Nuclear accidents and acts of terrorism have the potential to expose thousands of people to high-dose total-body iradiation (TBI). Those who survive the acute radiation syndrome are at risk of developing chronic, degenerative radiation-induced injuries [delayed effects of acute radiation (DEARE)] that may negatively affect quality of life. A growing body of literature suggests that the brain may be vulnerable to radiation injury at survivable doses, yet the long-term consequences of high-dose TBI on the adult brain are unclear. Herein we report the occurrence of lesions consistent with cerebrovascular injury, detected by susceptibility-weighted magnetic resonance imaging (MRI), in a cohort of non-human primate [(NHP); rhesus macaque, Macaca mulatta] long-term survivors of high-dose TBI (1.1–8.5 Gy). Animals were monitored longitudinally with brain MRI (approximately once every three years). Susceptibility-weighted images (SWI) were reviewed for hypointensities (cerebral microbleeds and/or focal necrosis). SWI hypointensities were noted in 13% of irradiated NHP; lesions were not observed in control animals. A prior history of exposure was correlated with an increased risk of developing a lesion detectable by MRI (P = 0.003). Twelve of 16 animals had at least one brain lesion present at the time of the first MRI evaluation; a subset of animals (n = 7) developed new lesions during the surveillance period (3.7–11.3 years postirradiation). Lesions occurred with a predilection for white matter and the gray–white matter junction. The majority of animals with lesions had one to three SWI hypointensities, but some animals had multifocal disease (n = 2). Histopathologic evaluation of deceased animals within the cohort (n = 3) revealed malformation of the cerebral vasculature and remodeling of the blood vessel walls. There was no association between comorbid diabetes mellitus or hypertension with SWI lesion status. These data suggest that long-term TBI survivors may be at risk of developing cerebrovascular injury years after irradiation.
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September 2020
Research Article|
July 21 2020
Non-Human Primates Receiving High-Dose Total-Body Irradiation are at Risk of Developing Cerebrovascular Injury Years Postirradiation
Rachel N. Andrews
;
Rachel N. Andrews
1
Departments of a Radiation Oncology, Section of Radiation Biology
b Departments of Pathology, Section on Comparative Medicine
c Departments of Wake Forest Baptist Comprehensive Cancer Center, Wake Forest School of Medicine, Medical Center Boulevard, Winston-Salem, North Carolina 27157
1 Address for correspondence: Department of Radiation Oncology, Section of Radiation Biology, Wake Forest University School of Medicine, Medical Center Blvd., Winston-Salem, NC 27157; email: rnandrew@wakehealth.edu.
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Ethan G. Bloomer
;
Ethan G. Bloomer
d University of Florida, College of Veterinary Medicine, Gainesville, Florida 32608
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John D. Olson
;
John D. Olson
b Departments of Pathology, Section on Comparative Medicine
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David B. Hanbury
;
David B. Hanbury
e Department of Psychology, Averett University, Danville, Virginia 24541
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Gregory O. Dugan
;
Gregory O. Dugan
b Departments of Pathology, Section on Comparative Medicine
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Christopher T. Whitlow
;
Christopher T. Whitlow
c Departments of Wake Forest Baptist Comprehensive Cancer Center, Wake Forest School of Medicine, Medical Center Boulevard, Winston-Salem, North Carolina 27157
Departments of f Radiology, Section of Neuroradiology
g Departments of Biomedical Engineering
h Departments of Biostatistics and Data Science, Wake Forest School of Medicine, Medical Center Boulevard, Winston-Salem, North Carolina 27157
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J. Mark Cline
J. Mark Cline
b Departments of Pathology, Section on Comparative Medicine
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Radiat Res (2020) 194 (3): 277–287.
Article history
Received:
February 19 2020
Accepted:
June 08 2020
Citation
Rachel N. Andrews, Ethan G. Bloomer, John D. Olson, David B. Hanbury, Gregory O. Dugan, Christopher T. Whitlow, J. Mark Cline; Non-Human Primates Receiving High-Dose Total-Body Irradiation are at Risk of Developing Cerebrovascular Injury Years Postirradiation. Radiat Res 1 September 2020; 194 (3): 277–287. doi: https://doi.org/10.1667/RADE-20-00051.1
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