Amygdala subnuclei development in adolescents with autism spectrum disorder: Association with social communication and repetitive behaviors
Introduction The amygdala subnuclei regulate emotional processing and are widely implicated in social cognitive impairments often seen in children with autism spectrum disorder (ASD). Dysregulated amygdala development has been reported in young children with ASD; less is known about amygdala maturat...
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Published in | Brain and behavior Vol. 11; no. 8; pp. e2299 - n/a |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Los Angeles
John Wiley & Sons, Inc
01.08.2021
John Wiley and Sons Inc Wiley |
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Abstract | Introduction
The amygdala subnuclei regulate emotional processing and are widely implicated in social cognitive impairments often seen in children with autism spectrum disorder (ASD). Dysregulated amygdala development has been reported in young children with ASD; less is known about amygdala maturation in later adolescence, a sensitive window for social skill development.
Methods
The macrostructural development of the amygdala subnuclei was assessed at two time points in a longitudinal magnetic resonance imaging (MRI) study of adolescents with ASD (n = 23) and typically‐developing adolescents (n = 15) . In adolescents with ASD, amygdala subnuclei growth was assessed in relation to ASD symptomatology based on standardized diagnostic assessments. Participants were scanned with MRI at median age of 12 years and returned for a second scan at a median age of 15 years. The volumes of nine amygdala subnuclei were extracted using an automatic segmentation algorithm.
Results
When examining the longitudinal data acquired across two time points, adolescents with ASD had larger basolateral amygdala (BLA) nuclei volumes compared to typically developing adolescents (B = 46.8, p = 0.04). When examining ASD symptomatology in relation to the growth of the amygdala subnuclei, reciprocal social interaction scores on the ADI‐R were positively associated with increased growth of the BLA nuclei (B = 8.3, p < 0.001). Growth in the medial nucleus negatively predicted the communication (B = −46.9, p = 0.02) and social (B = −47.7, p < 0.001) domains on the ADOS‐G. Growth in the right cortical nucleus (B = 26.14, p = 0.02) positively predicted ADOS‐G social scores. Central nucleus maturation (B = 29.9, p = 0.02) was associated with the repetitive behaviors domain on the ADOS‐G.
Conclusions
Larger BLA volumes in adolescents with ASD may reflect underlying alterations in cellular density previously reported in post‐mortem studies. Furthermore, findings demonstrate an association between regional growth in amygdala subnuclei volumes and ASD symptomatology. Improved understanding of the developmental trajectories of the amygdala subnuclei may aid in identifying key windows for interventions, particularly for social communication, in adolescents with ASD.
Amygdala subnuclei maturation was examined in adolescents with and without ASD. The volumes of the BLA nuclei were larger in adolescents with ASD compared to controls. BLA, cortical, and medial nuclei predicted social and/or communication skills. Larger central nuclei volumes positively predicted repetitive behaviors. |
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AbstractList | Introduction
The amygdala subnuclei regulate emotional processing and are widely implicated in social cognitive impairments often seen in children with autism spectrum disorder (ASD). Dysregulated amygdala development has been reported in young children with ASD; less is known about amygdala maturation in later adolescence, a sensitive window for social skill development.
Methods
The macrostructural development of the amygdala subnuclei was assessed at two time points in a longitudinal magnetic resonance imaging (MRI) study of adolescents with ASD (n = 23) and typically‐developing adolescents (n = 15) . In adolescents with ASD, amygdala subnuclei growth was assessed in relation to ASD symptomatology based on standardized diagnostic assessments. Participants were scanned with MRI at median age of 12 years and returned for a second scan at a median age of 15 years. The volumes of nine amygdala subnuclei were extracted using an automatic segmentation algorithm.
Results
When examining the longitudinal data acquired across two time points, adolescents with ASD had larger basolateral amygdala (BLA) nuclei volumes compared to typically developing adolescents (B = 46.8, p = 0.04). When examining ASD symptomatology in relation to the growth of the amygdala subnuclei, reciprocal social interaction scores on the ADI‐R were positively associated with increased growth of the BLA nuclei (B = 8.3, p < 0.001). Growth in the medial nucleus negatively predicted the communication (B = −46.9, p = 0.02) and social (B = −47.7, p < 0.001) domains on the ADOS‐G. Growth in the right cortical nucleus (B = 26.14, p = 0.02) positively predicted ADOS‐G social scores. Central nucleus maturation (B = 29.9, p = 0.02) was associated with the repetitive behaviors domain on the ADOS‐G.
