Journal of Affective Disorders 132 (2011) 223–230
Contents lists available at ScienceDirect
Journal of Affective Disorders
j o u r n a l h o m e p a g e : w w w. e l s ev i e r. c o m / l o c a t e / j a d
Research report
Prevalence and correlates of generalized anxiety disorder among older
adults in the Australian National Survey of Mental Health and Well-Being
Daniela C. Gonçalves a,⁎, Nancy A. Pachana b, Gerard J. Byrne a,c
a
b
c
School of Medicine, University of Queensland, Brisbane, Q 4029, Australia
School of Psychology, University of Queensland, Brisbane, Q 4067, Australia
Older Persons Mental Health Service, Royal Brisbane & Women's Hospital, Brisbane, Q 4029, Australia
a r t i c l e
i n f o
Article history:
Received 24 December 2010
Received in revised form 23 February 2011
Accepted 23 February 2011
Available online 22 March 2011
Keywords:
Aging
Generalized anxiety disorder
Older adult
CIDI
a b s t r a c t
Background: Generalized anxiety disorder (GAD) occurs commonly, with widespread consequences including decreased functioning and wellbeing, and increased consumption of health
resources. Notwithstanding its prevalence and impact, knowledge about GAD in older adults is
still scarce. Accordingly, the main goals of this study were to estimate the prevalence and
analyze the correlates of 12-month DSM-IV GAD in older community-residing adults.
Methods: The sample was drawn from the 2007 Australian National Survey of Mental Health
and Well-Being and consisted of 3035 participants aged between 55 and 85 years, assessed by
lay interviewers with the fully-structured Composite International Diagnostic Interview.
Results: Eighty-four participants were diagnosed with GAD, equivalent to a weighted 12-month
population prevalence of 2.8% (95% CI: 2.0, 3.7). In a multivariate logistic regression model
older age (OR = 0.24, p = 0.006), functional limitations (OR = 1.07, p = 0.001), lifetime
depression comorbidity (OR = 5.31, p b 0.001), concerns about having a serious illness despite
doctor's reassurance (OR = 2.29, p = 0.021), and family history of anxiety or depression
(OR = 2.41, p = 0.007) were the most significant predictors of 12-month GAD in older adults.
Limitations: This was a cross sectional study, limiting causal inferences.
Conclusions: In community-residing older adults GAD is highly prevalent and strongly associated with functional limitations, psychiatric comorbidity and increased medication intake.
These findings suggest the need for greater clinical awareness of GAD among older adults.
© 2011 Elsevier B.V. All rights reserved.
1. Introduction
Despite a recent increase in activity, research on anxiety
disorders in older adults is still relatively underdeveloped
(Byrne and Pachana, 2010). This is reflected in the limited
number of publications and scarceness of empirical data on
this topic, which partially explain why many obsolete beliefs
are still uncritically accepted. These include the belief that
anxiety disorders have a lower prevalence in older adults or
⁎ Corresponding author at: Academic Discipline of Psychiatry, School of
Medicine, University of Queensland, K Floor, Mental Health Centre, Royal
Brisbane & Women's Hospital, Herston, Q 4029, Australia. Tel.: + 61 7 3365
5572; fax: + 61 7 3365 5488.
E-mail address: d.goncalves@uqconnect.edu.au (D.C. Gonçalves).
0165-0327/$ – see front matter © 2011 Elsevier B.V. All rights reserved.
doi:10.1016/j.jad.2011.02.023
that anxiety disorders occur mainly within a depressive
context (Wetherell et al., 2005). Although prevalence studies
indicated that anxiety disorders in general (e.g., Regier et al.,
1988), and generalized anxiety disorder (GAD) in particular
(e.g., Hunt et al., 2002), decline in older, community-residing
cohorts, relative prevalence is still high in later life (e.g., Byers
et al., 2010; for a recent review about the prevalence of
anxiety disorders in older adults, see Bryant et al., 2008).
