Psychological Correlates of Sleep Apnea
Psychological Correlates of Sleep Apnea
Psychological Correlates of Sleep Apnea
583596, 1999
Copyright 1999 Elsevier Science Inc.
All rights reserved.
0022-3999/99 $see front matter
S0022-3999(99)00062-8
AbstractRelationships were examined between psychological and sleep variables in individuals with
sleep apnea (n572, 24 with hypertension; Respiratory Disturbance Index515) and without sleep apnea
(n540, 16 with hypertension; respiratory disturbance index,15). Subjects were 3264 years old, 100
150% of ideal weight, with no other major illness. For subjects with sleep apnea, depression, anger, and
total mood disturbance correlated positively with deep sleep, rapid eye movement sleep, and/or hypoxemia. For subjects without sleep apnea, vigor correlated positively with sleep quantity and negatively
with hypoxemia. When age, body mass, and hypertension were controlled, results changed little for subjects without sleep apnea; for subjects with sleep apnea, depression and total mood disturbance no longer
correlated with sleep measures. Although various psychological measures correlate with sleep variables
in sleep apnea subjects, many are explained by controlling age, body mass, and hypertension. Anger and
vigor, however, remain associated with sleep variables. 1999 Elsevier Science Inc.
Keywords:
INTRODUCTION
Obstructive sleep apnea is a devastating illness that leaves patients exhausted from
sleep deprivation and, at times, cognitively impaired [1]. The literature is mixed on
the role psychological factors play in this illness. Some researchers have observed
that sleep apnea is associated with clinical depression [25] or increased levels of
depressive symptoms [612], either as a direct consequence of the sleep deprivation
or indirectly as a consequence of social effects of this illness. Others have reported
that patients with sleep apnea do not show clinically significant levels of depression,
or have levels of depressive symptoms no higher than control groups [1315] or patients with other chronic illnesses [16]. In addition, some investigators have asserted
that sleep apnea patients have certain other associated psychological characteristics,
namely irritability [6, 9, 12, 16], tendency toward conflict with others [9], anxiety [2,
3, 7, 9, 10, 17], and fatigue or diminished energy [1, 7, 11, 14, 18]. Others have reported that sleep apnea patients show a somaticneurotic personality pattern [12,
17]. However, one researcher reported finding no correlation between presence/absence of sleep apnea and any personality factors [19].
Departments of * Psychiatry and Family and Preventive Medicine, University of California, San
Diego, California, USA.
Veterans Affairs San Diego Healthcare System, San Diego, California, USA.
Address correspondence to: Dr. Joel Dimsdale, Department of Psychiatry, University of California,
San Diego, La Jolla, CA 92093-0804. Phone: (619)-543-5592; Fax: 619-543-5462; E-mail: jdimsdale@
ucsd.edu.
583
584
W. A. BARDWELL et al.
Problems with these studies include sample characteristics, small sample size, lack
of control groups, and inconsistent or undisclosed criteria for diagnosing sleep apnea. Subjects have also suffered from other comorbid disorders and the studies have
rarely controlled for hypertension (HTN)frequently found in sleep apnea patientswhich has certain psychological characteristics in its own right [20, 21]. Previous studies have also not examined the influence of weight and age, which are associated with both sleep apnea and psychological factors.
Table I summarizes findings from several studies of sleep apnea and psychological variables. Eleven studies found elevated levels of depression in patients with
sleep apnea [2, 3, 5, 6, 8, 10] and/or improvement in depressive symptoms after
treatment (continuous positive airway pressure [CPAP], uvulopalatopharyngoplasty [UPPP], or tracheostomy) [4, 7, 9, 11, 16], whereas three studies did not [13
15]. Six studies found elevated levels of anxiety or tension or else improvement in
these symptoms after treatment in patients with sleep apnea [2, 3, 7, 9, 10, 17]. Three
investigations indicated that sleep apnea patients reported or were observed to be
irritable, frustrated, or prone to conflict [6, 9, 16].
