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Schizophrenia Bulletin vol. 36 no. 1 pp.

173–181, 2010
doi:10.1093/schbul/sbn066
Advance Access publication on June 17, 2008

Smoking in Schizophrenia: Diagnostic Specificity, Symptom Correlates, and Illness


Severity

Roman Kotov1,2, Lin T. Guey2, Evelyn J. Bromet2, and Key words: depression/psychosis/severe mental illness/
Joseph E. Schwartz2 epidemiology
2
Department of Psychiatry and Behavioral Sciences, Stony
Brook University, Putnam Hall-South Campus, Stony Brook,
NY 11794-8790
Introduction
Smoking is the leading cause of preventable mortality in
Background: Cigarette smoking was consistently found to developed countries, and it remains highly prevalent
be more prevalent in individuals with schizophrenia than in among patients with schizophrenia despite a steep decline
other psychiatric groups and the general population. These in the general US population.1–5 A quantitative review of
findings have been interpreted as evidence of a specific as- 42 studies from 20 countries reported a 62% pooled rate
sociation between schizophrenia and smoking. However, of smoking in patients with schizophrenia, which was sig-
the supporting data come primarily from cross-sectional nificantly elevated relative to general population and psy-
studies, which are susceptible to confounding. Our aim chiatric comparison groups.2 These data have been
was to test specificity of this link longitudinally in an ep- interpreted as evidence of a specific link between smoking
idemiologic sample. Methods: A cohort of 542 inpatients and schizophrenia. It was hypothesized that schizo-
with psychosis was followed for 10 years after first hospi- phrenia leads to smoking, presumably, because nicotine
talization, completing 5 face-to-face interviews. Assess- reduces symptoms of the illness (ie, self-medication),6
ments included ratings of specific symptoms (psychotic, that smoking may contribute to development of the dis-
negative, disorganized, and depressive), Global Assessment order by altering neurochemical systems in the brain,7
of Functioning, and a categorical measure of cigarette con- and that both conditions could arise from a common
sumption. All participants were assigned longitudinal con- genetic vulnerability.2
sensus diagnoses by study psychiatrists, and 229 were However, these hypotheses are based primarily on
diagnosed with schizophrenia spectrum disorders (SZ). cross-sectional comparisons of smoking rates in schizo-
Results: At baseline, 52.4% of participants were current phrenia and various other psychiatric disorders.2 Elevated
smokers and 69.3% were lifetime smokers. Smoking rates rates found in such studies may be due to confounders,
did not differ among the diagnostic groups (schizophrenia such as illness severity or impoverished environment.4,8,9
spectrum, major depressive, bipolar, or other psychotic dis- Several investigations attempted to control for potential
order) at any assessment point. Smokers were more se-
confounders statistically, but the selection of variables var-
verely ill than nonsmokers but did not differ in specific
ied widely. Typically, adjustments were made for age and
symptoms either cross-sectionally or longitudinally.
gender, but some studies also controlled for socioeco-
Among smokers, changes in cigarette consumption were
nomic status (SES), low IQ, education, marital status,
linked only with changes in depression (b = .16,
comorbid diagnoses, and several other characteris-
P < .001). Conclusions: Rates of smoking were elevated
tics.4,10–13 The effect almost invariably persisted after cor-
in subjects with schizophrenia but were just as high with
rections. However, no study controlled for illness severity.
other psychotic disorders. Smoking was not associated
Prospective investigations can provide more direct evi-
with psychotic symptoms, but cigarette consumption
dence of the connection, but 2 studies conducted to
covaried with depression over time. Given the devastating
date produced contradictory results. Weiser et al12 found
health consequences of cigarette use, smoking cessation
that smokers were at an increased risk for developing the
interventions are urgently needed in this population and
illness, whereas Zammit et al13 reported that smoking had
should specifically address depression.
a protective effect. Moreover, investigations of associa-
tions between smoking and severity of schizophrenia
1
To whom correspondence should be addressed; tel: 631-632- symptoms have also produced inconsistent results. One
7763, fax: 631-632-9433, e-mail: roman.kotov@stonybrook.edu. study reported a link to both negative and positive
Ó The Author 2008. Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center. All rights reserved.
For permissions, please email: journals.permissions@oxfordjournals.org.
173
R. Kotov et al.

