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Neural Response to Inflammatory Challenge in Major Depressive Disorder

Primary Purpose

Major Depressive Disorder

Status
Recruiting
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
LPS
Saline
Sponsored by
Laureate Institute for Brain Research, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Major Depressive Disorder

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

Both healthy controls and depressed participants will be required to be in good general health (as evaluated during Visit 1, including EKG) and to be 18-65 years of age. A DSM-V diagnosis of MDD will be made with the MINI International Neuropsychiatric Interview and current symptoms of depression will be measured with the clinician-administered MADRS and the self-report PHQ-9. Depressed participants will be required to have symptoms of depression (i.e. a PHQ-9 score ≥10) and/or a MADRS score of ≥7.

Exclusion Criteria:

General Exclusion Criteria:

  • Pregnancy
  • A history of fainting during blood draws will be evaluated by the clinical team and may be deemed exclusionary.

Medical Conditions:

  • Moderate to severe traumatic brain injury (>30 min. loss of consciousness or >24 hours posttraumatic amnesia) or other neurocognitive disorder with evidence of neurological deficits.
  • Presence of co-morbid medical conditions not limited to but including cardiovascular (e.g., history of acute coronary event, stroke) and neurological diseases (e.g., Parkinson's disease), as well as pain disorders.
  • Presence of co-morbid inflammatory disorders such as rheumatoid arthritis or other autoimmune disorders.
  • Presence of an uncontrolled medical condition that is deemed by the investigators to interfere with the proposed study procedures, or to put the study participant at undue risk.
  • Presence of chronic infection that may elevate pro-inflammatory cytokines.
  • Presence of an acute infectious illness or receipt of a vaccination in the two weeks prior to an experimental session.

Psychiatric Disorders:

  • Current severe suicidal ideation or attempt within the past 12 months.
  • Psychosis
  • Bipolar disorder
  • Substance abuse or dependence within the previous 6 months

Contraindications for MRI:

  • Cardiac pacemaker, metal fragments in eyes/skin/body (shrapnel), aortic/aneurysm clips, prosthesis, by-pass surgery/coronary artery clips, hearing aid, heart valve replacement, shunt (ventricular or spinal), electrodes, metal plates/pins/screws/wires, or neuro/bio-stimulators (TENS unit), persons who have ever been a professional metal worker/welder, history of eye surgery/eyes washed out because of metal, vision problems uncorrectable with lenses, inability to lie still on one's back for 60 minutes; prior neurosurgery; tattoos or cosmetic makeup with metal dyes, unwillingness to remove body piercings, and pregnancy.
  • Claustrophobia that is severe enough to preclude MRI scanning.

Medications:

  • Current and/or past regular use of hormone-containing medications (excluding contraceptives)
  • Use of medications such as oral corticosteroids which may have immunosuppressive effects.
  • Current use of non-steroid anti-inflammatory drugs that is deemed by the investigators to potentially confound the results of the study (e.g. > 3 days/week)
  • Current and/or past regular use of immune modifying drugs that target specific immune responses such as TNF antagonists
  • Current use of analgesics such as opioids or history of addiction to opioids or other analgesics
  • Current and/or past regular use of cardiovascular medications, including antihypertensive, antiarrhythmic, anti-anginal, and anticoagulant drugs (does not apply where medications are taken for different purpose e.g. anti-hypertensives for migraine).
  • Chronic use of antibiotics such as isotretinoin or minocycline because of their potential effects on the microbiome and immune function.
  • Evidence of recreational drug use from urine test.
  • Lifetime use of methamphetamine
  • Inclusion of individuals reporting other types of medications or supplements not listed or considered thus far will be at the discretion of the PI based on their potential to affect immune function, the microbiome, brain function or brain blood flow.

Health Factors:

  • BMI > 35 because of the effects of obesity on pro-inflammatory cytokine activity
  • Clinically significant abnormalities on screening laboratory tests
  • Abnormal EKG
  • In addition, participants who on arrival to the study, show any of the following symptoms will not be allowed to complete the study:

    1. screening supine systolic blood pressure >140 mmHg or <100 mmHg
    2. screening supine diastolic blood pressure >90 mmHg or <60 mmHg
    3. 12-lead EKG demonstrating a PR interval > 0.2 msec QTc >450 or QRS >120 msec (Bazett) If the QTc exceeds 450 msec, or QRS exceeds 120 msec, the EKG will be repeated 2 more times and the median value will be used
    4. pulse less than 50 beats/minute or greater than 100 beats/minute
    5. temperature greater than 99.5 degrees F.

