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MicroRNA Correlates of Childhood Maltreatment and Suicidality

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04923685
Recruitment Status : Recruiting
First Posted : June 11, 2021
Last Update Posted : April 7, 2023
Sponsor:
Collaborator:
National Institute of Mental Health (NIMH)
Information provided by (Responsible Party):
Yogesh Dwivedi, PhD, University of Alabama at Birmingham

Brief Summary:
This is a research study to find out if childhood trauma and stress are associated with depression or suicidal risk. The study will assess the effects of both short-term and long-term stress on biomarker (e.g. miRNA [MiRNA]) levels. miRNAs are a type of RNA (genetic material that is translated into protein) that are found in throughout the body and blood. They are called microRNA because their size is much smaller than typical RNA molecules. miRNAs are highly responsive to environment. This responsiveness is reflected in their expression in individuals who are affected by environment such as stress. The investigators are gathering genetic material, including DNA and RNA, from each participant. The RNA will be taken from the small vesicles and cells in the participant's blood and analyzed. The vesicles are small objects that occur normally in the blood and that contain RNA. This information may help us to understand the cause of mental illness and to improve medical and psychiatric care in the future. There will be 450 participants enrolled in this study.

Condition or disease Intervention/treatment
Major Depressive Disorder Suicidal Ideation Other: Trier Social Stress Test

Detailed Description:
The purpose of the study is to determine if the relationship between a history of childhood maltreatment (CM) and suicide risk is associated with alterations in the expression and epigenetic modification of specific microRNAs (miRNAs), thereby providing a molecular signature of suicide risk in people with CM. miRNAs are short regulatory RNAs that transduce environmental events into changes in protein synthesis in cells. The environment can induce permanent changes in miRNA expression. Aim 1 is to identify a set of neural-derived exosomal miRNAs that are associated with the interaction of suicidality and CM. Aim 2 is to examine whether an acute experimental stressor, the Trier Social Stress Test (TSST), impacts the expression of these miRNAs in suicidal patients with and without CM. Aim 3 will examine potential mechanisms by which altered miRNAs may contribute to CM-associated suicidal behavior. Aim 4 will examine if changes in CM-associated miRNAs are explained by modifications in their DNA methylation.

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Study Type : Observational
Estimated Enrollment : 450 participants
Observational Model: Cohort
Time Perspective: Other
Official Title: MicroRNA Correlates of Childhood Maltreatment and Suicidality
Actual Study Start Date : February 26, 2021
Estimated Primary Completion Date : September 2025
Estimated Study Completion Date : September 2025

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Suicide

Group/Cohort Intervention/treatment
MDD with elevated CM and suicidality scores
Major Depressive Disorder with elevator childhood maltreatment and suicidality scores.
Other: Trier Social Stress Test
The TSST is a standardized test to induce acute psychological stress in humans. Participants will abstain from caffeine for 12 hours and nicotine for 2 hours prior to the test. An IV butterfly catheter will be placed in an arm vein and flushed with saline. Participants will rest for 15 minutes. A 10ml baseline blood sample will be drawn. They will perform the TSST task and then have 10ml of blood drawn at 0, 15, 30, 60, and 90 minutes post-TSST.
Other Name: TSST

MDD with CM history but lower suicidality
Major Depressive disorder with childhood maltreatment history but lower suicidality scores.
Other: Trier Social Stress Test
The TSST is a standardized test to induce acute psychological stress in humans. Participants will abstain from caffeine for 12 hours and nicotine for 2 hours prior to the test. An IV butterfly catheter will be placed in an arm vein and flushed with saline. Participants will rest for 15 minutes. A 10ml baseline blood sample will be drawn. They will perform the TSST task and then have 10ml of blood drawn at 0, 15, 30, 60, and 90 minutes post-TSST.
Other Name: TSST

MDD without CM but with elevated suicidality
Major Depressive Disorder without childhood maltreatment, but with elevated suicidality scores.
Other: Trier Social Stress Test
The TSST is a standardized test to induce acute psychological stress in humans. Participants will abstain from caffeine for 12 hours and nicotine for 2 hours prior to the test. An IV butterfly catheter will be placed in an arm vein and flushed with saline. Participants will rest for 15 minutes. A 10ml baseline blood sample will be drawn. They will perform the TSST task and then have 10ml of blood drawn at 0, 15, 30, 60, and 90 minutes post-TSST.
Other Name: TSST

MDD without CM but with lower suicidality
Major Depressive Disorder without childhood maltreatment but with lower suicidality scores.
Other: Trier Social Stress Test
The TSST is a standardized test to induce acute psychological stress in humans. Participants will abstain from caffeine for 12 hours and nicotine for 2 hours prior to the test. An IV butterfly catheter will be placed in an arm vein and flushed with saline. Participants will rest for 15 minutes. A 10ml baseline blood sample will be drawn. They will perform the TSST task and then have 10ml of blood drawn at 0, 15, 30, 60, and 90 minutes post-TSST.
Other Name: TSST