Baseline Interview
N = 675

Excluded
31 ineligible
55 insufficient longitudinal data
47 substance-induced or
organic psychosis

Analysis Sample
N = 542

Incomplete Data
Intermediate 28 Died
6 months N = 423 29 Lost
2 years N = 387 47 Refused
4 years N = 319 8 Unable to consent
73 Contacted but insufficient data

Year 10 Interview
N = 357

Fig. 1. Derivation of the Sample and Its Retention by the 10-Year Follow-up.

symptoms,14 4 found associations with one type of symp- rate of current smoking remained stable across the
toms but not the others,11,15–17 and another 4 did not find 6-year enrollment period (b = .01, P = .83).
any significant relations.18–21 In contrast, the link between The purpose of the parent study was to investigate the
smoking and depression is well established both cross- course of schizophrenia longitudinally in an epidemio-
sectionally22 and prospectively.23–27 In fact, it was sug- logic sample of first-admission cases. To obtain a repre-
gested that depression may contribute to the high rates sentative sample, all new patients with psychosis were
of smoking in patients with schizophrenia,14,17 but this enrolled, and thus, a variety of psychotic disorders are
hypothesis has not been directly tested. present in this cohort. The inclusion criteria were aged
The objective of this study was to test the belief that 15–60, first admission either concurrent or during the
schizophrenia has a specific connection to smoking. First, 6 months prior to the index admission, clinical evidence
we examined the specificity of elevated smoking rates to of psychosis, ability to understanding the assessment pro-
schizophrenia by comparing it to disorders of similar se- cedures in English, and capacity to provide written in-
verity (eg, mood disorders with psychosis). Second, we formed consent. The procedures for obtaining
tested associations of smoking with schizophrenia and de- informed consent were approved annually by the Institu-
pression symptoms both cross-sectionally and longitudi- tional Review Boards at Stony Brook University and all
nally. Third, we evaluated links between changes in hospitals where respondents were recruited. For partici-
these symptoms and fluctuations in cigarette consump- pants aged 15–17, written consent of parents was also re-
tion over time among smokers. quired. The response rate was 72%. Overall, 675
individuals met the inclusion criteria and were inter-
viewed at the baseline. Of those, 31 were later found
Methods to be ineligible, primarily because it became clear that
they never suffered from psychosis. Another 55 partici-
Sample and Procedure pants were excluded because of insufficient follow-up in-
Data for this study came from a first-admission cohort formation to permit a longitudinal diagnosis (15 of them
described in detail elsewhere.28–31 The patients were died in the first 24 months of the study), and 47 were re-
recruited from all 12 psychiatric inpatient units of Suffolk moved because they had a substance-induced or organic
County, NY, between 1989 and 1995. The units included psychosis. Hence, the analysis sample is composed of 542
state, community, and university facilities. At the begin- participants (figure 1).
ning of the study, all facilities permitted smoking, but in In addition to baseline, face-to-face interviews were
late 1991 and early 1992, policies changed to prohibit performed at month 6 and years 2, 4, and 10 by trained
smoking on the units. Instead, patients were regularly master’s level mental health professionals. Study psychia-
taken outside to smoke. They were also offered nicotine trists formulated longitudinal consensus Diagnostic and
replacement (gum or patch). Despite these changes, the Statistical Manual of Mental Disorders, Fourth Edition,
174
Smoking in Schizophrenia

55 Measures
50 Smoking was assessed with items adapted from the Na-
tional Household Survey on Drug Abuse interview.32 All
45 participants were asked how much they smoked per day
in the past 30 days (past 6 months at waves 2, 3, and 4) on
GAF

