TY - JOUR
T1 - Neurocognition after motor vehicle collision and adverse post-traumatic neuropsychiatric sequelae within 8 weeks
T2 - Initial findings from the AURORA study
AU - Germine, Laura T.
AU - Joormann, Jutta
AU - Passell, Eliza
AU - Rutter, Lauren A.
AU - Scheuer, Luke
AU - Martini, Paolo
AU - Hwang, Irving
AU - Lee, Sue
AU - Sampson, Nancy
AU - Barch, Deanna M.
AU - House, Stacey L.
AU - Beaudoin, Francesca L.
AU - An, Xinming
AU - Stevens, Jennifer S.
AU - Zeng, Donglin
AU - Linnstaedt, Sarah D.
AU - Jovanovic, Tanja
AU - Clifford, Gari D.
AU - Neylan, Thomas C.
AU - Rauch, Scott L.
AU - Lewandowski, Christopher
AU - Hendry, Phyllis L.
AU - Sheikh, Sophia
AU - Storrow, Alan B.
AU - Musey, Paul I.
AU - Jones, Christopher W.
AU - Punches, Brittney E.
AU - McGrath, Meghan E.
AU - Pascual, Jose L.
AU - Mohiuddin, Kamran
AU - Pearson, Claire
AU - Peak, David A.
AU - Domeier, Robert M.
AU - Bruce, Steven E.
AU - Rathlev, Niels K.
AU - Sanchez, Leon D.
AU - Pietrzak, Robert H.
AU - Pizzagalli, Diego A.
AU - Harte, Steven E.
AU - Elliott, James M.
AU - Koenen, Karesten C.
AU - Ressler, Kerry J.
AU - McLean, Samuel A.
AU - Kessler, Ronald C.
N1 - Funding Information:
Data and/or research tools used in the preparation of this manuscript were obtained from the National Institute of Mental Health (NIMH) Data Archive (NDA). NDA is a collaborative informatics system created by the National Institutes of Health to provide a national resource to support and accelerate research in mental health. Dataset identifier: NIMH Data Archive 10.15154/1521156. This manuscript reflects the views of the authors and may not reflect the opinions or views of the NIH or of the Submitters submitting original data to NDA.
Funding Information:
Over the past three years, LTG has served on the scientific advisory board of Sage Bionetworks, a nonprofit 501c3. RCK was a consultant for Datastat, Inc, Sage Pharmaceuticals, and Takeda. CWJ reports no direct conflicts related to this paper, and no ongoing conflicts. CWJ has been an investigator on studies funded by Roche Diagnostics, AstraZeneca, Janssen, and Hologic Inc, for which his department has received research funding. Over the past three years, DAP has received consulting fees from Akili Interactive Labs, BlackThorn Therapeutics, Boehringer Ingelheim, Posit Science, and Takeda Pharmaceuticals, as well as an honorarium from Alkermes for activities unrelated to the current project. JME reports support from the National Institutes of Health (NIH) through Grant Nos. R01HD079076 and R03HD094577: Eunice Kennedy Shriver National Institute of Child Health & Human Development, National Center for Medical Rehabilitation Research. SS has received funding from the Florida Medical Malpractice Joint Underwriter's Association Dr. Alvin E. Smith Safety of Healthcare Services Grant, the NIH/NIA-funded Jacksonville Aging Studies Center (JAX-ASCENT, R33AG05654), and the Florida Blue Foundation. There are no known direct conflicts related to this paper.
Publisher Copyright:
© 2021
PY - 2022/2/1
Y1 - 2022/2/1
N2 - Background: Previous work has indicated that differences in neurocognitive functioning may predict the development of adverse post-traumatic neuropsychiatric sequelae (APNS). Such differences may be vulnerability factors or simply correlates of APNS-related symptoms. Longitudinal studies that measure neurocognitive functioning at the time of trauma are needed to determine whether such differences precede the development of APNS. Methods: Here, we present findings from a subsample of 666 ambulatory patients from the AURORA (Advancing Understanding of RecOvery afteR trumA) study. All patients presented to EDs after a motor vehicle collision (MVC). We examined associations of neurocognitive test performance shortly after MVC with peritraumatic symptoms in the ED and APNS (depression, post-traumatic stress, post-concussive symptoms, and pain) 2 weeks and 8 weeks later. Neurocognitive tests assessed processing speed, attention, verbal reasoning, memory, and social perception. Results: Distress in the ED was associated with poorer processing speed and short-term memory. Poorer short-term memory was also associated with depression at 2 weeks post-MVC, even after controlling for peritraumatic distress. Finally, higher vocabulary scores were associated with pain 2 weeks post-MVC. Limitations: Self-selection biases among those who present to the ED and enroll in the study limit generalizability. Also, it is not clear whether observed neurocognitive differences predate MVC exposure or arise in the immediate aftermath of MVC exposure. Conclusions: Our results suggest that processing speed and short-term memory may be useful predictors of trauma-related characteristics and the development of some APNS, making such measures clinically-relevant for identifying at-risk individuals.
AB - Background: Previous work has indicated that differences in neurocognitive functioning may predict the development of adverse post-traumatic neuropsychiatric sequelae (APNS). Such differences may be vulnerability factors or simply correlates of APNS-related symptoms. Longitudinal studies that measure neurocognitive functioning at the time of trauma are needed to determine whether such differences precede the development of APNS. Methods: Here, we present findings from a subsample of 666 ambulatory patients from the AURORA (Advancing Understanding of RecOvery afteR trumA) study. All patients presented to EDs after a motor vehicle collision (MVC). We examined associations of neurocognitive test performance shortly after MVC with peritraumatic symptoms in the ED and APNS (depression, post-traumatic stress, post-concussive symptoms, and pain) 2 weeks and 8 weeks later. Neurocognitive tests assessed processing speed, attention, verbal reasoning, memory, and social perception. Results: Distress in the ED was associated with poorer processing speed and short-term memory. Poorer short-term memory was also associated with depression at 2 weeks post-MVC, even after controlling for peritraumatic distress. Finally, higher vocabulary scores were associated with pain 2 weeks post-MVC. Limitations: Self-selection biases among those who present to the ED and enroll in the study limit generalizability. Also, it is not clear whether observed neurocognitive differences predate MVC exposure or arise in the immediate aftermath of MVC exposure. Conclusions: Our results suggest that processing speed and short-term memory may be useful predictors of trauma-related characteristics and the development of some APNS, making such measures clinically-relevant for identifying at-risk individuals.
KW - Cognition
KW - Digital cognitive assessment
KW - Digital neuropsychology
KW - Longitudinal
KW - Neuropsychology
KW - Trauma
UR - http://www.scopus.com/inward/record.url?scp=85120975375&partnerID=8YFLogxK
U2 - 10.1016/j.jad.2021.10.104
DO - 10.1016/j.jad.2021.10.104
M3 - Article
C2 - 34800569
AN - SCOPUS:85120975375
SN - 0165-0327
VL - 298
SP - 57
EP - 67
JO - Journal of Affective Disorders
JF - Journal of Affective Disorders
ER -