Perimenopausal Depression Clinical Trial
Official title:
Effects of Estradiol on Neural Reward System and Depression in the Perimenopause
Using neuroimaging, the investigator will study the effects of estrogen on mood and brain function in perimenopausal women either with or without depression.
Despite decades of research, affective disorders are prevalent and associated with
significant morbidity and mortality. Unraveling the pathophysiology of affective disorders
has been uniquely challenging because depressive syndromes are heterogeneous and have diverse
etiologies. Thus, past studies aimed at identifying neural and genetic biomarkers that would
improve the prediction of susceptibility, course of illness, and treatment response have
yielded inconsistent results. The investigator proposes to address this problem by studying
perimenopausal major depressive disorder (MDD), a depression subtype with a specific
endocrine trigger (i.e., ovarian hormone withdrawal). Evidence supporting ovarian hormone
withdrawal as a trigger for affective dysfunction in perimenopausal MDD includes the
following: perimenopausal women show a temporal association between ovarian hormone
withdrawal and the onset of mood symptoms; treatment with estrogen reduces mood symptoms; and
blinded estradiol withdrawal re-precipitates depression in women with a history of
perimenopausal MDD (manuscript in preparation). Focusing on perimenopausal MDD, a more
homogeneous subtype with a specific endocrine trigger, will increase the likelihood of
identifying meaningful neurobiological markers.One of the most powerful tools for
understanding the neural mediators of MDD is brain imaging. Prior research suggests that the
frontostriatal reward system is regulated by estradiol and implicated in MDD. However, neural
mechanisms of perimenopausal MDD have never been studied. We will assess the neural reward
system in perimenopausal women with and without MDD using functional magnetic resonance
imaging (fMRI) at baseline and following estradiol treatment. The central hypothesis is that
the neural reward system is hypoactive in perimenopausal MDD, and the antidepressant effects
of a three-week transdermal estradiol intervention will be mediated by increased activity in
the neural reward system, assessed using fMRI. The investigator will test the hypothesis by
executing the following aims:
Aim 1: To measure the frontostriatal response to reward in perimenopausal MDD and test the
effects of estradiol on neural activation in perimenopausal women. The investigator will use
fMRI at baseline and following estradiol treatment in women with and without MDD to probe
frontostriatal reward circuitry.
Aim 2: To quantify motivated behavior at baseline and following estradiol administration in
perimenopausal women with and without MDD. Motivated behavior will be operationally defined
as the response latency to reward versus non-reward during the fMRI reward task.
Aim 3: To measure the psychological correlates of the frontostriatal response to reward in
women with perimenopausal MDD at baseline and following estradiol administration. Depressive
symptoms will be assessed at baseline and following estradiol administration.
The results will provide critical information about the neuroendocrine pathophysiology of
perimenopausal depression and may subsequently contribute to the development of novel
pharmacologic interventions.
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Status | Clinical Trial | Phase | |
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Completed |
NCT00060736 -
The Effects of Estrogen Withdrawal on Mood Symptoms in Women
|
||
Completed |
NCT03526523 -
Testing the Efficacy of Mindfulness-based Stress Reduction in the Prevention of Perimenopausal Depression
|
N/A | |
Terminated |
NCT01368068 -
Investigation of Tibolone and Escitalopram in Perimenopausal Depression
|
Phase 4 | |
Completed |
NCT00030147 -
Raloxifene and Rimostil for Perimenopause-Related Depression
|
Phase 4 |