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1 and rho = 0.83 [0.68-0.92] for cone-function anxiety).
2 problems (eg, cognitive decline, depression, anxiety).
3 N = 42), all had co-morbid depression and/or anxiety.
4 therapeutic target for meaningfully reducing anxiety.
5 mensions and a second relatively specific to anxiety.
6 expressing feelings of depression and health anxiety.
7 open-field and plus maze were used to assess anxiety.
8 Questionnaire for symptoms of depression and anxiety.
9 nd inform neurodevelopmental perspectives on anxiety.
10 other pain syndromes, as well as stress and anxiety.
11 tional therapy on a patient's vision-related anxiety.
12 in separate studies, for modulating fear and anxiety.
13 r cingulate cortex in patients with clinical anxiety.
14 rall effectiveness or harms of screening for anxiety.
15 body weight, without altering locomotion and anxiety.
16 tion, lower visit happiness and higher visit anxiety.
17 e treatment of depression and cancer-related anxiety.
18 dentifying and predicting risk for pediatric anxiety.
19 s mirrored by decreases of negative mood and anxiety.
20 ls, such as hypertension, heart failure, and anxiety.
21 ty in networks that underlie sociability and anxiety.
22 marginal reliability (0.81 for rod-function anxiety, 0.83 for cone-function anxiety) and exhibits mi
23 lows: depression 41.8% (95% CI 35.8%-48.0%), anxiety 21.0% (95% CI: 4.8%-58.4%), PTSD 19.7% (95% CI 3
24 moderately to highly accurate in identifying anxiety (33 individual studies and 2 systematic reviews;
25 ociated with elevated self-report scores for anxiety (55.2 vs. 50.0), depression (50.2 vs. 46.1), and
27 varied over time between those with/without anxiety after accounting for baseline dissimilarities in
29 s and processes thought to underlie fear and anxiety, along with the promise of translational researc
33 e prevalence and new onset of depression and anxiety among subjects with age-related macular degenera
34 ment (i.e., an association between pediatric anxiety and a specific neurocognitive process), and then
39 ighly conserved regulatory mechanism linking anxiety and alcohol intake that might contribute to incr
41 tes that early neural measures implicated in anxiety and anxious temperament may be incorporated with
42 , fatigue (Checklist Individual Strength-8), anxiety and depression (Hospital Anxiety and Depression
43 e of insomnia, excessive daytime sleepiness, anxiety and depression among African gamers, (2) the ass
45 ernalizing factor, with high loadings across anxiety and depression items, were linked to impoverishe
46 antly improved depressive symptoms (Hospital Anxiety and Depression Rating Scale HADS) at both 24-h (
48 R23] and Fatigue module [QLQ-FA12], Hospital Anxiety and Depression Scale) collected 1 year after dia
49 trength-8), anxiety and depression (Hospital Anxiety and Depression Scale), cognitive functioning (Co
51 Montreal Cognitive Assessment test; Hospital Anxiety and Depression Scale; Impact of Event Scale-Revi
53 pression, and conversely, they should assess anxiety and depression when they present with GI complai
54 f "GI health" when young adults present with anxiety and depression, and conversely, they should asse
55 asthma and food allergy were associated with anxiety and depression, atopic dermatitis was associated
56 c risk factor for adult internalizing (i.e., anxiety and depression, beta = 0.20) psychopathology, ra
57 d from fatigue, 28% and 26% from symptoms of anxiety and depression, respectively, and 6% from cognit
58 role for accumbal MFN2 on the regulation of anxiety and depression-like behaviors through actions on
62 understanding, treating, and even preventing anxiety and fear-related disorders offer great opportuni
64 plaining the intimate link between sleep and anxiety and further highlight the prospect of non-rapid
65 nferior temporal cortex differed between the anxiety and healthy groups at relatively younger ages.
67 r understanding the behavioral expression of anxiety and its neural circuitry, the ethical and techni
68 s over 5% of women, with symptoms similar to anxiety and major depression, and is associated with dif
72 into maladaptive plasticities that underlie anxiety and post-traumatic stress disorders in humans.
