TY - JOUR
T1 - Subcortical brain atrophy in Gulf War Illness
AU - Christova, Peka
AU - James, Lisa M
AU - Engdahl, Brian
AU - Lewis, Scott M.
AU - Carpenter, Adam
AU - Georgopoulos, Apostolos P
PY - 2017/9/1
Y1 - 2017/9/1
N2 - Gulf War Illness (GWI) is a multisystem disorder that has affected a substantial number of veterans who served in the 1990–1991 Gulf War. The brain is prominently affected, as manifested by the presence of neurological, cognitive and mood symptoms. Although brain dysfunction in GWI has been well documented (EBioMedicine 12:127–32, 2016), abnormalities in brain structure have been debated. Here we report a substantial (~10%) subcortical brain atrophy in GWI comprising mainly the brainstem, cerebellum and thalamus, and, to a lesser extent, basal ganglia, amygdala and diencephalon. The highest atrophy was observed in the brainstem, followed by left cerebellum and right thalamus, then by right cerebellum and left thalamus. These findings indicate graded atrophy of regions anatomically connected through the brainstem via the crossed superior cerebellar peduncle (left cerebellum → right thalamus, right cerebellum → left thalamus). This distribution of atrophy, together with the observed systematic reduction in volume of other subcortical areas (basal ganglia, amygdala and diencephalon), resemble the distribution of atrophy seen in toxic encephalopathy (Am J Neuroradiol 13:747–760, 1992) caused by a variety of substances, including organic solvents. Given the potential exposure of Gulf War veterans to “a wide range of biological and chemical agents including sand, smoke from oil-well fires, paints, solvents, insecticides, petroleum fuels and their combustion products, organophosphate nerve agents, pyridostigmine bromide, …” (Institute of Medicine National Research Council. Gulf War and Health: Volume 1. Depleted uranium, pyridostigmine bromide, sarin, and vaccines. National Academies Press, Washington DC, 2000), it is reasonable to suppose that such exposures, alone or in combination, could underlie the subcortical atrophy observed.
AB - Gulf War Illness (GWI) is a multisystem disorder that has affected a substantial number of veterans who served in the 1990–1991 Gulf War. The brain is prominently affected, as manifested by the presence of neurological, cognitive and mood symptoms. Although brain dysfunction in GWI has been well documented (EBioMedicine 12:127–32, 2016), abnormalities in brain structure have been debated. Here we report a substantial (~10%) subcortical brain atrophy in GWI comprising mainly the brainstem, cerebellum and thalamus, and, to a lesser extent, basal ganglia, amygdala and diencephalon. The highest atrophy was observed in the brainstem, followed by left cerebellum and right thalamus, then by right cerebellum and left thalamus. These findings indicate graded atrophy of regions anatomically connected through the brainstem via the crossed superior cerebellar peduncle (left cerebellum → right thalamus, right cerebellum → left thalamus). This distribution of atrophy, together with the observed systematic reduction in volume of other subcortical areas (basal ganglia, amygdala and diencephalon), resemble the distribution of atrophy seen in toxic encephalopathy (Am J Neuroradiol 13:747–760, 1992) caused by a variety of substances, including organic solvents. Given the potential exposure of Gulf War veterans to “a wide range of biological and chemical agents including sand, smoke from oil-well fires, paints, solvents, insecticides, petroleum fuels and their combustion products, organophosphate nerve agents, pyridostigmine bromide, …” (Institute of Medicine National Research Council. Gulf War and Health: Volume 1. Depleted uranium, pyridostigmine bromide, sarin, and vaccines. National Academies Press, Washington DC, 2000), it is reasonable to suppose that such exposures, alone or in combination, could underlie the subcortical atrophy observed.
KW - Brain atrophy
KW - Brainstem
KW - Cerebellum
KW - Gulf War Illness
KW - Thalamus
KW - Toxic encephalopathy
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U2 - 10.1007/s00221-017-5010-8
DO - 10.1007/s00221-017-5010-8
M3 - Article
C2 - 28634886
AN - SCOPUS:85021139293
SN - 0014-4819
VL - 235
SP - 2777
EP - 2786
JO - Experimental Brain Research
JF - Experimental Brain Research
IS - 9
ER -