The impact of anxiety in older adults has been found to be
pervasive, being associated with memory impairment (Mantella
et al., 2007), burden of disability (Brenes et al., 2005), and the use
of both mental health services and general health services
(Porensky et al., 2009). GAD had also been reported to worsen
the prognosis of major depressive disorder (MDD) (Steffens and
McQuoid, 2005) and increase the risk of adverse cardiac events
224
D.C. Gonçalves et al. / Journal of Affective Disorders 132 (2011) 223–230
(Frasure-Smith and Lesperance, 2008), independently of MDD
(Barger and Sydeman, 2005). It is therefore important to identify
the factors that increase or decrease the likelihood of GAD
diagnosis in order to better understand the condition and design
of clinical intervention strategies with a higher likelihood of
success (Smit et al., 2007).
Factors associated with anxiety disorders in older cohorts
have been investigated in several clinical and epidemiological
studies, often with contradictory results. A recent study
reviewed risk factors for anxiety disorders and symptoms in
subjects aged 50 years and older (Vink et al., 2008). These
authors considered that a set of biological (chronic health
conditions, poor self perceived health, and functional limitations), psychological (external locus of control, neuroticism,
lack of self-efficacy, and past psychiatric history), and social
(social network, stressful events, and demographic characteristics) factors were evidence based for anxiety disorders in
community residing older adults. Cognitive impairment, high
blood pressure, sensory loss, limited coping strategies, poor
self-image, and low income were judged as risk factors for
anxiety symptoms (Vink et al., 2008). The same study also
analyzed factors associated with depressive symptoms and
disorders in older adults. These include exercise, use of
psychotropic medicine, alcohol use and smoking (Vink et al.,
2008).
Against this background, the principal goals of the present
study were to estimate the 12-month prevalence of DSM-IV
GAD and analyze the factors associated with this diagnosis in
a representative sample of community-dwelling adults aged
55 years and older. We defined a model for GAD in older
adults with putative factors derived from social, psychological, and biological dimensions. Socio-demographic factors
included age, gender, education, marital status, country of
birth, living arrangements, urbanization, financial problems,
stressful life events, social network, and caregiver status.
Psychological factors were past or current history of major
depressive disorder and worry about illness despite doctor's
reassurance. Biological factors included chronic diseases,
functional limitations, self-assessed physical health, intake
of anxiety related medication, lifestyle characteristics (exercise, alcohol intake, and smoking), and family history of
anxiety or depression. These factors were established based
on previous reported results concerning GAD in older adults,
and additional putative factors were also included, selected
for their relevance for mental health in older cohorts.
2. Methods
2.1. Sample and measures
The sample was drawn from the Confidentialised Unit
Record File (CURF) of the National Survey of Mental Health
and Wellbeing (NSMHWB), conducted by the Australian
Bureau of Statistics (ABS) in 2007, through a multi-stage
sampling of people aged 16–85 years old living in private
dwellings (ABS, 2007). A detailed description of the survey
has been provided elsewhere (Slade et al., 2009). A total of
14,805 private households were randomly selected, with a
national response rate of 60%, including 8841 full responses.
For the present analyses, participants aged 55 years or older
were considered (N = 3178; 53% female).
Data were collected by trained lay interviewers. The
Composite International Diagnostic Interview, version 3.0
(CIDI 3.0), (Kessler and Ustun, 2004), was employed to collect
self-report data regarding anxiety, affective, and substance
abuse disorders, generating ICD-10 and DSM-IV diagnoses.
Additional information collected included socio-demographic
characteristics, chronic medical conditions, disability, lifetime
and current use of health services, traumatic life experiences,
social network, and family history of mental illness.
2.2. Putative associated factors
Social factors were assessed through demographic information (age, gender, education, marital status, country of birth,
number of persons in the household, urbanization level, and
financial problems) and social characteristics (stressful life
events, social network, and caregiver status). For the present
analysis, educational level (completion of 8 years or less of
formal schooling or below vs. completion of 9 years or more),
marital status [not married (single, divorced, widowed) vs.
married], country of birth (Australia vs. other), number of
persons in the household (living alone vs. living with others),
urbanization level (major urban center vs. other), and financial
problems (none vs. one or more) were dichotomized. Financial
problems were ascertained by a list of ten questions concerning
money shortage over the last 12 months (e.g., inability to pay
bills). Lifetime significant life events were queried through a list
of 27 potentially stressful experiences, including traumatic
personal experiences (e.g., combat experience), events involving personal violence (e.g., beaten up as a child), and events
affecting others (e.g., child's serious illness). Social network
composition was ascertained by asking about the frequency of
contact with family members (never; monthly or less; weekly;
or daily). Caregiver status was defined as spending time
providing instrumental or emotional care to close relatives
because of their health problems.
