1. Quantitative Imaging Biomarkers of Damage to Critical Memory Regions Are Associated With Post–Radiation Therapy Memory Performance in Brain Tumor Patients
- Author
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Tringale, Kathryn R, Nguyen, Tanya T, Karunamuni, Roshan, Seibert, Tyler, Huynh-Le, Minh-Phuong, Connor, Michael, Moiseenko, Vitali, Gorman, Mary Kay, Marshall, Anisa, Tibbs, Michelle Devereux, Farid, Nikdokht, Simpson, Daniel, Sanghvi, Parag, McDonald, Carrie R, and Hattangadi-Gluth, Jona A
- Subjects
Biomedical and Clinical Sciences ,Oncology and Carcinogenesis ,Mental Health ,Neurodegenerative ,Radiation Oncology ,Behavioral and Social Science ,Minority Health ,Neurosciences ,Clinical Research ,Brain Disorders ,Rare Diseases ,Biomedical Imaging ,Acquired Cognitive Impairment ,Cancer ,Brain Cancer ,Adult ,Aged ,Agnosia ,Anisotropy ,Antineoplastic Agents ,Brain Neoplasms ,Cranial Irradiation ,Diffusion Magnetic Resonance Imaging ,Dose Fractionation ,Radiation ,Entorhinal Cortex ,Female ,Functional Neuroimaging ,Hippocampus ,Humans ,Male ,Memory ,Memory Disorders ,Mental Recall ,Middle Aged ,Neuropsychological Tests ,Prospective Studies ,Radiation Injuries ,Seizures ,Temporal Lobe ,White Matter ,Young Adult ,Other Physical Sciences ,Clinical Sciences ,Oncology & Carcinogenesis ,Oncology and carcinogenesis ,Theoretical and computational chemistry ,Medical and biological physics - Abstract
PurposeWe used quantitative magnetic resonance imaging to prospectively analyze the association between microstructural damage to memory-associated structures within the medial temporal lobe and longitudinal memory performance after brain radiation therapy (RT).Methods and materialsPatients with a primary brain tumor receiving fractionated brain RT were enrolled on a prospective trial (n = 27). Patients underwent high-resolution volumetric brain magnetic resonance imaging, diffusion-weighted imaging, and neurocognitive testing before and 3, 6, and 12 months post-RT. Medial temporal lobe regions (hippocampus; entorhinal, parahippocampal, and temporal pole white matter [WM]) were autosegmented, quantifying volume and diffusion biomarkers of WM integrity (mean diffusivity [MD]; fractional anisotropy [FA]). Reliable change indices measured changes in verbal (Hopkins Verbal Learning Test-Revised) and visuospatial (Brief Visuospatial Memory Test-Revised [BVMT-R]) memory. Linear mixed-effects models assessed longitudinal associations between imaging parameters and memory.ResultsVisuospatial memory significantly declined at 6 months post-RT (mean reliable change indices, -1.3; P = .012). Concurrent chemotherapy and seizures trended toward a significant association with greater decline in visuospatial memory (P = .053 and P = .054, respectively). Higher mean dose to the left temporal pole WM was significantly associated with decreased FA (r = -0.667; P = .002). Over all time points, smaller right hippocampal volume (P = .021), lower right entorhinal FA (P = .023), greater right entorhinal MD (P = .047), and greater temporal pole MD (BVMT-R total recall, P = .003; BVMT-R delayed recall, P = .042) were associated with worse visuospatial memory. The interaction between right entorhinal MD (BVMT-R total recall, P = .021; BVMT-R delayed recall, P = .004) and temporal pole FA (BVMT-R delayed recall, P = .024) significantly predicted visuospatial memory performance.ConclusionsBrain tumor patients exhibited visuospatial memory decline post-RT. Microstructural damage to critical memory regions, including the hippocampus and medial temporal lobe WM, were associated with post-RT memory decline. The integrity of medial temporal lobe structures is critical to memory performance post-RT, representing possible avoidance targets for memory preservation.
- Published
- 2019