TY - JOUR
T1 - Deep Transcranial Magnetic Stimulation Combined With Brief Exposure for Posttraumatic Stress Disorder
T2 - A Prospective Multisite Randomized Trial
AU - Isserles, Moshe
AU - Tendler, Aron
AU - Roth, Yiftach
AU - Bystritsky, Alexander
AU - Blumberger, Daniel M.
AU - Ward, Herbert
AU - Feifel, David
AU - Viner, Laura
AU - Duffy, Walter
AU - Zohar, Joseph
AU - Keller, Corey J.
AU - Bhati, Mahendra T.
AU - Etkin, Amit
AU - George, Mark S.
AU - Filipcic, Igor
AU - Lapidus, Kyle
AU - Casuto, Leah
AU - Vaishnavi, Sandeep
AU - Stein, Ahava
AU - Deutsch, Lisa
AU - Deutsch, Frederic
AU - Morales, Oscar
AU - Daskalakis, Zafiris J.
AU - Zangen, Abraham
AU - Ressler, Kerry J.
N1 - Funding Information:
This work was supported by BrainsWay , Inc.
Funding Information:
This work was supported by BrainsWay, Inc. AZ and YR are inventors of deep TMS coils and have financial interest in BrainsWay Ltd. AT reports financial interest in Advanced Mental Health Care, BrainsWay, and DTMS Center and receives consulting fees for BrainsWay and Clinical TMS Society. DMB reports in-kind equipment support from MagVenture for investigator-initiated research, previous research grant and in-kind equipment support from BrainsWay, and site principal investigator for three sponsored clinical trials. JZ reports receiving grants/research support from Lundbeck, Servier, BrainsWay, and Pfizer; honoraria/consultation fees from Servier, Pfizer, Abbott, Eli Lilly and Company, Actelion, AstraZeneca, SunPharma, Roche, and BrainsWay; and speaker fees from Lundbeck, Roche, Eli Lilly and Company, Servier, Pfizer, Abbott, SunPharma, and BrainsWay. CJK reports equity from Alto Neuroscience. AE reports equity from Alto Neuroscience, Mindstrong Health, Akili Interactive, and Sizung and salary from Alto Neuroscience. MSG reports research equipment loans from BrainsWay, Magstim, and MECTA Corporation and research grants to Medical University of South Carolina from BrainsWay. KL reports grants, personal fees, nonfinancial support, and other from Affective Care during the conduct of the study; grants, personal fees, nonfinancial support, and other from BrainsWay Ltd.; nonfinancial support and other from Halo Neuroscience; nonfinancial support from Medtronic, Neuronetics, and Roche; personal fees from FCB Health; personal fees and nonfinancial support from SmartAnalyst and Cipla; personal fees from LCN Consulting; other from New York Neuromodulation Medical PLLC, Psychiatric Care Medical PLLC, Sol2rise, and Victory Recovery Partners; and grants and personal fees from Fisher Wallace, outside the submitted work. AS serves as Food and Drug Administration regulatory and clinical consultant to BrainsWay. LD and FD received consultant fees from BrainsWay for statistical services. OM reports receiving occasional consulting (lectures) work from BrainsWay. In the last 5 years, ZJD has received research and equipment in-kind support for an investigator-initiated study through Brainsway, Inc. and Magventure, Inc. ZJD's work is supported by the Canadian Institutes of Health Research, National Institutes of Mental Health, Brain Canada, Temerty Family Foundation, Grant Family Foundation, Centre for Addiction and Mental Health Foundation, and Campbell Institute. KJR has received unrelated consulting income or sponsored research from Alkermes, BrainsWay, BioXcel Therapeutics, Inc. and Genomind, Inc. and is on scientific advisory boards for Janssen, Takeda, and Verily. All other authors report no biomedical financial interests or potential conflicts of interest. ClinicalTrials.gov: A Safety & Efficacy Study With Deep Transcranial Magnetic Stimulation for the Treatment of Post-Traumatic Stress Disorder (PTSD); https://clinicaltrials.gov/ct2/show/NCT02479906; NCT02479906.
