Generalized Anxiety Disorder in Adults: Epidemiology, Pathogenesis, Clinical Manifestations, Course, Assessment, and Diagnosis
Generalized Anxiety Disorder in Adults: Epidemiology, Pathogenesis, Clinical Manifestations, Course, Assessment, and Diagnosis
Generalized Anxiety Disorder in Adults: Epidemiology, Pathogenesis, Clinical Manifestations, Course, Assessment, and Diagnosis
All topics are updated as new evidence becomes available and our peer review process is complete.
Literature review current through: Feb 2023. | This topic last updated: Apr 18, 2022.
INTRODUCTION
Generalized anxiety disorder (GAD) is characterized by excessive and persistent worry that is
difficult to control, causes significant distress or impairment, and occurs on more days than not
for at least six months. Other features include psychological symptoms such as apprehension
and irritability, and physical (or somatic) symptoms such as increased fatigue and muscular
tension.
This topic addresses the epidemiology, pathogenesis, clinical manifestations, and diagnosis of
GAD. Pharmacotherapy for GAD, psychotherapy for GAD, and issues concerning treatment and
assessment of comorbid disorders are discussed separately:
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EPIDEMIOLOGY
Prevalence — Generalized anxiety disorder (GAD) is one of the most common mental disorders
in both community and clinical settings. It is associated with increased use of health care
services [1,2].
Epidemiologic studies of nationally representative samples in the United States report a past-
year prevalence of GAD to be 2.7 to 3.1 percent [3,4] and a lifetime prevalence of GAD of 5.1
[2,5] to 11.9 percent [6]. A review of epidemiological studies in Europe found a past-year
prevalence of 1.7 to 3.4 percent [7], and a lifetime prevalence of 4.3 to 5.9 percent [8].
Worldwide, estimates of the lifetime and 12-month prevalence are 3.7 and 1.8 percent,
respectively [9].
Major depressive disorder appears to be the most common comorbidity in individuals with
current or lifetime GAD. Comorbid major depression is reported in 39 percent of individuals
with current GAD and 62 percent of individuals with lifetime GAD [2,7]. Worldwide, mood
disorders have an estimated lifetime comorbidity of 63 percent [9].
Other disorders found to co-occur in individuals with GAD (rates over previous 30 days and
lifetime) include [2,13]:
GAD may also be associated with increased rates of alcohol and other substance use disorders,
posttraumatic stress disorder, and obsessive-compulsive disorder.
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GAD is common among patients with “medically unexplained” chronic pain [14] and with
chronic physical illness [15].
PATHOGENESIS
Biological factors
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Other data suggests the role of acid-sensing ion channels in the amygdala [28] and
elevated levels of C reactive protein and other proinflammatory cytokines [29] as
potentially involved in the development of GAD.
Additionally, alterations in glucose metabolism in the cortex, limbic system, and basal
ganglia suggest their role in the development of anxiety. For example, in one study,
positron emission tomography (PET) of 18 individuals with GAD were compared with PET
of 15 individuals without GAD (control group) [31]. PET scans of individuals with GAD
demonstrated a relative increase in glucose metabolism in parts of the occipital, right
posterior temporal lobe, inferior gyrus, cerebellum and right frontal gyrus, and an
absolute decrease in the basal ganglia versus control group.
In a separate functional MRI study, individuals with GAD showed greater anticipatory
activity in the bilateral dorsal amygdala to both aversive and neutral pictures [32]. This
suggests an enhanced anticipatory emotional responsiveness in GAD [31,32]. A systematic
review of neuroimaging studies found that GAD patients show difficulties in engaging the
prefrontal cortex and anterior cingulate cortex during emotional regulation tasks [33].
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● Developmental and personality factors – GAD in adults is associated with a higher than
average number of traumatic experiences and other undesirable life events in childhood,
compared with individuals without GAD [40]. Childhood maltreatment confers an
increased risk of developing GAD following stressful experiences [41].
GAD is more likely to occur in individuals with “behavioral inhibition” (the tendency to be
timid and shy in novel situations), than without this trait. Additionally, neuroticism (an
enduring tendency to worry and feel anxious, sad, or guilty) is associated with comorbid
GAD and major depression [42-44]. (See "Social anxiety disorder in adults: Epidemiology,
clinical manifestations, and diagnosis", section on 'Behavioral inhibition'.)
