Effect of Insomnia on Repetitive Transcranial Magnetic Stimulation Treatment Outcomes for Depression

Abstract

While repetitive transcranial magnetic stimulation (rTMS) is safe and effective for 50-60% of those treatment-resistant depression, it is critical to identify factors to optimize therapy to help those who do not respond. Baseline sleep characteristics have been investigated as a potential predictor of TMS efficacy but results from various studies have been conflicting. We aimed to explore whether baseline sleep quality, specifically insomnia related symptoms, is associated with TMS outcomes in a naturalistic sample of 975 patients receiving a standard course of rTMS from two sites. One site recorded information on concurrent medication use. Among these 353 patients, we also examined whether pharmacological treatment of insomnia affected TMS treatment response. Depression was measured using the 30-item Inventory of Depressive Symptomology Self Report (IDS-SR) in site one and an abbreviated 16-item Quick Inventory of Depressive Symptomology (QIDS) in site two. Sleep disturbances were measured using three sleep-related questions overlapping between the two questionnaires. We found that sleep quality improves after TMS and correlates with improvement in depression. Upon dichotomous categorization of the sample by insomnia and hypnotics use, we found that among those who had significant insomnia at baseline, those not using sleep medications had significantly worse post-treatment IDS-SR scores compared to those receiving pharmacological treatments for sleep (p=.021). Together, our results suggest that while baseline insomnia is not associated with response to TMS treatment, treating insomnia may affect the trajectory of TMS therapy. Future prospective studies are necessary to examine the effect of insomnia treatment alongside TMS for depression.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This study did not receive any funding

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

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The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

Institutional Review Board of Butler Hospital waived ethical approval for this work

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I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

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I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

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Data Availability

All data produced in the present study are available upon request to the authors

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