40
the following scale: none, <1 cigarette, 1–5 cigarettes,
35 ½ a pack, 1 pack, 1½ packs, and 2 or more packs. A par-
abstaining ticipant reporting any usage was considered a smoker at
30 fluctuating
persisting
that wave. At baseline, participants were also asked
25 whether they ever smoked on a regular basis. Those
0 2 4 6 8 10 who responded yes or reported cigarette usage at baseline
Years were considered lifetime smokers. Responses were
Fig. 2. Trajectory of Illness Severity (GAF) in the 3 Smoking Pattern
recoded as the number of cigarettes consumed on an
Groups of the Total Sample: Abstaining (N 5 191), Fluctuating average day using the mid-point of the corresponding in-
(N 5 127), and Persisting (N 5 224). terval except for the highest level, which was coded as 40.
Symptoms of schizophrenia in the 4-week period pre-
ceding the interview were measured with the Scale for the
Assessment of Positive Symptoms (SAPS)33 and the Scale
research diagnoses after the year 2 assessment. The rat-
for the Assessment of Negative Symptoms (SANS).34 The
ings were made independently by at least 2 psychiatrists
SAPS consists of 31 items tapping 4 symptom domains
and were discussed by the whole team. The raters based
diagnoses on all available information from structured and a global rating for each domain. The SANS is com-
clinical interviews, medical records, and significant posed of 19 items measuring 5 domains as well as the
others collected at baseline, month 6, and year 2.30 global ratings. SAPS and SANS items are rated on
The diagnoses were grouped as schizophrenia spectrum a 6-point scale (0 = none, 5 = severe). The validity of
(SZ; schizoaffective disorder, and schizophreniform these measures is well established.35–37 Specifically, the
disorder; N = 229), bipolar disorder with psychosis SANS is unidimensional, whereas the SAPS taps 2 fac-
(N = 148), major depressive disorder with psychosis tors: psychotic symptoms (hallucinations and delusions)
(N = 104), and other psychotic disorders (delusional dis- and disorganized symptoms (bizarre behavior and formal
order, brief psychotic reaction, and psychotic disorder thought disorder). Consistent with prior studies, we used
not otherwise specified; N = 61). The SZ group is the fo- individual items but not the global items.38–40 Common
cus of the present study. factor analysis supported the established structure in the
With extensive efforts to track the sample and keep present data. We removed 3 items that had consistently
respondents invested in the study, we were able to main- poor loadings in these analyses: SANS item 13 (inatten-
tain contact with the vast majority of participants. By the tiveness during mental status testing), SAPS item 9 (per-
10-year point, 28 respondents had died, 29 were lost to the secutory delusions), and SAPS item 10 (delusions of
study, 47 refused to be interviewed, and 8 were too ill to jealousy). Thus, the final SANS composite consisted of
give informed consent. Half of the 28 participants died of 18 items (internal consistency reliability ranged
medical illnesses (most commonly cardiovascular disease, a = .88–.90 over the 5 waves), SAPS psychotic of 16 items
various forms of cancer, and liver failure), but only one of (a = .79–.85), and SAPS disorganized of 13 items
them died of lung cancer. Due to relatively low mortality (a = .71–.76). The interrater reliability of these ratings
and absence of a clear connection to tobacco use, we do was very good (average interrater r = .72).41
not expect that mortality biased our findings. Of 430 con- Symptoms of depression in the month preceding
tacted respondents, 73 provided limited data and could not the interview were assessed with the Structured Clinical
be analyzed. Thus, all necessary information at year 10 Interview for DSM-III-R (SCID)42 depression module
was available for 357 respondents (completers), and 147 administered without skip-outs. Depression was opera-
of them had an SZ diagnosis. We compared excluded par- tionalized as a composite of the 9 DSM criterion symp-
ticipants (N = 185) with completers on all variables used toms. Items were rated on a 3-point scale: 1 = not
in this study and found no significant differences (all present, 2 = questionable, and 3 = definite. Internal
P > .10), which suggests that attrition had little systematic consistency reliability of the composite ranged from
impact on the results. For instance, the prevalence of cur- .83 to .86, and the interrater reliability was very
rent smoking at baseline was 51.6% among noncomplet- good.28 The composite correlated .74–.80 with the Ham-
ers, as compared with 52.8% among completers ilton Rating Scale for Depression (HAM-D)43 across dif-
(v2(1) = .07, P = .80). Missing data were handled with ferent waves. The HAM-D was not administered at year
maximum likelihood methods, and thus, all available 4, and hence, depression was assessed with the SCID-
data were utilized without deleting any records. based scale. However, we repeated all analyses with the
175
R. Kotov et al.

