TY - JOUR
T1 - Subclinical Anxiety and Posttraumatic Stress Influence Cortical Thinning During Adolescence
AU - Taylor, Brittany K.
AU - Eastman, Jacob A.
AU - Frenzel, Michaela R.
AU - Embury, Christine M.
AU - Wang, Yu Ping
AU - Stephen, Julia M.
AU - Calhoun, Vince D.
AU - Badura-Brack, Amy S.
AU - Wilson, Tony W.
N1 - Funding Information:
This work was supported by the National Science Foundation (#1539067 to TWW, YPW, JMS, and VDC), the National Institutes of Health (R01-MH121101 to TWW; R01-MH103220 to TWW; R01-MH116782 to TWW; R01-MH118013 to TWW; P20-GM103472 to VDC; and R01-EB020407 to VDC), and At Ease, USA (ABB). Funding agencies had no part in the study design or the writing of this report. Author ContributionsConceptualization: Stephen, Calhoun, Badura-Brack, WilsonData curation: Eastman, Frenzel, Embury, Stephen, Calhoun, WilsonFormal analysis: Taylor, CalhounFunding acquisition: Wang, Stephen, Calhoun, WilsonInvestigation: WilsonMethodology: Calhoun, Badura-Brack, WilsonProject administration: Stephen, Calhoun, WilsonResources: WilsonSoftware: CalhounSupervision: Stephen, WilsonValidation: TaylorVisualization: TaylorWriting – original draft: TaylorWriting – review and editing: Eastman, Frenzel, Embury, Wang, Stephen, Calhoun, Badura-Brack, Wilson Disclosure: Drs. Taylor, Wang, Stephen, Calhoun, Badura-Brack, Wilson, Mr. Eastman, and Mss. Frenzel and Embury have reported no biomedical financial interests or potential conflicts of interest.
Publisher Copyright:
© 2020 The Authors
PY - 2021/10
Y1 - 2021/10
N2 - Objective: Adolescence is a sensitive period for the development and emergence of anxiety and mood disorders. Research suggests that symptoms ranging from subclinical to clinical levels are associated with pathological developmental changes in the neocortex. However, much of this research has been cross-sectional, limiting the field's ability to identify the neurodevelopmental impacts of these symptoms. The present study examined how early reported symptoms predict baseline cortical thickness and surface area, and trajectories of change in these measures during adolescence. Method: A total of 205 typically developing individuals 9 to 15 years of age (103 male and 102 female participants) completed 3T structural magnetic resonance imaging annually for 3 years. From these, we extracted mean cortical thickness and total surface area for each year. Youth self-reported their anxiety, depressive, and posttraumatic stress symptoms during their first visit. We used latent growth curve modeling to determine how these symptoms along with sex interactions predicted baseline thickness and surface area, and rates of change in these measures over the 3-year period. Results: Higher anxiety was associated with lower baseline thickness and slowed cortical thinning over time. Conversely, greater posttraumatic stress predicted higher baseline thickness and accelerated thinning over time. Sex interactions suggested that the effects were dampened among female compared to male participants. Depressive symptoms were not related to cortical thickness or surface area. Conclusion: Female adolescents may express more regionally specific effects of symptoms sets on cortical thickness, although this requires further investigation. Cortical thickness in male adolescents appears to be preferentially susceptible to anxiety and posttraumatic stress symptoms, exhibiting global changes across multiple years.
AB - Objective: Adolescence is a sensitive period for the development and emergence of anxiety and mood disorders. Research suggests that symptoms ranging from subclinical to clinical levels are associated with pathological developmental changes in the neocortex. However, much of this research has been cross-sectional, limiting the field's ability to identify the neurodevelopmental impacts of these symptoms. The present study examined how early reported symptoms predict baseline cortical thickness and surface area, and trajectories of change in these measures during adolescence. Method: A total of 205 typically developing individuals 9 to 15 years of age (103 male and 102 female participants) completed 3T structural magnetic resonance imaging annually for 3 years. From these, we extracted mean cortical thickness and total surface area for each year. Youth self-reported their anxiety, depressive, and posttraumatic stress symptoms during their first visit. We used latent growth curve modeling to determine how these symptoms along with sex interactions predicted baseline thickness and surface area, and rates of change in these measures over the 3-year period. Results: Higher anxiety was associated with lower baseline thickness and slowed cortical thinning over time. Conversely, greater posttraumatic stress predicted higher baseline thickness and accelerated thinning over time. Sex interactions suggested that the effects were dampened among female compared to male participants. Depressive symptoms were not related to cortical thickness or surface area. Conclusion: Female adolescents may express more regionally specific effects of symptoms sets on cortical thickness, although this requires further investigation. Cortical thickness in male adolescents appears to be preferentially susceptible to anxiety and posttraumatic stress symptoms, exhibiting global changes across multiple years.
KW - MRI
KW - adolescent development
KW - longitudinal
KW - structural equation modeling
KW - subclinical symptoms
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U2 - 10.1016/j.jaac.2020.11.020
DO - 10.1016/j.jaac.2020.11.020
M3 - Article
C2 - 33383162
AN - SCOPUS:85103429048
SN - 0890-8567
VL - 60
SP - 1288
EP - 1299
JO - Journal of the American Academy of Child Psychiatry
JF - Journal of the American Academy of Child Psychiatry
IS - 10
ER -