TY - JOUR
T1 - Altered Periodic Dynamics in the Default Mode Network in Autism and Attention-Deficit/Hyperactivity Disorder
AU - Curtin, Paul
AU - Neufeld, Janina
AU - Curtin, Austen
AU - Arora, Manish
AU - Bölte, Sven
N1 - Funding Information:
This work was supported by the Swedish Research Council, Vinnova, Formas, FORTE, Swedish Brain Foundation (Hjärnfonden), Stockholm Brain Institute, Autism and Asperger Association Stockholm, Queen Silvia's Jubilee Fund, Solstickan Foundation, PRIMA Child and Adult Psychiatry, Pediatric Research Foundation at Astrid Lindgren Children's Hospital, Swedish Foundation for Strategic Research, Jerring Foundation, Swedish Order of Freemasons, Kempe-Carlgrenska Foundation, Sunnderdahls Handikappsfond, Jeansson Foundations, EU-AIMS (European Autism Intervention) (with support from Innovative Medicines Initiative Joint Undertaking [Grant No. 115300], the resources of which are composed of financial contributions from the European Union's Seventh Framework Programme [Grant No. FP7/2007–2013], European Federation of Pharmaceutical Industries and Associations companies’ in-kind contributions, and Autism Speaks), Innovative Medicines Initiative–EU-AIMS AIMS-2-TRIALS, and National Institute of Environmental Health Sciences (Grant Nos. P30ES023515, R01ES026033, U2CES030859, and R35ES030435 [to MA]). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Genotyping was performed by the SNP&SEQ Technology Platform in Uppsala (www.genotyping.se). The facility is part of the National Genomics Infrastructure Sweden and Science for Life Laboratory. The SNP&SEQ Platform is also supported by the Swedish Research Council and the Knut and Alice Wallenberg Foundation. We thank all twins and parents who have participated in this research. We also thank the RATSS team at the Center of Neurodevelopmental Disorders at Karolinska Institutet for their valuable contribution to the work presented in this study. The authors report no biomedical financial interests or potential conflicts of interest.
Funding Information:
This work was supported by the Swedish Research Council , Vinnova , Formas , FORTE , Swedish Brain Foundation (Hjärnfonden), Stockholm Brain Institute , Autism and Asperger Association Stockholm , Queen Silvia’s Jubilee Fund , Solstickan Foundation , PRIMA Child and Adult Psychiatry, Pediatric Research Foundation at Astrid Lindgren Children’s Hospital, Swedish Foundation for Strategic Research , Jerring Foundation , Swedish Order of Freemasons , Kempe-Carlgrenska Foundation , Sunnderdahls Handikappsfond, Jeansson Foundations , EU-AIMS (European Autism Intervention) (with support from Innovative Medicines Initiative Joint Undertaking [Grant No. 115300 ], the resources of which are composed of financial contributions from the European Union’s Seventh Framework Programme [Grant No. FP7/2007–2013 ], European Federation of Pharmaceutical Industries and Associations companies’ in-kind contributions, and Autism Speaks ), Innovative Medicines Initiative–EU-AIMS AIMS-2-TRIALS, and National Institute of Environmental Health Sciences (Grant Nos. P30ES023515 , R01ES026033 , U2CES030859 , and R35ES030435 [to MA]). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Funding Information:
Genotyping was performed by the SNP&SEQ Technology Platform in Uppsala ( www.genotyping.se ). The facility is part of the National Genomics Infrastructure Sweden and Science for Life Laboratory. The SNP&SEQ Platform is also supported by the Swedish Research Council and the Knut and Alice Wallenberg Foundation .
Publisher Copyright:
© 2022 Society of Biological Psychiatry
PY - 2022/6/1
Y1 - 2022/6/1
N2 - Background: Altered resting-state functional connectivity in the default mode network (DMN) is characteristic of both autism spectrum disorder (ASD) and attention-deficit/hyperactivity disorder (ADHD). Standard analytical pipelines for resting-state functional connectivity focus on linear correlations in activation time courses between neural networks or regions of interest. These features may be insensitive to temporally lagged or nonlinear relationships. Methods: In a twin cohort study comprising 292 children, including 52 with a diagnosis of ASD and 70 with a diagnosis of ADHD, we applied nonlinear analytical methods to characterize periodic dynamics in the DMN. Using recurrence quantification analysis and related methods, we measured the prevalence, duration, and complexity of periodic processes within and between DMN regions of interest. We constructed generalized estimating equations to compare these features between neurotypical children and children with ASD and/or ADHD while controlling for familial relationships, and we leveraged machine learning algorithms to construct models predictive of ASD or ADHD diagnosis. Results: In within-pair analyses of twins with discordant ASD diagnoses, we found that DMN signal dynamics were significantly different in dizygotic twins but not in monozygotic twins. Considering our full sample, we found that these patterns allowed a robust predictive classification of both ASD (81.0% accuracy; area under the curve = 0.85) and ADHD (82% accuracy; area under the curve = 0.87) cases. Conclusions: These findings indicate that synchronized periodicity among regions comprising the DMN relates both to neurotypical function and to ASD and/or ADHD, and they suggest generally that a dynamical analysis of network interconnectivity may be a useful methodology for future neuroimaging studies.
AB - Background: Altered resting-state functional connectivity in the default mode network (DMN) is characteristic of both autism spectrum disorder (ASD) and attention-deficit/hyperactivity disorder (ADHD). Standard analytical pipelines for resting-state functional connectivity focus on linear correlations in activation time courses between neural networks or regions of interest. These features may be insensitive to temporally lagged or nonlinear relationships. Methods: In a twin cohort study comprising 292 children, including 52 with a diagnosis of ASD and 70 with a diagnosis of ADHD, we applied nonlinear analytical methods to characterize periodic dynamics in the DMN. Using recurrence quantification analysis and related methods, we measured the prevalence, duration, and complexity of periodic processes within and between DMN regions of interest. We constructed generalized estimating equations to compare these features between neurotypical children and children with ASD and/or ADHD while controlling for familial relationships, and we leveraged machine learning algorithms to construct models predictive of ASD or ADHD diagnosis. Results: In within-pair analyses of twins with discordant ASD diagnoses, we found that DMN signal dynamics were significantly different in dizygotic twins but not in monozygotic twins. Considering our full sample, we found that these patterns allowed a robust predictive classification of both ASD (81.0% accuracy; area under the curve = 0.85) and ADHD (82% accuracy; area under the curve = 0.87) cases. Conclusions: These findings indicate that synchronized periodicity among regions comprising the DMN relates both to neurotypical function and to ASD and/or ADHD, and they suggest generally that a dynamical analysis of network interconnectivity may be a useful methodology for future neuroimaging studies.
KW - Attention-deficit/hyperactivity disorder
KW - Autism
KW - Default mode network
KW - Dynamical systems
KW - Recurrence quantification analysis
KW - Resting-state connectivity
UR - http://www.scopus.com/inward/record.url?scp=85125419183&partnerID=8YFLogxK
U2 - 10.1016/j.biopsych.2022.01.010
DO - 10.1016/j.biopsych.2022.01.010
M3 - Article
C2 - 35227462
AN - SCOPUS:85125419183
VL - 91
SP - 956
EP - 966
JO - Biological Psychiatry
JF - Biological Psychiatry
SN - 0006-3223
IS - 11
ER -