Various measures of sleep quality and quantity, such as sleep fragmentation [2,
5, 9, 11] or hypoxemia [2, 9, 11], have been found to be associated with psychological
and cognitive impairment in this population. One study reported that depression,
anxiety, and cognitive deficits were related to time spent in rapid eye movement
(REM) and deep sleep (stages 3 and 4), as well as to hypoxemia [9]. Another study
found that cognitive deficits were correlated with frequency of apneas/hypopneas,
arousals, and hypoxemia [2]. One group reported that depressive symptoms and fatigue decreased after CPAP. They found that the decrease in depressive symptoms
correlated with an increase in deep sleep, whereas the decrease in fatigue correlated
with improvement in oxyhemoglobin saturation [11]. Finally, another team found
depression correlated with REM time, REM latency, and the presence/absence of
HTN medications [5].
Although psychiatrists and behavioral medicine researchers are very interested
in links between various mood states and physiology, it has been striking that observations have almost entirely ignored sleepa behavioral and physiological state
comprising one third of the dayand sleep disorders. Certainly, the most common
of these sleep disorders is obstructive sleep apnea.
For these reasons, we thought it important to examine psychological and sleep
variables in a group of individuals with and without sleep apnea, some normotensive and some hypertensive. All participants fell into a common age range and were
free of other significant illnesses. Compared with most studies, we had a larger sample size and we collected data on hypertension so we could tease out the effect of
this illness from that associated with sleep apnea alone.
METHOD
Study methodology
Subjects (n5112) included 61 men and 11 women with sleep apnea (defined as a respiratory disturbance index [RDI]>15), 24 of whom had HTN; and 27 men and 13 women with no sleep apnea (RDI,
15) or other sleep disorder, 16 of whom had HTN. Subjects ranged from 32 to 54 years of age (see Table
II). Subjects with a history suggestive of sleep apnea were recruited by advertising and word of mouth.
To qualify, subjects had to be in the range of 100150% of ideal body weight as determined by Metropolitan Life Insurance tables [22]. Although sleep apnea is more common among the obese, subjects .150%
1993/ 20 males
1994
1993
Borak
Gall
20 males
w/ mild
apnea
38 males
1994
180 apneic
Edinger
1994
Flemons
100 apneic
32 w/
apnea
1997
Flemons
Subjects
Engelman 1994
Year
Authors
Interview/questionnaire
Instruments
Polysomnography:
AHI . 10/hour
Polysomnography
GHQ-12
AHI/hour > 10
Polysomnography:
HADS, GHQ-28,
AHI/hour > 5,
Nottingham Health
AHI median 5 28,
Profile (QOL),
AHI range 5
UWIST Mood
7129
Adjective Checklist
Polysomnography
MMPI
Apnea verification
7 males
Polysomnography:
referred
AHI , 20
due to
snoring,
but
negative
polysomnography
Controls
CPAP
CPAP vs.
oral
placebo
(crossover
design)
Treatment
(continued)
Findings
585
1992 25 males, 4
females
Cheshire
30 w/ AHI
,10
Controls
Polysomnography:
AHI > 15/hour
Apnea verification
HADS
Freiberger Personality
Inventory
Instruments
1992 23 males
1987 10 males
preop.
for UPP
1985 43 males, 7
female
Platon
Klonoff
Kales
10 males
preop.
for
CABG
Apnea warranting
tracheostomy
Polysomnography:
AHI > 15/hour
MMPI, SCL-90-R
MMPI, BDI
1993 76 w/ AHI
>10
Cassel
Subjects
Year
Authors
Table I.(Continued)
UPP
CPAP
CPAP
CPAP
Treatment
(continued)