HAM-D (without the year 4 data), and none of our find- Although the SZ group was the focus of the study, all
ings changed. analyses were also repeated for the total sample.
Illness severity was operationalized as psychiatrists’
consensus Global Assessment of Functioning (GAF) rat-
ing for the worst week in the past month. This score had Results
little variability at baseline because all participants were Prevalence of Smoking Across Diagnoses
hospitalized. Thus, we also report on baseline GAF for
the best month (GAF Best) in the year prior to hospital- In the total sample, the lifetime prevalence of smoking
ization in some analyses. was 69.3%. It did not differ by diagnosis, although the
GAF correlated strongly with the SANS (average con- SZ group had the lowest rate (67.4%; table 1). Current
current r = .61) but had only moderate associations prevalence of smoking at baseline was 52.4% and was
with the other symptom scales (average r = .33). The similar across the diagnoses. In fact, there were no diag-
concurrent correlations among the symptom scales nostic differences in rates of current smoking at any of the
were low to moderate (average r = .19), which is consis- follow-up assessments. Adjusting these comparisons for
tent with the literature.35–37 age, sex, and SES did not change the findings, except that
We examined 3 demographic variables: sex, age at at year 4 the SZ group had a significantly lower rate of
baseline, and SES of the head of the household. SES smoking that the ‘‘other psychoses’’ group (adjusted
was assessed at baseline using the 7-point occupational odds ratio = .32, confidence interval = .12–.86). We also
scale of the Hollingshead Four Factor Index of Social Po- stratified the sample by age (15–18, 19–25, 26–44, and
sition.44 It refers to the participant unless he or she is sup- 45–58 years) and repeated the analyses but observed no
ported by someone else. diagnostic differences in either of these strata (table 1).

