Bipolar Depression Clinical Trial
Official title:
Functional Connectivity in Mood Regulating Circuit In Bipolar Depression and Mania Before and After Lithium Treatment: An Brain fMRI Study
The purpose of this study is to find out what parts of the brain have increased or decreased activity with individuals who have bipolar disorder and how medicine changes this activity in bipolar subjects. Another purpose of this study is to compare data obtained from bipolar depressed subjects with data obtained from healthy subjects. In this study we will measure activity in different parts of the brain, while participants see pictures, using Magnetic Resonance Imaging (MRI) scan. We will do two MRI scans with each subject before and after treatment for eight weeks with a standard bipolar disorder medication called lithium.
Aim 1: Our first aim is to use a novel fMRI experimental paradigm to investigate the
pathophysiology of bipolar disorder (BD) in terms of the strength of connectivity (as
measured by LFBF correlations) between the different emotion regulating areas of the brain
rather than in terms of increase or decrease in localized brain activity.
Specific Aim 2: Our second aim is to investigate whether lithium works by altering the
connectivity of areas of the brain implicated in the pathophysiology of BD, thereby leading
to changes in the abnormal positive or negative emotional reactions to the environment seen
in mania and depression respectively.
Specific Aim 3: Out third aim is to investigate whether patients with the s/s or s/L alleles
of the 5-HTTLPR polymorphism will have greater amygdalar activation and decreased
cortico-amygdala connectivity compared to patients with L/L genotype. We will also
investigate whether lithium treatment differentially affects these fMRI measures in the s/s
or s/L and L/L genotypes.
Methods:
We will study unmedicated subjects satisfying DSM-IV criteria for Bipolar Disorder current
episode depressed or hypomanic/manic or who are euthymic. Subjects will undergo fMRI before
and after 8 weeks of treatment with lithium a mood stabilizer that is known to be effective
in both phases of BD. Healthy subjects will have a scan at baseline and after 8 weeks but
will not be treated with any medication. We will also test for the serotonin transporter
gene (the gene that controls the availability of a chemical called serotonin in the brain),
which has been shown to effect how lithium works.
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Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention
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