      Non-English speaking participants:

  • The majority of the assessments proposed for this study have not been translated from English, thus, non-English speaking volunteers will be excluded.

Sites / Locations

  • Laureate Institute for Brain ResearchRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

LPS

Placebo

Arm Description

Lipopolysaccharide (LPS) (0.8ng/kg of body weight; E. coli group O:113) administered as an intravenous bolus.

Placebo (same volume of 0.9% saline) administered as an intravenous bolus

Outcomes

Primary Outcome Measures

Inflammatory response
Serum interleukin 6 (IL-6) (pg/mL)
Neural response to interoceptive vs exteroceptive stimuli (interoceptive awareness task)
BOLD Signal Change in the Insula and Posterior Cingulate Cortex measured using MRI
Symptoms of anhedonia
Snaith-Hamilton Pleasure Scale Score

Secondary Outcome Measures

Full Information

First Posted
February 8, 2021
Last Updated
October 5, 2023
Sponsor
Laureate Institute for Brain Research, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT04751331
Brief Title
Neural Response to Inflammatory Challenge in Major Depressive Disorder
Official Title
Neural Response to Inflammatory Challenge in Major Depressive Disorder
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 15, 2021 (Actual)
Primary Completion Date
April 30, 2026 (Anticipated)
Study Completion Date
April 30, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Laureate Institute for Brain Research, Inc.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a parallel group, double-blinded, placebo-controlled study. Participants with MDD (n=90) and HC (n=90) will be randomly assigned (2:1) to receive either lipopolysaccharide (LPS) (0.8ng/kg of body weight) or placebo (same volume of 0.9% saline) administered as an intravenous bolus. This will yield the following groups: MDD-LPS (n=60), MDD-Placebo (n=30), HC-LPS (n=60), HC-placebo (n=30). There are three main aims: to identify immune pathways and neural circuits that respond differently to LPS in MDD vs. HC subjects; (2) to test whether the strength of inflammatory changes induced by LPS is associated with degree of change in anhedonic symptoms and neural circuits in the MDD group, and (3) to identify a biotype of MDD that shows a differential immunological and neurophysiological response to LPS. The main outcome variables are symptoms of anhedonia measured with the Snaith-Hamilton Pleasure Scale (SHAPS), cytokines (Il-6, IL-8, IL-10, and TNF), and BOLD signal change in the neural circuitry mediating interoceptive processing, i.e. the insula and cingulate cortex. The exploratory aim is to determine whether the acute inflammatory response to LPS can predict the clinical course of depression over a period of six months. The main outcome of this component of the study is self-reported depressive symptoms assessed with the QIDS-SR.
Detailed Description
This is a parallel group, double-blinded, placebo-controlled study. Participants with MDD (n=90) and HC (n=90) will be randomly assigned (2:1) to receive either lipopolysaccharide (LPS) (0.8ng/kg of body weight; E. coli group O:113) or placebo (same volume of 0.9% saline) administered as an intravenous bolus. This will yield the following groups: MDD-LPS (n=60), MDD-Placebo (n=30), HC-LPS (n=60), HC-placebo (n=30). Individuals who are eligible for the study will be randomly assigned through the use of a block randomization scheme to ensure the inclusion of equal numbers of HC and MDD participants in each group. MDD participants will complete up to 10 study visits (V1-V10) while the HCs will complete up to four visits (V1-V4). At visit 1 (V1), each subject will be consented and will complete the following: self-report and clinician-administered scales (including the Columbia Suicide Severity Rating Scale), a physical exam that includes an EKG and vital signs (temperature, pulse, blood pressure), safety labs (CBC, CMP, TSH, HbA1C, HIV, HCV, SARS CoV-2), a urine drug screen, an alcohol breathalyzer, and a baselineMRI session comprising the following scans: clinical, anatomical, visceral interoceptive attention (VIA) task, and resting state fMRI. Vital signs will be assessed in a supine position with a completely automated device. Blood pressure and heart-rate measurements will be preceded by at least five minutes of rest in a quiet setting without distractions. Blood will be drawn via venipuncture using