Identifying Brain and Genetic Markers of Sertraline Treatment Response in People With Social Anxiety Disorder

University of Michigan200 enrolled

Overview

This study will attempt to identify gene and brain activity markers that predict whether people with social anxiety disorder will respond to selective serotonin reuptake inhibitor medications.

Social anxiety disorder (SAD) is an anxiety disorder characterized by excessive fear and avoidance of social situations. Selective serotonin reuptake inhibitors (SSRIs) are a medication commonly prescribed to treat social anxiety disorder, but as many as 50% of people with SAD do not respond to SSRIs. Current theory suggests that neurological functioning and genetics may influence a patient's response to treatment. This study will examine variations in genetics and brain reactivity among people with SAD who do and do not respond to SSRIs. Through this, the study will identify neurological and genetic biomarkers that can predict responsiveness to SSRI treatment in people with SAD. Participation in this study will last 14 weeks. Both healthy people and people with SAD will be recruited to participate. All participants will complete similar study visits at entry, within 2 weeks of entry, and 12 weeks after that. The first visit, which will occur at study entry, will include screening questionnaires, an interview with research staff, a medical screening, a urine test, and collection of saliva samples for genotyping. The second visit and the last visit, which will be separated by 12 weeks, will involve MRI scans and behavioral tasks to be conducted inside and outside the MRI scanner. Over the 12 weeks between MRI scanning sessions, participants with SAD will take sertraline, a common SSRI, on a daily basis. They will also attend five additional visits during this time to complete assessments of their symptoms. These visits will occur 1, 2, 4, 8, and 12 weeks after starting sertraline treatment. Participants with SAD will therefore be completing a symptom assessment, MRI scans, and behavioral tasks all on the final visit, 12 weeks after the second visit.

Study Type

OBSERVATIONAL

Enrollment

200

Conditions

Anxiety Disorders

Interventions

SertralineDRUG

Oral sertraline will begin at 50 mg per day, then increase to 75 mg per day on Day 8, then increase to 100 mg per day on Day 15. The dose may be increased to 150 mg per day on Week 8, based on clinical response and medication toleration.

Eligibility

Sex: ALLMin age: 18 YearsMax age: 55 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: For social anxiety disorder group: * Current diagnosis of social anxiety disorder, generalized subtype * Physically healthy, as confirmed by comprehensive medical history, physical exam, and laboratory testing For healthy control group: * Never been diagnosed with either Axis I or Axis II mental disorders * Physically healthy, as confirmed by comprehensive medical history, physical exam, and laboratory testing Exclusion Criteria: * Clinically significant medical or neurologic condition * Diagnosis of primary comorbid anxiety disorder, defined by which disorder is the more debilitating and clinically salient * History of bipolar disorder or schizophrenia * Presence of an organic mental syndrome, mental retardation, or pervasive developmental disorder * Current major depressive disorder or major depression within the past 6 months * Hamilton Rating Scale for Depression score greater than 18 * Alcohol or drug abuse or dependence within the past year * Current suicidal ideation * Diagnosis of an Axis II personality disorder, except for avoidant personality disorder * Treatments with psychotropic or psychoactive medications within the 2 weeks before screening (or 8 weeks for fluoxetine and 4 weeks for monoamine oxidase inhibitors) * Positive urine drug screen results * Pregnancy Additional exclusion criteria for the functional MRI studies: * Left-handedness, as determined by standard questionnaire * Presence of ferrous-containing metals within the body, such as aneurysm clips, shrapnel, or retained particles * Claustrophobia

Locations (1)

University of Michigan

Ann Arbor, Michigan, United States

Outcomes

Primary Outcomes

Clinical Global Impression (CGI) Scale

Time frame: Measured before treatment, at five treatment study visits, and 12 weeks after starting treatment

Secondary Outcomes

Liebowitz Social Anxiety Scale (LSAS)

Time frame: Measured before treatment, at five treatment study visits, and 12 weeks after starting treatment

Data from ClinicalTrials.gov

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