Findings
586
W. A. BARDWELL et al.
1983 15 male, 5
female
1981 20 males
Sachs
Beutler
Polysomnography
Association of
Sleep Disorder
apnea criteria
Apnea verification
10 males
Polygraphic
monitoring
Polysomnography:
50 apneas/night >
10 seconds
63 males, 2 Polysomnography
females
Controls
MMPI
Eyesenck Personality
Questionnaire,
Karolinska Scales of
Personality, CA
Psychological
Inventory,
MarloweCrowne
MMPI, POMS
SADS-L
KDS-1,2,3A
Instruments
Tracheostomy
(8 subjects)
Treatment
Findings
AHI, Apnea/Hypopnea Index; BDI, Beck Depression Inventory; GHQ, General Health Questionnaire; HADS, Hospital Anxiety & Depression Scale;
KDS, KupferDetre Self-Rating Scale; MMPI, Minnesota Multiphasic Personality Inventory; MOS, Medical Outcome Study; POMS, Profile of Mood
States; QOL, Quality of Life; SADS-L, Schedule for Affective Disorders and Schizophrenia; SCL-90-R, Symptom Checklist90, Revised; SIP, Sickness
Impact Profile; UWIST, University of Wales Institute of Science and Technology.
1984 25 male
Reynolds
Subjects
Year
Authors
Table I.(Continued)
587
3359
21.831.1
25
112.5
99133
6489
12062.0
7561.2
Range
44.061.3
26.960.6
3.560.2
5.160.7
Mean
14661.8
9561.1
46.861.4
28.461.0
2.960.3
6.861.0
Mean
131159
84100
4059
22.136.1
15
1.314.5
Range
HTN (n516)
12161.5
7861.0
49.061.2
29.260.6
3.060.1
46.463.7
Mean
90137
6289
3464
2038.9
15
15110.7
Range
No HTN (n548)
14961.8
9361.2
49.961.6
31.160.9
2.760.2
61.066.8
Mean
90170
62104
3264
2040.1
15
17.6142.5
Range
HTN (n524)
HTN, hypertension (mean systolic blood pressure>140 mmHg or mean diastolic blood pressure>90 mmHg).
a
Age: main effect for apnea (p50.008).
b
Body mass index: main effects for apnea (p,0.003) and HTN (p50.039).
c
Respiratory disturbance index: main effects for apnea (p,0.001) and HTN (p50.042).
d
Systolic blood pressure: main effect for HTN (p,0.001).
e
Diastolic blood pressure: main effect for HTN (p,0.001).
Age
Body mass indexb
Social class
Respiratory Disturbance Indexc
Screen blood pressure
Systolicd
Diastolice
No HTN (n524)
588
W. A. BARDWELL et al.
589
of ideal body weight were excluded due to the possibility of confounding by other conditions associated
with obesity. Subjects were also excluded if they had any other major illness such as diabetes or depression.
Subjects had their sleep monitored for two nights in the Clinical Research Center. Polysomnography
included central and occipital electroencephalogram (EEG); bilateral electrooculogram (EOG); submental electromyogram (EMG); airflow, thoracic, and abdominal excursions with Respitrace; and tibialis EMG. Sleep records were scored according to the criteria of Rechtshaffen and Kales [23], and the
numbers of apneas and hypopneas were recorded. The majority of subjects had obstructive apneas only,
but some also showed evidence of central apneas. Subjects were classified as having sleep apnea if their
two-night average RDI was>15.
Blood pressure (BP) was measured with a Dinamap 845 XT monitor. BPs obtained from the Dinamap
correlate well (r.0.95) with mercury sphygmomanometry readings [24]. Subjects were seated for at least
5 minutes and acclimated to the equipment prior to BP determinations. Three consecutive readings were
taken on each of two occasions approximately 1 week apart. The BP used in the current investigation
was the mean of the six readings. Hypertension was defined as mean systolic BP (SBP)>140 mmHg or
mean diastolic BP (DBP)>90 mmHg. Participants who were hypertensive were tapered from their medication prior to participating in the study.
Variable selection
Psychological variables. In our behavioral variables, we employed a set of commonly used measures
of dysphoric mood: the Spielberger Trait Anxiety Scale; Center for Epidemiological StudiesDepression (CESD) Scale; CookMedley (CM) Stress Subscale; Profile of Mood States (POMS) Tension,
Depression, Fatigue, and Vigor Subscales; and POMS Total Mood Disturbance Factor. We also looked
at a set of behavioral medicine variables that focus on aspects of anger: BussDurkee (BD) Irritability
Subscale and BD Total Anger, Experience of Anger, and Expression of Anger Factors; CM Hostility
and Cynicism Subscales; and POMS Anger.
