Ketamine Treatment Effects on Synaptic Plasticity in Depression

Phase

Condition

Depression

Mood Disorders

Depression (Adult And Geriatric)

Treatment

Ketamine

Clinical Study ID

NCT04091971

7847

Ages 18-55
All Genders

Study Summary

Depression is the leading cause of disability globally (1, 2). One-third to one-half of patients suffering from major depressive disorder (MDD) do not achieve remission even after multiple antidepressant trials (3). Ketamine is a commonly-used FDA-approved anesthetic medication that at subanesthetic doses leads to rapid antidepressant and anti-suicidal ideation effects in hours, rather than weeks, following administration. Despite these promising findings, a key limitation of ketamine treatment is that it only yields an antidepressant response in approximately 50% of those treated. The goal of this project is to A) elucidate ketamine's mechanism of action and B) identify biomarkers predicting treatment outcome to ketamine which could be used to match patients to treatment based on the likelihood of effectiveness at the individual level. Data from animal models suggests that ketamine acts by enhancing the connections between neurons through a process known as synaptic plasticity (4-7), and that these biological changes are responsible for the sustained behavioral effects of ketamine (8). A newly available tool allows us to image the density of these synaptic connections in the living brain using PET (positron emission tomography) imaging with a radiotracer called [11C]UCB-J, which is a marker of synaptic density. We propose to directly quantify synaptic density in depressed patients before and after a course of ketamine, to examine changes in density following treatment. In exploratory analyses, we will examine synaptic density as a mediator of the sustained antidepressant effects of ketamine and as a predictor of treatment outcome. To study these questions, we will quantify synaptic density using PET imaging before and after a course of 4 sequential intravenous infusions of ketamine administered over a two week period. Study participation involves an inpatient stay of approximately three weeks at the New York State Psychiatric Institute at no cost.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Unipolar, major depressive episode (MDE), with 17-item Hamilton Depression RatingScale score ≥16. Patients may be psychiatric medication- free, or if currently takingpsychiatric medication, not responding adequately as evidenced by current MDE.
18-55 years old
Female patients of child-bearing potential must be willing to use an acceptable formof birth control during study participation such as condoms, diaphragm, oralcontraceptive pills.
Must be enrolled in division's umbrella research protocol
Able to provide informed consent
Agrees to voluntary admission to an inpatient research unit at The New York StatePsychiatric Institute (NYSPI) for baseline PET imaging and Magnetic Resonance Imaging (MRI), ketamine infusion, and repeat PET imaging

Exclusion

Exclusion Criteria:

Unstable medical or neurological illness including: A) baseline hypertension (BP>140/90); B) significant history of cardiovascular illness; C) Platelet count < 80,000 cells/uL; and D) Hemoglobin < 11 g/dL for females and < 12 g/dL for males
Significant electrocardiogram (ECG) abnormality (e.g., Ventricular tachycardia,evidence of myocardial ischemia, symptomatic bradycardia, unstable tachycardia, seconddegree (or greater) atrioventricular (AV) block).
Pregnancy, currently lactating, or planning to conceive during the course of studyparticipation.
Diagnosis of bipolar disorder or current psychotic symptoms.
Current or past ketamine use disorder (lifetime); any drug or alcohol use disorderwithin past 6 months
Inadequate understanding of English.
Prior ineffective trial of or adverse reaction to ketamine.
A neurological disease or prior head trauma with evidence of cognitive impairment. Subjects who endorse a history of prior head trauma and score ≥ 1.5 standard deviationsbelow the mean on the Trailmaking A&B will be excluded from study participation.
Metal implants or paramagnetic objects contained within the body (including heartpacemaker, shrapnel, or surgical prostheses) which may present a risk to the subject orinterfere with the MRI scan, according to the guidelines set forth in the followingreference book commonly used by neuroradiologists: "Guide to MR procedures and metallicobjects," F.G. Shellock, Lippincott Williams and Wilkins NY 2001. Additionally transdermalpatches will be removed during the MR study at the discretion of the investigator.
Current, past, or anticipated exposure to radiation, that may include: **
being badged for radiation exposure in the workplace
participation in nuclear medicine research protocols in the last year
Claustrophobia significant enough to interfere with MRI scanning
Weight that exceeds 325 lbs or inability to fit into MRI scanner
Individuals taking prescribed opioid medication, using opioids recreationally, ortaking naltrexone at the time of enrollment 14. Daily use of: benzodiazepine, zolpidem (Ambien), zaleplon (Sonata), or eszopiclone (Lunesta) for ≥2 weeks at time of consent

