TY - JOUR
T1 - The problem of axonal injury in the brains of veterans with histories of blast exposure
AU - Ryu, Jiwon
AU - Horkayne-Szakaly, Iren
AU - Xu, Leyan
AU - Pletnikova, Olga
AU - Leri, Francesco
AU - Eberhart, Charles
AU - Troncoso, Juan C.
AU - Koliatsos, Vassilis E.
N1 - Funding Information:
This work was supported from the Johns Hopkins Alzheimer’s Disease Research Center grant RFA AG-09-001 and generous gifts from the Kate Sidran Family Foundation and Sam and Sheila Giller family. The antibodies against phosphorylated tau; PHF1, CP13 and MC1, were generous gift from Dr. Peter Davies (Albert Einstein College of Medicine, Bronx, NY).
Publisher Copyright:
© 2014 Ryu et al.; licensee BioMed Central.
PY - 2014/1/27
Y1 - 2014/1/27
N2 - Introduction: Blast injury to brain, a hundred-year old problem with poorly characterized neuropathology, has resurfaced as health concern in recent deployments in Iraq and Afghanistan. To characterize the neuropathology of blast injury, we examined the brains of veterans for the presence of amyloid precursor protein (APP)-positive axonal swellings typical of diffuse axonal injury (DAI) and compared them to healthy controls as well as controls with opiate overdose, anoxic-ischemic encephalopathy, and non-blast TBI (falls and motor vehicle crashes). Results: In cases with blast history, we found APP (+) axonal abnormalities in several brain sites, especially the medial dorsal frontal white matter. In white matter, these abnormalities were featured primarily by clusters of axonal spheroids or varicosities in a honeycomb pattern with perivascular distribution. Axonal abnormalities colocalized with IBA1 (+) reactive microglia and had an appearance that was distinct from classical DAI encountered in TBI due to motor vehicle crashes. Opiate overdose cases also showed APP (+) axonal abnormalities, but the intensity of these lesions was lower compared to cases with blast histories and there was no clear association of such lesions with microglial activation. Conclusions: Our findings demonstrate that many cases with history of blast exposure are featured by APP (+) axonopathy that may be related to blast exposure, but an important role for opiate overdose, antemortem anoxia, and concurrent blunt TBI events in war theater or elsewhere cannot be discounted.
AB - Introduction: Blast injury to brain, a hundred-year old problem with poorly characterized neuropathology, has resurfaced as health concern in recent deployments in Iraq and Afghanistan. To characterize the neuropathology of blast injury, we examined the brains of veterans for the presence of amyloid precursor protein (APP)-positive axonal swellings typical of diffuse axonal injury (DAI) and compared them to healthy controls as well as controls with opiate overdose, anoxic-ischemic encephalopathy, and non-blast TBI (falls and motor vehicle crashes). Results: In cases with blast history, we found APP (+) axonal abnormalities in several brain sites, especially the medial dorsal frontal white matter. In white matter, these abnormalities were featured primarily by clusters of axonal spheroids or varicosities in a honeycomb pattern with perivascular distribution. Axonal abnormalities colocalized with IBA1 (+) reactive microglia and had an appearance that was distinct from classical DAI encountered in TBI due to motor vehicle crashes. Opiate overdose cases also showed APP (+) axonal abnormalities, but the intensity of these lesions was lower compared to cases with blast histories and there was no clear association of such lesions with microglial activation. Conclusions: Our findings demonstrate that many cases with history of blast exposure are featured by APP (+) axonopathy that may be related to blast exposure, but an important role for opiate overdose, antemortem anoxia, and concurrent blunt TBI events in war theater or elsewhere cannot be discounted.
KW - APP
KW - Axon bulbs
KW - Diffuse axonal injury
KW - Microglia
KW - Opiate
KW - Traumatic brain injury
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U2 - 10.1186/s40478-014-0153-3
DO - 10.1186/s40478-014-0153-3
M3 - Article
C2 - 25422066
AN - SCOPUS:84964697590
SN - 2051-5960
VL - 2
JO - Acta Neuropathologica Communications
JF - Acta Neuropathologica Communications
IS - 1
M1 - 153
ER -