73 ity (rho = 0.81 [0.64-0.91] for rod-function anxiety and rho = 0.83 [0.68-0.92] for cone-function anx
74 ed best to stimulation of one circuit, while anxiety and somatic symptoms responded best to stimulati
75 between measures of psychological distress (anxiety and/or depressive symptoms) and normalized chara
76 rod-function anxiety, 0.83 for cone-function anxiety) and exhibits minimal test-retest variability (r
77 emergent disorders, specifically depression, anxiety, and deliberate self-harm (nonsuicidal self-inju
79 ative psychological states including stress, anxiety, and depression-is a substantial prenatal exposu
82 -one individuals with comparable depression, anxiety, and ELM scores were used as psychiatric control
84 hreat responses including autonomic arousal, anxiety, and freezing behavior, while thalamic and basal
86 revalence estimates of PTSD, depression, and anxiety, and limited covariates were reported in the inc
87 y-induced locomotor activity, lower baseline anxiety, and motivational deficits in operant conditioni
91 ondary outcomes of alcohol craving and mood, anxiety, and sleep disturbances, which are predictive of
92 hizophrenia, bipolar or unipolar depression, anxiety, and substance use) to matched healthy control p
98 ation study (GWAS) of a continuous trait for anxiety (based on score on the Generalized Anxiety Disor
99 etic resonance imaging scanner, and assessed anxiety [Beck Anxiety Inventory], depressive symptoms [B
101 zures, hyperactivity, repetitive and reduced anxiety behaviours, plus several unexpected features, in
102 cific mental disorder, including depression, anxiety, bipolar, borderline personality disorder, schiz
103 ures and IBS symptom severity or GI-specific anxiety but we found a significant difference in the rel
104 lth disorders (CMDs), such as depression and anxiety, but we know little about nature-related motivat
105 ent of AEA signaling rescued seizure-induced anxiety by restoring the tonic control of the eCB signal
107 Trait scores, - 23.5 (13.2), indicating less anxiety, compared to placebo group, - 8.8 (14.7); result
108 unknown, but if they do, induced (adaptive) anxiety could be used as an intermediate translational m
111 understanding the emergence of pathological anxiety depends on the availability of paradigms effecti
115 ociated with lower prevalence of symptoms of anxiety, depression, and peritraumatic dissociation (odd
116 nd 6 months later demonstrated low levels of anxiety, depression, distress, and uncertainty and high
117 bers of ICU patients may have high levels of anxiety, depression, posttraumatic stress disorders, and
118 at birth and the trajectories of children's anxiety-depression symptoms between ages 3 to 8 years (a
119 rbance (MD -7.29; 95% CI -8.23 to -6.35) and anxiety/depression (MD -3.08; 95% CI -4.41 to -1.75) and
121 onal outcomes included any neuropsychiatric, anxiety, depressive, personality, or substance use disor
122 not in juvenile or adult windows, increased anxiety-, despair-, and schizophrenia-like behavior in a
123 ales with a primary diagnosis of generalized anxiety disorder (GAD) and nonpsychiatric controls.
124 a genome-wide association study of Lifetime Anxiety Disorder (n(case) = 25 453, n(control) = 58 113)
125 is and self-report of physician diagnosis of anxiety disorder (N=224,330) as a secondary analysis.
126 r anxiety (based on score on the Generalized Anxiety Disorder 2-item scale [GAD-2], N=199,611) as the
127 psychiatric disorders, including generalized anxiety disorder and posttraumatic stress disorder.