Several scales related to anger were intentionally selected. There are subtle differences in these measures: whereas one may measure a persons experience of anger (e.g., BD Experience of Anger Factor,
POMS Anger), another may measure how one expresses anger (e.g., BD Expression of Anger Factor),
and yet another may include several dimensions of anger (e.g., BD Total Anger Factor).
Sleep variables
The following sleep variables were chosen because they have been commonly used in other studies
of sleep and psychological/cognitive factors: deep sleep and REM sleep (each calculated as a percentage
of total sleep time [TST]); TST; wake time after sleep onset (WASO); RDI; and hypoxemia (defined as
the percent of time that oxygen saturation was ,90%).
Data analysis
Data analysis involved four phases. First, an omnibus test was conducted of the relationship between
sleep variables and psychological variables. This provides protection against type I error due to multiple
comparisons of these variables. Specifically, the maximal canonical correlation between sleep variables
and psychological variables was computed. Its statistical significance was determined from its permutation distribution under the null hypothesis (see chapter 15 of Efron and Tibshirani [25] for a review of
permutation testing).
Second, patients with and without sleep apnea were contrasted in terms of the psychological variables
using t-tests and then using analysis of covariance (ANCOVA), while controlling for age, body mass index (BMI), and hypertension (HTN). Third, correlations between the psychological and sleep variables
were examined as follows:
1.
2.
3.
4.
In
In
In
In
patients
patients
patients
patients
Finally, multiple regression analysis was used to determine if the presence/absence of sleep apnea affected the relationships between individual psychological variables and individual sleep variables. Unlike
the correlations, the multiple regression analyses used a single data set consisting of patients with and
without sleep apnea, using a dummy variable to differentiate the groups. Each model included a psychological variable, the dummy variable (indicating presence/absence of sleep apnea), and an interaction
term (dummy variable multiplied by the psychological variable). If the interaction terms proved to be
significant, this would indicate that the presence/absence of sleep apnea is important in understanding
the relationship between sleep and psychological variables.
590
W. A. BARDWELL et al.
RESULTS
591
Several design aspects characterize this study: ample sample size; control of confounders likely related to sleep apnea; and demonstration of the implications of different methods of analysis. Our sample consisted of 72 subjects with sleep apnea
and 40 subjects without sleep apnea. Most previous studies have used fewer subjects, often with no control group.
r50.26, p50.036
Deep sleep
(% of TST)
r50.26, p50.039
r50.37, p50.003a
r50.28, p50.022
r50.27, p50.026
REM
(% of TST)
r50.32, p50.043
r520.39, p50.017
Total sleep
time
(TST)
Respiratory
disturbance
index
r520.36, p50.042
r50.26, p50.041
r50.26, p50.046
Percentage
of time
with oxygen
saturation of
,90%
592
W. A. BARDWELL et al.
Deep
Sleep
(% of TST)
r50.35, p50.005a
REM
(% of TST)
r50.39, p50.016
r520.35, p50.040
r50.27, p50.035
Total sleep
time
(TST)
r50.33, p50.050
Respiratory
disturbance
index
Percentage of time
with oxygen
saturation,90%
Table IV.Correlations between sleep variables and psychosocial variablescontrolling for age BMI, and HTN
593
594
W. A. BARDWELL et al.
Without covariates
Sleep
variable
Apnea
Deep sleep
REM
1
1
REM
RDI
Hypoxemia
TST
Hypoxemia
REM
REM
Nonapnea
1
1
1
TST
Hypoxemia
Nonapnea
1
2
2
1
1
2
Other potential confounding factors (age, BMI, and HTN) were measured,
allowing us to compare results when these variables were controlled and when they
were not controlled in the analyses. Our results showed that these covariates are important for patients with sleep apnea, but relatively unimportant for patients without sleep apnea. Because reproductive hormonal status (i.e., menstrual cycle, menopause, and hormone replacement therapy) can potentially influence both sleep and
mood, it might be of interest for future studies to examine this area explicitly. We
did not examine this area in the current study and feel that the statistical power
is lacking to make these judgments with confidence, given the small number of
women included.
