Glutamate Probes in Adolescent Depression

NCT ID: NCT02307617

Last Updated: 2021-04-23

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 57 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2014-08-01
• Study Completion Date: 2017-04-17

Brief Summary

The purpose of this study is to learn if measures of brain chemicals from a brain scan called Magnetic Resonance Imaging and Spectroscopy (MRI/MRS) and brain activity (known as cortical excitability and inhibition) collected by Transcranial Magnetic Stimulation (TMS) are different in adolescents with depression who are in different stages of treatment.

Researchers are conducting this study to learn more about how the brain works in adolescents with depression and without depression (healthy controls). This is important because it may identify a biological marker (a measure of how bad an illness is) for depression that could one day be used to identify depressed adolescents who would benefit from certain treatments (medications for example) or to monitor how well treatments are working.

Detailed Description

This is a cross-sectional and longitudinal neurophysiology research study of 200 adolescent subjects in varying stages of major depressive disorder (MDD). The aims of this study are designed to gain an understanding of (1) the role of glutamate in the neurophysiology and pharmacologic treatment of child and adolescent MDD; (2) the role of gamma-aminobutyric acid (GABA) in the neurophysiology and pharmacologic treatment of child and adolescent MDD; (3) the trajectory of glutamatergic and GABAergic functioning in human development with MDD.

Glutamate concentrations in the anterior cingulate cortex (ACC) and left dorsolateral prefrontal (L-DLPFC) cortex will be evaluated using proton magnetic resonance spectroscopy (MRS) at 3 Tesla (3T). Glutamatergic cortical excitability measures (with motor threshold and intracortical facilitation paradigms), and GABAergic cortical inhibitory measures (with cortical silent period and intracortical inhibition paradigms) will be studied using single and paired-pulse transcranial magnetic stimulation (TMS) paradigms.

Conditions

Major Depressive Disorder; Major Depressive Disorder, Recurrent; Major Depressive Disorder, Remitted

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: OTHER

Study Groups

Group 2

Adolescent participants who plan to start selective serotonin reuptake inhibitor (SSRI) treatment for their depression. Data will be collected prior to the start of the medication and again 6 weeks after the start of the medication.

No interventions assigned to this group

Medication Responders

Adolescent participants who have responded to SSRI treatment for their depression.

No interventions assigned to this group

Medication Non-Responders

Adolescent participants with depression that has not responded to SSRI treatment.

No interventions assigned to this group

Healthy Controls

Adolescent participants who have no current or past mental health diagnoses.

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

1. Adolescents from the ages of 13 to 21, male or female.

2. Subjects with MDD (Groups 2, 3 & 4):

• Must have a diagnosis of Major Depressive Disorder (MDD)
• Single episode or recurrent; moderate to severe.
• The MDD diagnosis is based on the Kiddie Schedule for Affective Disorders and Schizophrenia for School Aged Children - Past and Lifetime (K-SADS-PL).
• This semi-structured psychiatric interview will be administered by a psychiatrist, Ph.D. level psychologist, or equivalent professional with extensive clinical experience.
• Must have a Childhood Depression Rating Scale-Revised (CDRS-R) score of ≥ 40
• Must have a Clinical Global Impression Severity (CGI-S) Scale of ≥ 4

3. Group 1: (Healthy Controls; 50 Subjects): Healthy volunteers who are 13-21 years of age with no current or lifetime mental health diagnoses and no current or lifetime psychotropic medication treatment.

4. Group 2: (50 subjects): Subjects with moderate to severe MDD for which an SSRI has been clinically indicated.

• If initiating SSRI treatment, medication must be started ± 7 days of the baseline visit
• Subjects and parents in group 2 will be eligible to return in 6-8 weeks for a follow up visit that includes mood assessments and evaluations.
• Subjects who have been adherent to their clinically prescribed medication will be eligible for a second MRI/MRS scan and TMS measures within 7 days of the second visit.
• Subjects who choose not to initiate treatment with an SSRI will have a baseline visit only
• Subjects who discontinue or change their medication after the baseline will not be eligible for a follow-up visit

Group 3: (50 subjects): Subjects with moderate to severe MDD that has responded to treatment with an SSRI.

• Response will be defined as a 1 (very much) or 2 (much) improved on a CGI-Improvement Scale. This is the current acceptable standard in child and adolescent psychopharmacological research.

Group 4: (50 subjects): Subjects with moderate to severe MDD that has not responded to treatment with an SSRI as defined above with CGI scale score.

5. Subject and parent or guardian (if under age 18) must be capable of providing informed consent

6. Subjects and at least 1 parent must be fluent in English. • Subjects 18 years of age or older do not require an English-speaking parent

Exclusion Criteria

1. Contraindications to MRI/MRS, as determined by the MRI safety screen and MRI safety codes.

2. Subjects who are judged by the Principal Investigator to be at imminent risk for self-harm or suicide as indicated by interview or C-SSRS.

3. Pregnancy or suspected pregnancy in females.

4. Metal in the head (except the mouth*), implanted medication pumps, cardiac pacemaker (*subjects with braces will be excluded from MRI/MRS portion of the study only)

5. Prior brain surgery.

6. Risk for increased intracranial pressure such as a brain tumor.

7. Any unstable medical condition.

1. Current or past mental health diagnoses in subjects or first degree relatives of subjects.

2. Current or past mental health medications.

1. Primary Axis I or II disorder other than MDD.

2. Unprovoked seizure history, seizure disorder, history of febrile seizures, first degree relative with epilepsy

3. Taking medication(s) that lower seizure threshold

4. Any significant findings on the TMS adult safety screen (TASS).

1. Subject has started SSRI medication more than 7 days prior to the baseline visit.

• Minimum Eligible Age: 13 Years
• Maximum Eligible Age: 21 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Mayo Clinic

OTHER

Sponsor Role: lead

Responsible Party

Paul E. Croarkin

Principal Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Paul E Croarkin, D.O.

Role: PRINCIPAL_INVESTIGATOR

Mayo Clinic

Locations

Mayo Clinic

Rochester, Minnesota, United States

Countries

United States

Related Links

https://www.mayo.edu/research/clinical-trials

Mayo Clinic Clinical Trials

Other Identifiers

14-004662

Identifier Type: -

Identifier Source: org_study_id