Oxytocin Suppresses Substance Use Disorders Associated With Chronic Stress
| Status: | Completed |
|---|---|
| Conditions: | Psychiatric, Psychiatric |
| Therapuetic Areas: | Psychiatry / Psychology |
| Healthy: | No |
| Age Range: | 21 - 65 |
| Updated: | 3/16/2019 |
| Start Date: | February 2014 |
| End Date: | April 2017 |
In comparison to the general population, military personnel and veterans are at increased
risk of developing both substance use disorders (SUDs) and post-traumatic stress disorder
(PTSD). Despite promising developments in the past decade, the treatment of patients with
SUDs and comorbid PTSD is woefully inadequate (Back, 2010; Back et al., 2014; Brady et al.,
2007; McCauley et al., 2012). One of the adverse effects of abused drugs is their long-term
negative impact on social behavior that is thought to involve oxytocin (OT) dysregulation
(McGregor et al., 2008). In preclinical and clinical experiments, local, intra-nasal, or
systemic OT administration decreases activation of the amygdala in response to visual
fearful/threatening stimuli (Kirsch et al., 2005), ameliorates the effects of stressful
events, and decreases drug-taking and seeking behavior (McGregor et al., 2008; Baskerville
and Douglas, 2010; Carson et al., 2010a; Bowen et al., 2011; Cox et al 2013). However, little
attention has been focused on whether OT decreases SUD vulnerability after exposure to
traumatic stress in preclinical or clinical studies. This clinical project will determine
whether intra-nasally administered OT will decrease craving (Aim 1) to use alcohol and
decrease stress reactivity (Aim 2) following exposure to laboratory-induced stress (Trier
Social Stress Task) among veterans with a dual diagnosis of alcohol use disorder and PTSD.
risk of developing both substance use disorders (SUDs) and post-traumatic stress disorder
(PTSD). Despite promising developments in the past decade, the treatment of patients with
SUDs and comorbid PTSD is woefully inadequate (Back, 2010; Back et al., 2014; Brady et al.,
2007; McCauley et al., 2012). One of the adverse effects of abused drugs is their long-term
negative impact on social behavior that is thought to involve oxytocin (OT) dysregulation
(McGregor et al., 2008). In preclinical and clinical experiments, local, intra-nasal, or
systemic OT administration decreases activation of the amygdala in response to visual
fearful/threatening stimuli (Kirsch et al., 2005), ameliorates the effects of stressful
events, and decreases drug-taking and seeking behavior (McGregor et al., 2008; Baskerville
and Douglas, 2010; Carson et al., 2010a; Bowen et al., 2011; Cox et al 2013). However, little
attention has been focused on whether OT decreases SUD vulnerability after exposure to
traumatic stress in preclinical or clinical studies. This clinical project will determine
whether intra-nasally administered OT will decrease craving (Aim 1) to use alcohol and
decrease stress reactivity (Aim 2) following exposure to laboratory-induced stress (Trier
Social Stress Task) among veterans with a dual diagnosis of alcohol use disorder and PTSD.
Inclusion Criteria:
- Male or female; any race or ethnicity; age 21-65 years.
- Female subjects will be required to complete the laboratory testing during the early
to mid-follicular phase of their menstrual cycle (days 1-7 following the onset of
menses).
- Veteran of the US military; any service branch.
- Able to provide informed consent and function at an intellectual level sufficient to
allow accurate completion of the assessment instruments.
- Subjects must be able to comprehend English.
- Meet DSM-5 criteria for a current alcohol use disorder (assessed via the Mini
International Neuropsychiatric Interview; MINI). Note that we will use the currently
available diagnostic measure (MINI for DSM-IV) and will make appropriate modifications
to update for compatibility with DSM-5.
- Meet DSM-5 criteria for current PTSD (assessed via the Clinician Administered PTSD
Scale; CAPS). Note that we will use the currently available assessment instrument
(CAPS for DSM-IV), and will make appropriate modifications to update for compatibility
with DSM-5.
- A CAPS score of 50 or greater.
- Subjects will be required to have at least 5 days of abstinence from alcohol or other
substances (except caffeine or nicotine) prior to completing the laboratory testing,
as verified by multiple methods including self-report, breathalyzer tests, and urine
drug screen tests.
- Subjects may also meet criteria for a mood disorder (except bipolar affective
disorder, see Exclusion Criteria) or anxiety disorders (e.g., agoraphobia, social
phobia, generalized anxiety disorder). The inclusion of subjects with affective and
anxiety disorders is essential because of the marked frequency of the co-existence of
mood and other anxiety disorders among patients with PTSD and alcohol use disorders.
- Subjects taking psychotropic medications will be required to be maintained on a stable
dose for at least eight weeks before study initiation. This is because initiation or
change of psychotropic medications during the course of the trial may interfere with
interpretation of results.
- Must consent to random assignment to oxytocin or placebo.
Exclusion Criteria:
- Subjects meeting DSM-5 criteria for a history of or current psychotic or bipolar
affective disorders, or with current suicidal or homicidal ideation and intent. Those
subjects will be referred clinically.
- Subjects who would present a serious suicide risk or who are likely to require
hospitalization during the course of the study. Those subjects will be referred
clinically.
- Subjects on maintenance anxiolytic, antidepressant, or mood stabilizing medications,
which have been initiated during the past 8 weeks.
- Subjects with a history of a major medical illness (e.g., endocrine, cardiovascular,
central nervous system disorders, peripheral neuropathy, or pulmonary disease) or
other acute or unstable medical condition that might interfere with safe conduct of
the study or accurate interpretation of the results.
- Subjects meeting DSM-5 criteria for another substance use disorder, except caffeine or
nicotine, within the past 12 months.
- Subjects experiencing withdrawal symptoms, as evidence by a score of 10 or above on
the Clinical Institute Withdrawal Assessment of Alcohol (CIWA)
- Females who are unable or unwilling to be scheduled for lab testing during the early
to mid-follicular phase of their menstrual cycle.
- Pregnant women will be excluded from the proposed study.
We found this trial at
1
site
171 Ashley Avenue
Charleston, South Carolina 29425
Charleston, South Carolina 29425
843-792-1414
Phone: 843-792-9383
Medical University of South Carolina The Medical University of South Carolina (MUSC) has grown from...
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