Microstructural Injury to Corpus Callosum and Intrahemispheric White Matter Tracts Correlate With Attention and Processing Speed Decline After Brain Radiation

Minh-Phuong Huynh-Le, Michelle D Tibbs, Roshan Karunamuni, Mia Salans, Kathryn R Tringale, Anthony Yip, Michael Connor, Aaron B Simon, Lucas K Vitzthum, Anny Reyes, Anna Christina Macari, Vitali Moiseenko, Carrie R McDonald, Jona A Hattangadi-Gluth, Minh-Phuong Huynh-Le, Michelle D Tibbs, Roshan Karunamuni, Mia Salans, Kathryn R Tringale, Anthony Yip, Michael Connor, Aaron B Simon, Lucas K Vitzthum, Anny Reyes, Anna Christina Macari, Vitali Moiseenko, Carrie R McDonald, Jona A Hattangadi-Gluth

Abstract

Purpose: The corpus callosum (CC) and intrahemispheric white matter tracts (IHWM) subserve critical aspects of attention and processing speed. We analyzed imaging biomarkers of microstructural injury within these regions and association with attention and processing speed performance before and after radiation therapy in primary brain tumor patients.

Methods and materials: In a prospective clinical trial, 44 primary brain tumor patients underwent cognitive testing and magnetic resonance imaging/diffusion-weighted imaging at baseline (pre-radiation therapy) and 3-, 6-, and 12-months post-radiation therapy. CC (subregions, total) and IHWM tracts (left/right without CC, total) were autosegmented; tumor, tumor bed, and edema were censored. Biomarkers included volume changes (cm3), mean diffusivity ([MD]; higher values indicate white matter injury), fractional anisotropy ([FA]; lower values indicate white matter injury). Reliable-change indices measured changes in attention (Weschler Adult Intelligence Scale [WAIS-IV] digits-forward; Delis-Kaplan Executive Function System Trail Making [D-KEFS-TM] visual-scanning), and processing speed (WAIS-IV coding; D-KEFS-TM number-sequencing, letter-sequencing), accounting for practice effects. Linear mixed-effects models evaluated associations between mean radiation dose and biomarkers (volume, MD, FA) and imaging biomarkers and neurocognitive performance. Statistics were corrected for multiple comparisons.

Results: Processing speed declined at 6 months following radiation therapy (number sequencing, letter sequencing; P < .04). Seizures and antiepileptic drug therapy were associated with lower visual-scanning attention reliable-change indices at 6 months (P = .039). Higher radiation dose correlated with smaller midanterior CC volume (P = .023); lower FA in posterior CC, anterior CC, and total CC (all P < .03); and higher MD in anterior CC (P = .012). Smaller midanterior CC and left IHWM volume correlated with worse processing speed (coding, letter-sequencing, number-sequencing; all P < .03). Higher FA in right, left, and total IHWM correlated with better coding scores (all P < .01). Lower FA in total IHWM (P = .009) was associated with worse visual-scanning attention scores. Higher FA in midposterior CC (P = .029) correlated with better digits-forward attention scores.

Conclusions: The CC demonstrated radiation dose-dependent atrophy and WM injury. Microstructural injury within the CC and IHWM was associated with attention and processing speed decline after radiation therapy. These areas represent possible avoidance regions for preservation of attention and processing speed.

Copyright © 2021 Elsevier Inc. All rights reserved.

Figures

Fig. 1.
Fig. 1.
Overlay of autosegmentation of total corpus callosum (CC) and intrahemispheric white matter (IHWM) tracts on magnetic resonance images taken from a representative patient in the cohort. (A) Total CC and its subregions: anterior, midanterior, central, midposterior, and posterior, derived from FreeSurfer. (B) Axial, (C) coronal, and (D) sagittal images of left and right IHWM tracts generated from diffusion weighted imaging using AtlasTract. Right IHWM is shown in red, left IHWM is blue, and CC is gray.

Source: PubMed

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