24 OCD patients and 24 healthy subjects will be submitted to a two-day fear conditioning paradigm during acquisition of functional magnetic resonance imaging (fMRI). OCD patients will be submitted to the paradigm at two timepoints: baseline and 4 weeks after treatment initiation with sertraline up to 200mg/day or maximum tolerated dosage. OCD patients are expected to demonstrate worsened extinction retention compared to healthy subjects at baseline. Sertraline treatment is expected to improve extinction retention compared to baseline and to normalize the brain regions being recruited with the conditioned stimuli presented during the recall phase.
Fear conditioning paradigms are used to investigate the learning process of the fear response in patients with psychiatric disorders and healthy subjects. Patients with post traumatic stress disorder have been shown to fail to retrieve the memory of fear extinction during the recall phase of the fear conditioning paradigm when compared to healthy subjects. In one previous trial, obsessive-compulsive disorder (OCD) patients have demonstrated the same failure to recall extinction and the results from functional magnetic resonance imaging (fMRI) activation maps have shown different regions being recruited during recall when compared with healthy subjects. However, in that previous trial, some of the OCD patients included were already taking medication for OCD. In the current trial, we will evaluate 24 unmedicated OCD patients with a two-day fear conditioning paradigm before and after 4-weeks of treatment initiation with sertraline up to 200mg/day or maximum tolerated dosage. Sertraline is a first-line treatment option for OCD. At baseline, OCD patients will be compared to 24 healthy subjects. At post treatment, fear conditioning and fMRI results wil be compared to baseline. OCD patients are expected to demonstrate worsened extinction retention compared to healthy subjects at baseline. Sertraline treatment is expected to improve extinction retention compared to baseline and to normalize the brain regions being recruited with the conditioned stimuli presented during the recall phase. By "normalize" we mean that after treatment the regions being recruited will be the same as the ones recruited by healthy subjects during baseline, in other words, differences found at baseline regarding brain activation by the conditioned stimuli are expected to disappear after treatment. Abbreviations: CS= conditioned stimuli, CS+= conditioned stimuli to shock, CS-=neutral conditioned stimuli, CS+E= extinguished conditioned stimuli to shock, CS+U=unextinguished conditioned stimuli to shock
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
OTHER
Masking
NONE
Enrollment
69
first week: sertraline hydrochloride 50mg/day, second week: sertraline hydrochloride 100mg/day, third week: sertraline hydrochloride 150mg/day, fourth week: sertraline hydrochloride 200mg/day OBS.: Other SSRIs (fluoxetine, paroxetine, escitalopram) with equivalent dosage schedules can be used if patients report prior intolerance to sertraline
Institute of Psychiatry, Hospital das Clínicas, Faculdade de Medicina da Universidade de São Paulo
São Paulo, Brazil
Main behavioral measure (extinction retention index)
Equation: 100-((MEAN(2 first CS+E during recall)/MAXIMUM(2 last CS+E during extinction))\*100)
Time frame: Baseline for both groups (OCD and helthy subjects), change from baseline to 4 weeks after treatment initiation only for intervention group
Main functional neuroimaging measure
ventro medial prefrontal cortex (vmPFC) activation during recall phase
Time frame: Baseline for both groups (OCD and helthy subjects), change from baseline to 4 weeks after treatment initiation only for intervention group
Main treatment outcome measure
Yale Brown Obsessive Compulsive Scale reduction (final score minus initial score)
Time frame: Change from baseline to 4 weeks after treatment initiation (only interventional group)
Main behavioral measure baseline comparison (extinction retention index OCD patients versus healthy subjects)
Equation: 100-((MEAN(2 first CS+E during recall)/MAXIMUM(2 last CS+E during extinction))\*100)
Time frame: Baseline
Main functional neuroimaging measure (activation maps for contrast CS+E versus CS-during recall phase,OCD patients versus healthy subjects)
ventro medial prefrontal cortex (vmPFC) activation during recall phase
Time frame: Baseline (all subjects)
Secondary behavioral measure (learning- conditioning index, OCD patients pre and post treatment)
Equation: MEAN(all CS+ during conditioning)-MEAN(all CS- during conditioning)
Time frame: Change from baseline to 4 weeks after treatment initiation (only interventional group)
Secondary behavioral measure (learning- conditioning index, OCD patients versus healthy subjects)
Equation: MEAN(all CS+ during conditioning)-MEAN(all CS- during conditioning)
Time frame: Baseline (all subjects)
Secondary Behavioral Measure (context discrimination index based on skin conductance, OCD patients pre and post treatment)
Equation: MEAN(first two CS+U during renewal)-MEAN(first two CS+U during recall)
Time frame: Change from baseline to 4 weeks after treatment initiation (only interventional group)
Secondary Behavioral Measure (context discrimination index based on skin conductance, OCD patients versus healthy subjects)
Equation: MEAN(first two CS+U during renewal)-MEAN(first two CS+U during recall)
Time frame: Baseline (all subjects)
Secondary functional neuroimaging measure (functional activation maps for contrast CS+/CS- during conditioning phase, OCD patients pre and post treatment)
Gain in amygdala activation during conditioning for CS+ presentations
Time frame: Change from baseline to 4 weeks after treatment initiation (only interventional group)
Secondary functional neuroimaging measure (functional activation maps for contrast CS+/CS- during conditioning phase, OCD patients versus healthy subjects)
Gain in amygdala activation during conditioning for CS+ presentations
Time frame: Baseline (all subjects)
Secondary functional neuroimaging measure (functional activation maps for contrast CS+E/CS- during recall phase of baseline measurement, OCD patients versus healthy subjects)
Alternative activations (OCD patients versus controls), regions other than the vmPFC, activated with CS+ presentations during recall
Time frame: Baseline (all subjects)
Secondary functional neuroimaging measure (functional activation maps for contrast CS+E/CS- during recall phase comparing change between post and pre treatment)
Alternative activations (OCD patients post treatment compared with baseline), regions other than the vmPFC, activated with CS+E presentations during recall
Time frame: Change between baseline and 4 weeks after treatment initiation (only interventional group)
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