Thalamic volume and fear extinction interact to predict acute posttraumatic stress severity
Posttraumatic stress disorder (PTSD) is associated with lower gray matter volume (GMV) in brain regions critical for extinction of learned threat. However, relationships among volume, extinction learning, and PTSD symptom development remain unclear. We investigated subcortical brain volumes in regio...
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Veröffentlicht in: | Journal of psychiatric research 2021-09, Vol.141, p.325-332 |
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creator | Steuber, Elizabeth R. Seligowski, Antonia V. Roeckner, Alyssa R. Reda, Mariam Lebois, Lauren A.M. van Rooij, Sanne J.H. Murty, Vishnu P. Ely, Timothy D. Bruce, Steven E. House, Stacey L. Beaudoin, Francesca L. An, Xinming Zeng, Donglin Neylan, Thomas C. Clifford, Gari D. Linnstaedt, Sarah D. Germine, Laura T. Rauch, Scott L. Lewandowski, Christopher Sheikh, Sophia Jones, Christopher W. Punches, Brittany E. Swor, Robert A. McGrath, Meghan E. Hudak, Lauren A. Pascual, Jose L. Chang, Anna M. Pearson, Claire Peak, David A. Domeier, Robert M. O'Neil, Brian J. Rathlev, Niels K. Sanchez, Leon D. Pietrzak, Robert H. Joormann, Jutta Barch, Deanna M. Pizzagalli, Diego A. Elliott, James M. Kessler, Ronald C. Koenen, Karestan C. McLean, Samuel A. Ressler, Kerry J. Jovanovic, Tanja Harnett, Nathaniel G. Stevens, Jennifer S. |
description | Posttraumatic stress disorder (PTSD) is associated with lower gray matter volume (GMV) in brain regions critical for extinction of learned threat. However, relationships among volume, extinction learning, and PTSD symptom development remain unclear. We investigated subcortical brain volumes in regions supporting extinction learning and fear-potentiated startle (FPS) to understand brain-behavior interactions that may impact PTSD symptom development in recently traumatized individuals. Participants (N = 99) completed magnetic resonance imaging and threat conditioning two weeks following trauma exposure as part of a multisite observational study to understand the neuropsychiatric effects of trauma (AURORA Study). Participants completed self-assessments of PTSD (PTSD Checklist for DSM-5; PCL-5), dissociation, and depression symptoms two- and eight-weeks post-trauma. We completed multiple regressions to investigate relationships between FPS during late extinction, GMV, and PTSD symptom development. The interaction between thalamic GMV and FPS during late extinction at two weeks post-trauma predicted PCL-5 scores eight weeks (t (75) = 2.49, β = 0.28, p = 0.015) post-trauma. Higher FPS predicted higher PCL-5 scores in the setting of increased thalamic GMV. Meanwhile, lower FPS also predicted higher PCL-5 scores in the setting of decreased thalamic GMV. Thalamic GMV and FPS interactions also predicted posttraumatic dissociative and depressive symptoms. Amygdala and hippocampus GMV by FPS interactions were not associated with posttraumatic symptom development. Taken together, thalamic GMV and FPS during late extinction interact to contribute to adverse posttraumatic neuropsychiatric outcomes. Multimodal assessments soon after trauma have the potential to distinguish key phenotypes vulnerable to posttraumatic neuropsychiatric outcomes. |
doi_str_mv | 10.1016/j.jpsychires.2021.07.023 |
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However, relationships among volume, extinction learning, and PTSD symptom development remain unclear. We investigated subcortical brain volumes in regions supporting extinction learning and fear-potentiated startle (FPS) to understand brain-behavior interactions that may impact PTSD symptom development in recently traumatized individuals. Participants (N = 99) completed magnetic resonance imaging and threat conditioning two weeks following trauma exposure as part of a multisite observational study to understand the neuropsychiatric effects of trauma (AURORA Study). Participants completed self-assessments of PTSD (PTSD Checklist for DSM-5; PCL-5), dissociation, and depression symptoms two- and eight-weeks post-trauma. We completed multiple regressions to investigate relationships between FPS during late extinction, GMV, and PTSD symptom development. The interaction between thalamic GMV and FPS during late extinction at two weeks post-trauma predicted PCL-5 scores eight weeks (t (75) = 2.49, β = 0.28, p = 0.015) post-trauma. Higher FPS predicted higher PCL-5 scores in the setting of increased thalamic GMV. Meanwhile, lower FPS also predicted higher PCL-5 scores in the setting of decreased thalamic GMV. Thalamic GMV and FPS interactions also predicted posttraumatic dissociative and depressive symptoms. Amygdala and hippocampus GMV by FPS interactions were not associated with posttraumatic symptom development. Taken together, thalamic GMV and FPS during late extinction interact to contribute to adverse posttraumatic neuropsychiatric outcomes. Multimodal assessments soon after trauma have the potential to distinguish key phenotypes vulnerable to posttraumatic neuropsychiatric outcomes.