and somatic dimensions of state and trait anxiety: development and validation of the State-Trait Inventory for Cognitive and Somatic Anxiety (STICSA) Behav. Cogn. Psychoth. 2008;36:313–332. [Google Scholar]
  32. Schulte-van Maaren YW, Carlier IV, Zitman FG, van Hemert AM, de Waal MW, van Noorden MS, Giltay EJ. Reference values for generic instruments used in routine outcome monitoring: the Leiden routine outcome monitoring study. BMC Psychiatry. 2012;12:203. doi: 10.1186/1471-244X-12-203. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Shafer AB. Meta-analysis of the factor structures of four depression questionnaires: Beck, CES-D, Hamilton, and Zung. J. Clin. Psychol. 2006;62:123–146. doi: 10.1002/jclp.20213. [DOI] [PubMed] [Google Scholar]
  34. Shiffman S, Hufford M, Hickcox M, Paty JA, Gnys M, Kassel JD. Remember that? A comparison of real-time versus retrospective recall of smoking lapses. J. Consult. Clin. Psychol. 1997;65:292–300. doi: 10.1037/0022-006x.65.2.292.a. [DOI] [PubMed] [Google Scholar]
  35. SRNT. Biochemical verification of tobacco use and cessation. Nicotine Tob. Res. 2002;4:149–159. doi: 10.1080/14622200210123581. [DOI] [PubMed] [Google Scholar]
  36. Strong DR, Kahler CW, Leventhal AM, Abrantes AM, Lloyd-Richardson E, Niaura R, Brown RA. Impact of bupropion and cognitive-behavioral treatment for depression on positive affect, negative affect, and urges to smoke during cessation treatment. Nicotine Tob. Res. 2009;11:1142–1153. doi: 10.1093/ntr/ntp111. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Strong DR, Leventhal AM, Evatt DP, Haber S, Greenberg BD, Abrams D, Niaura R. Positive reactions to tobacco predict relapse after cessation. J. Abnorm. Psychol. 2011;120:999–1005. doi: 10.1037/a0023666. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Wacker J, Dillon DG, Pizzagalli DA. The role of the nucleus accumbens and rostral anterior cingulate cortex in anhedonia: integration of resting EEG, fMRI, and volumetric techniques. Neuroimage. 2009;46:327–337. doi: 10.1016/j.neuroimage.2009.01.058. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Wardenaar KJ, van Veen T, Giltay EJ, de Beurs E, Penninx BW, Zitman FG. Development and validation of a 30-item short adaptation of the Mood and Anxiety Symptoms Questionnaire (MASQ) Psychiatry Res. 2010;179:101–106. doi: 10.1016/j.psychres.2009.03.005. [DOI] [PubMed] [Google Scholar]
  40. Watson D, Clark LA, Weber K, Assenheimer JS, Strauss ME, McCormick RA. Testing a tripartite model: II. Exploring the symptom structure of anxiety and depression in student, adult, and patient samples. J. Abnorm. Psychol. 1995;104:15–25. doi: 10.1037//0021-843x.104.1.15. [DOI] [PubMed] [Google Scholar]
  41. Weinberger AH, Desai RA, McKee SA. Nicotine withdrawal in U.S. smokers with current mood, anxiety, alcohol use, substance use disorders. Drug Alcohol Depend. 2010;108:7–12. doi: 10.1016/j.drugalcdep.2009.11.004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Xian H, Scherrer JF, Madden PA, Lyons MJ, Tsuang M, True WR, Eisen SA. Latent class typology of nicotine withdrawal: genetic contributions and association with failed smoking cessation and psychiatric disorders. Psychol. Med. 2005;35:409–419. doi: 10.1017/s0033291704003289. [DOI] [PubMed] [Google Scholar]
  43. Zvolensky MJ, Gibson LE, Vujanovic AA, Gregor K, Bernstein A, Kahler C, Legues CW, Brown RA, Feldner MT. Impact of Posttraumatic Stress Disorder on early smoking lapse and relapse during a self-guided quit attempt among community-recruited daily smokers. Nicotine Tob. Res. 2008;10:1415–1427. doi: 10.1080/14622200802238951. [DOI] [PubMed] [Google Scholar]
  44. Zvolensky MJ, Stewart SH, Vujanovic AA, Gavric D, Steeves D. Anxiety sensitivity and anxiety and depressive symptoms in the prediction of early smoking lapse and relapse during smoking cessation treatment. Nicotine Tob. Res. 2009;11:323–331. doi: 10.1093/ntr/ntn037. [DOI] [PMC free article] [PubMed] [Google Scholar]

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