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Deep Transcranial Magnetic Stimulation Combined With Brief Exposure for Posttraumatic Stress Disorder: A Prospective Multisite Randomized Trial

暴露疗法 随机对照试验 磁刺激 安慰剂 消光(光学矿物学) 深部经颅磁刺激 刺激 经颅直流电刺激 前额叶皮质 创伤后应激 医学 麻醉 心理学 精神科 内科学 焦虑 认知 病理 生物 古生物学 替代医学
作者
Moshe Isserles,Aron Tendler,Yiftach Roth,Alexander Bystritsky,Daniel M. Blumberger,Herbert E. Ward,David Feifel,Laura Viner,Walter Duffy,Joseph Zohar,Corey J. Keller,Mahendra T. Bhati,Amit Etkin,Mark S. George,Igor Filipčić,Kyle Lapidus,Leah Casuto,Sandeep Vaishnavi,Ahava Stein,Lisa Deutsch,Frederic Deutsch,Oscar Morales,Zafiris J. Daskalakis,Abraham Zangen,Kerry J. Ressler
出处
期刊:Biological Psychiatry [Elsevier BV]
卷期号:90 (10): 721-728 被引量:55
标识
DOI:10.1016/j.biopsych.2021.04.019
摘要

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.

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