Conclusions
Larger BLA volumes in adolescents with ASD may reflect underlying alterations in cellular density previously reported in post‐mortem studies. Furthermore, findings demonstrate an association between regional growth in amygdala subnuclei volumes and ASD symptomatology. Improved understanding of the developmental trajectories of the amygdala subnuclei may aid in identifying key windows for interventions, particularly for social communication, in adolescents with ASD.
Amygdala subnuclei maturation was examined in adolescents with and without ASD. The volumes of the BLA nuclei were larger in adolescents with ASD compared to controls. BLA, cortical, and medial nuclei predicted social and/or communication skills. Larger central nuclei volumes positively predicted repetitive behaviors. Abstract Introduction The amygdala subnuclei regulate emotional processing and are widely implicated in social cognitive impairments often seen in children with autism spectrum disorder (ASD). Dysregulated amygdala development has been reported in young children with ASD; less is known about amygdala maturation in later adolescence, a sensitive window for social skill development. Methods The macrostructural development of the amygdala subnuclei was assessed at two time points in a longitudinal magnetic resonance imaging (MRI) study of adolescents with ASD (n = 23) and typically‐developing adolescents (n = 15) . In adolescents with ASD, amygdala subnuclei growth was assessed in relation to ASD symptomatology based on standardized diagnostic assessments. Participants were scanned with MRI at median age of 12 years and returned for a second scan at a median age of 15 years. The volumes of nine amygdala subnuclei were extracted using an automatic segmentation algorithm. Results When examining the longitudinal data acquired across two time points, adolescents with ASD had larger basolateral amygdala (BLA) nuclei volumes compared to typically developing adolescents (B = 46.8, p = 0.04). When examining ASD symptomatology in relation to the growth of the amygdala subnuclei, reciprocal social interaction scores on the ADI‐R were positively associated with increased growth of the BLA nuclei (B = 8.3, p < 0.001). Growth in the medial nucleus negatively predicted the communication (B = −46.9, p = 0.02) and social (B = −47.7, p < 0.001) domains on the ADOS‐G. Growth in the right cortical nucleus (B = 26.14, p = 0.02) positively predicted ADOS‐G social scores. Central nucleus maturation (B = 29.9, p = 0.02) was associated with the repetitive behaviors domain on the ADOS‐G. Conclusions Larger BLA volumes in adolescents with ASD may reflect underlying alterations in cellular density previously reported in post‐mortem studies. Furthermore, findings demonstrate an association between regional growth in amygdala subnuclei volumes and ASD symptomatology. Improved understanding of the developmental trajectories of the amygdala subnuclei may aid in identifying key windows for interventions, particularly for social communication, in adolescents with ASD. Amygdala subnuclei maturation was examined in adolescents with and without ASD. The volumes of the BLA nuclei were larger in adolescents with ASD compared to controls. BLA, cortical, and medial nuclei predicted social and/or communication skills. Larger central nuclei volumes positively predicted repetitive behaviors. IntroductionThe amygdala subnuclei regulate emotional processing and are widely implicated in social cognitive impairments often seen in children with autism spectrum disorder (ASD). Dysregulated amygdala development has been reported in young children with ASD; less is known about amygdala maturation in later adolescence, a sensitive window for social skill development.MethodsThe macrostructural development of the amygdala subnuclei was assessed at two time points in a longitudinal magnetic resonance imaging (MRI) study of adolescents with ASD (n = 23) and typically-developing adolescents (n = 15) . In adolescents with ASD, amygdala subnuclei growth was assessed in relation to ASD symptomatology based on standardized diagnostic assessments. Participants were scanned with MRI at median age of 12 years and returned for a second scan at a median age of 15 years. The volumes of nine amygdala subnuclei were extracted using an automatic segmentation algorithm.ResultsWhen examining the longitudinal data acquired across two time points, adolescents with ASD had larger basolateral amygdala (BLA) nuclei volumes compared to typically developing adolescents (B = 46.8, p = 0.04). When examining ASD