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Clinical Trials/NCT03336918
NCT03336918
Active, not recruiting
Not Applicable

Lithium Effects on the Brain's Functional and Structural Connectome in the Treatment of Bipolar Disorder

Brigham and Women's Hospital1 site in 1 country120 target enrollmentDecember 7, 2017

Overview

Phase
Not Applicable
Intervention
Lithium
Conditions
Bipolar Disorder
Sponsor
Brigham and Women's Hospital
Enrollment
120
Locations
1
Primary Endpoint
Functional Connectivity (Fc) changes
Status
Active, not recruiting
Last Updated
2 months ago

Overview

Brief Summary

Lithium is highly effective in the treatment of bipolar disorder. This study aims to investigate, for the first time, the impact of lithium monotherapy on the structural and functional connectivity of the brain using MRI imaging.

Detailed Description

The premise of this proposal is that the clinical efficacy of lithium in bipolar disorder, and its complex effects on multiple brain physiological functions, may be best deciphered using a network properties-metric approach. This approach is critical because it provides insight into the function of brain networks (e.g., resilience to disruption, central hubs), which is likely to be more closely linked to behavioral outcomes. Furthermore, we will conduct an exploratory investigation of the in vivo molecular effects of lithium by measuring peripheral gene expression. To bring these together, we will also explore whether connectome changes serve as mediator between molecular changes (i.e., gene expression) induced by lithium treatment and behavioral changes (e.g., depression, mood stability, suicidality).

Registry
clinicaltrials.gov
Start Date
December 7, 2017
End Date
June 1, 2026
Last Updated
2 months ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Amit Anand

Principal Investigator

Brigham and Women's Hospital

Eligibility Criteria

Inclusion Criteria

  • for BD subjects:
  • ages 18-60 years (inclusive) and able to give voluntary informed consent;
  • Satisfy criteria for Diagnostic and Statistical Manual 5th edition (DSM-V) for BD I or II, current Depressive Episode;
  • 17-item Hamilton Depression Rating Scale (HAM-D) score \>15 and \<25;
  • Young Mania Rating Scale (YMRS) \< 8;
  • no psychotropics in the last 2 weeks (if previously on fluoxetine then medication free for 5 weeks) OR on stable psychotropic medications for 12 weeks
  • no lithium treatment for past 6 months;
  • satisfy criteria to undergo an MRI scan based on MRI screening questionnaire;
  • able to be managed as outpatients during the study as ascertained by Clinical Global Severity Scale \< 5 (i.e., moderately ill) and no significant suicidal or homicidal ideation or gross disability.

Exclusion Criteria

  • for BD subjects are:
  • meeting DSM-IV criteria for schizophrenia, schizoaffective disorder, or an anxiety disorder as
  • a primary diagnosis;
  • requiring inpatient treatment;
  • meeting DSM-V criteria for substance dependence within the past 3 months, except caffeine or nicotine;
  • positive urinary toxicology screening at screening visit;
  • use of alcohol in the past 1 week;
  • serious medical or neurological illness;
  • current pregnancy or breast feeding;
  • metallic implants or other contraindications to MRI.

Arms & Interventions

Bipolar Disorder I or II Depressed

DSM-V Bipolar I or II Depressed treated with lithium

Intervention: Lithium

Healthy Controls

Healthy Controls with no psychiatric history

Outcomes

Primary Outcomes

Functional Connectivity (Fc) changes

Time Frame: 2, 8, 26 weeks

Investigate effects of lithium monotherapy treatment of BD on changes in Fc through fMRI imaging from baseline after 2, 8, and 26 weeks of treatment and test whether these changes correlate with improvement in state-related symptoms and longer term mood stability. Healthy controls will also be scanned at the same time points but not treated.

Structural Connectivity (Sc) changes

Time Frame: 2, 8, 26 weeks

Investigate effects of lithium monotherapy treatment of BD depression on changes in the diffusion weighted imaging Sc through fMRI imaging from baseline after 2, 8, and 26 weeks and test whether these changes correlate with depression severity and mood stability. Healthy controls will also be scanned at the same time points but not treated.

Secondary Outcomes

  • Changes in peripheral gene expression(2, 8, 26 weeks)

Study Sites (1)

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