● Cognitive origins of worry – Many explanations of the origin and persistence of the
excessive and pervasive worrying that characterize GAD have been proposed. As
examples, affected individuals may:
Other presenting symptoms may include restlessness or hyperarousal, fatigue, irritability, poor
concentration, sleep disturbance, and muscle tension. These are often chronic and unexplained
despite repeated presentation to health care professionals.
Onset — The average age of onset of GAD is 30 years, although the range is broad [50]. While
subsyndromal anxiety symptoms are common before the age of 20, full syndromal disorder
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typically occurs later than other anxiety disorders (eg, separation anxiety disorder, phobias,
panic disorder) [51,52].
Studies examining the effect of age of onset on the course of GAD have shown mixed results.
While some studies have suggested that earlier age of onset is associated with a more
protracted course [53], others find that early-onset GAD does not constitute a more severe
subtype [54].
In a community survey including 1974 adults age ≥65 years, nearly 25 percent reported a
late onset of generalized anxiety symptoms [58]. Factors associated with late-onset GAD
include female sex, chronic physical illness (eg, respiratory, cardiovascular, cognitive),
current major depression or phobia, recent adverse life events, negative childhood events
(eg, parental loss or separation, parental mental health problems), financial difficulties,
and past history of GAD [56,59].
In one prospective study of 179 individuals with GAD, approximately 60 percent of patients
recovered over 12 years (ie, had no more than residual symptoms for eight consecutive weeks),
but approximately one-half of recovered patients subsequently relapsed during the 12-year
period [60].
In another prospective study involving 142 subjects with GAD followed for 14 years, the severity
of anxiety symptoms over time decreased only modestly [61].
However, studies of individuals in community samples suggest a better prognosis than studies
of clinical populations. In one 22-year follow-up study of 105 community living individuals with
GAD found that less than 20 percent had persistent GAD (defined by the presence of daily
symptoms over the previous 12 months) [52].
Effects of illness
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cases, the level of impairment is greater than is seen in individuals with major depression
[63,64].
For example, in a national epidemiologic survey of adult mental health in Germany (n = 4181),
the impact of psychiatric symptoms on daily functioning and perceived quality of life was
assessed [64]. A greater percentage of respondents with the diagnosis of GAD reported six or
more days with impairment (defined as inability to work or carry out everyday activities) over
the past month than respondents with major depression or no diagnosis (34 versus 21 versus 2
percent respectively). Furthermore, lower scores on measures of quality of life including general
health and mental health (as measured on the 100-point Medical Outcomes Study Short Form-
36) were seen in individuals with GAD versus major depression versus no diagnosis (general
health: 47 versus 59 versus 68 respectively; mental health: 34 versus 42 versus 51, respectively).
The presence of comorbid disorders such as major depression appear to be associated with
more severe and prolonged course of illness and greater functional impairment [6,12,60]. For
example, in a national survey, a greater percentage of individuals with both GAD and major
depression reported six or more days of impairment in the past month than individuals with
either GAD or major depression (48 versus 34 versus 21 percent respectively) [64]. Additionally,
the survey showed that a greater percentage of individuals with both disorders had over 50
percent reduction in overall activities than individuals with generalized anxiety or major
depression (23 versus 11 versus 8 percent respectively). (See 'Comorbidity' above.)
Systemic effects — GAD is associated with poor cardiovascular health, coronary heart disease
[65], and cardiovascular mortality [66]. Relationships between worry and cardiovascular
changes include observations that excessive worrying leads to diminished heart rate variability,
elevated heart rate, hypertension, and increased antihypertensive use [65]. Additionally, greater
severity of worry has been associated with higher rates of fatal and nonfatal coronary heart
disease. Evidence to support the contention that worry may be beneficial to cardiovascular
function or health promoting behaviors has not been found [65].
Prospective studies suggest that clinically significant anxiety in the midlife period may be an
independent risk factor for the development of dementia [67].
Assessment
History — Our primary goal in assessing individuals with anxiety is differentiating anxiety due
to generalized anxiety disorder (GAD) from anxiety that may be due to other causes and
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determining if the anxiety warrants treatment or not. We use history as the primary tool to
accomplish these goals.
● First, we assess the frequency, character, and severity of symptoms to raise or lower
suspicion for the diagnosis of GAD by asking the following questions. Using a symptom
scale, such as the GAD seven-item (GAD-7) scale (calculator 1), can also be helpful to try to
quantify the severity of symptoms (see 'Quantifying the severity of symptoms' below):
• Does the anxiety concern every day or routine circumstances or events (eg, job
responsibility, health of self or family members, finances, misfortunes, or other minor
tasks such as household chores)?
• Have the symptoms been present for more than six months?
