Working memory performance in glioma patients is associated with functional connectivity between the right dorsolateral prefrontal cortex and default mode network

Author:

Smolders Lars12ORCID,De Baene Wouter3ORCID,van der Hofstad Remco2,Florack Luc2,Rutten Geert‐Jan1

Affiliation:

1. Department of Neurosurgery Elisabeth‐TweeSteden Hospital Tilburg The Netherlands

2. Department of Mathematics and Computer Science Eindhoven University of Technology Eindhoven The Netherlands

3. Department of Cognitive Neuropsychology Tilburg University Tilburg The Netherlands

Abstract

AbstractIn healthy subjects, activity in the default mode network (DMN) and the frontoparietal network (FPN) has consistently been associated with working memory (WM). In particular, the dorsolateral prefrontal cortex (DLPFC) is important for WM. The functional–anatomical basis of WM impairment in glioma patients is, however, still poorly understood. We investigated whether WM performance of glioma patients is reflected in resting‐state functional connectivity (FC) between the DMN and FPN, additionally focusing on the DLPFC. Resting‐state functional MRI data were acquired from 45 glioma patients prior to surgery. WM performance was derived from a pre‐operative N‐back task. Scans were parcellated into ROIs using both the Gordon and Yeo atlas. FC was calculated as the average Pearson correlation between functional time series. The FC between right DLPFC and DMN was inversely related to WM performance for both the Gordon and Yeo atlas (p = .010). No association was found for FC between left DLPFC and DMN, nor between the whole FPN and DMN. The results are robust and not dependent on atlas choice or tumor location, as they hold for both the Gordon and Yeo atlases, and independently of location variables. Our findings show that WM performance of glioma patients can be quantified in terms of interactions between regions and large‐scale networks that can be measured with resting‐state fMRI. These group‐based results are a necessary step toward development of biomarkers for clinical management of glioma patients, and provide additional evidence that global disruption of the DMN relates to cognitive impairment in glioma patients.

Funder

ZonMw

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience

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