TY - JOUR
T1 - Neurobiological Correlates of Change in Adaptive Behavior in Autism
AU - Pretzsch, Charlotte M
AU - Schäfer, Tim
AU - Lombardo, Michael V
AU - Warrier, Varun
AU - Mann, Caroline
AU - Bletsch, Anke
AU - Chatham, Chris H
AU - Floris, Dorothea L
AU - Tillmann, Julian
AU - Yousaf, Afsheen
AU - Jones, Emily
AU - Charman, Tony
AU - Ambrosino, Sara
AU - Bourgeron, Thomas
AU - Dumas, Guillaume
AU - Loth, Eva
AU - Oakley, Bethany
AU - Buitelaar, Jan K
AU - Cliquet, Freddy
AU - Leblond, Claire S
AU - Baron-Cohen, Simon
AU - Beckmann, Christian F
AU - Banaschewski, Tobias
AU - Durston, Sarah
AU - Freitag, Christine M
AU - Murphy, Declan G M
AU - Ecker, Christine
N1 - Publisher Copyright:
© 2022 American Psychiatric Association. All rights reserved.
PY - 2022/5
Y1 - 2022/5
N2 - OBJECTIVE: Autism spectrum disorder (ASD) is a lifelong neurodevelopmental condition that is associated with significant difficulties in adaptive behavior and variation in clinical outcomes across the life span. Some individuals with ASD improve, whereas others may not change significantly, or regress. Hence, the development of "personalized medicine" approaches is essential. However, this requires an understanding of the biological processes underpinning differences in clinical outcome, at both the individual and subgroup levels, across the lifespan.METHODS: The authors conducted a longitudinal follow-up study of 483 individuals (204 with ASD and 279 neurotypical individuals, ages 6-30 years), with assessment time points separated by ∼12-24 months. Data collected included behavioral data (Vineland Adaptive Behavior Scale-II), neuroanatomical data (structural MRI), and genetic data (DNA). Individuals with ASD were grouped into clinically meaningful "increasers," "no-changers," and "decreasers" in adaptive behavior. First, the authors compared neuroanatomy between outcome groups. Next, they examined whether deviations from the neurotypical neuroanatomical profile were associated with outcome at the individual level. Finally, they explored the observed neuroanatomical differences' potential genetic underpinnings.RESULTS: Outcome groups differed in neuroanatomical features (cortical volume and thickness, surface area), including in "social brain" regions previously implicated in ASD. Also, deviations of neuroanatomical features from the neurotypical profile predicted outcome at the individual level. Moreover, neuroanatomical differences were associated with genetic processes relevant to neuroanatomical phenotypes (e.g., synaptic development).CONCLUSIONS: This study demonstrates, for the first time, that variation in clinical (adaptive) outcome is associated with both group- and individual-level variation in anatomy of brain regions enriched for genes relevant to ASD. This may facilitate the move toward better targeted/precision medicine approaches.
AB - OBJECTIVE: Autism spectrum disorder (ASD) is a lifelong neurodevelopmental condition that is associated with significant difficulties in adaptive behavior and variation in clinical outcomes across the life span. Some individuals with ASD improve, whereas others may not change significantly, or regress. Hence, the development of "personalized medicine" approaches is essential. However, this requires an understanding of the biological processes underpinning differences in clinical outcome, at both the individual and subgroup levels, across the lifespan.METHODS: The authors conducted a longitudinal follow-up study of 483 individuals (204 with ASD and 279 neurotypical individuals, ages 6-30 years), with assessment time points separated by ∼12-24 months. Data collected included behavioral data (Vineland Adaptive Behavior Scale-II), neuroanatomical data (structural MRI), and genetic data (DNA). Individuals with ASD were grouped into clinically meaningful "increasers," "no-changers," and "decreasers" in adaptive behavior. First, the authors compared neuroanatomy between outcome groups. Next, they examined whether deviations from the neurotypical neuroanatomical profile were associated with outcome at the individual level. Finally, they explored the observed neuroanatomical differences' potential genetic underpinnings.RESULTS: Outcome groups differed in neuroanatomical features (cortical volume and thickness, surface area), including in "social brain" regions previously implicated in ASD. Also, deviations of neuroanatomical features from the neurotypical profile predicted outcome at the individual level. Moreover, neuroanatomical differences were associated with genetic processes relevant to neuroanatomical phenotypes (e.g., synaptic development).CONCLUSIONS: This study demonstrates, for the first time, that variation in clinical (adaptive) outcome is associated with both group- and individual-level variation in anatomy of brain regions enriched for genes relevant to ASD. This may facilitate the move toward better targeted/precision medicine approaches.
KW - Autism Spectrum Disorder
KW - Biological Markers
KW - Genetics/Genomics
KW - Neuroanatomy
KW - Neurodevelopmental Disorders
KW - Neuroimaging
UR - http://www.scopus.com/inward/record.url?scp=85129781004&partnerID=8YFLogxK
U2 - 10.1176/appi.ajp.21070711
DO - 10.1176/appi.ajp.21070711
M3 - Article
C2 - 35331004
SN - 0002-953X
VL - 179
SP - 336
EP - 349
JO - American Journal of Psychiatry
JF - American Journal of Psychiatry
IS - 5
ER -