Volume 52, Issue 2 pp. 380-396
Review Article

MRI findings in posttraumatic stress disorder

Akira Kunimatsu MD, PhD

Corresponding Author

Akira Kunimatsu MD, PhD

Department of Radiology, IMSUT Hospital, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan

Department of Radiology, The University of Tokyo Hospital, Tokyo, Japan

Address reprint requests to: A.K., Department of Radiology, IMSUT Hospital, The Institute of Medical Science, The University of Tokyo, 4-6-1, Shirokanedai, Minato-ku, Tokyo 108-8639, Japan. E-mail: [email protected]Search for more papers by this author
Koichiro Yasaka MD, PhD

Koichiro Yasaka MD, PhD

Department of Radiology, IMSUT Hospital, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan

Department of Radiology, The University of Tokyo Hospital, Tokyo, Japan

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Hiroyuki Akai MD, PhD

Hiroyuki Akai MD, PhD

Department of Radiology, IMSUT Hospital, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan

Department of Radiology, The University of Tokyo Hospital, Tokyo, Japan

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Natsuko Kunimatsu MD, PhD

Natsuko Kunimatsu MD, PhD

Department of Radiology, International University of Health and Welfare, Mita Hospital, Tokyo, Japan

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Osamu Abe MD, PhD

Osamu Abe MD, PhD

Department of Radiology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan

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First published: 12 September 2019
Citations: 112

Abstract

Posttraumatic stress disorder (PTSD) is a psychiatric condition that develops after a person experiences one or more traumatic events, characterized by intrusive recollection, avoidance of trauma-related events, hyperarousal, and negative cognitions and mood. Neurophysiological evidence suggests that the development of PTSD is ascribed to functional abnormalities in fear learning, threat detection, executive function and emotional regulation, and contextual processing. Magnetic resonance imaging (MRI) plays a primary role in both structural and functional neuroimaging for PTSD, demonstrating focal atrophy of the gray matter, altered fractional anisotropy, and altered focal neural activity and functional connectivity. MRI findings have implicated that brain regions associated with PTSD pathophysiology include the medial and dorsolateral prefrontal cortex, orbitofrontal cortex, insula, lentiform nucleus, amygdala, hippocampus and parahippocampus, anterior and posterior cingulate cortex, precuneus, cuneus, fusiform and lingual gyri, and the white matter tracts connecting these brain regions. Of these, alterations in the anterior cingulate, amygdala, hippocampus, and insula are highly reproducible across structural and functional MRI, supporting the hypothesis that abnormalities in fear learning and reactions to threat play an important role in the development of PTSD. In addition, most of these structures have been known to belong to one or more intrinsic brain networks regulating autobiographical memory retrieval and self-thought, salience detection and autonomic responses, or attention and emotional control. Altered functional brain networks have been shown in PTSD. Therefore, in PTSD MRI is expected to reflect disequilibrium among functional brain networks, malfunction within an individual network, and impaired brain structures closely interacting with the networks.

Level of Evidence: 3

Technical Efficacy Stage: 3

J. Magn. Reson. Imaging 2019. J. Magn. Reson. Imaging 2020;52:380–396.

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