In individuals who answer yes to all of the above questions we further consider the
diagnosis of GAD and rule out other diagnoses that present with similar or overlapping
syndromes and other comorbid diseases. (See 'Diagnostic criteria' below and 'Differential
diagnosis' below.)
Individuals who answer no to any of these questions probably do not meet the American
Psychiatric Association’s Diagnostic and Statistical Manual of Mental Disorders, Fifth
Edition (DSM-5) criteria for GAD.
● For people who would meet DSM-5 criteria for GAD or have a likely diagnosis of GAD
based on the severity and frequency of symptoms as above, we review prior psychiatric
history and rule out other psychiatric diagnoses as potential causes of anxiety. We do this
by establishing the presence or absence of symptoms that may differentiate between
disorders:
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• Specific worries about potential medical illness or somatic symptoms – These suggest a
focused anxiety disorder (eg, illness-anxiety disorder) rather than a GAD.
• Rapid onset and resolution of symptoms – Symptoms that start rapidly, sharply rise in
intensity, peak within an hour, and then decline are suggestive of discrete anxiety
attacks which suggests panic disorder rather than GAD.
These and other psychiatric disorders that can share symptomatology with GAD are
discussed in further detail elsewhere. It is also possible for these disorders to coexist with
GAD. (See 'Differential diagnosis' below.)
● We ask about physical health problems (eg, thyroid disease, asthma) and their effects. We
review the individual’s use of prescribed medications (eg, steroids, bronchodilators) as
these may be causing or worsening the anxiety. We also ask about alcohol and other
substance use or recent abstinence from alcohol or other substances.
Physical examination and laboratory testing in select individuals — For individuals with
suspected physical cause of anxiety (eg, individuals with weight loss, cognitive impairment,
shortness of breath) and in individuals with later onset of generalized anxiety (eg, older than 50
years) we do a general physical screening examination and laboratory testing to screen for
underlying medical disorders. We typically obtain a complete blood count, chemistry panel,
serum thyrotropin, urinalysis, electrocardiogram (in patients over 40 with chest pain or
palpitations), and urine toxicology. In cases with suspected underlying medical cause, we refer
to the appropriate specialist for further evaluation.
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Quantifying the severity of symptoms — In all individuals with symptoms suspicious for
GAD, we use the GAD-7 scale (calculator 1) as a means of measuring the level of anxiety.
Additionally, in individuals with confirmed GAD we use the GAD-7 periodically, to monitor
symptoms and judge the response to treatment. The GAD-7 has acceptable reliability and
validity [68] and is sensitive to change in symptoms [69].
The Penn State Worry Questionnaire is available in a number of languages but does not assess
all key symptoms and may be less sensitive to change than the GAD-7 [69].
For hospitalized individuals with active medical disorders, we use the Hospital Anxiety and
Depression Scale to assess and monitor the severity of anxiety and depression. It is useful in
identifying pathological anxiety, has separate subscales for anxiety and depression, and
includes questions that can distinguish symptoms of GAD from anxiety associated with other
medical conditions [68].
Diagnostic criteria — We diagnose GAD in individuals with excessive anxiety and worry that
occur on more days than not for at least six months, are associated with somatic symptoms
(muscle tension, irritability, sleep disturbance), are not due to effects of substances or another
medical condition, and cause clinically significant distress or impairment in social, occupation,
or other important areas of functioning. In patients who “fall short” of the severity or duration
thresholds, further review is advisable, particularly in those who are significantly distressed or
impaired in functioning.
● A. Excessive anxiety and worry (apprehensive expectation), occurring more days than not
for at least six months, about a number of events or activities (such as work or school
performance).
● C. The anxiety and worry are associated with three (or more) of the following six
symptoms (with at least some symptoms having been present for more days than not for
the past six months):
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• 4. Irritability
• 5. Muscle tension
● F. The disturbance is not better explained by another mental disorder (eg, anxiety or worry
about having panic attacks in panic disorder, negative evaluation in social anxiety disorder
[social phobia], contamination or other obsessions in OCD, separation from attachment
figures in separation anxiety disorder, reminders of traumatic events in posttraumatic
stress disorder, gaining weight in anorexia nervosa, physical complaints in somatic
symptom disorder, perceived appearance flaws in body dysmorphic disorder, having a
serious illness in illness anxiety disorder, or the content of delusional beliefs in
schizophrenia or delusional disorder). Because the majority of the anxiety symptoms are
not specific to GAD, it is important to exclude the other anxiety disorders before making
the diagnosis.