</description><identifier>ISSN: 0022-3956</identifier><identifier>EISSN: 1879-1379</identifier><identifier>DOI: 10.1016/j.jpsychires.2021.07.023</identifier><identifier>PMID: 34304036</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Amygdala ; Extinction ; Extinction, Psychological ; Fear ; Fear-potentiated startle ; Gray matter volume ; Hippocampus ; Humans ; Magnetic Resonance Imaging ; Posttraumatic stress disorder ; Stress Disorders, Post-Traumatic - diagnostic imaging ; Thalamus</subject><ispartof>Journal of psychiatric research, 2021-09, Vol.141, p.325-332</ispartof><rights>2021 Elsevier Ltd</rights><rights>Copyright © 2021 Elsevier Ltd. 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However, relationships among volume, extinction learning, and PTSD symptom development remain unclear. We investigated subcortical brain volumes in regions supporting extinction learning and fear-potentiated startle (FPS) to understand brain-behavior interactions that may impact PTSD symptom development in recently traumatized individuals. Participants (N = 99) completed magnetic resonance imaging and threat conditioning two weeks following trauma exposure as part of a multisite observational study to understand the neuropsychiatric effects of trauma (AURORA Study). Participants completed self-assessments of PTSD (PTSD Checklist for DSM-5; PCL-5), dissociation, and depression symptoms two- and eight-weeks post-trauma. We completed multiple regressions to investigate relationships between FPS during late extinction, GMV, and PTSD symptom development. The interaction between thalamic GMV and FPS during late extinction at two weeks post-trauma predicted PCL-5 scores eight weeks (t (75) = 2.49, β = 0.28, p = 0.015) post-trauma. Higher FPS predicted higher PCL-5 scores in the setting of increased thalamic GMV. Meanwhile, lower FPS also predicted higher PCL-5 scores in the setting of decreased thalamic GMV. Thalamic GMV and FPS interactions also predicted posttraumatic dissociative and depressive symptoms. Amygdala and hippocampus GMV by FPS interactions were not associated with posttraumatic symptom development. Taken together, thalamic GMV and FPS during late extinction interact to contribute to adverse posttraumatic neuropsychiatric outcomes. Multimodal assessments soon after trauma have the potential to distinguish key phenotypes vulnerable to posttraumatic neuropsychiatric outcomes.</description><subject>Amygdala</subject><subject>Extinction</subject><subject>Extinction, Psychological</subject><subject>Fear</subject><subject>Fear-potentiated startle</subject><subject>Gray matter volume</subject><subject>Hippocampus</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging</subject><subject>Posttraumatic stress disorder</subject><subject>Stress Disorders, Post-Traumatic - diagnostic 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volume and fear extinction interact to predict acute posttraumatic stress severity</title><author>Steuber, Elizabeth R. ; Seligowski, Antonia V. ; Roeckner, Alyssa R. ; Reda, Mariam ; Lebois, Lauren A.M. ; van Rooij, Sanne J.H. ; Murty, Vishnu P. ; Ely, Timothy D. ; Bruce, Steven E. ; House, Stacey L. ; Beaudoin, Francesca L. ; An, Xinming ; Zeng, Donglin ; Neylan, Thomas C. ; Clifford, Gari D. ; Linnstaedt, Sarah D. ; Germine, Laura T. ; Rauch, Scott L. ; Lewandowski, Christopher ; Sheikh, Sophia ; Jones, Christopher W. ; Punches, Brittany E. ; Swor, Robert A. ; McGrath, Meghan E. ; Hudak, Lauren A. ; Pascual, Jose L. ; Chang, Anna M. ; Pearson, Claire ; Peak, David A. ; Domeier, Robert M. ; O'Neil, Brian J. ; Rathlev, Niels K. ; Sanchez, Leon D. ; Pietrzak, Robert H. ; Joormann, Jutta ; Barch, Deanna M. ; Pizzagalli, Diego A. ; Elliott, James M. ; Kessler, Ronald C. ; Koenen, Karestan C. ; McLean, Samuel A. ; Ressler, Kerry J. ; Jovanovic, Tanja ; Harnett, Nathaniel G. ; Stevens, 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Jennifer S.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of psychiatric research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Steuber, Elizabeth R.</au><au>Seligowski, Antonia V.</au><au>Roeckner, Alyssa R.</au><au>Reda, Mariam</au><au>Lebois, Lauren A.M.</au><au>van Rooij, Sanne J.H.</au><au>Murty, Vishnu P.</au><au>Ely, Timothy D.</au><au>Bruce, Steven E.</au><au>House, Stacey L.</au><au>Beaudoin, Francesca L.</au><au>An, Xinming</au><au>Zeng, Donglin</au><au>Neylan, Thomas C.</au><au>Clifford, Gari D.