Psychological factors consisted of past or current history of
major depressive disorder (MDD) and worry about illness
despite receiving reassurance from a doctor. Past or current
history of MDD was derived from the lifetime diagnosis of
MDD, based on DSM-IV criteria. Illness concerns were
determined by a dichotomous question. Biological factors
were ascertained through lifetime history of chronic diseases,
functional limitations, frequency of weekly exercise, selfassessed physical health, intake of anxiety related medication, smoking and alcohol intake frequency, and family
history of anxiety or depression. Chronic diseases were
based on the Australian National Health Priority Areas.
Participants were asked whether they were ever told by a
doctor or a nurse that they had asthma, cancer, stroke, heart
or circulatory condition, rheumatism, or diabetes. Obesity,
also being a national priority area, was included and defined
as having a body mass index (BMI) of 30 or more, calculated
from self-reported height and weight information. Functional
limitations were measured on the 12-item WHO Disability
Assessment Schedule, using the simple sum method to obtain
the total score (Andrews et al., 2009). Frequency of vigorous
weekly exercise was inquired through an open question and
answers were converted into ordinal categories (never; 1–3
times per week; more than 3 times per week). Self-assessed
physical health was assessed on a 3-point Likert scale (poor/
D.C. Gonçalves et al. / Journal of Affective Disorders 132 (2011) 223–230
fair, good, very good/excellent). Intake of tablets for sleep and
anxiety or nerves was used to dichotomously determine
medication intake, whereas alcohol and smoking habits were
determined by their frequency (never; weekly or less; daily).
Family history of anxiety or depression was obtained by
inquiring about the presence of these disorders in close
relatives.
2.3. Data analyses
Data analyses were conducted in Stata 11.1 (StataCorp,
2009) using survey data routines. Individualized person
weights were used to allow population estimates to be
calculated. Standard errors of prevalence estimates and
confidence intervals around odds ratios were calculated on
the basis of 60 delete-one jackknife replications using
replicate weights provided by the Australian Bureau of
Statistics. Reported results for the prevalence estimates take
into account the probability of being sampled and have been
standardized to the projected 2007 age and sex distribution of
the Australian population based on the 2006 national
population census (ABS, 2007). Data were analyzed through
logistic regression models, using the 12-month prevalence of
GAD as the outcome variable and the previously described
factors as the putative associated variables. The hierarchical
rule, which states that GAD cannot occur exclusively during a
mood disorder (APA, 1994), was suspended. Previous studies
indicated that there were no significant differences between
outpatients diagnosed with GAD with or without this
hierarchical rule applied, but they were quite distinct from
225
outpatients diagnosed with MDD, namely reporting more
impaired social functioning (Zimmerman and Chelminski,
2003). In order to decrease confounding, participants who did
not present with 12-month GAD symptoms but were
diagnosed with lifetime GAD were excluded from subsequent
analysis (n = 143), rendering a sample of 3035 participants
aged 55 years and older. Bivariate logistic regression analyses
were used to assess the statistical significance of each of the
variables against the presence of GAD, after which all the
significant variables were included in a multivariate logistic
regression model. An inclusive alpha level for statistical
significance was established at α b 0.25 (Hosmer and Lemeshow, 2000) on the bivariate analysis. For the multivariate
model statistical significance was considered at α b 0.05.
3. Results
3.1. Sample characteristics
The sample consisted of 3035 older adults (M = 68,
SD = 8, range 55–85 years, 52% female), the majority of
whom were born in Australia (70%) and lived in a major
urban center (59%). Approximately one fifth of the participants had completed 8 years or less of formal schooling.
Almost 56% of the participants were married, and approximately 40% lived alone, although almost all participants (90%)
were in contact with family members at least weekly. A
minority of the participants (15%) reported one or more
financial problems. One fifth of the participants reported no
stressful life events, whereas more than half reported two or
Table 1
Socio-demographic characteristics of older adults with and without GAD and bivariate logistic regression analyses.