sterile techniques by a trained phlebotomist or nurse. Subjects that pass the safety screen return two days later for the experimental session (V2). Prior to infusion of LPS or saline, the Columbia, EKG, urine drug screen, and breathalyzer are repeated, vital signs are taken, and baseline (T0) rating scales and blood draws are completed. A nurse will insert a catheter with a heparin lock into the non-dominant forearm for blood draws and a continuous saline flush, and one into the dominant forearm for LPS or saline administration. Prior to the LPS/saline infusion, participants will be hydrated with 500cc of saline. The LPS to be used in the study will be obtained from the NIH Clinical Center. Vital signs will be assessed every 30 min post infusion of LPS/saline for the first 2 hours (and thereafter every hour). Blood samples will be taken at baseline (T0), at T1, and then at T2 and T3 (~ peak response) and prior to discharge at T6. Participants also will complete hourly measures of sickness symptoms (e.g., fatigue, pain), anxiety, depression, and anhedonia. Symptoms will be recorded and graded according to FDA criteria. Two hours post-infusion at the approximate peak of the inflammatory response, the participants will complete the same MRI scans as at baseline. Subject to the judgment of a physician, the participants will be discharged 6 hours post injection so that the total experimental procedure will take ~8 hours to complete. Participants return the following day (V3) and one week later (V4) for mood ratings, blood draws, and identical MRI sessions. MDD participants will also be followed longitudinally for 6 months (phase 2), in the process completing remote or in-person psychological assessments at months 1 through 6 post LPS-infusion. Participants will be recruited from the Tulsa metropolitan area through internet, radio, print advertisements and will be evaluated at LIBR. We may also advertise the study to students on Tulsa-area campuses using flyers and potentially also recruitment tables on campus, and discussions with organizations, classes, and faculty where permission from the appropriate university officials is obtained. A total of 200 human participants (180 completers of phase I) will be involved in the proposed research. Half the participants will be males or females between the ages of 18 and 65 with MDD and current symptoms of depression (mild to severe) and half the participants will be HC with no personal history of psychiatric illness. A DSM-V diagnosis of MDD will be made with the MINI International Neuropsychiatric Interview and current symptoms of depression will be measured with the clinician-administered Montgomery Asberg Depression Rating Scale (MADRS), the self-report Patient Health Questionnaire (PHQ-9), and the Quick Inventory of Depressive Symptoms (QIDS-SR). Depressed participants will be required to be in good general health (as evaluated during the screening visit, including physical exam, safety labs and EKG) and to be 18-65 years of age. MDD participants will be required to have symptoms of depression, that is, a MADRS score of ≥7 or a PHQ-9 score ≥10. MDD participants are also required to be unmedicated for at least 4 weeks (8 weeks for fluoxetine) or currently receiving treatment with only one anti-depressant medication. HC participants will be required to be in good general health and to be 18-65 years of age. There are three main aims: to identify immune pathways and neural circuits that respond differently to LPS in MDD vs. HC subjects; (2) to test whether the strength of inflammatory changes induced by LPS is associated with degree of change in anhedonic symptoms and neural circuits in the MDD group, and (3) to identify a biotype of MDD that shows a differential immunological and neurophysiological response to LPS. The main outcome variables are symptoms of anhedonia measured with the Snaith-Hamilton Pleasure Scale (SHAPS), cytokines (Il-6, IL-8, IL-10, and TNF), and BOLD signal change in the neural circuitry mediating interoceptive processing, i.e. the insula and cingulate cortex. The exploratory aim is to determine whether the acute inflammatory response to LPS can predict the clinical course of depression over a period of six months. The main outcome of this component of the study is self-reported depressive symptoms assessed with the QIDS-SR.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Major Depressive Disorder

