Document Detail


Functional connectivity magnetic resonance imaging classification of autism.
MedLine Citation:
PMID:  22006979     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Group differences in resting state functional magnetic resonance imaging connectivity between individuals with autism and typically developing controls have been widely replicated for a small number of discrete brain regions, yet the whole-brain distribution of connectivity abnormalities in autism is not well characterized. It is also unclear whether functional connectivity is sufficiently robust to be used as a diagnostic or prognostic metric in individual patients with autism. We obtained pairwise functional connectivity measurements from a lattice of 7266 regions of interest covering the entire grey matter (26.4 million connections) in a well-characterized set of 40 male adolescents and young adults with autism and 40 age-, sex- and IQ-matched typically developing subjects. A single resting state blood oxygen level-dependent scan of 8 min was used for the classification in each subject. A leave-one-out classifier successfully distinguished autism from control subjects with 83% sensitivity and 75% specificity for a total accuracy of 79% (P = 1.1 × 10(-7)). In subjects <20 years of age, the classifier performed at 89% accuracy (P = 5.4 × 10(-7)). In a replication dataset consisting of 21 individuals from six families with both affected and unaffected siblings, the classifier performed at 71% accuracy (91% accuracy for subjects <20 years of age). Classification scores in subjects with autism were significantly correlated with the Social Responsiveness Scale (P = 0.05), verbal IQ (P = 0.02) and the Autism Diagnostic Observation Schedule-Generic's combined social and communication subscores (P = 0.05). An analysis of informative connections demonstrated that region of interest pairs with strongest correlation values were most abnormal in autism. Negatively correlated region of interest pairs showed higher correlation in autism (less anticorrelation), possibly representing weaker inhibitory connections, particularly for long connections (Euclidean distance >10 cm). Brain regions showing greatest differences included regions of the default mode network, superior parietal lobule, fusiform gyrus and anterior insula. Overall, classification accuracy was better for younger subjects, with differences between autism and control subjects diminishing after 19 years of age. Classification scores of unaffected siblings of individuals with autism were more similar to those of the control subjects than to those of the subjects with autism. These findings indicate feasibility of a functional connectivity magnetic resonance imaging diagnostic assay for autism.
Authors:
Jeffrey S Anderson; Jared A Nielsen; Alyson L Froehlich; Molly B DuBray; T Jason Druzgal; Annahir N Cariello; Jason R Cooperrider; Brandon A Zielinski; Caitlin Ravichandran; P Thomas Fletcher; Andrew L Alexander; Erin D Bigler; Nicholas Lange; Janet E Lainhart
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't     Date:  2011-10-17
Journal Detail:
Title:  Brain : a journal of neurology     Volume:  134     ISSN:  1460-2156     ISO Abbreviation:  Brain     Publication Date:  2011 Dec 
Date Detail:
Created Date:  2011-12-15     Completed Date:  2012-02-09     Revised Date:  2014-09-05    
Medline Journal Info:
Nlm Unique ID:  0372537     Medline TA:  Brain     Country:  England    
Other Details:
Languages:  eng     Pagination:  3742-54     Citation Subset:  AIM; IM    
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Autistic Disorder / classification*,  diagnosis,  physiopathology
Brain / physiopathology*
Brain Mapping
Humans
Image Processing, Computer-Assisted
Magnetic Resonance Imaging*
Male
Neural Pathways / physiopathology
Sensitivity and Specificity
Young Adult
Grant Support
ID/Acronym/Agency:
K08 MH092697/MH/NIMH NIH HHS; K08 MH092697/MH/NIMH NIH HHS; K08 MH092697-02/MH/NIMH NIH HHS; P50MH60450/MH/NIMH NIH HHS; R01MH080826/MH/NIMH NIH HHS; R01NS34783/NS/NINDS NIH HHS; T32DC008553/DC/NIDCD NIH HHS
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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