Neuroanatomical Diversity of Corpus Callosum and Brain Volume in Autism: Meta-analysis, Analysis of the Autism Brain Imaging Data Exchange Project, and Simulation

• Published in: Biological psychiatry (1969) Vol. 78; no. 2; pp. 126 - 134
• Main Authors: Lefebvre, Aline, Beggiato, Anita, Bourgeron, Thomas, Toro, Roberto
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 15.07.2015; Elsevier
• Subjects: Adolescent; Adult; Autism; Autistic Disorder; Autistic Disorder - pathology; Autistic Disorder - psychology; Brain; Brain - pathology; Brain volume; Child; Child, Preschool; Cognitive science; Computational neuroanatomy; Corpus Callosum; Corpus Callosum - pathology; Databases, Factual; Female; Human health and pathology; Humans; Intelligence; Life Sciences; Male; Meta-analysis; Psychiatric/Mental Health; Psychiatrics and mental health; Statistical power; Young Adult; Autism; Brain volume; Computational neuroanatomy; Statistical power; Corpus callosum; Meta-analysis
• ISSN: 0006-3223; 1873-2402; 1873-2402
• DOI: 10.1016/j.biopsych.2015.02.010

Patients with autism have been often reported to have a smaller corpus callosum (CC) than control subjects. We conducted a meta-analysis of the literature, analyzed the CC in 694 subjects of the Autism Brain Imaging Data Exchange project, and performed computer simulations to study the effect of different analysis strategies. Our meta-analysis suggested a group difference in CC size; however, the studies were heavily underpowered (20% power to detect Cohen’s d = .3). In contrast, we did not observe significant differences in the Autism Brain Imaging Data Exchange cohort, despite having achieved 99% power. However, we observed that CC scaled nonlinearly with brain volume (BV): large brains had a proportionally smaller CC. Our simulations showed that because of this nonlinearity, CC normalization could not control for eventual BV differences, but using BV as a covariate in a linear model would. We also observed a weaker correlation of IQ and BV in cases compared with control subjects. Our simulations showed that matching populations by IQ could then induce artifactual BV differences. The lack of statistical power in the previous literature prevents us from establishing the reality of the claims of a smaller CC in autism, and our own analyses did not find any. However, the nonlinear relationship between CC and BV and the different correlation between BV and IQ in cases and control subjects may induce artifactual differences. Overall, our results highlight the necessity for open data sharing to provide a more solid ground for the discovery of neuroimaging biomarkers within the context of the wide human neuroanatomical diversity.