Brain Imaging Techniques That Predict Antidepressant Responsiveness (WyethKolden)

• ClinicalTrials.gov Identifier: NCT00909155
• Recruitment Status: Completed
• First Posted: May 27, 2009
• Results First Posted: December 15, 2014
• Last Update Posted: August 3, 2018
• Sponsor: University of Wisconsin, Madison
• Collaborator: Wyeth is now a wholly owned subsidiary of Pfizer
• Information provided by (Responsible Party): University of Wisconsin, Madison

Study Description

Brief Summary:

Do functional brain changes occur during Venlafaxine ER (extended release) versus Fluoxetine treatment and do changes in selective structures, such as the amygdala, predict treatment response?

Condition or disease	Intervention/treatment	Phase
Major Depressive Disorder	Drug: Venlafaxine ERT; Drug: Fluoxetine	Not Applicable

Detailed Description:

This is a single site, controlled, double-blind study of outpatients. There are two arms:

1. Forty participants who have a current Diagnostic and Statistical Manual of Mental Disorders, 4th edition, text revised (DSM-IV-TR) diagnosis of Major Depression will be recruited. These subjects will be randomized to receive one of two antidepressant medications: Fluoxetine or Venlafaxine ER for the duration of the study. Subjects will gradually be titrated onto the medications and will be seen in the clinic up to 18 times for medication checks, to monitor side effects and depressive symptoms, including suicidal ideation. In the event of suicidal ideation, subjects will be withdrawn from the study and referred for immediate treatment.
2. Twenty normal control subjects with no current or past DSM-IV-TR diagnosis and will receive no medication. Normal control subjects will have up to 5 visits while in the study.

Subjects will contact study staff to complete a phone screen and then eligible subjects will complete a clinic screen. Subjects will then be scheduled to attend the magnetic resonance imaging (MRI) simulation visit and if subjects continue to meet entrance criteria, they will be scheduled for the first MRI. Following the first MRI, subjects in the medication conditions will begin receiving medication.

All subjects will undergo 3 functional magnetic resonance imaging (fMRI)s during the study: at the beginning of the study, approximately 8 weeks and 26 weeks later. During the MRI, subjects will view slides with positive and negative emotional content. Subjects will complete various clinical interviews or rating scales assessing mood and side effects at each of the visits.

Study Design

• Study Type: Interventional (Clinical Trial)
• Actual Enrollment: 50 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
• Primary Purpose: Basic Science
• Official Title: Non-Invasive Brain Imaging Techniques That Predict Antidepressant Responsiveness and Provide Insights Into the Mechanism of Action of Venlafaxine ER vs. Fluoxetine
• Study Start Date: July 2002
• Actual Primary Completion Date: December 2009
• Actual Study Completion Date: December 2009

Arms and Interventions

Arm	Intervention/treatment
Active Comparator: Depressed; Venlafaxine treatment; Currently depressed subjects; Randomized medication treatment with Venlafaxine extended release tablets (Venlafaxine ERT). Dosage 75-300mg/day for up to 6 months.	Drug: Venlafaxine ERT; Titrated to a minimum dose of 75mg. Further titration based on clinician assessment at followup visits. Intervention to continue through completion of study (180 days). Initial titration: Days 1-7: 37.5 mg; Days 7-14: 75 mg; Days 15-180: 75-300mg based on clinician assessment. Titration rate is a maximum of 75mg/7d.; Other Name: Effexor ER
Active Comparator: Depressed; Fluoxetine treatment; Currently depressed subjects; Randomized medication treatment with Fluoxetine tablets. Dosage 20-80mg/day for up to 6 months.	Drug: Fluoxetine; Titrated to a minimum dose of 20mg. Further titration based on clinician assessment at followup visits. Intervention to continue through completion of study (180 days). Initial titration: Days 1-7: 20mg; Days 7-14: 20mg; Days 15-180: 20-80mg based on clinician assessment. Titration rate is a maximum of 20mg/7d; Other Name: Prozac
No Intervention: Control; Non-psychiatric subjects with no past or current history of depression. Subjects will receive no medication

Outcome Measures

Primary Outcome Measures :

1. Hamilton Depression (HAM-D) and Anxiety (HAM-A) Rating Scales [ Time Frame: Study entry, 2 months, and at end of study (6 mos) ]

   Hamilton Depression rating scale is a clinician assessment tool to measure severity of depression symptoms. Minimum score is 0 (no symptoms); maximum score is 52 (severe symptoms of depression).

   Hamilton Anxiety rating scale is a clinician assessment tool to measure severity of anxiety symptoms. Minimum score is 0 (no symptoms); maximum score is 56 (severe symptoms of anxiety).

2. Functional Magnetic Resonance Imaging (fMRI) Response to an Emotional Regulation Task. [ Time Frame: At study entry, 2 months and end of study (6 months) ]

   Depressed participants were scanned while viewing a sequence of positive and negative images; they were instructed to enhance or supress their emotional response to the image or to continue to attend. To examine brain function when regulating negative affect, we created contrast maps for each participant at all 3 time points by subtracting the attend condition from the suppress condition in response to negative stimuli. Data from all 3 scan sessions were used to assess treatment-induced change in brain activity when regulating emotion. Analyses examining change using difference scores (end vs. starting points), we subtracted initial HAMD score from final HAMD score. For fMRI analyses, in a voxelwise manner, we subtracted initial negative suppress vs attend from final negative suppress vs attend.

