Study: Folding-compensated cortical thickness
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FULL TITLE:
Compensating Cortical Thickness for Cortical Folding-Related Variation

SPECIES:
Human

DESCRIPTION:
The local multiple regression-based folding-compensated cortical thickness pipeline is now part of the HCP Pipelines (Glasser et al., 2013) on GitHub (https://github.com/Washington-University/HCPpipelines) and is now a default output of new runs of the HCP Structural Preprocessing pipelines (specifically the PostFreeSurfer pipeline). The pipeline can also be run on existing HCP Pipelines outputs using the global/scripts/CorrThick.sh pipeline module. An example script is provided at Examples/Scripts/CorrThickPipelineBatch.sh. In the HCP Pipelines’ outputs and HCP data releases, the global linear folding-compensated cortical thickness file contains the tag corrThickness. Our new measure of local, nonlinear, folding-compensated cortical thickness file contains the tag MRcorrThickness. Related publication is available at https://www.biorxiv.org/content/10.1101/2025.05.03.651968v1.abstract

ABSTRACT:
Cortical thickness is a widely used biomarker of brain morphology and health, yet it is dependent on local cortical folding. Because gyral crowns are consistently thicker than sulcal fundi and cortical folds vary widely across individuals, these fluctuations introduce unmodeled nuisance variance that can obscure meaningful biological effects of interest. Previous global methods of folding compensation incompletely compensate for folding effects on cortical thickness. Spatial smoothing is commonly used to reduce these effects in the literature, but this markedly degrades spatial localization precision. To address these limitations, we developed a novel method for folding-compensated cortical thickness estimation that uses nonlinear local multiple regression with five folding measures to model and more completely remove folding-related variance from cortical thickness. This approach estimates what cortical thickness would have been in the absence of folding, yielding a more biologically interpretable measure of cortical architecture. We applied this new approach to data from the Young Adult Human Connectome Project (HCP-YA) and Aging Human Connectome Project (HCA), demonstrating substantial reductions in intra-areal and inter-individual variability, substantially increasing standardized effect sizes of age on cortical thickness (41% increase) while preserving neurobiologically expected patterns, and avoiding the loss of spatial precision that occurs with the spatial smoothing that has traditionally been used in the literature. The method has been integrated into the HCP pipelines, facilitating its widespread use. By attenuating folding-induced variability, this technique enhances cortical thickness as a structural phenotype and may support more accurate cortical parcellation, longitudinal tracking, and biomarker discovery in brain health and disease.

PUBLICATION:
BioRxiv - DOI: 10.1101/2025.05.03.651968