The current study is a placebo-controlled, double-blind, randomized controlled study using a cross-over design, including Healthy Controls (HC) and participants with Panic Disorder (PD). The primary aim of the study is to investigate the neural correlates and behavioral effects of caffeine (versus placebo), and its impact on emotional reactivity, decision-making, and interoception, and compare the effects in individuals with PD vs HCs. Subjective anxiety and the occurrence of panic attacks will also be measured. Multimodal neuroimaging methods, such as structural and functional MRI, will be used to address the aims of the study. Emotional reactivity, emotional decision-making and interoception will be measured with experimental tasks in a 7 Tesla (7T) magnetic resonance (MR) scanner, jointly with measures of skin conductance, heart rate, respiratory rate, and self-reported ratings of anxiety and interoception. Emotional reactivity will be assessed using emotional and neutral faces. Emotional decision-making will be assessed with an approach-avoidance conflict task. Changes in interoception (bodily sensation, such as pulse and respiration) will be explored using a task in which participants are asked to focus on their breathing or an external stimulus. Caffeine effects on brain resting-state activity will also be assessed. All tasks will be conducted while in the 7T MR scanner. A secondary aim of the study is to examine the impact of genetic variability in the adenosine A2A receptor (ADORA2A) genotype (e.g., rs5751876 T/T) on the effects of caffeine (vs placebo), as ADORA2A genotype has previously been associated with elevated caffeine-induced anxiety.
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Task-related BOLD fMRI signal
Timeframe: Session 1 (day 1)
Task-related BOLD fMRI signal
Timeframe: Session 2 (day 2; minimum of 36 hours after session/day 1)
Self-reported anxiety
Timeframe: Session 1 (day 1)
Self-reported anxiety
Timeframe: Session 2 (day 2; minimum of 36 hours after session/day 1)
Self-reported interoceptive awareness
Timeframe: Session 1 (day 1)
Self-reported interoceptive awareness
Timeframe: Session 2 (day 2; minimum of 36 hours after session/day 1)
Self-reported interoceptive functional impairment
Timeframe: Session 1 (day 1)
Self-reported interoceptive functional impairment
Timeframe: Session 2 (day 2; minimum of 36 hours after session/day 1)
Skin conductance responses (SCR)
Timeframe: Session 1 (day 1)
Skin conductance responses (SCR)
Timeframe: Session 2 (day 2; minimum of 36 hours after session/day 1)
Occurrence of panic attacks
Timeframe: Session 1 (day 1)
Occurrence of panic attacks
Timeframe: Session 2 (day 2; minimum of 36 hours after session/day 1)