Publisher Copyright:
© 2021 Society of Biological Psychiatry
PY - 2021/11/15
Y1 - 2021/11/15
N2 - Background: Posttraumatic stress disorder (PTSD) is both prevalent and debilitating. While deep transcranial magnetic stimulation (dTMS) has shown preliminary efficacy, exposure therapy remains the most efficacious, though limited, treatment in PTSD. The medial prefrontal cortex (mPFC) is implicated in extinction learning, suggesting that concurrent mPFC stimulation may enhance exposure therapy. In this randomized controlled multicenter trial, the efficacy and safety of mPFC dTMS combined with a brief exposure procedure were studied in patients with PTSD. Methods: Immediately following exposure to their trauma narrative, 125 outpatients were randomly assigned to receive dTMS or sham. Twelve sessions were administered over 4 weeks, with a primary end point of change in 5-week Clinician-Administered PTSD Scale for DSM-5 score. This clinical study did not include biological markers. Results: Clinician-Administered PTSD Scale for DSM-5 score improved significantly in both groups at 5 weeks, though the improvement was smaller in the dTMS group (16.32) compared with the sham group (20.52; p =.027). At 9 weeks, improvement continued in Clinician-Administered PTSD Scale for DSM-5 score in both groups but remained smaller in dTMS (19.0) versus sham (24.4; p =.024). Conclusions: Both groups showed significant PTSD symptom improvement, possibly from the brief script-driven imagery exposure. While our design was unable to rule out placebo effects, the magnitude and durability of improvement suggest that repeated ultrabrief exposure therapy alone may be an effective treatment for PTSD, warranting additional study. The surprising and unexpected effect in the dTMS group also suggests that repeated mPFC stimulation with the H7 coil may interfere with trauma memory–mediated extinction. Our results provide new insight for dTMS approaches for possible future avenues to treat PTSD.
AB - Background: Posttraumatic stress disorder (PTSD) is both prevalent and debilitating. While deep transcranial magnetic stimulation (dTMS) has shown preliminary efficacy, exposure therapy remains the most efficacious, though limited, treatment in PTSD. The medial prefrontal cortex (mPFC) is implicated in extinction learning, suggesting that concurrent mPFC stimulation may enhance exposure therapy. In this randomized controlled multicenter trial, the efficacy and safety of mPFC dTMS combined with a brief exposure procedure were studied in patients with PTSD. Methods: Immediately following exposure to their trauma narrative, 125 outpatients were randomly assigned to receive dTMS or sham. Twelve sessions were administered over 4 weeks, with a primary end point of change in 5-week Clinician-Administered PTSD Scale for DSM-5 score. This clinical study did not include biological markers. Results: Clinician-Administered PTSD Scale for DSM-5 score improved significantly in both groups at 5 weeks, though the improvement was smaller in the dTMS group (16.32) compared with the sham group (20.52; p =.027). At 9 weeks, improvement continued in Clinician-Administered PTSD Scale for DSM-5 score in both groups but remained smaller in dTMS (19.0) versus sham (24.4; p =.024). Conclusions: Both groups showed significant PTSD symptom improvement, possibly from the brief script-driven imagery exposure. While our design was unable to rule out placebo effects, the magnitude and durability of improvement suggest that repeated ultrabrief exposure therapy alone may be an effective treatment for PTSD, warranting additional study. The surprising and unexpected effect in the dTMS group also suggests that repeated mPFC stimulation with the H7 coil may interfere with trauma memory–mediated extinction. Our results provide new insight for dTMS approaches for possible future avenues to treat PTSD.
KW - Deep TMS
KW - Exposure therapy
KW - PTSD
KW - Posttraumatic stress disorder
KW - Script-driven imagery
KW - mPFC
UR - http://www.scopus.com/inward/record.url?scp=85111107671&partnerID=8YFLogxK
U2 - 10.1016/j.biopsych.2021.04.019
DO - 10.1016/j.biopsych.2021.04.019
M3 - Article
C2 - 34274108
AN - SCOPUS:85111107671
SN - 0006-3223
VL - 90
SP - 721
EP - 728
JO - Biological Psychiatry
JF - Biological Psychiatry
IS - 10
ER -