   Control subjects were not depressed, repeat scans to assess change were not completed.

   Reported results are from BA10, one of our areas of interest.

Eligibility Criteria

• Ages Eligible for Study: 18 Years to 70 Years (Adult, Older Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Criteria

Inclusion Criteria:

• Intervention Group:

  • Right-handed,
  • Be able to lie still on their back for about 120 minutes,
  • Meet DSM-IV criteria for major depression (single or recurrent),
  • Have had depressive symptoms for at least 1 month prior to screen visit,
  • Must score an 18 or above on the Hamilton-D at both the initial screening visit and first fMRI scanning session,
  • Able to understand and speak English.
• Control Group: same as above with the exception of no diagnosis of psychiatric disorder.

Exclusion Criteria:

• Any history of seizures,
• Current medical disorders that might make interpretation of scan data difficult,
• Diabetes requiring insulin treatment,
• A serious heart disorder or subjects who have had a heart attack within the last 3 months,
• Subjects who meet DSM-IV criteria for alcohol/drug abuse or dependence within the last six months,
• Other current DSM-IV Axis I or Axis II diagnoses,
• A personal or family history of bipolar disorder,
• Current use of medication that affects central nervous system (CNS) function,
• Participation in the last 30 days in a clinical study involving an investigational drug,
• A subject with metallic implants, such as prostheses, shrapnel or aneurysm clip-S, or persons with electronic implants, such as cardiac pacemakers. The magnetic field generated by the MRI machine can cause a displacement or malfunctioning of these devices.
• A subject who is claustrophobic,
• Female subjects who are pregnant,
• A subject at serious risk for suicide,
• Diagnosis of cancer in the past 3 years and/or has active neoplastic disease,
• Nonresponse to 2 adequate trials of antidepressant treatment,
• Nonresponse to 2 adequate trials of an empirically supported psychotherapy.

Contacts and Locations

Locations

United States, Wisconsin

University of Wisconsin Madison Psychiatry Department

Madison, Wisconsin, United States, 53719

Sponsors and Collaborators

University of Wisconsin, Madison

Wyeth is now a wholly owned subsidiary of Pfizer

Investigators

• Principal Investigator: Gregory Kolden, Ph.D.; University of Wisconsin Madison Psychiatry Department
• Principal Investigator: Michael Peterson, MD, Ph.D.; University of Wisconsin Madison Psychiatry Department

More Information

Publications of Results:

Heller AS, Johnstone T, Peterson MJ, Kolden GG, Kalin NH, Davidson RJ. Increased prefrontal cortex activity during negative emotion regulation as a predictor of depression symptom severity trajectory over 6 months. JAMA Psychiatry. 2013 Nov;70(11):1181-9. doi: 10.1001/jamapsychiatry.2013.2430.

Heller AS, Johnstone T, Light SN, Peterson MJ, Kolden GG, Kalin NH, Davidson RJ. Relationships between changes in sustained fronto-striatal connectivity and positive affect in major depression resulting from antidepressant treatment. Am J Psychiatry. 2013 Feb;170(2):197-206. doi: 10.1176/appi.ajp.2012.12010014.

Light SN, Heller AS, Johnstone T, Kolden GG, Peterson MJ, Kalin NH, Davidson RJ. Reduced right ventrolateral prefrontal cortex activity while inhibiting positive affect is associated with improvement in hedonic capacity after 8 weeks of antidepressant treatment in major depressive disorder. Biol Psychiatry. 2011 Nov 15;70(10):962-8. doi: 10.1016/j.biopsych.2011.06.031. Epub 2011 Aug 25.

Heller AS, Johnstone T, Shackman AJ, Light SN, Peterson MJ, Kolden GG, Kalin NH, Davidson RJ. Reduced capacity to sustain positive emotion in major depression reflects diminished maintenance of fronto-striatal brain activation. Proc Natl Acad Sci U S A. 2009 Dec 29;106(52):22445-50. doi: 10.1073/pnas.0910651106. Epub 2009 Dec 22.

• Responsible Party: University of Wisconsin, Madison
• ClinicalTrials.gov Identifier: NCT00909155
• Other Study ID Numbers: 0600B-100953; 2001-294 ( Other Identifier: HS IRB )
• First Posted: May 27, 2009
• Results First Posted: December 15, 2014
• Last Update Posted: August 3, 2018
• Last Verified: July 2018

Keywords provided by University of Wisconsin, Madison:

Major Depressive Disorder

Additional relevant MeSH terms:

Depressive Disorder; Depression; Depressive Disorder, Major; Mood Disorders; Mental Disorders; Behavioral Symptoms; Fluoxetine; Venlafaxine Hydrochloride; Serotonin Uptake Inhibitors; Neurotransmitter Uptake Inhibitors; Membrane Transport Modulators; Molecular Mechanisms of Pharmacological Action; Neurotransmitter Agents; Serotonin Agents; Physiological Effects of Drugs; Antidepressive Agents, Second-Generation; Antidepressive Agents; Psychotropic Drugs; Cytochrome P-450 CYP2D6 Inhibitors; Cytochrome P-450 Enzyme Inhibitors; Enzyme Inhibitors; Serotonin and Noradrenaline Reuptake Inhibitors