Variable
Age
55–64
65–74
75–85
Gender
Female
Education
9 years or more
Marital status
Married
Country of birth
Outside Australia
Living arrangements
Living with someone
Urbanicity
Outside major urban center
Financial problems
One or more
Frequency family contact
Never
Monthly
Weekly
Daily
Caregiver status
Does not provide care
Life events
No 12-month GAD (n = 2951)
12-month GAD (n = 84)
N (%) a
N (%) a
OR (95% CI)
t
p
−3.1
−3.6
1132 (47.6%)
1044 (30.9%)
775 (21.5%)
58 (76.4%)
16 (16.2%)
10 (7.4%)
1
0.33 (0.16, 0.67)
0.22 (0.09, 0.50)
1523 (50.5%)
55 (66.2%)
1.91 (1.01, 3.61)
2.05
0.045
2282 (78.3%)
68 (80.8%)
1.17 (0.56, 2.43)
0.42
0.673
1652 (69.5%)
40 (66.3%)
0.86 (0.49, 1.51)
− 0.54
0.590
878 (32.3%)
26 (38.9%)
1.33 (0.68, 2.61)
0.85
0.396
1810 (77.2%)
42 (70.2%)
0.70 (0.42, 1.16)
− 1.41
0.164
1206 (37.8%)
41 (37.8%)
1.00 (0.57, 1.77)
− 0.00
0.999
155 (4.58%)
20 (24.2%)
6.65 (3.17, 13.96)
5.12
b 0.001
4 (3.0%)
9 (6.2%)
23 (25.0%)
48 (65.8%)
1
0.24 (0.05, 1.26)
0.28 (0.06, 1.24)
0.34 (0.08, 1.38)
−1.72
−1.71
−1.54
0.091
0.092
0.128
20 (31.4%)
M (SD)
3.32 (2.63)
2.48 (1.32, 4.68)
2.87
0.006
1.21 (1.12, 1.31)
5.06
b 0.001
37
280
945
1689
(1.0%)
(8.1%)
(29.0%)
(62.0%)
418 (15.6)
M (SD)
2.11 (2.04)
GAD: generalized anxiety disorder; OR: odds ratio; CI: confidence interval.
a
Values correspond to raw numbers and population weighted prevalence.
0.003
0.001
226
D.C. Gonçalves et al. / Journal of Affective Disorders 132 (2011) 223–230
more. Almost 10% of the participants were diagnosed with
lifetime MDD, which included both past and current episodes.
Almost 80% of the participants reported one or more chronic
diseases and mean disability score on the WHODAS was 4
(SD = 6, range 0–48). Less than one fifth of the participants
assessed their health as “fair” or “poor”, whereas half
reported “very good” or “excellent” physical health. Family
history of either anxiety or depression was reported by 23% of
the participants.
3.2. Prevalence and correlates of GAD
Eighty-four participants were diagnosed with 12-month
GAD, according to DSM-IV criteria with the hierarchical rule
suspended, which is equivalent to a raw prevalence of 2.8%
(95% CI: 2.2, 3.4) and a weighted population prevalence of
2.8% (95% CI: 2.0, 3.7). The majority of those diagnosed with
GAD were women (n = 55, corresponding to two thirds of the
participants diagnosed with GAD). Forty-five participants,
which is equivalent to 54% of the GAD sub-sample, had both
12-month GAD and MDD, the majority of whom were also
women (n = 27, 26% of the GAD subsample).
