The DOI matches its Crossref record; 191 of the 191 references it cites were found in a registry or an index.
Development of Anterior Cingulate Functional Connectivity from Late Childhood to Early Adulthood
Abstract
Human cerebral development is remarkably protracted. Although microstructural processes of neuronal maturation remain accessible only to morphometric post-mortem studies, neuroimaging tools permit the examination of macrostructural aspects of brain development. The analysis of resting-state functional connectivity (FC) offers novel possibilities for the investigation of cerebral development. Using seed-based FC methods, we examined the development of 5 functionally distinct cingulate-based intrinsic connectivity networks (ICNs) in children (n = 14, 10.6 +/- 1.5 years), adolescents (n = 12, 15.4 +/- 1.2) and young adults (n=14, 22.4 +/- 1.2). Children demonstrated a more diffuse pattern of correlation with voxels proximal to the seed region of interest (ROI) ("local FC"), whereas adults exhibited more focal patterns of FC, as well as a greater number of significantly correlated voxels at long distances from the seed ROI. Adolescents exhibited intermediate patterns of FC. Consistent with evidence for different maturational time courses, ICNs associated with social and emotional functions exhibited the greatest developmental effects. Our findings demonstrate the utility of FC for the study of developing functional organization. Moreover, given that ICNs are thought to have an anatomical basis in neuronal connectivity, measures of FC may provide a quantitative index of brain maturation in healthy subjects and those with neurodevelopmental disorders.
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In the citing paper
“Prior to 2012, multiple studies had found that functional connectivity between anatomically proximate ROIs gradually decreased, whereas long-range functional connections, especially anterior-posterior links, gradually increased until adulthood (Dosenbach et al., 2010; Fair et al., 2009; Kelly et al., 2009; Supekar et al., 2009).”
From Development of large-scale functional networks from birth to adulthood: A guide to the neuroimaging literature (2017) · cites this paper as Kelly et al., 2009
In the citing paper
“Also, the greatest development occurred in those ICNs associated with social and emotional functions.”
From Emerging Adulthood, a Pre-adult Life-History Stage (2020) · cites this paper as [35]
In the citing paper
“They found that the pattern of correlation with voxels proximal to the seed region of interest was age-dependent: the pattern was diffuse in children (mean age 10.6 years), was less diffuse in adolescents (mean age 15.4 years), and showed signs of becoming focal in young adults (mean age 22.4 years).”
From Emerging Adulthood, a Pre-adult Life-History Stage (2020) · cites this paper as [35]
In the citing paper
“Kelly and colleagues provide additional evidence that brain maturation extends beyond adolescence into young adulthood (35).”
From Emerging Adulthood, a Pre-adult Life-History Stage (2020) · cites this paper as [35]
In the citing paper
“diffuse patterns of local FC are gradually replaced by a distributed architecture, dominated by focal long-range connections (3-6).”
From Aberrant Striatal Functional Connectivity in Children with Autism (2011) · cites this paper as [5]
In the citing paper
“Since development is characterized by an overall increase in long-range functional connections (3-5;25), these studies suggest dysmaturation as a core feature of ASD pathophysiology.”
From Aberrant Striatal Functional Connectivity in Children with Autism (2011) · cites this paper as [5]
In the citing paper
“This resembles TDC functional architecture rather than that of TA (3;5;25), suggesting developmental immaturity in ASD.”
From Aberrant Striatal Functional Connectivity in Children with Autism (2011) · cites this paper as [5]
In the citing paper
“initial R-fMRI studies of adults with ASD demonstrated reduced long-range FC in large-scale networks (3;e.g., 5;50).”
From Aberrant Striatal Functional Connectivity in Children with Autism (2011) · cites this paper as [5]
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Cited by
Sorted by citations
Toward discovery science of human brain function
Biswal, B. B., Mennes, M., Zuo, X.-N., Gohel, S., Kelly, C., Smith, S. M., Beckmann, C. F., Adelstein, J. S., Buckner, R. L., Colcombe, S., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0911855107 · Cited by 2,970
Self-citationNeurodegenerative Diseases Target Large-Scale Human Brain Networks
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“, 2008) and remodel itself (Kelly et al., 2008; Lerch et al., 2006) in response to core inherited projection map formation scripts (Ruthazer and Cline, 2004) that interact with the environment to drive individual differences in cognitive, emotional, and motor function (Seeley et al.”
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Functional brain networks develop from a local to distributed organization
Fair, D. A., Cohen, A. L., Power, J. D., Dosenbach, N. U. F., Church, J. A., Miezin, F. M., Schlaggar, B. L., & Petersen, S. E. (2009) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000381 · Cited by 1,530
“These results have now been replicated in a developmental resting connectivity study targeting sub-regions of the anterior cingulate [34].”
BackgroundMethodResultInfluentialNormal development of brain circuits
Tau, G. Z., & Peterson, B. S. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.115 · Cited by 1,391
“Sets of regions that share temporally correlated activity at rest are believed to constitute functional networks (Beckmann et al, 2005; Damoiseaux et al, 2006; Deluca et al, 2006; Fox et al, 2005, 2006; Fox and Raichle, 2007; Greicius et al, 2003; Kelly et al, 2008; Raichle et al, 2001).”
Background
Metadata
- Authors
- Kelly, A. M. C., Di Martino, A., Uddin, L. Q., Shehzad, Z., Gee, D. G., Reiss, P. T., Margulies, D. S., Castellanos, F. X., & Milham, M. P.
- Affiliations
- NYU Langone Health (US)
- New York University (US)
- Humboldt-Universität zu Berlin (DE)
- Nathan Kline Institute for Psychiatric Research (US)
- Venue
- Cerebral Cortex
- Publisher
- Oxford University Press (OUP)
- Published
- 2008-07-24
- Volume
- 19
- Issue
- 3
- Pages
- 640-657
- ISSN
- 1047-3211 (ISSN-L)
- 1460-2199
- OpenAlex
- W2113490642
- Cited by
- 572
- References
- 191
- Citations by year
- 2026: 10 · 2025: 16 · 2024: 17 · 2023: 22 · 2022: 20 · 2021: 34 · 2020: 25 · 2019: 33 · 2018: 37 · 2017: 37 · 2016: 36 · 2015: 37 · 2014: 63 · 2013: 51 · 2012: 43
- FWCI
- 15.68
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Cerebral Cortex (publishedVersion)
- PubMed (publishedVersion)
- Max Planck Digital Library (submittedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Keywords
- anterior cingulate cortex, resting-state functional connectivity, resting-state networks, brain maturation, developmental trajectories, children, adolescents, young adults, seed-based functional connectivity
- MeSH terms
- Adolescent, Age Factors, Child, Female, Gyrus Cinguli, Humans, Functional Laterality, Male, Nerve Net, Young Adult
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