Individualized Targeting and Neuromodulation of Late-Life Depression

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Approximately 10-15% of elderly persons will suffer from late life depression (LLD), which is often complicated by simultaneous cognitive impairment (so-called "pseudodementia" of depression). Unfortunately, the treatments for moderate to severe LDD have not changed significantly in the past sixty y...

Approximately 10-15% of elderly persons will suffer from late life depression (LLD), which is often complicated by simultaneous cognitive impairment (so-called "pseudodementia" of depression). Unfortunately, the treatments for moderate to severe LDD have not changed significantly in the past sixty years, and are accompanied by either systemic side effects (antidepressant medications), or prominent memory loss (electroconvulsive therapy; ECT). Newer therapies such as transcranial magnetic stimulation (TMS) have a superior side effect profile, but lack robust efficacy in LLD (only 40% remission) compared to 60-80% remission rates with ECT. Moreover, few studies have attempted to measure target engagement of effective therapeutics for LLD, leading to critical gaps in understanding of the biological mechanisms underlying this disease. The long-term goal is to develop safer, more effective treatments for LLD that engage the brain's pathophysiology, improve functioning, and prolong quality of life. Findings from the investigators' studies of structural and connectivity changes associated with depression treatment and others suggest that when noninvasive neurostimulation is precisely focused on specific neural circuits governing mood, more robust antidepressant results can be achieved. The brain region determined to have the greatest functional relevance in depression is the anterior cingulate cortex (ACC), with multiple imaging and stimulation studies over two decades supporting its crucial role. However, its mesial location makes direct stimulation difficult; consequently, TMS in its most common form attempts to modulate the ACC through a more superficial "cortical window," namely the dorsolateral prefrontal cortex (DLPFC). However, modest remission rates for TMS in LLD (<40%) may be related to the current practice of using external scalp landmarks to target the DLPFC, causing imprecision and inaccuracy in finding and accessing the true DLPFC. Based on recent clinical trials and brain stimulation modeling methods developed in an ongoing study, the investigators propose a pilot study of structural and functional MRI (sfMRI) to identify individual-specific targets for TMS to treat LDD. A total of 24 elderly depressed patients recruited from the UNM Treatment Resistant Depression (TRD) Clinic and the Geriatric Psychiatry Clinic will undergo sfMRI and cognitive/behavioral assessment prior to TMS treatment. Utilizing analytical techniques already implemented in other studies, the investigators will identify each person's cortical "fingerprint" or hotspot in the DLPFC that demonstrates maximum functional anti-correlated connectivity with the ACC. The participants with LLD will each receive 30 sessions of TMS targeted to this functional network. Following the 15th and the 30th stimulation session, participants will repeat clinical and imaging assessments. Changes in depressive symptoms will be correlated with changes in connectivity, as well as the amount of induced electrical current projected to reach depression network nodes using finite element modeling methods. This precision medicine approach is crucial for reducing variability in the actual amount of delivered energy and will have a significant impact on efficacy, making TMS the "go-to" treatment of choice for LLD.

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