129 t six times as likely to have had a mood and anxiety disorder health care visit, more than three time
130 was to ascertain the prevalence of mood and anxiety disorder health care visits and antidepressant a
132 ate to high accuracy for adults (Generalized Anxiety Disorder scale: sensitivity, 70% to 97%; specifi
134 ve explanatory account of the development of anxiety disorders and addiction, but such models also fa
136 odels of information processing in pediatric anxiety disorders and highlight the particular value of
137 eports of burnout, musculoskeletal injuries, anxiety disorders and sleep disturbances compared to les
144 for the onset of psychiatric disorders, with anxiety disorders being the most common and affecting as
145 being considered as a novel therapeutic for anxiety disorders due to its ability to promote affiliat
146 hough both pediatric and adult patients with anxiety disorders exhibit similar neural responding to t
147 thy subjects compared with participants with anxiety disorders exhibited greater amygdala-ventromedia
148 pes.SIGNIFICANCE STATEMENT Predisposition to anxiety disorders has both a neurodevelopmental and a ge
149 ponse to unpredictable threats, pathological anxiety disorders occur when symptoms adversely affect d
150 cognitive training treatments for pediatric anxiety disorders rely on accurate and reliable identifi
153 mechanisms that might contribute to fear and anxiety disorders transmission in clinically affected fa
155 mpulsive disorder (OCD) and various types of anxiety disorders, but phenomenological overlap, high ra
156 rs of cognitive control in pediatric OCD and anxiety disorders, including before and after treatment.
157 = 326) included treatment-seeking youth with anxiety disorders, with disruptive mood dysregulation di
165 plicated in sleep impairment and in mood and anxiety disorders: the default mode network and negative
166 l changes in threat learning to pathological anxiety, findings from studies in patients inconsistentl
168 estigated the implication of beta4*nAChRs in anxiety-, food reward- and nicotine reward-related behav
173 food restriction activates SIRT1, promoting anxiety, hyperactivity, and addiction to starvation, exa
174 quality of life, symptoms of depression and anxiety, illness understanding, and end-of-life care.
175 articularly when investigating the impact of anxiety in a diversity of cognitive functions and popula
176 ilability of paradigms effective in inducing anxiety in a simple, consistent and sustained manner.
177 developed a recommendation on screening for anxiety in adolescent and adult women to improve detecti
179 ct, crossover experiment, the study measured anxiety in healthy subjects before and after a session o
180 for screening and monitoring vision-related anxiety in patients with inherited retinal degenerations
182 n respondents from Ireland, highest rates of anxiety in respondents from Germany, and social exclusio
188 ential Organ Failure Assessment, State-Trait Anxiety Inventory State greater than or equal to 40 was
189 imaging scanner, and assessed anxiety [Beck Anxiety Inventory], depressive symptoms [Beck Depression
190 than impaired threat learning, pathological anxiety involves heightened skin conductance response to
191 ctivity manifests with pediatric symptoms of anxiety, irritability, and attention-deficit/hyperactivi
194 ainstem nuclei involved in the regulation of anxiety is the dorsal raphe, which contains different su
197 We assessed how individual differences in anxiety-like (measured via the elevated plus maze and op
198 plash test, we show that E2 add-back induces anxiety-like and depression-like behavior in Het-Met mic
200 implicate vHIP-NAc in social interaction and anxiety-like behavior and identify markers of vulnerabil
201 xtual fear, as well as persistently elevated anxiety-like behavior and impaired spatial memory at rem
202 hypersensitivity in the caudal abdomen, mild anxiety-like behavior and substantial memory deficits as
203 ns in voluntary alcohol intake and decreased anxiety-like behavior associated with alcohol dependence
205 igra pars reticulata (SNR), accompanied with anxiety-like behavior in aged PD-related alpha-syn A53T
206 did not show a significant relationship with anxiety-like behavior in any of the targeted brain regio
207 38) also reversed ethanol withdrawal-induced anxiety-like behavior in ethanol-dependent rats, but did
208 Ac afferents during tests of depressive- and anxiety-like behavior in male and female mice, both befo
209 of IL-17a by these cells was correlated with anxiety-like behavior in mice and was partially dependen
210 f rats as susceptible and resilient based on anxiety-like behavior in the elevated plus maze and cont
211 ard sensitivity, perseverative behavior, and anxiety-like behavior using saccharin preference testing
212 n adult mature neurons resulted in increased anxiety-like behavior with concomitant hypercorticalism,
213 thways on reward sensitivity, locomotion, or anxiety-like behavior, but inhibiting DRN-projecting LHb
214 notype in offspring characterized by reduced anxiety-like behavior, fragmented social behavior, and a
222 dule of food reward, locomotor activity, and anxiety-like behavior], dopamine function [striatal expr
223 in the ventral hippocampus without affecting anxiety-like behaviors and basolateral amygdala firing.