</au><au>Linnstaedt, Sarah D.</au><au>Germine, Laura T.</au><au>Rauch, Scott L.</au><au>Lewandowski, Christopher</au><au>Sheikh, Sophia</au><au>Jones, Christopher W.</au><au>Punches, Brittany E.</au><au>Swor, Robert A.</au><au>McGrath, Meghan E.</au><au>Hudak, Lauren A.</au><au>Pascual, Jose L.</au><au>Chang, Anna M.</au><au>Pearson, Claire</au><au>Peak, David A.</au><au>Domeier, Robert M.</au><au>O'Neil, Brian J.</au><au>Rathlev, Niels K.</au><au>Sanchez, Leon D.</au><au>Pietrzak, Robert H.</au><au>Joormann, Jutta</au><au>Barch, Deanna M.</au><au>Pizzagalli, Diego A.</au><au>Elliott, James M.</au><au>Kessler, Ronald C.</au><au>Koenen, Karestan C.</au><au>McLean, Samuel A.</au><au>Ressler, Kerry J.</au><au>Jovanovic, Tanja</au><au>Harnett, Nathaniel G.</au><au>Stevens, Jennifer S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Thalamic volume and fear extinction interact to predict acute posttraumatic stress severity</atitle><jtitle>Journal of psychiatric research</jtitle><addtitle>J Psychiatr Res</addtitle><date>2021-09-01</date><risdate>2021</risdate><volume>141</volume><spage>325</spage><epage>332</epage><pages>325-332</pages><issn>0022-3956</issn><eissn>1879-1379</eissn><abstract>Posttraumatic stress disorder (PTSD) is associated with lower gray matter volume (GMV) in brain regions critical for extinction of learned threat. However, relationships among volume, extinction learning, and PTSD symptom development remain unclear. We investigated subcortical brain volumes in regions supporting extinction learning and fear-potentiated startle (FPS) to understand brain-behavior interactions that may impact PTSD symptom development in recently traumatized individuals. Participants (N = 99) completed magnetic resonance imaging and threat conditioning two weeks following trauma exposure as part of a multisite observational study to understand the neuropsychiatric effects of trauma (AURORA Study). Participants completed self-assessments of PTSD (PTSD Checklist for DSM-5; PCL-5), dissociation, and depression symptoms two- and eight-weeks post-trauma. We completed multiple regressions to investigate relationships between FPS during late extinction, GMV, and PTSD symptom development. The interaction between thalamic GMV and FPS during late extinction at two weeks post-trauma predicted PCL-5 scores eight weeks (t (75) = 2.49, β = 0.28, p = 0.015) post-trauma. Higher FPS predicted higher PCL-5 scores in the setting of increased thalamic GMV. Meanwhile, lower FPS also predicted higher PCL-5 scores in the setting of decreased thalamic GMV. Thalamic GMV and FPS interactions also predicted posttraumatic dissociative and depressive symptoms. Amygdala and hippocampus GMV by FPS interactions were not associated with posttraumatic symptom development. Taken together, thalamic GMV and FPS during late extinction interact to contribute to adverse posttraumatic neuropsychiatric outcomes. Multimodal assessments soon after trauma have the potential to distinguish key phenotypes vulnerable to posttraumatic neuropsychiatric outcomes.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>34304036</pmid><doi>10.1016/j.jpsychires.2021.07.023</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-5295-7072</orcidid><orcidid>https://orcid.org/0000-0002-4990-9165</orcidid><orcidid>https://orcid.org/0000-0002-6494-9843</orcidid><orcidid>https://orcid.org/0000-0003-3810-8482</orcidid><orcidid>https://orcid.org/0000-0002-8807-0913</orcidid><orcidid>https://orcid.org/0000-0001-7699-6754</orcidid><orcidid>https://orcid.org/0000-0002-1613-7912</orcidid><orcidid>https://orcid.org/0000-0002-5807-4382</orcidid><orcidid>https://orcid.org/0000-0003-4831-2305</orcidid><orcidid>https://orcid.org/0000-0001-9752-5257</orcidid><orcidid>https://orcid.org/0000-0001-5346-2012</orcidid><orcidid>https://orcid.org/0000-0002-5717-6168</orcidid><orcidid>https://orcid.org/0000-0002-5690-5234</orcidid><orcidid>https://orcid.org/0000-0001-9482-3582</orcidid><orcidid>https://orcid.org/0000-0002-7546-1966</orcidid><orcidid>https://orcid.org/0000-0002-5531-8513</orcidid><orcidid>https://orcid.org/0000-0003-1939-3126</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-3956 |
ispartof | Journal of psychiatric research, 2021-09, Vol.141, p.325-332 |
issn | 0022-3956 1879-1379 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8513112 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Amygdala Extinction Extinction, Psychological Fear Fear-potentiated startle Gray matter volume Hippocampus Humans Magnetic Resonance Imaging Posttraumatic stress disorder Stress Disorders, Post-Traumatic - diagnostic imaging Thalamus |
title | Thalamic volume and fear extinction interact to predict acute posttraumatic stress severity |
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