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
180 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
LPS
Arm Type
Experimental
Arm Description
Lipopolysaccharide (LPS) (0.8ng/kg of body weight; E. coli group O:113) administered as an intravenous bolus.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo (same volume of 0.9% saline) administered as an intravenous bolus
Intervention Type
Biological
Intervention Name(s)
LPS
Intervention Description
Lipopolysaccharide (LPS) (0.8ng/kg of body weight; E. coli group O:113)
Intervention Type
Biological
Intervention Name(s)
Saline
Intervention Description
0.9% saline administered as an intravenous bolus
Primary Outcome Measure Information:
Title
Inflammatory response
Description
Serum interleukin 6 (IL-6) (pg/mL)
Time Frame
Two hours post infusion
Title
Neural response to interoceptive vs exteroceptive stimuli (interoceptive awareness task)
Description
BOLD Signal Change in the Insula and Posterior Cingulate Cortex measured using MRI
Time Frame
Two hours post infusion
Title
Symptoms of anhedonia
Description
Snaith-Hamilton Pleasure Scale Score
Time Frame
Two hours post infusion

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Both healthy controls and depressed participants will be required to be in good general health (as evaluated during Visit 1, including EKG) and to be 18-65 years of age. A DSM-V diagnosis of MDD will be made with the MINI International Neuropsychiatric Interview and current symptoms of depression will be measured with the clinician-administered MADRS and the self-report PHQ-9. Depressed participants will be required to have symptoms of depression (i.e. a PHQ-9 score ≥10) and/or a MADRS score of ≥7. Exclusion Criteria: General Exclusion Criteria: Pregnancy A history of fainting during blood draws will be evaluated by the clinical team and may be deemed exclusionary. Medical Conditions: Moderate to severe traumatic brain injury (>30 min. loss of consciousness or >24 hours posttraumatic amnesia) or other neurocognitive disorder with evidence of neurological deficits. Presence of co-morbid medical conditions not limited to but including cardiovascular (e.g., history of acute coronary event, stroke) and neurological diseases (e.g., Parkinson's disease), as well as pain disorders. Presence of co-morbid inflammatory disorders such as rheumatoid arthritis or other autoimmune disorders. Presence of an uncontrolled medical condition that is deemed by the investigators to interfere with the proposed study procedures, or to put the study participant at undue risk. Presence of chronic infection that may elevate pro-inflammatory cytokines. Presence of an acute infectious illness or receipt of a vaccination in the two weeks prior to an experimental session. Psychiatric Disorders: Current severe suicidal ideation or attempt within the past 12 months. Psychosis Bipolar disorder Substance abuse or dependence within the previous 6 months Contraindications for MRI: Cardiac pacemaker, metal fragments in eyes/skin/body (shrapnel), aortic/aneurysm clips, prosthesis, by-pass surgery/coronary artery clips, hearing aid, heart valve replacement, shunt (ventricular or spinal), electrodes, metal plates/pins/screws/wires, or neuro/bio-stimulators (TENS unit), persons who have ever been a professional metal worker/welder, history of eye surgery/eyes washed out because of metal, vision problems uncorrectable with lenses, inability to lie still on one's back for 60 minutes; prior neurosurgery; tattoos or cosmetic makeup with metal dyes, unwillingness to remove body piercings, and pregnancy. Claustrophobia that is severe enough to preclude MRI scanning. Medications: Current and/or past regular use of hormone-containing medications (excluding contraceptives) Use of medications such as oral corticosteroids which may have immunosuppressive effects. Current use of non-steroid anti-inflammatory drugs that is deemed by the investigators to potentially confound the results of the study (e.g. > 3 days/week) Current and/or past regular use of immune modifying drugs that target specific immune responses such as TNF antagonists Current use of analgesics such as opioids or history of addiction to opioids or other analgesics Current and/or past regular use of cardiovascular medications, including antihypertensive, antiarrhythmic, anti-anginal, and anticoagulant drugs (does not apply where medications are taken for different purpose e.g. anti-hypertensives for migraine). Chronic use of antibiotics such as isotretinoin or minocycline because of their potential effects on the microbiome and immune function. Evidence of recreational drug use from urine test. Lifetime use of methamphetamine Inclusion of individuals reporting other types of medications or supplements not listed or considered thus far will be at the discretion of the PI based on their potential to affect immune function, the microbiome, brain function or brain blood flow. Health Factors: BMI > 35 because of the effects of obesity on pro-inflammatory cytokine activity Clinically significant abnormalities on screening laboratory tests Abnormal EKG In addition, participants who on arrival to the study, show any of the following symptoms will not be allowed to complete the study: screening supine systolic blood pressure >140 mmHg or <100 mmHg screening supine diastolic blood pressure >90 mmHg or <60 mmHg 12-lead EKG demonstrating a PR interval > 0.2 msec QTc >450 or QRS >120 msec (Bazett) If the QTc exceeds 450 msec, or QRS exceeds 120 msec, the EKG will be repeated 2 more times and the median value will be used pulse less than 50 beats/minute or greater than 100 beats/minute temperature greater than 99.5 degrees F. Non-English speaking participants: The majority of the assessments proposed for this study have not been translated from English, thus, non-English speaking volunteers will be excluded.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jonathan Savitz, PhD
Phone
918 502 5104
Email
jsavitz@laureateinstitute.org
Facility Information:
Facility Name
Laureate Institute for Brain Research
City
Tulsa
State/Province
Oklahoma
ZIP/Postal Code
74136
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jonathan Savitz, PhD
Phone
918-502-5104
Email
jsavitz@laureateinstitute.org

12. IPD Sharing Statement

Plan to Share IPD
No

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Neural Response to Inflammatory Challenge in Major Depressive Disorder

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