Sex differences in the functional topography of association networks in youth

Author:

Shanmugan Sheila123,Seidlitz Jakob123,Cui Zaixu1234,Adebimpe Azeez123ORCID,Bassett Danielle S.25678ORCID,Bertolero Maxwell A.123,Davatzikos Christos57910,Fair Damien A.11,Gur Raquel E.236910ORCID,Gur Ruben C.23610ORCID,Larsen Bart123ORCID,Li Hongming910ORCID,Pines Adam123,Raznahan Armin12,Roalf David R.23,Shinohara Russell T.1013,Vogel Jacob123,Wolf Daniel H.2310,Fan Yong910ORCID,Alexander-Bloch Aaron23ORCID,Satterthwaite Theodore D.12310ORCID

Affiliation:

1. Penn Lifespan Informatics and Neuroimaging Center, University of Pennsylvania, Philadelphia, PA 19104

2. Department of Psychiatry, University of Pennsylvania, Philadelphia, PA 19104

3. Penn-Children's Hospital of Philadelphia Lifespan Brain Institute, University of Pennsylvania, Philadelphia, PA 19104

4. Chinese Institute for Brain Research, Beijing,102206, China

5. Department of Bioengineering, University of Pennsylvania, Philadelphia, PA 19104

6. Department of Neurology, University of Pennsylvania, Philadelphia, PA 19104

7. Department of Electrical and Systems Engineering, University of Pennsylvania, Philadelphia, PA 19104

8. Department of Physics and Astronomy, University of Pennsylvania, Philadelphia, PA 19104

9. Department of Radiology, University of Pennsylvania, Philadelphia, PA 19104

10. Center for Biomedical Image Computation and Analytics, University of Pennsylvania, Philadelphia, PA 19104

11. Department of Behavioral Neuroscience, Department of Psychiatry, Advanced Imaging Research Center, Oregon Health and Science University, Portland, OR 97239

12. Section on Developmental Neurogenomics Unit, Intramural Research Program, National Institutes of Mental Health, Bethesda, MD 20892

13. Penn Statistics in Imaging and Visualization Center, Department of Biostatistics, Epidemiology, and Informatics, University of Pennsylvania, Philadelphia, PA 19104

Abstract

Prior work has shown that there is substantial interindividual variation in the spatial distribution of functional networks across the cerebral cortex, or functional topography. However, it remains unknown whether there are sex differences in the topography of individualized networks in youth. Here, we leveraged an advanced machine learning method (sparsity-regularized non-negative matrix factorization) to define individualized functional networks in 693 youth (ages 8 to 23 y) who underwent functional MRI as part of the Philadelphia Neurodevelopmental Cohort. Multivariate pattern analysis using support vector machines classified participant sex based on functional topography with 82.9% accuracy ( P < 0.0001). Brain regions most effective in classifying participant sex belonged to association networks, including the ventral attention, default mode, and frontoparietal networks. Mass univariate analyses using generalized additive models with penalized splines provided convergent results. Furthermore, transcriptomic data from the Allen Human Brain Atlas revealed that sex differences in multivariate patterns of functional topography were spatially correlated with the expression of genes on the X chromosome. These results highlight the role of sex as a biological variable in shaping functional topography.

Funder

HHS | NIH | National Institute of Mental Health

HHS | NIH | National Institute of Biomedical Imaging and Bioengineering

HHS | NIH | National Institute of Neurological Disorders and Stroke

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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