226 osphorylation, cAMP inhibition) and in vivo (anxiety-like behaviors, cannabimimetic effects, novel en
229 ssing stress hyper-reactive-, depressive- or anxiety-like phenotypes may possess more translational v
231 valuated THC effects on behavioral assays of anxiety, locomotion, and place conditioning, as well as
237 t, with no change in sociability, olfaction, anxiety, or several hippocampal-dependent behaviors.
243 al care, which were directly associated with anxiety, perceived stress, and post-traumatic symptomato
244 and completing a survey assessing optimism, anxiety, personality traits, and sociodemographics using
245 n of two key features of the high trait-like anxiety phenotype: high responsivity to anxiety-provokin
246 ce estimates were calculated for depression, anxiety, post-traumatic stress disorder (PTSD), and suic
247 ur hypotheses, results showed an increase in anxiety-potentiated startle following active but not sha
249 like anxiety phenotype: high responsivity to anxiety-provoking uncertain threat and responsivity to c
250 ar year of surgery, history of depression or anxiety, psychosis, schizophrenia, mania, or bipolar dis
252 and "anxiety." The subset of vision-related anxiety questions was analyzed by a graded response mode
253 Depression Rating Scale (HAMD-17), Hamilton Anxiety Rating Scale (HAMA), and mean reaction time/accu
254 ary effectiveness measures included Hamilton Anxiety Rating Scale, Hamilton Depression Rating Scale,
255 ity, 64%), and adolescents (Screen for Child Anxiety Related Emotional Disorders: sensitivity, 64% to
256 cilitates gregarious song and reduces stress/anxiety-related behavior in male and female European sta
257 administration of BHB attenuated SPS-induced anxiety-related behaviors evaluated by the elevated plus
259 ons and anaesthesia negated the reduction in anxiety-related behaviour in tunnel compared with tail h
260 Regarding the F1 offspring, screening for anxiety-related behaviours using the elevated-plus maze,
264 of cholinergic modulators on the function of anxiety-related networks in humans have not been investi
266 al but not immediately present threats; this anxiety-related potentiation of anticipatory responding
269 Secondary endpoints included the Hamilton Anxiety Scale (HAM-A), Hamilton Depression Rating Scale
270 QI), Symptom Checklist 90 (SCL-90), Hamilton Anxiety Scale (HAMA) and Hamilton Depression Scale (HAMD
271 isk genotype, circulating PACAP, and somatic anxiety severity were stronger among females than males.
272 Whether or not adaptive and pathological anxiety share mechanisms remains unknown, but if they do
274 cannabinoids and reverses the stress-induced anxiety state in a cannabinoid receptor-dependent manner
275 patients (51.9%) reported moderate to severe anxiety (State-Trait Anxiety Inventory State >= 40).
276 tion and reward-based learning, we show that anxiety states in humans impair learning by attenuating
277 cal co-morbidities, a history of depression, anxiety, substance use disorder, and chronic pain (all P
279 f activation across induced and pathological anxiety, supporting the proposition that some neurobiolo
280 8 113) and an additional analysis of Current Anxiety Symptoms (n(case) = 19 012, n(control) = 58 113)
281 c computational model, while trait cognitive anxiety symptoms are associated with enhanced learning f
283 with a greater reduction in clinician-rated anxiety symptoms pre-to-post CBT and SSRI treatment.
288 Current diagnostic criteria for mood and anxiety tend to lump different forms of sleep disturbanc
289 etic variants associated with high levels of anxiety/tension, and high levels of worry/vulnerability
290 re mediated by spinal afferents and fear and anxiety (the affective aspects of visceral pain) are the
291 which pertained to concepts of "worry" and "anxiety." The subset of vision-related anxiety questions
292 very, impaired spatial memory, and increased anxiety through 8 wk poststroke compared to wild type (W
295 may underlie individual differences in trait anxiety using the common marmoset (Callithrix jacchus, m
300 atients who screened positive for depression/anxiety (without PTSD) were more likely to have chronic