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Prognostic neuroimaging biomarkers of trauma-related psychopathology: resting-state fMRI shortly after trauma predicts future PTSD and depression symptoms in the AURORA study.


ABSTRACT: Neurobiological markers of future susceptibility to posttraumatic stress disorder (PTSD) may facilitate identification of vulnerable individuals in the early aftermath of trauma. Variability in resting-state networks (RSNs), patterns of intrinsic functional connectivity across the brain, has previously been linked to PTSD, and may thus be informative of PTSD susceptibility. The present data are part of an initial analysis from the AURORA study, a longitudinal, multisite study of adverse neuropsychiatric sequalae. Magnetic resonance imaging (MRI) data from 109 recently (i.e., ~2 weeks) traumatized individuals were collected and PTSD and depression symptoms were assessed at 3 months post trauma. We assessed commonly reported RSNs including the default mode network (DMN), central executive network (CEN), and salience network (SN). We also identified a proposed arousal network (AN) composed of a priori brain regions important for PTSD: the amygdala, hippocampus, mamillary bodies, midbrain, and pons. Primary analyses assessed whether variability in functional connectivity at the 2-week imaging timepoint predicted 3-month PTSD symptom severity. Left dorsolateral prefrontal cortex (DLPFC) to AN connectivity at 2 weeks post trauma was negatively related to 3-month PTSD symptoms. Further, right inferior temporal gyrus (ITG) to DMN connectivity was positively related to 3-month PTSD symptoms. Both DLPFC-AN and ITG-DMN connectivity also predicted depression symptoms at 3 months. Our results suggest that, following trauma exposure, acutely assessed variability in RSN connectivity was associated with PTSD symptom severity approximately two and a half months later. However, these patterns may reflect general susceptibility to posttraumatic dysfunction as the imaging patterns were not linked to specific disorder symptoms, at least in the subacute/early chronic phase. The present data suggest that assessment of RSNs in the early aftermath of trauma may be informative of susceptibility to posttraumatic dysfunction, with future work needed to understand neural markers of long-term (e.g., 12 months post trauma) dysfunction. Furthermore, these findings are consistent with neural models suggesting that decreased top-down cortico-limbic regulation and increased network-mediated fear generalization may contribute to ongoing dysfunction in the aftermath of trauma.

SUBMITTER: Harnett NG 

PROVIDER: S-EPMC8134491 | biostudies-literature | 2021 Jun

REPOSITORIES: biostudies-literature

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Prognostic neuroimaging biomarkers of trauma-related psychopathology: resting-state fMRI shortly after trauma predicts future PTSD and depression symptoms in the AURORA study.

Harnett Nathaniel G NG   van Rooij Sanne J H SJH   Ely Timothy D TD   Lebois Lauren A M LAM   Murty Vishnu P VP   Jovanovic Tanja T   Hill Sarah B SB   Dumornay Nathalie M NM   Merker Julia B JB   Bruce Steve E SE   House Stacey L SL   Beaudoin Francesca L FL   An Xinming X   Zeng Donglin D   Neylan Thomas C TC   Clifford Gari D GD   Linnstaedt Sarah D SD   Germine Laura T LT   Bollen Kenneth A KA   Rauch Scott L SL   Lewandowski Christopher C   Hendry Phyllis L PL   Sheikh Sophia S   Storrow Alan B AB   Musey Paul I PI   Haran John P JP   Jones Christopher W CW   Punches Brittany E BE   Swor Robert A RA   McGrath Meghan E ME   Pascual Jose L JL   Seamon Mark J MJ   Mohiuddin Kamran K   Chang Anna M AM   Pearson Claire C   Peak David A DA   Domeier Robert M RM   Rathlev Niels K NK   Sanchez Leon D LD   Pietrzak Robert H RH   Joormann Jutta J   Barch Deanna M DM   Pizzagalli Diego A DA   Sheridan John F JF   Harte Steven E SE   Elliott James M JM   Kessler Ronald C RC   Koenen Karestan C KC   Mclean Samuel S   Ressler Kerry J KJ   Stevens Jennifer S JS  

Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 20210121 7


Neurobiological markers of future susceptibility to posttraumatic stress disorder (PTSD) may facilitate identification of vulnerable individuals in the early aftermath of trauma. Variability in resting-state networks (RSNs), patterns of intrinsic functional connectivity across the brain, has previously been linked to PTSD, and may thus be informative of PTSD susceptibility. The present data are part of an initial analysis from the AURORA study, a longitudinal, multisite study of adverse neuropsy  ...[more]

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