TY - JOUR
T1 - Sequential decreases in basolateral amygdala response to threat predict failure to recover from PTSD
AU - Roeckner, Alyssa R.
AU - Lin, Esther R.H.
AU - Hinrichs, Rebecca
AU - Harnett, Nathaniel G.
AU - Lebois, Lauren A.M.
AU - van Rooij, Sanne J.H.
AU - Ely, Timothy D.
AU - Jovanovic, Tanja
AU - Murty, Vishnu P.
AU - Bruce, Steven E.
AU - House, Stacey L.
AU - Beaudoin, Francesca L.
AU - An, Xinming
AU - Neylan, Thomas C.
AU - Clifford, Gari D.
AU - Linnstaedt, Sarah D.
AU - Germine, Laura T.
AU - Rauch, Scott L.
AU - Haran, John P.
AU - Storrow, Alan B.
AU - Lewandowski, Christopher
AU - Musey, Paul I.
AU - Hendry, Phyllis L.
AU - Sheikh, Sophia
AU - Jones, Christopher W.
AU - Punches, Brittany E.
AU - Swor, Robert A.
AU - Hudak, Lauren A.
AU - Pascual, Jose L.
AU - Seamon, Mark J.
AU - Datner, Elizabeth M.
AU - Pearson, Claire
AU - Peak, David A.
AU - Merchant, Roland C.
AU - Domeier, Robert M.
AU - Rathlev, Niels K.
AU - O’Neil, Brian J.
AU - Sergot, Paulina
AU - Sanchez, Leon D.
AU - Joormann, Jutta
AU - Sheridan, John F.
AU - Harte, Steven E.
AU - Koenen, Karestan C.
AU - Kessler, Ronald C.
AU - McLean, Samuel A.
AU - Ressler, Kerry J.
AU - Stevens, Jennifer S.
N1 - Publisher Copyright:
© This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2025.
PY - 2025/9
Y1 - 2025/9
N2 - Amygdala hyperreactivity early-post trauma has been a demonstrable neurobiological correlate of future posttraumautic stress disorder (PTSD). The basolateral amygdala (BLA) particularly is vital for fear memory and threat processing, but BLA functional dynamics following a traumatic event are unexplored. BLA reactivity to threat may be a trait that can predict PTSD and persist over time. Alternatively, BLA responsivity to threat cues may change over time and be related to PTSD severity. As part of a larger, multisite study, AURORA, participants 18–75 years old were enrolled in an emergency department (ED) within 72 h of a traumatic event (N = 304, 199 female). At 2-weeks and 6-months post-trauma, PTSD symptoms, BLA responses to threat (fearful>neutral faces), and functional connectivity (FC) during fMRI were assessed. Generalizability of findings was assessed in an external replication sample of ED patients (n = 33). Two weeks post-trauma right BLA reactivity positively predicted later PTSD severity. However, left BLA reactivity to threat at 6 months post-trauma was negatively associated with PTSD severity at that timepoint (ΔPseudo-R2 = 0.04, IRR = 0.38, p < 0.001). In addition, a decrease in BLA reactivity from 2-weeks to 6-months predicted greater PTSD severity at 6 months (ΔPseudo-R2 = 0.03, IRR = 0.58, p < 0.001). This replicated in the external sample. A reduction in left BLA FC with the dorsal attention network predicted increased PTSD severity over time. These findings support a shift in BLA function within the first 6 months post-trauma that predicts PTSD pathology and stand in contrast to prior conceptualizations of amygdala hyperreactivity as a trait-like PTSD risk factor.
AB - Amygdala hyperreactivity early-post trauma has been a demonstrable neurobiological correlate of future posttraumautic stress disorder (PTSD). The basolateral amygdala (BLA) particularly is vital for fear memory and threat processing, but BLA functional dynamics following a traumatic event are unexplored. BLA reactivity to threat may be a trait that can predict PTSD and persist over time. Alternatively, BLA responsivity to threat cues may change over time and be related to PTSD severity. As part of a larger, multisite study, AURORA, participants 18–75 years old were enrolled in an emergency department (ED) within 72 h of a traumatic event (N = 304, 199 female). At 2-weeks and 6-months post-trauma, PTSD symptoms, BLA responses to threat (fearful>neutral faces), and functional connectivity (FC) during fMRI were assessed. Generalizability of findings was assessed in an external replication sample of ED patients (n = 33). Two weeks post-trauma right BLA reactivity positively predicted later PTSD severity. However, left BLA reactivity to threat at 6 months post-trauma was negatively associated with PTSD severity at that timepoint (ΔPseudo-R2 = 0.04, IRR = 0.38, p < 0.001). In addition, a decrease in BLA reactivity from 2-weeks to 6-months predicted greater PTSD severity at 6 months (ΔPseudo-R2 = 0.03, IRR = 0.58, p < 0.001). This replicated in the external sample. A reduction in left BLA FC with the dorsal attention network predicted increased PTSD severity over time. These findings support a shift in BLA function within the first 6 months post-trauma that predicts PTSD pathology and stand in contrast to prior conceptualizations of amygdala hyperreactivity as a trait-like PTSD risk factor.
UR - https://www.scopus.com/pages/publications/105003917507
U2 - 10.1038/s41386-025-02115-1
DO - 10.1038/s41386-025-02115-1
M3 - Article
C2 - 40319171
AN - SCOPUS:105003917507
SN - 0893-133X
VL - 50
SP - 1573
EP - 1582
JO - Neuropsychopharmacology
JF - Neuropsychopharmacology
IS - 10
ER -