There were significant differences between survey participants with and without GAD on biological, psychological and
social factors. Women had greater odds of being diagnosed with
GAD than men (OR = 1.91, 95% CI: 1.01, 3.61). Older participants were less likely than younger participants to have GAD
(OR = 0.33, 95% CI: 0.16, 0.67, for the category 65–74 and
OR= 0.22, 95% CI: 0.09, 0.50, for the category 75–85, when
compared with 55–64). The odds of GAD increased as the
number of stressful life events experienced increased
(OR = 1.21, 95% CI: 1.12, 1.31), as the number of reported
chronic diseases increased (OR = 1.36, 95% CI: 1.05, 1.75),
and as functional limitations increased (OR = 1.10, 95% CI:
1.06, 1.13). Financial problems (OR = 6.65, 95% CI: 3.17, 13.96),
providing instrumental and emotional care to close relatives
(OR = 2.48, 95% CI: 1.32, 4.68), lifetime diagnosis of MDD
(OR = 12.45, 95% CI: 6.70, 23.12), and worrying about illness
despite reassurance from a doctor (OR = 6.22, 95% CI: 3.47,
11.14) were all significantly related with increased odds of 12month GAD. Conversely, living with someone (OR = 0.70, 95%
CI: 0.42, 1.16), higher frequency of family contact (OR = 0.24,
95% CI: 0.05, 1.26, for the category “monthly” when compared
with “never”), more exercise (OR = 0.19, 95% CI: 0.02, 1.59, for
the category “more than 3 times per week” when compared
with “never”), and better self-assessed health (OR = 0.53,
95% CI: 0.28, 1.00, for the category “good”, and OR = 0.19, 95%
CI: 0.08, 0.41, for the category “very good/excellent”, when
compared with “poor/fair”) were all associated with decreased
odds of 12-month GAD. Among putative biological factors,
smoking (OR = 2.24, 95% CI: 0.93, 5.44, for the category “daily”
when compared with “never”), family history of anxiety or
depression (OR = 4.30, 95% CI: 2.59, 7.12) and self-reported
anxiety medication intake (OR = 4.94, 95% CI: 2.59, 9.44) were
both associated with an increased odds of GAD. However,
country of birth, educational level, marital status, urban
location, and alcohol intake were not significantly associated
with GAD. There were also no significant results for some of
Table 2
Clinical characteristics of older adults with and without GAD and bivariate logistic regression analyses.
Variable
Lifetime MDD diagnosis
Yes
Worry about illness
Yes
Exercise frequency (per week)
Never
1–3 times week
More than 3 times
Self assessed health
Poor/fair
Good
Very good/excellent
Anxiety medication intake
Yes
Alcohol intake
Never
Weekly or less
Daily
Smoking
Never
Weekly or less
Daily
Family history anxiety/depression
Yes
Chronic diseases
Functional limitations
No 12-month GAD (n = 2951)
12-month GAD (n = 84)
N (%) a
N (%) a
OR (95% CI)
t
p
241 (7.4%)
45 (49.9%)
12.45 (6.70, 23.12)
8.15
b 0.001
242 (8.9%)
33 (37.7%)
6.22 (3.47, 11.14)
6.27
b 0.001
2422 (80.3%)
358 (13.7%)
171 (6.0%)
68 (84.2%)
14 (14.6%)
2 (1.1%)
1
1.02 (0.52, 1.98)
0.19 (0.02, 1.59)
0.05
−1.56
0.960
0.123
608 (20.3%)
1007 (34.3%)
1336 (45.4%)
36 (43.3%)
33 (38.7%)
15 (18.0%)
1
0.53 (0.28, 1.00)
0.19 (0.08, 0.41)
−1.99
−4.26
0.051
b 0.001
289 (8.8%)
28 (32.3%)
4.94 (2.59, 9.44)
4.94
b 0.001
967 (31.3%)
1198 (41.0%)
786 (27.6%)
32 (38.1%)
33 (37.7%)
19 (24.3%)
1
0.76 (0.40, 1.44)
0.72 (0.32, 1.66)
−0.86
−0.78
0.391
0.439
2576 (87.4%)
18 (1.7%)
337 (10.9%)
66 (76.9%)
2 (1.6%)
16 (21.6%)
1
1.07 (0.15, 7.68)
2.24 (0.93, 5.44)
0.07
1.83
0.942
0.072
4.30 (2.59, 7.12)
5.78
b 0.001
1.36 (1.05, 1.75)
1.10 (1.06, 1.13)
2.39
5.84
0.020
b 0.001
636
M
1.68
3.68
(22.1%)
(SD)
(1.26)
(5.74)
GAD: generalized anxiety disorder; OR: odds ratio; CI: confidence interval.
a
Values correspond to raw numbers and population weighted prevalence.
44
M
2.22
10.17
(55.0%)
(SD)
(1.60)
(9.88)
D.C. Gonçalves et al. / Journal of Affective Disorders 132 (2011) 223–230
the categories of ordinal variables, namely daily family contact
and smoking weekly or less. Tables 1 and 2 summarize the
frequencies for both groups as well as the results of the
bivariate analyses.