Smoking Status in the SZ Sample


Data Analysis
Smoking status was very stable over the 10 years with tet-
Cross-sectional comparisons were made with t tests and rachoric correlations between waves ranging .80–.97
chi-square tests. Adjustment for covariates was per- (table 2; top half). Indeed, 80% of baseline smokers, as
formed with logistic regression. Stability of smoking sta- compared with 21% of baseline nonsmokers, smoked
tus was evaluated with tetrachoric correlations, estimated at year 10. Of the 229 participants with SZ diagnoses,
in Mplus version 4.1.45 Tetrachoric correlations quantify 147 smoked at one or more waves and constitute the
associations between dichotomous variables on the met- smokers subsample.
ric of Pearson r while correcting for biasing effects of low Lifetime smokers did not differ from nonsmokers with
base rates. Longitudinal associations between smoking respect to sex, age, and SES (table 1). Moreover, smoking
status and symptom/illness severity were examined status was not related to symptom and illness severity at
with repeated-measures analysis of variance in SAS any assessments point, except for one significant finding
PROC MIXED.46 Changes in cigarette consumption for the GAF and one for the SANS (table 3). We also
over time and their correlates were evaluated with mul- examined these relationships longitudinally. Given the
tilevel growth curve analysis,47 estimated in PROC high stability of smoking status, participants were classi-
MIXED. Specifically, cigarette consumption was modeled fied according to their pattern of smoking across all avail-
on 2 levels as repeated observations (level 1) nested within able assessments as abstaining (never smoked during the
individuals (level 2). In level 1 (within subjects), cigarette study, N = 82), fluctuating (had a change in smoking sta-
consumption was evaluated as a function of time, symp- tus, N = 51), or persisting (always smoked, N = 96). The
toms, and illness severity, whereas level 2 (between sub- groups did not differ on diagnosis, gender, or SES, but
jects) modeled the mean and variance of the level 1 the fluctuating group was 5.0 years younger than the
intercept as a function of demographic variables. Longi- rest of the sample (P < .001). The groups also did not
tudinal trends in cigarette consumption were evaluated differ in their trajectories of symptom and illness severity.
with a modified model. We removed all clinical and de- Controlling for sex, age, and SES did not change the
mographic covariates, so that level 1 described cigarette findings.
consumption as a linear function of time alone, and level
2 included only mean and variance of the intercept. All
variables except time were standardized with respect to Cigarette Consumption Among SZ Smokers
their grand means and SDs (across all subjects and In the smokers subsample (N = 147), individual cigarette
waves) to facilitate interpretation. In both PROC consumption varied considerably over time, with Pearson
MIXED analyses, the random-effects covariance struc- correlations across waves ranging .33–.64 (table 2; bot-
ture was specified as an unstructured covariance matrix tom half). These results indicate that some participants
because it imposed the fewest assumptions and provided increased their use while other decreased it. However,
a better fit than various constrained covariance matrices. the group’s average daily cigarette consumption did
176
Smoking in Schizophrenia

Table 1. Demographic Characteristics of Lifetime Smokers

Odds Ratio
N Nonsmoker (%) Smoker (%) (confidence interval)

Total sample
Diagnosis
Schizophrenia spectrum 229 32.6 67.4 —
Bipolar disorder 148 30.8 69.2 1.09 (.69–1.70)
Major depression 104 26.9 73.1 1.31 (.79–2.20)
Other psychoses 61 29.5 70.5 1.16 (.62–2.14)
Sex
Male 302 31.1 68.9 —
Female 240 30.1 69.9 1.05 (.72–1.52)
Age
15–18 52 34.6 65.4 —
19–25 170 35.7 64.3 0.95 (.50–1.83)
26–44 272 28.5 71.5 1.33 (.71–2.49)
45–58 48 20.8 79.2 2.01 (.82–4.95)
SES
Blue collar or less 245 29.2 70.8 —
Above blue collar 297 31.9 68.1 0.88 (.61–1.28)
Schizophrenia spectrum group
Sex
Male 149 34.7 65.3 —
Female 80 28.8 71.3 1.32 (.73–2.38)
Age
15–18 20 40.0 60.0 —
19–25 88 33.0 67.0 1.36 (.50–3.68)
26–44 109 32.7 67.3 1.37 (.51–3.66)
45–58 12 16.7 83.3 3.33 (.57–19.41)
SES
Blue collar or less 121 29.4 70.6 —
Above blue collar 108 36.1 63.9 .74 (.42–1.29)

Note: SES, socioeconomic status. N = 542 (229 for the schizophrenia spectrum group). Dashes indicate reference category.