Healthy controls with CM history
Healthy controls with childhood maltreatment history,
Other: Trier Social Stress Test
The TSST is a standardized test to induce acute psychological stress in humans. Participants will abstain from caffeine for 12 hours and nicotine for 2 hours prior to the test. An IV butterfly catheter will be placed in an arm vein and flushed with saline. Participants will rest for 15 minutes. A 10ml baseline blood sample will be drawn. They will perform the TSST task and then have 10ml of blood drawn at 0, 15, 30, 60, and 90 minutes post-TSST.
Other Name: TSST

Healthy controls without CM history
Healthy controls without childhood maltreatment history.
Other: Trier Social Stress Test
The TSST is a standardized test to induce acute psychological stress in humans. Participants will abstain from caffeine for 12 hours and nicotine for 2 hours prior to the test. An IV butterfly catheter will be placed in an arm vein and flushed with saline. Participants will rest for 15 minutes. A 10ml baseline blood sample will be drawn. They will perform the TSST task and then have 10ml of blood drawn at 0, 15, 30, 60, and 90 minutes post-TSST.
Other Name: TSST




Primary Outcome Measures :
  1. MicroRNA response to stress [ Time Frame: 24 hours ]
    MiRNAs methylation levels will be examined


Biospecimen Retention:   Samples With DNA
Blood and urine collection


Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   18 Years to 60 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
People between the ages of 18 and 60 with either a history of Major Depressive Disorder or no lifetime history of any major mental illness.
Criteria

Inclusion Criteria:

  1. Age 18-60
  2. Physically healthy
  3. Willing and able to provide informed consent

5. Diagnosis of MDD or No history of mental illness

Exclusion Criteria:

  1. Pregnancy or lactation (women of reproductive potential must have a negative urine pregnancy screen)
  2. Post-partum state (being within 2 months of delivery or miscarriage)
  3. Homicide risk as determined by clinical interview
  4. A lifetime history of psychotic disorder
  5. Any history of dissociation or dissociative disorder
  6. Bipolar disorder
  7. Pervasive developmental disorder
  8. Cognitive disorder
  9. Cluster A personality disorder
  10. Borderline personality disorder
  11. Anorexia nervosa
  12. Alcohol or drug dependence (except nicotine and caffeine) within the last month or the use of any hallucinogen (except cannabis), including phencyclidine in the last month (NOTE that a positive UDS is not exclusionary except for hallucinogens, methamphetamine, or cocaine. People presenting intoxicated with alcohol may be included when a Breathalyzer test (Alco-Sensor IV) is negative as long as there is no history of recent dependence.
  13. Recent myocardial infarction
  14. Unstable angina
  15. Active neoplasm in the past 6 months
  16. Immunosuppressive or corticosteroid therapy within the last month, with the following exceptions: any inhaled, intranasal, topical or vaginal corticosteroids are allowed.
  17. Chemotherapy
  18. Head injury with loss of consciousness in the past 6 months

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04923685


Contacts
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Contact: Allison Stewart, BA 256-551-4428 allisonstewart@uabmc.edu
Contact: Richard C Shelton, MD 256-551-6630 rcshelton@uabmc.edu

Locations
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United States, Alabama
University of Alabama at Birmingham Recruiting
Birmingham, Alabama, United States, 35233
Contact: Melissa Alexander    205-934-2484    lalexander@uabmc.edu   
UAB Huntsville Regional Medical Campus Recruiting
Huntsville, Alabama, United States, 35294
Contact: Allison M Stewart, BA    256-551-4431    allisonstewart@uabmc.edu   
Contact: Jessica Weed, BA    256-551-4687    jcweed@uabmc.edu   
Principal Investigator: Yogesh Dwivedi, PhD         
Principal Investigator: Richard C Shelton, MD         
Sponsors and Collaborators
University of Alabama at Birmingham
National Institute of Mental Health (NIMH)
Investigators
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Principal Investigator: Yogesh Dwivedi, PhD University of Alabama at Birmingham
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Responsible Party: Yogesh Dwivedi, PhD, Professor, University of Alabama at Birmingham
ClinicalTrials.gov Identifier: NCT04923685    
Other Study ID Numbers: IRB-300006024
First Posted: June 11, 2021    Key Record Dates
Last Update Posted: April 7, 2023
Last Verified: April 2023

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Yogesh Dwivedi, PhD, University of Alabama at Birmingham:
Depression
Suicidal Ideation
Suicidality
Healthy Control
Depression and Anxiety
Childhood Maltreatment
Additional relevant MeSH terms:
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Depressive Disorder
Depressive Disorder, Major
Suicidal Ideation
Mood Disorders
Mental Disorders
Behavioral Symptoms
Suicide
Self-Injurious Behavior