The factors that attained statistical significance in the
bivariate analyses were then included in a multivariate
logistic regression model (Table 3). The Hosmer–Lemeshow
statistic indicated satisfactory goodness-of fit for the model
[χ2(2818) = 2580.47, p = 0.99], correctly classifying approximately 97% of the sample and presenting an area under the
receiver operating characteristic (ROC) curve of 0.89. The
model was free of multicollinearity, with a variance inflation
factor (VIF) of 1.14 and a tolerance value of 0.88. In the final
model, age (OR = 0.24, 95% CI: 0.09, 0.65, p = 0.006, for the
category 75–85 when compared with 55–65), lifetime
MDD (OR = 5.31, 95% CI: 2.39, 11.78, p b 0.001), worry about
illness (OR = 2.29, 95% CI: 1.14, 4.61, p = 0.021), functional
limitations (OR = 1.07, 95% CI: 1.03, 1.12, p = 0.001), and
family history of anxiety or depression (OR = 2.41, 95% CI:
1.28, 5.55, p = 0.007) were significantly associated with 12month GAD.
Table 3
Multivariate logistic regression analysis of generalized anxiety disorder.
Variable
Age
55–64
65–74
75–85
Gender
Female
Living arrangements
Living with someone
Financial problems
One or more
Frequency family contact
Never
Monthly
Weekly
Daily
Caregiver status
Yes
Stressful life events
Lifetime diagnosis of MDD
Yes
Worry about illness
Yes
Exercise frequency (per week)
Never
1–3 times week
More than 3 times
Chronic illnesses
Functional limitations
Self assessed health
Poor/fair
Good
Very good/excellent
Anxiety medication intake
Yes
Smoking
Never
Weekly or less
Daily
Family history of anxiety
or depression
Yes
OR (95% CI)
t
1
0.35 (0.14, 0.86)
0.24 (0.09, 0.65)
−2.33
−2.88
0.023
0.006
1.48 (0.59, 3.71)
0.86
0.394
0.76 (0.42, 1.42)
−0.84
0.403
1.10 (0.74, 1.66)
0.49
0.624
1
0.33 (0.07, 1.54)
0.45 (0.12, 1.72)
0.69 (0.19, 2.59)
−1.44
−1.19
−0.55
0.156
0.240
0.581
0.98 (0.52, 1.85)
1.04 (0.92, 1.17)
−0.07
0.56
0.946
0.575
5.31 (2.39, 11.78)
4.19
b0.001
2.29 (1.14, 4.61)
2.37
0.021
2.65)
2.39)
1.30)
1.12)
0.44
−1.28
0.23
3.41
0.662
0.205
0.817
0.001
1
1.57 (0.73, 3.38)
0.77 (0.32, 1.82)
1.18
−0.61
0.244
0.541
2.31 (0.99, 5.34)
1.98
0.053
1
1.10 (0.54, 2.23)
1.35 (0.40, 4.52)
0.26
0.50
0.792
0.622
2.41 (1.28, 5.55)
2.78
0.007
1
1.19
0.21
1.03
1.07
(0.54,
(0.02,
(0.81,
(1.03,
p
227
4. Discussion
In a population-based sample of community-dwelling older
adults the weighted 12-month prevalence of non-hierarchical
DSM-IV GAD was 2.8%, similar to values previously reported
(Byers et al., 2010). The present prevalence finding is
considerably lower than the one reported by the Longitudinal
Aging Study Amsterdam (LASA), which found a 6-month
prevalence for DSM-III GAD in community living adults aged
between 55 and 85 to be 7.3% (Beekman et al., 1998). This
significant difference is partially explained by changes in the
DSM criteria between DSM-III and DSM-IV, particularly the
introduction of the excessiveness criterion and the increase in
the minimum required duration of symptoms from one month
to six months, thus being more restrictive. A study that
manipulated DSM-IV diagnostic criteria for GAD found that
when the excessiveness criterion was suspended and the
duration of anxiety was changed to one month or more the
12-month prevalence of GAD in the entire sample of the NCS-R
rose from 3.0 to 6.2% (Ruscio et al., 2007).
In the current analysis, age, history of lifetime comorbid
MDD, functional limitations, and family history of anxiety or
depression were the factors most significantly associated
with GAD in older adults. Worry about illness despite a
doctor's reassurance was also associated with GAD, albeit
with relatively wide confidence intervals. These findings are
consistent with previously published work. Cross-sectional
studies usually provide lower prevalence estimates for GAD
in older adults in comparison with younger adults (Hunt
et al., 2002), and longitudinal findings indicate that increasing
age is associated with decreasing severity of GAD symptoms
in middle-aged adults (Ramsawh et al., 2009).
