Havana Syndrome Among Canadian Diplomats: Brain Imaging Reveals Acquired Neurotoxicity
Friedman, A.; Calkin, C.; Adams, A.; Suarez, G. A.; Bardouille, T.; Hacohen, N.; Green, A. L.; Gupta, R. R.; Hashmi, J.; Kamintsky, L.; Kim, J. S.; Laroche, R.; MacKenzie, D.; Milikovsky, D.; Oystreck, D.; Newton, J.; Noel, G.; Ofer, J.; Quraan, M.; Reardon, C.; Ross, M.; Rutherford, D.; Schmidt, M.; Serlin, Y.; Sweeney, C.; Verge, J.; Walsh, L.; Bowen, C.
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BACKGROUNDIn late 2016, US diplomats stationed in Havana began presenting with a variety of neurological manifestations that proved difficult to diagnose. Though previous studies suggested a likely association with brain injury, the mechanism of injury, brain regions involved, and etiology remained unknown. METHODSWe conducted a multimodal study examining 26 Canadian diplomats and their family members, the majority of whom presented with symptoms similar to their American counterparts while residing in Havana. Assessments included a medical history, self-reported symptom questionnaires, cognitive assessments, blood tests, and brain imaging assessments (magnetic resonance imaging (MRI) and magnetoencephalography (MEG)). Individuals showing signs of brain injury underwent further neurological, visual, and audio-vestibular assessments. Eight participants were tested both before and after living in Havana. RESULTSOur assessment documents multiple functional and structural impairments, including significant spatial memory impairment, abnormal brain-stem evoked potentials, degradation of fibre tracts in the fornix and posterior corpus callosum, blood-brain barrier injury to the right basal forebrain and anterior insula, and abnormal paroxysmal slowing events of cortical activity. Subsequent mass-spectrometry and blood analyses documented reduced serum cholinesterase activity and the presence of organophosphates (Temephos) and pyrethroid metabolites (3-phenoxybenzoic acid or 3-BPA). CONCLUSIONSOur findings confirm brain injury, specify the regions involved, and raise the hypothesis of overexposure to cholinesterase inhibitors as a plausible etiology. If correct, our hypothesis bears public health ramifications (see Discussion) and suggests a course of action for reducing exposure in the future. FUNDINGGlobal Affairs Canada.
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