Unknown

Dataset Information

0

Homotopic functional connectivity disruptions in glioma patients are associated with tumor malignancy and overall survival.


ABSTRACT:

Background

Gliomas exhibit widespread bilateral functional connectivity (FC) alterations that may be associated with tumor grade. Limited studies have examined the connection-level mechanisms responsible for these effects. Given the typically strong FC observed between mirroring/homotopic brain regions in healthy subjects, we hypothesized that homotopic connectivity (HC) is altered in low-grade and high-grade glioma patients and the extent of disruption is associated with tumor grade and predictive of overall survival (OS) in a cohort of de novo high-grade glioma (World Health Organization [WHO] grade 4) patients.

Methods

We used a mirrored FC-derived cortical parcellation to extract blood-oxygen-level-dependent (BOLD) signals and to quantify FC differences between homotopic pairs in normal-appearing brain in a retrospective cohort of glioma patients and healthy controls.

Results

Fifty-nine glioma patients (WHO grade 2, n = 9; grade 4 = 50; mean age, 57.5 years) and 30 healthy subjects (mean age, 65.9 years) were analyzed. High-grade glioma patients showed lower HC compared with low-grade glioma patients and healthy controls across several cortical locations and resting-state networks. Connectivity disruptions were also strongly correlated with hemodynamic lags between homotopic regions. Finally, in high-grade glioma patients with known survival times (n = 42), HC in somatomotor and dorsal attention networks were significantly correlated with OS.

Conclusions

These findings demonstrate an association between tumor grade and HC alterations that may underlie global FC changes and provide prognostic information.

SUBMITTER: Daniel AGS 

PROVIDER: S-EPMC8694208 | biostudies-literature |

REPOSITORIES: biostudies-literature

Similar Datasets

| S-EPMC7840474 | biostudies-literature
| S-EPMC7992880 | biostudies-literature
| S-EPMC8117153 | biostudies-literature
| S-EPMC5987867 | biostudies-literature
| S-EPMC10702213 | biostudies-literature
| S-EPMC6399443 | biostudies-literature
| S-EPMC4160382 | biostudies-literature
| S-EPMC8492970 | biostudies-literature
| S-EPMC10212507 | biostudies-literature
| S-EPMC5361870 | biostudies-literature