symptomatology in relation to the growth of the amygdala subnuclei, reciprocal social interaction scores on the ADI-R were positively associated with increased growth of the BLA nuclei (B = 8.3, p < 0.001). Growth in the medial nucleus negatively predicted the communication (B = −46.9, p = 0.02) and social (B = −47.7, p < 0.001) domains on the ADOS-G. Growth in the right cortical nucleus (B = 26.14, p = 0.02) positively predicted ADOS-G social scores. Central nucleus maturation (B = 29.9, p = 0.02) was associated with the repetitive behaviors domain on the ADOS-G.ConclusionsLarger BLA volumes in adolescents with ASD may reflect underlying alterations in cellular density previously reported in post-mortem studies. Furthermore, findings demonstrate an association between regional growth in amygdala subnuclei volumes and ASD symptomatology. Improved understanding of the developmental trajectories of the amygdala subnuclei may aid in identifying key windows for interventions, particularly for social communication, in adolescents with ASD. The amygdala subnuclei regulate emotional processing and are widely implicated in social cognitive impairments often seen in children with autism spectrum disorder (ASD). Dysregulated amygdala development has been reported in young children with ASD; less is known about amygdala maturation in later adolescence, a sensitive window for social skill development.INTRODUCTIONThe amygdala subnuclei regulate emotional processing and are widely implicated in social cognitive impairments often seen in children with autism spectrum disorder (ASD). Dysregulated amygdala development has been reported in young children with ASD; less is known about amygdala maturation in later adolescence, a sensitive window for social skill development.The macrostructural development of the amygdala subnuclei was assessed at two time points in a longitudinal magnetic resonance imaging (MRI) study of adolescents with ASD (n = 23) and typically-developing adolescents (n = 15) . In adolescents with ASD, amygdala subnuclei growth was assessed in relation to ASD symptomatology based on standardized diagnostic assessments. Participants were scanned with MRI at median age of 12 years and returned for a second scan at a median age of 15 years. The volumes of nine amygdala subnuclei were extracted using an automatic segmentation algorithm.METHODSThe macrostructural development of the amygdala subnuclei was assessed at two time points in a longitudinal magnetic resonance imaging (MRI) study of adolescents with ASD (n = 23) and typically-developing adolescents (n = 15) . In adolescents with ASD, amygdala subnuclei growth was assessed in relation to ASD symptomatology based on standardized diagnostic assessments. Participants were scanned with MRI at median age of 12 years and returned for a second scan at a median age of 15 years. The volumes of nine amygdala subnuclei were extracted using an automatic segmentation algorithm.When examining the longitudinal data acquired across two time points, adolescents with ASD had larger basolateral amygdala (BLA) nuclei volumes compared to typically developing adolescents (B = 46.8, p = 0.04). When examining ASD symptomatology in relation to the growth of the amygdala subnuclei, reciprocal social interaction scores on the ADI-R were positively associated with increased growth of the BLA nuclei (B = 8.3, p < 0.001). Growth in the medial nucleus negatively predicted the communication (B = -46.9, p = 0.02) and social (B = -47.7, p < 0.001) domains on the ADOS-G. Growth in the right cortical nucleus (B = 26.14, p = 0.02) positively predicted ADOS-G social scores. Central nucleus maturation (B = 29.9, p = 0.02) was associated with the repetitive behaviors domain on the ADOS-G.RESULTSWhen examining the longitudinal data acquired across two time points, adolescents with ASD had larger basolateral amygdala (BLA) nuclei volumes compared to typically developing adolescents (B = 46.8, p = 0.04). When examining ASD symptomatology in relation to the growth of the amygdala subnuclei, reciprocal social interaction scores on the ADI-R were positively associated with increased growth of the BLA nuclei (B = 8.3, p < 0.001). Growth in the medial nucleus negatively predicted the communication (B = -46.9, p = 0.02) and social (B = -47.7, p < 0.001) domains on the ADOS-G. Growth in the right cortical nucleus (B = 26.14, p = 0.02) positively predicted ADOS-G social scores. Central nucleus maturation (B = 29.9, p = 0.02) was associated with the repetitive behaviors domain on the ADOS-G.Larger BLA volumes in adolescents