Brain-phenotype predictions of language and executive function can survive across diverse real-world data: Dataset shifts in developmental populations

• Published in: Developmental cognitive neuroscience 2024-12, Vol.70, p.101464, Article 101464
• Main Authors: Adkinson, Brendan D., Rosenblatt, Matthew, Dadashkarimi, Javid, Tejavibulya, Link, Jiang, Rongtao, Noble, Stephanie, Scheinost, Dustin
• Format: Article
• Language: English
• Subjects: Adolescence; Adolescent; Adult; Brain - diagnostic imaging; Brain - growth & development; Brain - physiology; Child; Child, Preschool; Childhood; Cognition; Cohort Studies; Connectome - methods; Dataset shift; Datasets as Topic; Diversity; Executive Function - physiology; Female; Harmonization; Humans; Language; Machine learning; Magnetic Resonance Imaging - methods; Male; Original Research; Phenotype; Reproducibility of Results; Young Adult
• ISSN: 1878-9293; 1878-9307; 1878-9307
• DOI: 10.1016/j.dcn.2024.101464

Predictive modeling potentially increases the reproducibility and generalizability of neuroimaging brain-phenotype associations. Yet, the evaluation of a model in another dataset is underutilized. Among studies that undertake external validation, there is a notable lack of attention to generalization across dataset-specific idiosyncrasies (i.e., dataset shifts). Research settings, by design, remove the between-site variations that real-world and, eventually, clinical applications demand. Here, we rigorously test the ability of a range of predictive models to generalize across three diverse, unharmonized developmental samples: the Philadelphia Neurodevelopmental Cohort (n=1291), the Healthy Brain Network (n=1110), and the Human Connectome Project in Development (n=428). These datasets have high inter-dataset heterogeneity, encompassing substantial variations in age distribution, sex, racial and ethnic minority representation, recruitment geography, clinical symptom burdens, fMRI tasks, sequences, and behavioral measures. Through advanced methodological approaches, we demonstrate that reproducible and generalizable brain-behavior associations can be realized across diverse dataset features. Results indicate the potential of functional connectome-based predictive models to be robust despite substantial inter-dataset variability. Notably, for the HCPD and HBN datasets, the best predictions were not from training and testing in the same dataset (i.e., cross-validation) but across datasets. This result suggests that training on diverse data may improve prediction in specific cases. Overall, this work provides a critical foundation for future work evaluating the generalizability of brain-phenotype associations in real-world scenarios and clinical settings.