Several methodological explanations have been put
forward to explain the apparent decline of anxiety disorders
with age, including the systematic exclusion of impaired, frail
or institutionalized older adults (Jeste et al., 2005) and a
subtle shift in phenomenology that is not detected by the
traditionally employed diagnostic criteria (Flint, 2005). Even
though the present study did not survey institutionalized
older adults, many participants reported functional impairment and chronic disorders, thus frailty and impairment were
represented to some extent. The phenomenological characteristics of GAD in older adults, which might be overlooked by
the current assessment techniques, warrant further investigation to properly distinguish age effects from cohort effects.
Alternatively, decreasing prevalence might be attributable
to substantive rather than methodological factors. According
to the socioemotional selectivity theory emotional goals
become more salient with age, with older adults exhibiting
age-differentiated strategies of emotional control and tending
to engage in strategies to optimize social exchanges and
relationships (Carstensen et al., 1999). Additionally, it has
been shown that older adults display a memory bias that
favors positive information (Mather and Carstensen, 2003),
experiencing the same number of positive emotions and
fewer negative emotions than their younger counterparts
(Carstensen et al., 2000).
Functional limitations had a direct and significant association with GAD. Because functional limitations increase with
age they might create a specific vulnerability factor for older
cohorts. Functional limitations and their associated disability
228
D.C. Gonçalves et al. / Journal of Affective Disorders 132 (2011) 223–230
have been frequently reported in association with anxiety
disorders in older cohorts, in both cross-sectional and
longitudinal studies (Vink et al., 2008). The mechanisms
that underlie the interplay between functional limitations
and anxiety are not yet established but a dynamic and
reciprocal interaction between mental and physical health
has been postulated. Anxiety symptoms are themselves
disabling, as well as impacting on different physiological
systems, including the cardiovascular and respiratory systems, thus increasing the likelihood of disability (Culpepper,
2009). In a recent study that followed more than 1000 older
women for 3 years, anxiety symptoms were found to be an
independent predictor of disability, both in activities of daily
living and light housework chores (Brenes et al., 2005). On
the other hand, functional limitations at baseline and low
performance on basic or instrumental activities of daily living
were significant risk factors for GAD and mixed anxiety and
depression (Schoevers et al., 2005).
We also found that a comorbid lifetime diagnosis of MDD
was highly related with GAD in older adults. In addition,
almost half of those diagnosed with GAD were also diagnosed
with MDD, which is consistent with the findings of other
studies of older cohorts (Manela et al., 1996; Schoevers et al.,
2005). Several hypotheses exist to explain the high comorbidity between disorders, including shared genetic risk
factors (Cerda et al., 2010; Kendler et al., 1992) and social
and functional vulnerability created by GAD that subsequently triggers depression (Simon, 2009). However, biological
data corroborate that MDD and GAD are distinct disorders
(Goldberg, 2008). Furthermore, recent longitudinal findings
indicate that although the association between GAD and MDD
is significant, it is similar to that observed between GAD and
other anxiety disorders, and even MDD and other anxiety
disorders (Beesdo et al., 2010).
The impact of family history of anxiety or depression upon
the development of GAD can be explained by genetic and
behavioral mechanisms, and the interplay between the two. In
a study conducted with almost 4000 pairs of older twins,
approximately one fourth of the variation in GAD was explained by genetic factors (Mackintosh et al., 2006). Although
less evidence exists for the role played by family environment
(Hettema et al., 2002), it has been suggested that attachment
and vicarious learning during childhood increase the likelihood
of having GAD as an adult (McLaughlin et al., 2008). Another
relevant aspect to take into account is that participants
diagnosed with GAD might have a selective memory for family
history of mental disorder. The relevance of family history of
anxiety or depression for current anxiety disorders was found
to decrease with age (Beekman et al., 1998). This was also
partially replicated in our sample, as the stratified analysis for
age groups indicated that family history was more significant
for those aged between 55 and 65 years. These results might
indicate that as age increases environmental factors are more
relevant or reflect memory bias in older cohorts (Beekman
et al., 1998). It might also be the case that older adults are less
likely to identify and report anxiety symptoms in themselves
(Palmer et al., 1997).