with ASD may reflect underlying alterations in cellular density previously reported in post-mortem studies. Furthermore, findings demonstrate an association between regional growth in amygdala subnuclei volumes and ASD symptomatology. Improved understanding of the developmental trajectories of the amygdala subnuclei may aid in identifying key windows for interventions, particularly for social communication, in adolescents with ASD.CONCLUSIONSLarger BLA volumes in adolescents with ASD may reflect underlying alterations in cellular density previously reported in post-mortem studies. Furthermore, findings demonstrate an association between regional growth in amygdala subnuclei volumes and ASD symptomatology. Improved understanding of the developmental trajectories of the amygdala subnuclei may aid in identifying key windows for interventions, particularly for social communication, in adolescents with ASD. |
Author | Nicolson, Rob Duerden, Emma G. Martinez‐Trujillo, Julio Wang, Jianan Seguin, Diane Pac, Sara |
AuthorAffiliation | 5 Applied Psychology Faculty of Education, Western University London Canada 3 Biomedical Engineering Faculty of Engineering, Western University London Canada 1 Physiology and Pharmacology Schulich School of Medicine and Dentistry, Western University London Canada 2 Neuroscience Schulich School of Medicine and Dentistry, Western University London Canada 4 Psychiatry, Schulich School of Medicine and Dentistry University of Western Ontario London Canada |
AuthorAffiliation_xml | – name: 3 Biomedical Engineering Faculty of Engineering, Western University London Canada – name: 1 Physiology and Pharmacology Schulich School of Medicine and Dentistry, Western University London Canada – name: 2 Neuroscience Schulich School of Medicine and Dentistry, Western University London Canada – name: 4 Psychiatry, Schulich School of Medicine and Dentistry University of Western Ontario London Canada – name: 5 Applied Psychology Faculty of Education, Western University London Canada |
Author_xml | – sequence: 1 givenname: Diane surname: Seguin fullname: Seguin, Diane organization: Schulich School of Medicine and Dentistry, Western University – sequence: 2 givenname: Sara surname: Pac fullname: Pac, Sara organization: Schulich School of Medicine and Dentistry, Western University – sequence: 3 givenname: Jianan surname: Wang fullname: Wang, Jianan organization: Faculty of Engineering, Western University – sequence: 4 givenname: Rob surname: Nicolson fullname: Nicolson, Rob organization: University of Western Ontario – sequence: 5 givenname: Julio surname: Martinez‐Trujillo fullname: Martinez‐Trujillo, Julio organization: Schulich School of Medicine and Dentistry, Western University – sequence: 6 givenname: Emma G. orcidid: 0000-0002-9734-7865 surname: Duerden fullname: Duerden, Emma G. email: eduerden@uwo.ca organization: Faculty of Education, Western University |
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Snippet | Introduction
The amygdala subnuclei regulate emotional processing and are widely implicated in social cognitive impairments often seen in children with autism... IntroductionThe amygdala subnuclei regulate emotional processing and are widely implicated in social cognitive impairments often seen in children with autism... The amygdala subnuclei regulate emotional processing and are widely implicated in social cognitive impairments often seen in children with autism spectrum... Amygdala subnuclei maturation was examined in adolescents with and without ASD. The volumes of the BLA nuclei were larger in adolescents with ASD compared to... Abstract Introduction The amygdala subnuclei regulate emotional processing and are widely implicated in social cognitive impairments often seen in children... |
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StartPage | e2299 |
SubjectTerms | Adults Amygdala Anxiety Autism autism spectrum disorders Behavior Brain Child development Communication human magnetic resonance imaging Original Research Post traumatic stress disorder Rodents Schizophrenia social Teenagers |
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Title | Amygdala subnuclei development in adolescents with autism spectrum disorder: Association with social communication and repetitive behaviors |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fbrb3.2299 https://www.proquest.com/docview/2568444634 https://www.proquest.com/docview/2557540270 https://pubmed.ncbi.nlm.nih.gov/PMC8413788 https://doaj.org/article/3a85ca6e60b84dce9880356015f4d7dd |
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