Table 2.
Study | Data Source | n | Age, Years, Mean ± SD or Range | Male, % | Algorithm/Approach | Features | Validation | Symptoms/Phenotypes Predicted | Highlights |
---|---|---|---|---|---|---|---|---|---|
(27) | ABIDE, ADHD-200 | ABIDE: 122 autism, 230 NTa ADHD-200: 77 ADHD, 35 NT |
6–24 | 71%b | CPM (linear regression) | FC from 268 × 268 ROIs (Shen atlas) (148) | Internal (split half, leave-one-out CV); leave-one-site-out CV; external validation in independent sample | SRS, ADOS, ADHD-RS | SRS, ADOS predictive network models were largely distinct; SRS model generalized to predict inattention in a separate ADHD sample |
(54) | Lab-specific | 58 autismc | Not specified for dim. analyses | Not specified for dim. analyses | Linear regression | 16 FC | Internal (leave-one-out CV) | ADOS, ADI-R | Functional connections identified as correctly classifying autism vs. NT status generalized to predict the communication domain of ADOS |
(78) | ABIDE | 103 autism | 20.8 ± 8.1 | 100% | SVR | First score of principal connectivity gradient, stepwise connectivity maps | Internal (5-fold CV); leave-one-site-out CV | ADOS | Prediction of ADOS total and social cognition; DMN and primary visual areas highly represented in predictive models |
(86) | ABIDE, LEAP | 232 autismd | 14.8 ± 6.5 | 74% | CCA | FC from 415 × 415 ROIs [Schaefer atlas (149) 1 subcortical atlas] | Leave-one-site-out CV | Various autism, social abilities scales | Multiple canonical variates predictive of left-out-site; connections within and between somatomotor, DMN, attention, visual networks implicated in models |
(87) | Lab-specific | 31 autism | 17.9 ± 3.4 | 100% | Ridge regression | FC from DMN, SN, FPN networks (Power atlas) (140) | Internal (leave-one-out CV) | SRS, ABAS | Prediction of change in SRS and ABAS scores and prediction of time 2 SRS scores ~ 3 years after scanning |
(88) | ABIDE | 85 autism 191 NT |
8–13 | 66% | CPM (linear regression) | FC from 268 × 268 ROIs (Shen atlas) (148) | Internal (leave-one-out, split-half CV); site 1 to site 2 prediction | BRIEF | Complex, brain-wide model with many edges in somatomotor, visual, and cerebellar areas; also edges in DMN and temporal lobe |
(89) | ABIDE | 82 autism | 7–12 | 100% | Lasso regression | FC from 227 × 227 ROIs (Power atlas) (140) | Internal (leave-one-out CV) | ADOS | Separate predictive brain networks predicting communication and social interaction phenotypes can be merged to predict social affect scores |
ABAS, Adaptive Behavior Assessment System; ABIDE, Autism Brain Imaging Data Exchange; ADHD, attention-deficit/hyperactivity disorder; ADHD-RS, ADHD Rating Scale; ADI-R, Autism Diagnostic Interview–Revised; ADOS, Autism Diagnostic Observation Schedule; BRIEF, Behavior Rating Inventory of Executive Function; CCA, canonical correlation analysis; CPM, connectome-based predictive modeling; CV, cross-validation; dFC, dynamic functional connectivity; dim., dimension; DMN, default mode network; FC, functional connectivity; FPN, frontoparietal network; LEAP, European Autism Interventions Multicenter Study for Developing New Medications Longitudinal European Autism Project; NT, neurotypical; ROI, region of interest; SN, salience network; SRS, Social Responsiveness Scale; SVR, support vector regression.
Here, we report sample size used for most of the SRS analyses (SRS total scores as well as the following subscales: communication, motivation, and mannerisms). The sample size was n = 180 NT and 80 autism for predicting SRS cognition and awareness subscales and n = 79 autism and n = 58 autism for predicting ADOS modules 3 and 4, respectively.
Across SRS analyses, ~70% of the sample was male; in ADOS analyses, ~85% of the sample was male. Sex was not reported in the ADHD-200 sample.
We report the sample size used in the ADOS dimensional prediction analyses. A total of 27 participants with autism were used in the ADI-R dimensional prediction analyses.
A total of 125 individuals with autism and 78 control subjects from the LEAP cohort were used in Short Sensory Profile subscales analyses; demographics were roughly similar to the rest of the sample.