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Cholinergic Modulation of Condition and Emotion in Mood Disorders: Functional Neuroimaging Studies

Primary Purpose

Mood Disorders, Healthy, Unipolar Depression

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Scopolamine Nasal Spray
Sponsored by
National Institute of Mental Health (NIMH)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Mood Disorders focused on measuring Scopolamine, Depression, fMRI, Cognition, Emotion, Brain, Bipolar Disorder, Major Depressive Disorder, MDD, Healthy Volunteer, HV

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesAccepts Healthy Volunteers

INCLUSION CRITERIA: Patients with Major Depressive Disorder (MDD): Age 18-55 Current diagnosis of MDD, as defined by DSM-IV criteria for recurrent MDD Current depressive episode Current IDS score in the moderately-to-severely depressed range Right handed Able to provide informed consent Patients with Bipolar Disorder (BD): Age 18-55 Current diagnosis of bipolar disorder, as defined by DSM-IV Current depressive episode Current IDS score in the moderately-to-severely depressed range Right handed Able to provide informed consent Healthy Controls: Age 18-55 Able to provide informed consent Medically healthy EXCLUSION CRITERIA: Patients MDD & BD: Serious suicidal ideation or behavior (with a current plan or intent), or current delusions or hallucinations Medical or neurological illnesses likely to affect physiology or anatomy History of drug or alcohol abuse within 1 year or a lifetime history of alcohol or drug dependence (DSM IV criteria) Current or past history of other axis I disorders that preceded the onset of MDD or BD Current pregnancy (documented by pregnancy testing within 24 hours prior to pilot studies and 24 hours prior to scanning) Current breast feeding General MRI exclusion criteria (including the presence of pacemakers, cochlear implants, surgical clips or metal fragments in their eyes or body parts) Vision and/or hearing problems severe enough to interfere with testing Electrocardiographic evidence of ischemia, arrhythmia, conduction defect, or myocardial infarction Current blood pressure of >140 mm Hg or < 90 mm Hg systolic, or > 90 mm Hg diastolic (due to the potential cardiovascular effects of scopolamine and physostigmine) Clinically significant cerebrovascular or cardiovascular disease, hypertension, congestive heart disease, angina pectoris, advanced arteriosclerosis, gross neurological impairment, hyperthyroidism, known hypersensitivity or idiosyncrasy to anticholinergic agents, glaucoma, renal or hepatic impairment Clinical history of glaucoma or narrow angle glaucoma (due to the possibility of exacerbation of this condition by scopolamine) Age of onset greater than 45 years (to reduce the biological heterogeneity encompassed by the MDD and BD criteria, since subjects with a late age-at onset for depression have a far greater likelihood of having MRI correlates of cerebrovascular disease than age-matched, healthy controls or age-matched, early-onset depressives) Exposure within two weeks to medications likely to effect cerebral blood flow and metabolism or likely to interact with anti-cholinergic medications (e.g. narcotics or anti-cholinergic agents)- as verified by history and urine drug screen HIV positive status Weight over 275 pounds Healthy Controls: Medical or neurological illness Current pregnancy (documented by pregnancy testing within 24 hours prior to pilot studies and 24 hours prior to scanning) Current breast feeding General MRI exclusion criteria (including the presence of pacemakers, cochlear implants, surgical clips or metal fragments in their eyes or body parts) Vision and/or hearing problems severe enough to interfere with testing Electrocardiographic evidence of ischemia, arrhythmia, conduction defect, or myocardial infarction Current blood pressure of >140 mm Hg or < 90 mm Hg systolic, or > 90 mm Hg diastolic (due to the potential cardiovascular effects of scopolamine and physostigmine) Clinically significant cerebrovascular or cardiovascular disease, hypertension, congestive heart disease, angina pectoris, advanced arteriosclerosis, gross neurological impairment, hyperthyroidism, known hypersensitivity or idiosyncrasy to anticholinergic agents, glaucoma, renal or hepatic impairment Clinical history of glaucoma or narrow angle glaucoma (due to the possibility of exacerbation of this condition by scopolamine) HIV positive status Weight over 275 pounds For BD patients being recruited for the scopolamine efficacy trial, they may forgo imaging and thus will not be excluded for imaging related exclusion criteria (including general MRI exclusion criteria and vision and/or hearing problems).