not change. It was 16.1 cigarettes a day at baseline and group, cigarette consumption varied considerably over
showed no significant upward or downward trend over time (table 2). Average consumption at baseline was
the 10-year follow-up. 18.1 cigarettes a day and declined at the rate of 0.36 cig-
Cross-sectional analyses did not reveal any consistent arettes a year (P < .001) over the 10-year follow-up.
associations between cigarette consumption and clinical Lifetime smokers did not differ from nonsmokers with
variables (Appendix), including GAF Best at baseline respect to sex, age, and SES (table 1). On the other hand,
(r = .04). In the longitudinal analysis, we related smokers had consistently lower GAF scores, with com-
changes in cigarette consumption to changes in symptom parisons being significant at each wave except lifetime
and illness severity over time. Each association was and baseline (table 3). However, lifetime and baseline
adjusted for demographic characteristics and influence smokers had significantly lower GAF Best scores (d =
of the other variables. Only depression severity showed 0.23, P < .05 for both). Depression scores were consis-
a significant effect (b = .16, P < .001), which corre- tently elevated in smokers and the difference reached sig-
sponds to consuming an extra cigarette a day for each nificance at 3 time points. The SANS was also
additional DSM depression symptom (table 4). significantly elevated at years 4 and 10 (table 3). Control-
ling for sex, age, and SES did not change the findings,
except for the effect of year 2 GAF in the total sample,
Analyses in the Total Sample whose significance changed from P = .030 to .081. Al-
Given that the rates of smoking did not differ among the though more associations were statistically significant
diagnostic groups, we repeated all analyses in the total in the total sample than in the SZ subgroup, the effect
sample. We thus increased power and enhanced general- sizes remained essentially the same (see mean effects in
izability of the analyses. Smoking status was very stable table 3). Thus, the apparent difference in findings like-
in this sample (table 2), and 351 of the 542 participants ly reflects greater statistical power of the total sample.
smoked at least at one point during the study. In this To appreciate the magnitude of association between
177
R. Kotov et al.

Table 2. Stability of Smoking in the Schizophrenia Spectrum Results for cigarette consumption paralleled findings
Group (N = 229, above diagonal) and the Total Sample (N = 542, in the SZ group. Cross-sectional analyses did not reveal
below diagonal)
any consistent associations between cigarette consump-
tion and clinical variables because no links were repli-
Baseline Month 6 Year 2 Year 4 Year 10
cated across more than 2 waves (Appendix). In the
Smoking statusa longitudinal analysis, only depression severity had a sig-
Baseline — 0.95 0.94 0.88 0.80 nificant association with the amount of smoking while
6 mo 0.95 — 0.97 0.95 0.91 adjusting for other clinical variables and demographic
2y 0.94 0.96 — 0.97 0.97 characteristics (table 4).
4y 0.91 0.94 0.97 — 0.91
10 y 0.79 0.87 0.91 0.88 —
Additional Analyses
Consumptionb
Baseline — 0.62 0.47 0.36 0.33 All analyses were repeated in the completers subsample.
6 mo 0.64 — 0.61 0.55 0.42 The results were unchanged, except that a few cross-
2y 0.51 0.65 — 0.64 0.45 sectional comparisons became nonsignificant due to
4y 0.41 0.54 0.65 — 0.38
10 y 0.30 0.41 0.41 0.47 —
reduced power and without an appreciable change in
magnitude.
a
Top block = tetrachoric correlations among smoking status
variables (smoker/nonsmoker).
b Discussion
Bottom block = Pearson correlations of cigarette consumption
in the smokers subsample. Consistent with previous reports, the point prevalence
of smoking in the schizophrenia group of our epidemio-
logic first-admission sample (51.0% at year 10) was 2.5-
smoking and GAF, we compared prevalence of severe fold greater than in the US population (20.9% in 2005).1
illness (GAF  50) at year 10 between smokers and non- However, rates of smoking were just as high in the other
smokers. Many more smokers were severely ill (64.5% vs diagnostic groups. The present findings underscore the
45.1%, P < .001). significance of smoking as a public health problem
Longitudinal analyses also confirmed the association that cuts across psychotic disorders and possibly all se-
between smoking status and illness severity. Smoking vere mental illnesses. There was little change in smoking
pattern (abstaining, fluctuating, or persisting) had no as- status among participants with schizophrenia over the
sociation with symptom trajectories, but the persisting 10-year follow-up, and the average cigarette consump-
group had consistently lower GAF scores than the tion remained stable, although for individual smokers
abstaining (P < .01), with the fluctuating falling in be- the amount of consumption fluctuated notably over
tween (figure 1). Controlling for sex, age, and SES did time. Neither smoking status nor amount of consump-
not change the findings. tion was associated with schizophrenia symptoms.

