Altered bed nucleus of the stria terminalis and amygdala responses to threat in combat veterans with posttraumatic stress disorder

被引:3
作者
Feola, Brandee [1 ]
Flook, Elizabeth A. [1 ,2 ]
Gardner, Hannah [1 ]
Phan, K. Luan [3 ]
Gwirtsman, Harry [1 ,4 ]
Olatunji, Bunmi [5 ]
Blackford, Jennifer Urbano [1 ,6 ,7 ]
机构
[1] Vanderbilt Univ, Dept Psychiat & Behav Sci, Med Ctr, Nashville, TN USA
[2] Univ Penn, Dept Psychiat, Philadelphia, PA USA
[3] Ohio State Univ, Dept Psychiat, Columbus, OH USA
[4] US Dept Vet Affairs, Tennessee Valley HealthCare Syst, Nashville, TN USA
[5] Vanderbilt Univ, Dept Psychol, Nashville, TN USA
[6] Univ Nebraska Med Ctr, Munroe Meyer Inst, Omaha, NE USA
[7] 6902 Pine St, Omaha, NE 68104 USA
基金
美国国家卫生研究院;
关键词
FUNCTIONAL CONNECTIVITY; EXPOSURE THERAPY; ANXIETY; NEUROBIOLOGY; METAANALYSIS; PREDICTS; EMOTION; MEMORY; PTSD; TIME;
D O I
10.1002/jts.22918
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Posttraumatic stress disorder (PTSD) significantly impacts many veterans. Although PTSD has been linked to alterations in the fear brain network, the disorder likely involves alterations in both the fear and anxiety networks. Fear involves responses to imminent, predictable threat and is driven by the amygdala, whereas anxiety involves responses to potential, unpredictable threat and engages the bed nucleus of the stria terminalis (BNST). The BNST has been implicated in PTSD, but the role of the BNST in combat veterans with PTSD has yet to be examined. Identifying alterations in BNST responses to unpredictable threat could provide important new targets for treatment. The current study examined whether veterans with PTSD have altered BNST or amygdala responses (function and connectivity) to unpredictable and predictable threat. The fMRI task involved viewing predictable threat cues followed by threat images, predictable neutral cues followed by neutral images, and unpredictable threat cues followed by either a threat or neutral image. Participants included 32 combat-exposed veterans with PTSD and 13 combat-exposed controls without PTSD. Across all conditions, veterans with PTSD had heightened BNST activation and displayed stronger BNST and amygdala connectivity with multiple fear and anxiety regions (hypothalamus, hippocampus, insula, ventromedial prefrontal cortex) relative to controls. In contrast, combat controls showed a pattern of stronger connectivity during neutral conditions (e.g., BNST-vmPFC), which may suggest a neural signature of resilience to developing PTSD, eta(2)(p) = .087-.527, ps < .001. These findings have implications for understanding fear and anxiety networks that may contribute to the development and maintenance of PTSD.
引用
收藏
页码:359 / 372
页数:14
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