Study Design

Ketamine

October 09, 2020

May 01, 2022

Study Description

Depression is the leading cause of disability globally (1, 2). One-third to one-half of patients suffering from major depressive disorder (MDD) do not achieve remission even after multiple antidepressant trials (3). Ketamine is a commonly-used FDA-approved anesthetic and non-competitive N-methyl-D-aspartate (NMDA) glutamate receptor antagonist. Recent randomized trials demonstrate that subanesthetic doses of ketamine lead to rapid antidepressant and antisuicidal ideation effects in individuals with MDD and bipolar depression (reviewed in (9)). In contrast to current FDA-approved antidepressants, ketamine exerts antidepressant effects in hours, rather than weeks, following administration. Despite these promising findings, a key limitation of ketamine treatment is that it only yields an antidepressant response in approximately 50% of those treated. In addition, ketamine's clinical utility is limited by its acute dissociative side effects, a one to two-week duration of action as monotherapy, its addictive potential, and long term safety concerns related to cognition and interstitial cystitis (9-11). Given the profound benefit of ketamine for some individuals yet these key limitations, developing a precision medicine research strategy for ketamine's antidepressant effects could be of tremendous scientific and clinical benefit, in order to A) elucidate ketamine's mechanism of action, to advance the development of safer alternative agents and B) identify biomarkers predicting treatment outcome to ketamine, which could be used to match patients to treatment based on the likelihood of effectiveness at the individual level.

There is evidence of brain atrophy in depression: gray matter volume is reduced in the prefrontal cortex (PFC) and in the hippocampus (HC) in depressed individuals (12). Postmortem studies in depression show low expression of several genes related to synaptic function and decreased synapse number in the dorsolateral PFC (13). Chronic stress, a risk factor for depression, precipitates neuronal atrophy and dendritic spine loss in HC and PFC (14, 15). Preclinical work in rodents suggests that ketamine may exert antidepressant effects by reversing neuronal atrophy, specifically through the formation of new dendritic spine synapses in the brain. In rodents, ketamine induces rapid synaptogenesis via stimulation of mechanistic target of rapamycin (mTOR) and brain-derived neurotrophic factor (BDNF), leading to a reversal of chronic, stress-induced neuronal atrophy (4-7).

A recently developed research tool enables examination of synaptic density in vivo in humans. [11C]UCB-J is a PET radiotracer that is specific for synaptic vesicle glycoprotein 2A (SV2A) (16, 17), providing a quantitative measure of synaptic density in vivo in the brain in humans. A recent PET imaging pilot study identified low [11C]UCB-J binding in the PFC of individuals with current MDD as compared to healthy volunteers, providing early evidence that this synaptic density biomarker may quantify a disease-relevant process in depression (18). Furthermore, PET imaging with [11C]UCB-J displays outstanding test-retest reliability, with absolute test-retest variability of only 4-5% in brain regions of interest in this study (19), making it an outstanding tool for longitudinal studies of the effects of treatment interventions. We therefore propose to directly quantify synaptic density in depressed patients to investigate whether it is increased by treatment with ketamine in a regionally-specific manner. Moreover, we will examine synaptic density as a mediator of the sustained antidepressant effects of ketamine and as a predictor of treatment outcome. We will quantify synaptic density using PET imaging before and after a course of 4 sequential intravenous infusions of ketamine administered over a two-week period. Study participation involves an inpatient stay of approximately three weeks at the New York State Psychiatric Institute at no cost.

Connect with a study center

New York State Psychiatric Institute/Columbia University
New York, New York 10032
United States
Site Not Available

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