Table 3. Cross-sectional Comparisons of Smokers and Nonsmokers in Symptom and Illness Severity (Cohen d)

Lifetime Baseline Month 6 Year 2 Year 4 Year 10 Meana

Schizophrenia spectrum group


N 227 229 183 168 140 147
GAF 0.14 0.01 0.31* 0.10 0.29 0.22 0.16
Depression scale 0.22 0.11 0.27 0.13 0.34 0.03 0.18
SAPS psychotic 0.25 0.13 0.17 0.08 0.07 0.25 0.14
SAPS disorganized 0.11 0.02 0.12 0.16 0.00 0.03 0.01
SANS 0.13 0.08 0.16 0.26 0.26 0.34* 0.10
Total sample
N 540 542 423 387 319 357
GAF 0.07 0.03 0.28** 0.22* 0.32** 0.45*** 0.16
Depression scale 0.19* 0.15 0.20* 0.15 0.25* 0.10 0.17
SAPS psychotic 0.12 0.07 0.15 0.07 0.13 0.21 0.12
SAPS disorganized 0.01 0.02 0.04 0.03 0.02 0.10 0.01
SANS 0.05 0.05 0.14 0.18 0.25* 0.35* 0.11

Note: GAF, Global Assessment of Functioning; SAPS, Scale for the Assessment of Positive Symptoms; SANS, Scale for the
Assessment of Negative Symptoms.
a
Mean = sample size weighted mean of the 6 columns.
*P < .05, **P < .01, ***P < .001.