Sites / Locations

  • National Institutes of Health Clinical Center, 9000 Rockville Pike

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

Depressed Patients with Major Depression DIsorder

Depressed Patients with Bipolar Disorder

Healthy Control

Arm Description

Outcomes

Primary Outcome Measures

Evaluation of the antidepressant effects of the antimuscarinic agent scopolamine

Secondary Outcome Measures

Full Information

First Posted
March 6, 2003
Last Updated
March 17, 2021
Sponsor
National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT00055575
Brief Title
Cholinergic Modulation of Condition and Emotion in Mood Disorders: Functional Neuroimaging Studies
Official Title
Cholinergic Modulation of Cognition and Emotion in Mood Disorders: Functional Neuroimaging Studies
Study Type
Interventional

2. Study Status

Record Verification Date
February 2, 2015
Overall Recruitment Status
Terminated
Study Start Date
February 27, 2003 (undefined)
Primary Completion Date
February 2, 2015 (Actual)
Study Completion Date
February 2, 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Institute of Mental Health (NIMH)

4. Oversight

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

5. Study Description

Brief Summary
This study looks at the role of a specific brain chemical system in the mood and attention symptoms seen in major depression and bipolar disorders using functional brain imaging.
Detailed Description
Objective The goal of this research project is to evaluate the role of the cholinergic system in behavioral and cognitive symptoms observed in mood disorders in humans, using functional brain neuroimaging techniques. Specific aspects of behavior and cognition are impaired in mood disorders, including selective attention, set-shifting and memory; and there is also evidence that depressed subjects exhibit a mood congruent processing bias whereby they more readily process negatively toned information as compared to positively toned information. This cognitive pattern lends itself to evaluation with functional brain imaging, both in terms of identifying the anatomical correlates of the specific behavioral and cognitive deficits as well as characterizing the effects of pharmacological manipulation. Attention and memory functions are closely tied to the cholinergic neurotransmitter system. The cholinergic system is one of the neurotransmitter systems implicated in the pathophysiology of mood disorders. Evidence suggests that during major depressive episodes, the cholinergic system is hypersensitive to acetylcholine. Agents that enhance muscarinic cholinergic receptor function increase depressive symptoms in depressed subjects, and can produce symptoms of depression in healthy subjects. The preclinical literature more specifically implicates the muscarinic receptors and indicates that the use of muscarinic antagonists, in the context of animal models of depression, results in improvement in the behavioral analogs of depression. Study Population The accrual ceiling for this protocol is 388 participants. 143 currently depressed patients with major depressive disorder, 100 currently depressed patients with bipolar disorder, and 145 healthy controls will participate in this study. Design The antimuscarinic agent, scopolamine, will be administered in a double-blind, placebo controlled manner across all studies. Clinical ratings, cognitive tasks and neuroimaging will be conducted at various timepoints to evaluate the clinical effects of scopolamine on depression, to assess the acute mood response to scopolamine; and to study the neurobiological correlates of the clinical and behavioral drug effects. Outcome Measures The proposed inpatient or outpatient project investigates the role of cholinergic neurotransmission in the behavioral and cognitive symptoms observed in the depressed phase of both major depressive disorder (MDD) and bipolar disorder (BD). The studies proposed here will identify anatomical correlates of the mood congruent processing bias, working memory, attention and set-shifting deficits observed in depressed subjects. Further, these studies will evaluate the effects of the cholinergic antagonist, scopolamine, both on the performance deficits and on neural activity in brain regions recruited as subjects perform these tasks. Dose escalation studies will be conducted to determine if higher doses of scopolamine will increase the antidepressant response rate in patients with major depressive disorder. Based on earlier work showing the predictive value in baseline neuroimaging data to predict treatment outcome, we will stratify participants at baseline into groups based on expected response to scopolamine treatment. This approach is expected to reveal how neuromodulators influence processing in brain structures recruited to perform these tasks, both in healthy subjects and in major depressive disorders. The combined use of functional brain imaging and pharmacological manipulation to evaluate the role of neurotransmitter dysfunction in depression may direct us to potential therapeutic approaches.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mood Disorders, Healthy, Unipolar Depression, Bipolar Depression
Keywords
Scopolamine, Depression, fMRI, Cognition, Emotion, Brain, Bipolar Disorder, Major Depressive Disorder, MDD, Healthy Volunteer, HV