Our finding concerning worry about illness despite a
doctor's reassurance should be interpreted with caution, as it
was associated with a wide confidence interval. As excessive
worry is the cornerstone of GAD it is natural that concerns
about health and illness are frequently reported. However,
being worried about a serious illness even when there is no
medical evidence for it is also the main diagnostic criterion for
hypochondriasis, a disorder found in frequent comorbid
relation to GAD (Barsky et al., 1992). A similar trend was
found in our sample, where almost 40% of the participants
with GAD was worried about having a serious illness despite
doctor's reassurance, whereas less than one tenth of those
without the disorder expressed the same concern. There is
further evidence for the tight association between GAD and
illness worry. A study about the natural course of GAD
indicated that at 40-year follow-up somatoform disorders
were the most frequent outcome (Rubio and Lopez-Ibor,
2007). Because ours was a cross-sectional study and diagnosis
was not established for hypochondriasis, caution is required
when interpreting the results. However, it seems likely that
worrying about a serious illness creates an additional
vulnerability factor for those with GAD or that having GAD
increases concern about having a serious illness in the
absence of sufficient evidence for such.
The strengths of our study include its use of a large,
population-based, sample of older adults and a fully structured psychiatric interview. There are however some limitations. Although ours was a representative epidemiologic
sample, it was not specifically designed to assess risk factors
for GAD in older adults. Some factors previously identified as
relevant to the etiology of GAD, such as personality traits,
were not included. Biological variables were scarce in the
survey dataset and the inclusion of relevant information for
the understanding of anxiety disorders, namely imaging data,
would have provided a richer set of results. However, the
present dataset was comprehensive and comprised factors
from multiple domains, allowing for a comprehensive
analysis of GAD. The sampling strategy excluded people
aged 86 and older, as well as institutionalized persons, thus
excluding frailer or more impaired older adults. Nevertheless
frailty and impairment were represented in the sample
population, as indicated by the functional limitations and
cognitive screening results. Both the DSM-IV diagnostic
criteria themselves and the CIDI instrument used to assess
them were initially developed to assess younger populations,
and it remains uncertain whether either is entirely suitable
for use with older adults (O'Connor and Parslow, 2010). On
the other hand the CIDI is a detailed structured interview
especially developed for epidemiological research (Kessler
and Ustun, 2004), which has been used with older adults
before, and no consensus has yet emerged about how
younger and older adults might differ in their anxiety
symptom presentation (Wolitzky-Taylor et al., 2010). The
final limitation concerns the cross sectional nature of the
design, which limits causal inferences.
This study analyzed the factors associated with GAD in
older adults, using a population-based representative sample
of Australians. Along with depression, anxiety disorders are
the leading cause of incident non-fatal disease burden in
Australia (Mathers et al., 1999), representing over 14% of the
years lost due to disability. Unfortunately, the majority of the
identified factors are not modifiable. Nevertheless, by identifying risk factors for GAD it might be possible to design
effective preventive or early intervention strategies (Smit
et al., 2007), ultimately decreasing medical costs and
D.C. Gonçalves et al. / Journal of Affective Disorders 132 (2011) 223–230
increasing quality of life and disability-free years of life for
older people. Data support the efficacy of both behavioral and
pharmacological interventions for anxiety disorders in older
people (Pinquart and Duberstein, 2007). From a clinical
perspective, the model we have described allows the identification of community-residing older adults with a higher
likelihood of having GAD, thus making them potentially
identifiable and suitable candidates for interventions. Despite
the existence of previously published research, there are still
several unanswered questions about this topic, especially
when compared with the available data for other disorders on
this population, namely depressive disorders (Vink et al.,
2008). Furthermore, it provides timely information about
GAD on the Australian context.
Role of funding source
Daniela Gonçalves was supported by a scholarship from the Fundação
para a Ciência e Tecnologia, Portugal (SFRH/BD/30226/2006) and financial
support from an anonymous donor. Gerard Byrne was supported by grants
from the Australian National Health and Medical Research Council (456182)
and the US Alzheimer's Association (IIRG-07-59015). None of the institutions
had further role in study design; in the collection, analysis and interpretation
of data; in the writing of the report; and in the decision to submit the paper
for publication.
Conflict of interest
No conflict declared.
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