Literature DB >> 24096125

Sparse canonical correlation analysis relates network-level atrophy to multivariate cognitive measures in a neurodegenerative population.

Brian B Avants1, David J Libon, Katya Rascovsky, Ashley Boller, Corey T McMillan, Lauren Massimo, H Branch Coslett, Anjan Chatterjee, Rachel G Gross, Murray Grossman.   

Abstract

This study establishes that sparse canonical correlation analysis (SCCAN) identifies generalizable, structural MRI-derived cortical networks that relate to five distinct categories of cognition. We obtain multivariate psychometrics from the domain-specific sub-scales of the Philadelphia Brief Assessment of Cognition (PBAC). By using a training and separate testing stage, we find that PBAC-defined cognitive domains of language, visuospatial functioning, episodic memory, executive control, and social functioning correlate with unique and distributed areas of gray matter (GM). In contrast, a parallel univariate framework fails to identify, from the training data, regions that are also significant in the left-out test dataset. The cohort includes164 patients with Alzheimer's disease, behavioral-variant frontotemporal dementia, semantic variant primary progressive aphasia, non-fluent/agrammatic primary progressive aphasia, or corticobasal syndrome. The analysis is implemented with open-source software for which we provide examples in the text. In conclusion, we show that multivariate techniques identify biologically-plausible brain regions supporting specific cognitive domains. The findings are identified in training data and confirmed in test data.
© 2013.

Entities:  

Keywords:  Alzheimer disease; Frontotemporal lobar degeneration; MRI; PBAC; Philadelphia Brief Assessment of Cognition; Sparse canonical correlation analysis

Mesh:

Year:  2013        PMID: 24096125      PMCID: PMC3911786          DOI: 10.1016/j.neuroimage.2013.09.048

Source DB:  PubMed          Journal:  Neuroimage        ISSN: 1053-8119            Impact factor:   6.556


  71 in total

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  31 in total

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6.  White matter disease contributes to apathy and disinhibition in behavioral variant frontotemporal dementia.

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