178
Smoking in Schizophrenia

Table 4. Correlates of Cigarette Consumption Over Time in sive literature documenting cross-sectional and longitudi-
Smokers: Multilevel Growth Curve Analysisa nal correlations between smoking and depression in other
populations.22 It appears that depression may have an
Schizophrenia
etiologic connection with smoking behavior, and mech-
Spectrum Total Sample
anisms for this association have been proposed.22,50–52
GAF 0.01 0.02 These data highlight the importance of addressing de-
Depression scale 0.16*** 0.11***
pression in smoking cessation interventions.
We did not find differences between smokers and
SAPS psychotic 0.01 0.02
nonsmokers in SES and gender composition, although
SAPS disorganized 0.03 0.04 in the general population smoking is more prevalent
SANS 0.01 0.01 among men and in lower socioeconomic strata.1 The
gender difference was also observed in schizophrenia
Note: GAF, Global Assessment of Functioning; SAPS, Scale for samples.2 However, the patients in these studies have
the Assessment of Positive Symptoms; SANS, Scale for the
typically been ill for a long time. In contrast, our cohort
Assessment of Negative Symptoms.
a
All values are standardized b-weights and represent was assessed at the time of the first admission and was
independent contributions of each predictor. Associations are followed through the early stages of the illness. We ex-
also adjusted for age, sex, socioeconomic status, and time pect that gender and SES differences will emerge in our
(nominal variable). sample with time.
*P < .05, **P < .01, ***P < .001.
A notable caveat of this study is that the findings
should not be generalized to patients who have never
suffered from psychosis. With regard to our diagnostic
However, changes in the letter were linked with changes comparisons, it is important to note that the majority
in depression symptoms. of mood disorder patients did not have any psychotic
We did not find evidence of specificity of smoking to symptoms at the follow-up assessments, yet no diagnos-
schizophrenia relative to other psychotic disorders at any tic differences were observed. Furthermore, severity
point during the follow-up, although our study had the of psychotic symptoms was associated neither with
power of .93 to detect the level of difference reported smoking status nor with cigarette consumption. Never-
in a recent meta-analysis that compared schizophrenia theless, our conclusions should also be tested in nonpsy-
with other psychiatric disorders.2 Further examination chotic severely ill patients. The present findings do show
of smokers suggested that they were not different from that smoking is highly prevalent across psychotic
nonsmokers in severity of specific symptoms but were disorders rather than being specific to schizophrenia.
more severely ill overall. For instance, at the end of Another limitation of the study is that anxiety was
the follow-up, smokers were 43% more likely to be se- not assessed, despite growing evidence of its links to
verely ill than nonsmokers. Thus, it appears that reports smoking.5,48,53 Cigarette consumption is also associated
of elevated smoking rates in schizophrenia may have con- with substance use. Evaluation of this relationship was
founded diagnosis with illness severity. In support of this beyond the scope of the present study, but it would be
interpretation, smoking did not show specificity to non- very informative to examine the links between substance
affective psychosis in a nationally representative study of abuse and smoking over time. Finally, smoking was
mental illness in the United States.48 Furthermore, as measured with a single item and was rated on an ordinal
mentioned in the Introduction, prospective investigations scale rather that continuously. This likely limited reli-
of relations between smoking and schizophrenia pro- ability of the score and probably led to underestimation
duced contradictory results, and cross-sectional studies of the effect sizes.
failed to find consistent associations between smoking Despite these limitations, our findings suggest that
and severity of schizophrenia symptoms. On the other smoking is especially prevalent among those with severe
hand, smoking status has been linked to illness severity mental illness, and special intervention efforts should be
in general psychiatric samples, albeit assessed with proxy directed toward this group. It appears that factors con-
measures.4,8,49 For instance, Aguilar et al49 found no tributing to high rates of smoking are likely to be consis-
clear links between nicotine dependence and schizophre- tent across the diagnostic groups studied here. One factor
nia symptoms but observed an association between with potential etiological significance is depression, and it
smoking and frequent hospitalizations, an indirect mea- should be addressed specifically in smoking cessation
sure of illness severity. protocols. Importantly, emerging evidence suggests
Examination of cigarette consumption among smokers that smoking cessation interventions can be successfully
did not support the self-medication hypothesis with employed in psychiatric populations,54,55 and quitting
regard to schizophrenia symptoms. However, we found does not seem to impede recovery from mental illness.56
that increases in depression were associated with heavier Hence, provision of these services to severely mentally ill
smoking. This observation is consistent with the exten- is an imperative.
179
R. Kotov et al.

Appendix Cross-sectional Correlations (Pearson r) Between Cigarette Consumption and Clinical Variables in Smokers Subsample

Baseline Month 6 Year 2 Year 4 Year 10 Meana

Schizophrenia spectrum group


N 147 119 109 96 97
GAF 0.05 0.14 0.18 0.03 0.05 0.05
Depression scale 0.12 0.14 0.10 0.09 0.08 0.11
SAPS psychotic 0.10 0.06 0.04 0.14 0.04 0.04
SAPS disorganized 0.17* 0.04 0.02 0.21* 0.05 0.10
SANS 0.03 0.11 0.29** 0.01 0.13 0.11
Total sample
N 349 279 253 219 235
GAF 0.10 0.05 0.17** 0.10 0.23** 0.07
Depression scale 0.08 0.15** 0.19** 0.07 0.06 0.11
SAPS psychotic 0.03 .01 0.00 0.04 0.10 0.00
SAPS disorganized 0.12* 0.08 0.03 0.12 0.03 0.06
SANS 0.05 0.09 0.18** 0.13 0.24** 0.10

Note: GAF, Global Assessment of Functioning; SAPS, Scale for the Assessment of Positive Symptoms; SANS, Scale for the
Assessment of Negative Symptoms.
a
Mean = sample size weighted mean of the 5 columns.
*P < .05, **P < .01, ***P < .001.

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