We found several noteworthy patterns of relationships between sleep and psychological measures, and these patterns differed for patients with and without sleep
apnea. For patients with sleep apnea, dysphoric mood (anger, depression, and total
mood disturbance) was primarily associated with amount of REM sleep. Also, depression was related to deep sleep, and anger was related to hypoxemia. All of these
correlations were positive. These results agree with some previously reported findings in studies of patients with sleep apnea, but only partially agree with a recent
metaanalysis of sleep disorders in psychiatric patients. Keep in mind we did not
study psychiatric patients and most mood scores for our subjects were not in the
pathological range. Nonetheless, Benca et al. found that patients with affective disorders showed increased REM but less deep sleep and total sleep time [27].
Table V pictorially summarizes how relationships between sleep and mood variables are affected by the use of covariates. When we controlled for age, BMI, and
HTN in patients with sleep apnea, a new variable, vigor (i.e., ebullience, high energy), became positively correlated with TST. However, many of the relationships
between sleep and mood disappeared. The previously noted links between sleep
and depression, total mood disturbance, and all but one of the anger relationships
vanished when controlling for these factors. This suggests that depression and total
mood disturbance are related more to age, weight, and/or HTN than they are to
sleep apnea. It also suggests that anger is related to the amount of REM sleep in
595
patients with sleep apneaat least when using the POMS Anger Subscale, a measure of experience of anger.
For patients without sleep apnea, total sleep time was positively related to vigor
and negatively related to anger expression. These relationships remained even after
controlling for age, BMI, and HTN. It is plausible that the less one sleeps, the less
vigorous one feels and the more likely one is to express anger. However, the direction of causality may be the opposite, with increased anger and, less probably, a decreased sense of vigor, resulting in diminished total sleep time.
We have increased confidence that, for individuals without sleep apnea, deep
sleep, REM sleep, and hypoxemia are of relatively little importance vis-a`-vis dysphoric mood states. Total sleep time is the more important sleep variable for patients without sleep apnea. On the other hand, for patients with sleep apnea,
amount of REM sleep is related to anger, whereas total sleep time appears to be
important only in terms of the level of vigor they report. This supports findings by
other investigators who also found links between REM and anger [28] and between
TST and vigor [2932].
Our results lend some support to previous findings that patients with sleep apnea
experience more anger than patients without sleep apnea. However, when patients
without sleep apnea lose sleep, anger expression seems to be involvedeither as the
cause or the result of reduced sleep time. Both patients with and without sleep apnea experience increased vigor the more they sleep. Although this seems intuitively
obvious, it indirectly supports previous findings that patients with sleep apnea show
higher levels of fatigue. However, we were not able to find relationships between
sleep variables and our direct measure of fatigue, nor with our measures of stress,
tension, or anxiety.
Our reading of the data is that many of the previously reported links between
mood and sleep in individuals with sleep apnea disappear after controlling for covariates (age, BMI, HTN). Our second observation is that mood and sleep are variously linked, depending on the population being studied. For individuals with sleep
apnea, there are several more links between measures of dysphoric mood and sleep,
but most of these vanish after covarying age, BMI, and HTN. For individuals without sleep apnea, there are fewer relationships between dysphoric mood and sleep.
Psychiatrists and behavioral medicine researchers are likely to pay increasing attention to sleep. Our findings point to the implications of considering variables long
known to behavioral medicine researchers to be important covariates (i.e., age,
BMI, HTN). Table V demonstrates the profound impact they can haveparticularly for patients with sleep apnea. Future studies examining psychological correlates of sleep apnea must control for the effects of these confounders, which may
also be important in resolving disparities in findings from previous research.
AcknowledgmentsThis work was supported by grants HL44915, RR00827, AG08415, and AG02711
from the National Institutes of Health.
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