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Sequential Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Non-Randomized
Enrollment
197 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Depressed Patients with Major Depression DIsorder
Arm Type
Experimental
Arm Title
Depressed Patients with Bipolar Disorder
Arm Type
Experimental
Arm Title
Healthy Control
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
Scopolamine Nasal Spray
Primary Outcome Measure Information:
Title
Evaluation of the antidepressant effects of the antimuscarinic agent scopolamine
Time Frame
5 to 10 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
INCLUSION CRITERIA: Patients with Major Depressive Disorder (MDD): Age 18-55 Current diagnosis of MDD, as defined by DSM-IV criteria for recurrent MDD Current depressive episode Current IDS score in the moderately-to-severely depressed range Right handed Able to provide informed consent Patients with Bipolar Disorder (BD): Age 18-55 Current diagnosis of bipolar disorder, as defined by DSM-IV Current depressive episode Current IDS score in the moderately-to-severely depressed range Right handed Able to provide informed consent Healthy Controls: Age 18-55 Able to provide informed consent Medically healthy EXCLUSION CRITERIA: Patients MDD & BD: Serious suicidal ideation or behavior (with a current plan or intent), or current delusions or hallucinations Medical or neurological illnesses likely to affect physiology or anatomy History of drug or alcohol abuse within 1 year or a lifetime history of alcohol or drug dependence (DSM IV criteria) Current or past history of other axis I disorders that preceded the onset of MDD or BD Current pregnancy (documented by pregnancy testing within 24 hours prior to pilot studies and 24 hours prior to scanning) Current breast feeding General MRI exclusion criteria (including the presence of pacemakers, cochlear implants, surgical clips or metal fragments in their eyes or body parts) Vision and/or hearing problems severe enough to interfere with testing Electrocardiographic evidence of ischemia, arrhythmia, conduction defect, or myocardial infarction Current blood pressure of >140 mm Hg or < 90 mm Hg systolic, or > 90 mm Hg diastolic (due to the potential cardiovascular effects of scopolamine and physostigmine) Clinically significant cerebrovascular or cardiovascular disease, hypertension, congestive heart disease, angina pectoris, advanced arteriosclerosis, gross neurological impairment, hyperthyroidism, known hypersensitivity or idiosyncrasy to anticholinergic agents, glaucoma, renal or hepatic impairment Clinical history of glaucoma or narrow angle glaucoma (due to the possibility of exacerbation of this condition by scopolamine) Age of onset greater than 45 years (to reduce the biological heterogeneity encompassed by the MDD and BD criteria, since subjects with a late age-at onset for depression have a far greater likelihood of having MRI correlates of cerebrovascular disease than age-matched, healthy controls or age-matched, early-onset depressives) Exposure within two weeks to medications likely to effect cerebral blood flow and metabolism or likely to interact with anti-cholinergic medications (e.g. narcotics or anti-cholinergic agents)- as verified by history and urine drug screen HIV positive status Weight over 275 pounds Healthy Controls: Medical or neurological illness Current pregnancy (documented by pregnancy testing within 24 hours prior to pilot studies and 24 hours prior to scanning) Current breast feeding General MRI exclusion criteria (including the presence of pacemakers, cochlear implants, surgical clips or metal fragments in their eyes or body parts) Vision and/or hearing problems severe enough to interfere with testing Electrocardiographic evidence of ischemia, arrhythmia, conduction defect, or myocardial infarction Current blood pressure of >140 mm Hg or < 90 mm Hg systolic, or > 90 mm Hg diastolic (due to the potential cardiovascular effects of scopolamine and physostigmine) Clinically significant cerebrovascular or cardiovascular disease, hypertension, congestive heart disease, angina pectoris, advanced arteriosclerosis, gross neurological impairment, hyperthyroidism, known hypersensitivity or idiosyncrasy to anticholinergic agents, glaucoma, renal or hepatic impairment Clinical history of glaucoma or narrow angle glaucoma (due to the possibility of exacerbation of this condition by scopolamine) HIV positive status Weight over 275 pounds For BD patients being recruited for the scopolamine efficacy trial, they may forgo imaging and thus will not be excluded for imaging related exclusion criteria (including general MRI exclusion criteria and vision and/or hearing problems).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carlos A Zarate, M.D.
Organizational Affiliation
National Institute of Mental Health (NIMH)
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Institutes of Health Clinical Center, 9000 Rockville Pike
City
Bethesda
State/Province
Maryland
ZIP/Postal Code
20892
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
10852235
Citation
Elliott R, Rubinsztein JS, Sahakian BJ, Dolan RJ. Selective attention to emotional stimuli in a verbal go/no-go task: an fMRI study. Neuroreport. 2000 Jun 5;11(8):1739-44. doi: 10.1097/00001756-200006050-00028.
Results Reference
background
PubMed Identifier
10616937
Citation
Murphy FC, Sahakian BJ, Rubinsztein JS, Michael A, Rogers RD, Robbins TW, Paykel ES. Emotional bias and inhibitory control processes in mania and depression. Psychol Med. 1999 Nov;29(6):1307-21. doi: 10.1017/s0033291799001233.
Results Reference
background
PubMed Identifier
10645378
Citation
Murray LA, Whitehouse WG, Alloy LB. Mood congruence and depressive deficits in memory: a forced-recall analysis. Memory. 1999 Mar;7(2):175-96. doi: 10.1080/741944068.
Results Reference
background
PubMed Identifier
23364679
Citation
Furey ML, Drevets WC, Hoffman EM, Frankel E, Speer AM, Zarate CA Jr. Potential of pretreatment neural activity in the visual cortex during emotional processing to predict treatment response to scopolamine in major depressive disorder. JAMA Psychiatry. 2013 Mar;70(3):280-90. doi: 10.1001/2013.jamapsychiatry.60.
Results Reference
derived

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Cholinergic Modulation of Condition and Emotion in Mood Disorders: Functional Neuroimaging Studies

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