The essential feature of diagnostic criteria for GAD in the World Health Organization
International Classification of Diseases, 11th revision (ICD-11) is generalized apprehension or
excessive worry, together with additional symptoms such as muscular tension, subjective
experience of nervousness, difficulty maintaining concentration, irritability, or sleep
disturbance. Symptoms have to be present for most days over the preceding several months.
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The diagnosis of GAD in children and adolescents is discussed further separately. (See "Anxiety
disorders in children and adolescents: Epidemiology, pathogenesis, clinical manifestations, and
course".)
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involving multiple organ systems. (See "Panic disorder in adults: Epidemiology, clinical
manifestations, and diagnosis".)
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Links to society and government-sponsored guidelines from selected countries and regions
around the world are provided separately. (See "Society guideline links: Anxiety and anxiety
disorders in adults".)
● Clinical manifestations – Individuals with GAD experience worry about typical life
experiences such as work, health, and interpersonal relations. The symptoms are out of
proportion to the impact of the anticipated event. Other presenting symptoms commonly
include hyperarousal, autonomic hyperactivity, irritability, poor sleep, and unexplained
pain or muscle tension.
● Course – GAD usually has a gradual onset with subsyndromal anxiety commonly
presenting before age 20. The average onset of the disorder is 30. Late-onset GAD (eg, ≥50
years) is common and is associated with poor health-related quality of life. (See 'Onset'
above.)
GAD is associated with poor cardiovascular health, coronary heart disease, and
cardiovascular mortality. (See 'Systemic effects' above.)
● Assessment – For patients who present with anxiety, we assess whether the frequency,
character, and severity of symptoms are consistent with GAD. We also evaluate for other
alternative or comorbid psychiatric and medical conditions that may also contribute to
anxiety. In individuals with a suspected physical cause of anxiety (eg, weight loss,
confusion) and in individuals with later onset (>50 years old) of generalized anxiety, we do
a general physical screening examination and laboratory screening. (See 'Assessment'
above.)
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● Differential diagnosis – We differentiate anxiety due to GAD from other disorders that
may present with overlapping symptoms (eg, depression, panic disorder, adjustment
disorder) primarily by history. Major depression is particularly difficult to distinguish from
GAD due to shared symptoms of insidious onset, protracted course, and the presence of
dysphoria and anxiety. (See 'Differential diagnosis' above.)
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Topic 496 Version 29.0
Contributor Disclosures
David Baldwin, MA, DM FRCPsych Consultant/Advisory Boards: Anxiety UK [Anxiety disorder]; Idorsia
[Sleep]; National Clinical Audit of Anxiety and Depression [Anxiety and depression]. All of the relevant
financial relationships listed have been mitigated. Murray B Stein, MD, MPH Equity Ownership/Stock
Options: EpiVario [Substance use disorders and PTSD]; Oxeia Biopharmaceuticals [Traumatic brain injury].
Consultant/Advisory Boards: Acadia Pharmaceuticals [Anxiety and traumatic stress-related disorders];
Aptinyx [Anxiety and traumatic stress-related disorders]; atai Life Sciences [Anxiety and traumatic stress-
related disorders]; Bionomics [Anxiety and traumatic stress-related disorders]; BioXcel Therapeutics
[Anxiety and traumatic stress-related disorders]; Boehringer-Ingelheim [Anxiety and traumatic stress-
related disorders]; Clexio [Anxiety and traumatic stress-related disorders]; Eisai [Anxiety and traumatic
stress-related disorders]; EmpowerPharm [Anxiety and traumatic stress-related disorders]; Engrail
Therapeutics [Anxiety and traumatic stress-related disorders]; GABA Therapeutics [Anxiety and traumatic
stress-related disorders]; Jazz Pharmaceuticals [Anxiety and traumatic stress-related disorders]; Oxeia
Biopharmaceuticals [Traumatic brain injury]; Roche/Genentech [Anxiety and traumatic stress-related
disorders]. Other Financial Interest: Biological Psychiatry [Deputy Editor]; Depression and Anxiety [Editor-
in-chief]. All of the relevant financial relationships listed have been mitigated. Michael Friedman, MD No
relevant financial relationship(s) with ineligible companies to disclose.
Contributor disclosures are reviewed for conflicts of interest by the editorial group. When found, these are
addressed by vetting through a multi-level review process, and through requirements for references to be
provided to support the content. Appropriately referenced content is required of all authors and must
conform to UpToDate standards of evidence.
https://www.uptodate.com/contents/496/print 20/20